<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.1 20151215//EN" "https://jats.nlm.nih.gov/publishing/1.1/JATS-journalpublishing1.dtd">
<article xmlns:xlink="http://www.w3.org/1999/xlink" specific-use="sps-1.9" dtd-version="1.1" xml:lang="pt" article-type="research-article">
  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">abc</journal-id>
      <journal-title-group>
        <journal-title>Arquivos Brasileiros de Cardiologia</journal-title>
        <abbrev-journal-title abbrev-type="publisher">Arq. Bras. Cardiol.</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="ppub">0066-782X</issn>
      <issn pub-type="epub">1678-4170</issn>
      <publisher>
        <publisher-name>Sociedade Brasileira de Cardiologia - SBC</publisher-name>
        <publisher-loc>S&#227;o Paulo, SP, Brazil</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v3">frqNCdKgppcwkZ5LsHNXMyw</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2012000400006</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v1">S0066-782X(12)09800406</article-id>
      <article-id pub-id-type="doi">10.1590/S0066-782X2012000400006</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Artigos Originais</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Regula&#231;&#227;o auton&#244;mica das propriedades mec&#226;nicas em biopr&#243;tese valvar porcina</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Hu</surname>
            <given-names>Xiang</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Zhao</surname>
            <given-names>Qiang</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Ye</surname>
            <given-names>Xiaofeng</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
      </contrib-group>
      <aff id="aff01">
        <addr-line>
          <named-content content-type="city">Shanghai</named-content>
          <named-content content-type="state"/>
        </addr-line>
        <institution content-type="orgname">Shanghai Jiaotong University</institution>
        <institution content-type="orgdiv1">Rui Jin Hospital </institution>
        <institution content-type="orgdiv2">Department of Cardiac Surgery</institution>
        <country country="CN">China</country>
      </aff>
      <pub-date date-type="collection" publication-format="electronic">
        <month>04</month>
        <year>2012</year>
      </pub-date>
      <volume>98</volume>
      <issue>4</issue>
      <fpage>321</fpage>
      <lpage>328</lpage>
      <history>
        <date date-type="received">
          <day>01</day>
          <month>09</month>
          <year>2010</year>
        </date>
        <date date-type="accepted">
          <day>23</day>
          <month>11</month>
          <year>2010</year>
        </date>
        <date date-type="rev-recd">
          <day>01</day>
          <month>11</month>
          <year>2010</year>
        </date>
      </history>
      <permissions>
        <license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc/4.0/" xml:lang="en">
          <license-p>This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.</license-p>
        </license>
      </permissions>
      <abstract>
        <p>FUNDAMENTO: A presen&#231;a de nervos nas v&#225;lvulas card&#237;acas foi demonstrada pela primeira vez h&#225; d&#233;cadas e identificadas em subpopula&#231;&#245;es: simp&#225;ticas e parassimp&#225;ticas, e, portanto, &#233; esperado que as v&#225;lvulas sejam grandemente afetadas pelos nervos aut&#244;nomos. Entretanto, poucos estudos t&#234;m se concentrado na regula&#231;&#227;o de v&#225;lvulas card&#237;acas pelo sistema nervoso aut&#244;nomo. OBJETIVO: Buscamos identificar o papel do sistema nervoso aut&#244;nomo na regula&#231;&#227;o das propriedades mec&#226;nicas dos tecidos de v&#225;lvulas mitrais porcinas. M&#201;TODOS: As propriedades mec&#226;nicas dos folhetos de v&#225;lvulas mitrais porcinas foram avaliados em resposta &#224; norepinefrina (NE) e acetilcolina (ACH), os principais neurotransmissores. Ao mesmo tempo, fentolamina (FENT), metoprolol (Metop), atropina (Atrop) e desnudamento endotelial foram adicionados ao sistema reativo. RESULTADOS: Sob condi&#231;&#245;es fisiol&#243;gicas, a rigidez n&#227;o foi afetada pelo desnudamento endotelial (p &gt; 0,05). A NE significantemente aumentou a rigidez valvar por aumento de 10 vezes na concentra&#231;&#227;o (10-6 vs 10-7, p &lt; 0,05; 10-5 vs 10-6, p &lt; 0,05). Essa resposta foi amenizada por FENT, Metop ou desnudamento endotelial (p &lt; 0,05); entretanto, manteve-se aumentada de maneira significante quando comparada aos Controles (p &lt; 0,05). A ACH causou uma diminui&#231;&#227;o na rigidez acompanhada por um aumento em sua concentra&#231;&#227;o (altera&#231;&#227;o significante na rigidez por aumento de 10 vezes na concentra&#231;&#227;o de ACH, 10-6 vs Controle, p &lt; 0,05; 10-5 vs 10-6, p &lt; 0,05), que foi revertida pelo desnudamento endotelial e Atrop (p &gt; 0,05 vs Controle). CONCLUS&#195;O: Esses achados ressaltam o papel do sistema nervoso aut&#244;nomo na regula&#231;&#227;o das propriedades mec&#226;nicas das c&#250;spides de v&#225;lvula mitral porcina, o que refor&#231;a a import&#226;ncia do estado nervoso aut&#244;nomo no funcionamento ideal da v&#225;lvula.</p>
      </abstract>
      <kwd-group xml:lang="pt" kwd-group-type="author-generated">
        <kwd>Valva mitral</kwd>
        <kwd>vias aut&#244;nomas</kwd>
        <kwd>biopr&#243;tese</kwd>
        <kwd>sistema nervoso aut&#244;nomo</kwd>
      </kwd-group>
      <pub-date publication-format="electronic" date-type="pub">
        <day>21</day>
        <month>06</month>
        <year>2012</year>
      </pub-date>
    </article-meta>
  </front>
  <body>
    <p>
      <bold>ARTIGO ESPECIAL</bold>
    </p>
    <p>
      <bold>Regula&#231;&#227;o auton&#244;mica das propriedades mec&#226;nicas em biopr&#243;tese valvar porcina</bold>
    </p>
    <p>
      <bold>Xiang Hu; Qiang Zhao; Xiaofeng Ye</bold>
    </p>
    <p> Department of Cardiac Surgery, Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, PRC</p>
    <p>
      <xref ref-type="corresp" rid="end">Correspond&#234;ncia</xref>
    </p>
    <p>
      <bold>RESUMO</bold>
    </p>
    <p><bold>FUNDAMENTO:</bold> A presen&#231;a de nervos nas v&#225;lvulas card&#237;acas foi demonstrada pela primeira vez h&#225; d&#233;cadas e identificadas em subpopula&#231;&#245;es: simp&#225;ticas e parassimp&#225;ticas, e, portanto, &#233; esperado que as v&#225;lvulas sejam grandemente afetadas pelos nervos aut&#244;nomos. Entretanto, poucos estudos t&#234;m se concentrado na regula&#231;&#227;o de v&#225;lvulas card&#237;acas pelo sistema nervoso aut&#244;nomo. </p>
    <p><bold>OBJETIVO:</bold> Buscamos identificar o papel do sistema nervoso aut&#244;nomo na regula&#231;&#227;o das propriedades mec&#226;nicas dos tecidos de v&#225;lvulas mitrais porcinas. </p>
    <p><bold>M&#201;TODOS:</bold> As propriedades mec&#226;nicas dos folhetos de v&#225;lvulas mitrais porcinas foram avaliados em resposta &#224; norepinefrina (NE) e acetilcolina (ACH), os principais neurotransmissores. Ao mesmo tempo, fentolamina (FENT), metoprolol (Metop), atropina (Atrop) e desnudamento endotelial foram adicionados ao sistema reativo. </p>
    <p><bold>RESULTADOS:</bold> Sob condi&#231;&#245;es fisiol&#243;gicas, a rigidez n&#227;o foi afetada pelo desnudamento endotelial (p &gt; 0,05). A NE significantemente aumentou a rigidez valvar por aumento de 10 vezes na concentra&#231;&#227;o (10<sup>-6</sup><italic>vs</italic> 10<sup>-7</sup>, p &lt; 0,05; 10-5 <italic>vs</italic> 10<sup>-6</sup>, p &lt; 0,05). Essa resposta foi amenizada por FENT, Metop ou desnudamento endotelial (p &lt; 0,05); entretanto, manteve-se aumentada de maneira significante quando comparada aos Controles (p &lt; 0,05). A ACH causou uma diminui&#231;&#227;o na rigidez acompanhada por um aumento em sua concentra&#231;&#227;o (altera&#231;&#227;o significante na rigidez por aumento de 10 vezes na concentra&#231;&#227;o de ACH, 10<sup>-6</sup><italic>vs</italic> Controle, p &lt; 0,05; 10<sup>-5</sup><italic>vs</italic> 10<sup>-6</sup>, p &lt; 0,05), que foi revertida pelo desnudamento endotelial e Atrop (p &gt; 0,05 <italic>vs</italic> Controle). </p>
    <p><bold>CONCLUS&#195;O:</bold> Esses achados ressaltam o papel do sistema nervoso aut&#244;nomo na regula&#231;&#227;o das propriedades mec&#226;nicas das c&#250;spides de v&#225;lvula mitral porcina, o que refor&#231;a a import&#226;ncia do estado nervoso aut&#244;nomo no funcionamento ideal da v&#225;lvula. </p>
    <p><bold>Palavras-chave:</bold> Valva mitral, vias aut&#244;nomas, biopr&#243;tese, sistema nervoso aut&#244;nomo.</p>
    <p>
      <bold>Introdu&#231;&#227;o</bold>
    </p>
    <p>A fun&#231;&#227;o das v&#225;lvulas card&#237;acas &#233; bastante complicada, pois os movimentos passivos da v&#225;lvula n&#227;o levam em considera&#231;&#227;o sua capacidade de se adaptar ao ambiente hemodin&#226;mico e humoral. Isso &#233; exemplificado pela presen&#231;a de nervos nas v&#225;lvulas card&#237;acas, demonstrada pela primeira vez h&#225; d&#233;cadas e identificadas em subpopula&#231;&#245;es: simp&#225;ticas, parassimp&#225;ticas, sensoriais e marcadores colin&#233;rgicos nervosos<sup>1,2</sup>. A arritmia card&#237;aca &#233; frequentemente detectada em pacientes com doen&#231;as card&#237;acas, incluindo as coron&#225;rias e valvares. T&#244;nus aut&#244;nomo inadequado, a suposta etiologia, &#233; considerado prevalente na maioria das doen&#231;as card&#237;acas, ent&#227;o &#233; esperado que as v&#225;lvulas sejam grandemente afetadas pelos nervos aut&#244;nomos. Entretanto, poucas investiga&#231;&#245;es t&#234;m se concentrado na regula&#231;&#227;o de v&#225;lvulas card&#237;acas pelo sistema nervoso aut&#244;nomo. Estudos recentes indicaram que a adi&#231;&#227;o de norepinefrina (NE) e acetilcolina (ACH) produziu aumentos dose-dependentes na contratilidade da v&#225;lvula mitral e relaxamento do tecido da v&#225;lvula a&#243;rtica, em um modelo <italic>ex vivo</italic>, respectivamente<sup>3,4</sup>. O papel funcional dos neurotransmissores sobre as propriedades mec&#226;nicas do tecido das c&#250;spides permanece indeterminado. Isso poderia ser vital, considerando que a v&#225;lvula &#233; submetida a altas for&#231;as mec&#226;nicas em cada ciclo card&#237;aco. O entendimento das propriedades mec&#226;nicas valvares &#233; crucial para a abordagem de uma cada vez mais prevalente entidade de doen&#231;a valvar card&#237;aca, ainda mais quando se considera o aumento da expectativa de vida na popula&#231;&#227;o geral e a melhora na sobreviv&#234;ncia de longo prazo de pacientes com doen&#231;a valvar card&#237;aca, submetidos &#224; cirurgia de substitui&#231;&#227;o de v&#225;lvula card&#237;aca alog&#234;nica. O foco desse estudo &#233; principalmente em v&#225;lvulas mitrais, pois das quatro v&#225;lvulas card&#237;acas, a mitral &#233; a mais comumente afetada em processos patol&#243;gicos que requerem interven&#231;&#227;o cir&#250;rgica. </p>
    <p>Nossa hip&#243;tese &#233; que, sob condi&#231;&#245;es fisiol&#243;gicas, a rigidez do tecido da v&#225;lvula mitral (m&#243;dulo de elasticidade) varia em resposta a agentes nervosos aut&#244;nomos atrav&#233;s do endot&#233;lio valvar e respectivos receptores, e por conseguinte, o t&#244;nus do folheto e a fun&#231;&#227;o da v&#225;lvula s&#227;o modulados. Os objetivos do estudo s&#227;o avaliar as altera&#231;&#245;es neurotransmissor-dependentes nas propriedades mec&#226;nicas da v&#225;lvula mitral. </p>
    <p>
      <bold>M&#233;todos</bold>
    </p>
    <p>
      <bold>Isolamento de tecido</bold>
    </p>
    <p>Cora&#231;&#245;es porcinos (20 a 24 meses de idade) foram obtidos de um matadouro (FuXing Meats, Xangai, China). As c&#250;spides mitrais (folheto anterior ou posterior, randomicamente), sem evid&#234;ncia vis&#237;vel de les&#245;es, foram imersas imediatamente em solu&#231;&#227;o-tamp&#227;o de Krebs gelada e analisadas em at&#233; 24 horas ap&#243;s o sacrif&#237;cio dos animais. As amostras foram inicialmente preparadas, eliminado-se todas as cordas tend&#237;neas e divididas em tiras retangulares id&#234;nticas de 15 x 10 mm do ventre de cada c&#250;spide em dire&#231;&#227;o radial e circunferencial. A dire&#231;&#227;o circunferencial foi definida como paralela &#224; borda livre e a dire&#231;&#227;o radial, como da borda livre &#224; membrana basal da v&#225;lvula mitral. As tiras radiais e circunferenciais foram analisadas separadamente. Os cortes foram designados para diferentes grupos, de acordo com os neurotransmissores utilizados ao acaso: norepinefrina (NE) (10<sup>-7 </sup>- 10<sup>-4</sup> M; n = 10; SIGMA), acetilcolina (ACH) (10<sup>-6 </sup>- 10<sup>-4</sup> M; n = 10; SIGMA) e Controles normais (n = 10). A fim de identificar a localiza&#231;&#227;o e mecanismo dos neuroagentes envolvidos na rigidez, tiras submetidas a desnudamento endotelial, que foi obtido mecanicamente com a utiliza&#231;&#227;o de um raspador celular, tamb&#233;m foram empregadas (grupo com desnudamento endotelial, n = 10). Cada corte de tecido foi exposto somente a um &#250;nico neurotransmissor para evitar intera&#231;&#245;es entre os v&#225;rios agentes e a solu&#231;&#227;o seriada foi substitu&#237;da por uma nova de cada vez, no intuito de garantir a concentra&#231;&#227;o. Procedimentos envolvendo animais e seu cuidado foram aprovados pelo Comit&#234; de Cuidados e Uso de Animais da Faculdade de Medicina da Shanghai Jiao Tong University. </p>
    <p>
      <bold>Papel dos receptores dos neurotransmissores</bold>
    </p>
    <p>Para avaliar a contribui&#231;&#227;o dos receptores dos neurotransmissores nas mudan&#231;as das propriedades mec&#226;nicas dos tecidos, as tiras foram pr&#233;-incubadas por 1 hora com fentolamina (FENT, um inibidor n&#227;o-seletivo &#945;-adrenoceptor, SIGMA), prazosina (Praz, um inibidor seletivo &#945;1-adrenoceptor, SIGMA), metoprolol (Metop, um inibidor seletivo &#946;1-adrenoceptor, SIGMA), propranolol (Propr, um inibidor n&#227;o-seletivo &#946;-adrenoceptor, SIGMA) e atropina (Atrop, um inibidor do receptor colin&#233;rgico M, SIGMA), antes do teste.</p>
    <p>
      <bold>Protocolo experimental</bold>
    </p>
    <p>Ap&#243;s serem grampeados em ambas as extremidades com grampos de a&#231;o inoxid&#225;vel forrados com papel abrasivo, as amostras foram montadas em um dispositivo de teste mec&#226;nico modificado (modelo 8511; Instron, Canton, Mass) em um banho de solu&#231;&#227;o de Krebs a 37&#186;C e continuamente submetidos a 95% O<sub>2</sub> e 5% CO<sub>2</sub>. O pH das solu&#231;&#245;es foi estabilizado entre 7,35 e 7,45. Transdutores de for&#231;a para medida de tens&#227;o foram ligados ao longo dos eixos para monitorar em tempo real as altera&#231;&#245;es na tens&#227;o nas dire&#231;&#245;es radial e circunferencial, respectivamente. </p>
    <p>
      <bold>Medidas de rigidez tecidual (m&#243;dulo de elasticidade)</bold>
    </p>
    <p>Os grampos foram colocados inicialmente 1 a 2 cm mais pr&#243;ximos para enrugar levemente o tecido e assegurar aus&#234;ncia de pr&#233;-carga. As amostras foram ent&#227;o pr&#233;-condicionadas por carga e descarga cont&#237;nuas a 4 mm/s a uma carga pr&#233;-determinada (entre 200 e 400 g) por 20 ciclos para permitir que a resposta de tens&#227;o-deforma&#231;&#227;o da v&#225;lvula pudesse ser repetida. Outros tr&#234;s ciclos de medidas de tens&#227;o-deforma&#231;&#227;o foram ent&#227;o registrados para os eixos radial e cincunferencial (grupo basal). O tecido foi ent&#227;o submetido a concentra&#231;&#245;es progressivamente mais altas de neurotransmissores e respectivos bloqueadores de receptor. Tr&#234;s ciclos adicionais de tens&#227;o versus deforma&#231;&#227;o foram registrados (grupo de tratamento). Cada amostra serviu como seu pr&#243;prio controle e foi utilizada apenas uma vez. A rigidez das amostras foi calculada a partir do gradiente da por&#231;&#227;o linear da curva de tens&#227;o-deforma&#231;&#227;o (<xref ref-type="fig" rid="a06fig01m">Fig. 1</xref>). Nesse manuscrito, os termos rigidez, m&#243;dulo e m&#243;dulo de elasticidade s&#227;o utilizados de forma intercambi&#225;vel. </p>
    <p content-type="asset">
      <fig id="a06fig01m">
        <graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf01.jpg"/></fig>
    </p>
    <p>
      <bold>An&#225;lise dos dados</bold>
    </p>
    <p>Os dados s&#227;o expressos como m&#233;dia &#177; DP. As compara&#231;&#245;es das propriedades mec&#226;nicas entre tecidos normais e tratados foram realizadas atrav&#233;s de teste <italic>t</italic> de <italic>Student</italic> bilateral para duas amostras independentes ou teste ANOVA one-way para grupos m&#250;ltiplos. Todos os valores de p &lt; 0,05 foram considerados significantes. As an&#225;lises estat&#237;sticas foram realizadas com o <italic>software</italic> SPSS vers&#227;o 13.0 (SPSS Institute).</p>
    <p>
      <bold>Resultados</bold>
    </p>
    <p>
      <bold>Dados basais de rigidez em ambos os eixos</bold>
    </p>
    <p>A rigidez basal foi avaliada nos grupos iniciais: controles normais e folhetos ap&#243;s desnudamento endotelial. A rigidez nos controles n&#227;o foi afetada pelo desnudamento (Controle <italic>vs</italic> Desnudamento; Circunferencial: 5,08 &#177; 0,41 <italic>vs</italic> 4,71 &#177; 0,64, p &gt; 0,05; Radial: 2,40 &#177; 0,10 <italic>vs</italic> 2,18 &#177; 0,41, p &gt; 0,05). Al&#233;m disso, n&#227;o houve diferen&#231;a significante entre os eixos radial e circunferencial dentro do grupo em conformidade com a anisotropia desse tecido (Circunferencial <italic>vs</italic> Radial; Controle: 5,08 &#177; 0,41 <italic>vs</italic> 2,40 &#177; 0,10, p &lt; 0,05; Desnudamento: 4,71 &#177; 0,64 <italic>vs</italic> 2,18 &#177; 0,41, p &lt; 0,05). Ver <xref ref-type="table" rid="tab01">Tabela 1</xref>.</p>
    <table-wrap id="tab01">
      <graphic xlink:href="1678-4170-abc-98-04-0321-00006-gt01.jpg"/></table-wrap>
    <p>
      <bold>Regula&#231;&#227;o simp&#225;tica da altera&#231;&#227;o em rigidez tecidual</bold>
    </p>
    <p>Quando submetidos &#224; NE em concentra&#231;&#227;o de gradiente, as v&#225;lvulas apresentaram aumento na rigidez de forma concentra&#231;&#227;o-dependente (<xref ref-type="fig" rid="a06fig02">Fig. 2A</xref>). A NE aumentou a rigidez valvar por aumento de 10 vezes na concentra&#231;&#227;o (10<sup>-6</sup><italic>vs</italic> 10<sup>-7</sup>: Circunferencial: 6,15 &#177; 0,78 <italic>vs</italic> 5,34 &#177; 0,23, Radial: 3,28 &#177; 0,74 <italic>vs</italic> 2,64 &#177; 0,39, p &lt; 0,05; 10<sup>-5</sup><italic>vs</italic> 10<sup>-6</sup>: Circunferencial: 7,03 &#177; 0,51 <italic>vs</italic> 6,15 &#177; 0,78, Radial: 4,32 &#177; 0,99 <italic>vs</italic> 3,28 &#177; 0,74, p &lt; 0,05), atingindo o plat&#244; concentra&#231;&#227;o-efeito no final (10<sup>-4</sup><italic>vs</italic> 10<sup>-5</sup>, p &gt; 0,05).</p>
    <p><fig id="a06fig02"/>&#13;
&#160;&#13;
</p>
    <p>
      <fig id="a06fig02a_m">
        <graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf02.jpg"/></fig>
    </p>
    <p>&#13;
  <fig id="a06fig02xfig02b"/><fig id="a06fig02b_m"><graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf03.jpg"/></fig></p>
    <p>Entretanto, o desnudamento endotelial diminuiu a capacidade da NE em aumentar a rigidez (<xref ref-type="fig" rid="a06fig02">Fig. 2B</xref>), mantendo a NE de alta dose (10<sup>-5</sup>) significante quando comparada aos grupos de menor dose (10<sup>-5</sup><italic>vs</italic> 10<sup>-6</sup>: Circunferencial: 6,20 &#177; 0,67 <italic>vs</italic> 5,37 &#177; 0,35, Radial: 3,24 &#177; 0,66 <italic>vs</italic> 2,59 &#177; 0,55, p &lt; 0,05) com o efeito plat&#244; sem altera&#231;&#245;es. </p>
    <p>De forma similar, quando a FENT estava presente no banho do &#243;rg&#227;o, havia uma tend&#234;ncia &#224; diminui&#231;&#227;o da rigidez da c&#250;spide ap&#243;s a adi&#231;&#227;o de NE de resposta m&#225;xima (FENT <italic>vs</italic> 10<sup>-5</sup>; Circunferencial: 5,96 &#177; 1,06 <italic>vs</italic> 7,03 &#177; 0,51, Radial: 3,14 &#177; 0,64 <italic>vs</italic> 4,32 &#177; 0,99, p &lt; 0,05), ainda significante em compara&#231;&#227;o com os Controles (FENT <italic>vs</italic> controle; Circunferencial: 5,96 &#177; 1,06 <italic>vs</italic> 5,08 &#177; 0,41, Radial: 3,14 &#177; 0,64 <italic>vs</italic> 2,40 &#177; 0,10, p &lt; 0,05), ver <xref ref-type="fig" rid="a06fig03">Figura 3A</xref>. Entretanto, essa resposta n&#227;o ocorreu na presen&#231;a de Praz ou FENT, isoladamente.</p>
    <p><fig id="a06fig03"/>&#13;
&#160;&#13;
</p>
    <p>
      <fig id="a06fig03a_m">
        <graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf04.jpg"/></fig>
    </p>
    <p>&#13;
  <fig id="a06fig03xfig03b"/><fig id="a06fig03b_m"><graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf05.jpg"/></fig></p>
    <p>Finalmente, ap&#243;s incuba&#231;&#227;o das c&#250;spides com Metop, a adi&#231;&#227;o de NE resultou em uma diferen&#231;a significante na rigidez da c&#250;spide em compara&#231;&#227;o com NE isoladamente (Metop <italic>vs</italic> NE; Circunferencial: 5,67 &#177; 0,73 <italic>vs</italic> 7,03 &#177; 0,51, Radial: 3,09 &#177; 0,68 <italic>vs</italic> 4,32 &#177; 0,99, p &lt; 0,05). Entretanto, compara&#231;&#245;es diretas de altera&#231;&#245;es ap&#243;s Metop e NE <italic>versus </italic>controles ainda eram estatisticamente significantes (p &lt; 0,05). Ver <xref ref-type="fig" rid="a06fig03">Figura 3B</xref>. A rigidez n&#227;o foi afetada pela adi&#231;&#227;o isolada de Propr ou Metop. </p>
    <p>
      <bold>Contribui&#231;&#227;o vagal para rigidez tecidual</bold>
    </p>
    <p>A rigidez das c&#250;spides mitrais diminuiu significantemente em resposta ao aumento das concentra&#231;&#245;es de ACH (significante altera&#231;&#227;o em rigidez por aumento de 10 vezes na concentra&#231;&#227;o de ACH, 10<sup>-5</sup><italic>vs</italic> 10<sup>-6</sup>; Circunferencial: 3,40 &#177; 1,10 <italic>vs</italic> 4,35 &#177; 0,76, Radial: 1,05 &#177; 0,38 <italic>vs</italic> 1,80 &#177; 0,79, p &lt; 0,05). O grupo com escala mais baixa (10<sup>-6 </sup>mol/l) ainda exibia um efeito significante na diminui&#231;&#227;o do m&#243;dulo quando comparados com Controles (Circunferencial: 4,35 &#177; 0,76 <italic>vs</italic> 5,08 &#177; 0,41, Radial: 1,80 &#177; 0,79 <italic>vs</italic> 2,40 &#177; 0,10, p &lt; 0,05 <italic>vs</italic> controle) com o efeito plat&#244; na concentra&#231;&#227;o de 10<sup>-5 </sup>mol/l (10<sup>-5</sup><italic>vs</italic> 10<sup>-4</sup>, p &gt; 0,05). Ver <xref ref-type="fig" rid="a06fig04m">Figura 4</xref>.</p>
    <p content-type="asset">
      <fig id="a06fig04m">
        <graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf06.jpg"/></fig>
    </p>
    <p>Quando as amostras de v&#225;lvulas foram pr&#233;-incubadas em Atrop ou sofreram desnudamento endotelial por meios mec&#226;nicos, a resposta &#224; ACHO foi completamente revogada (p &gt; 0,05 <italic>vs</italic> controle) (<xref ref-type="fig" rid="a06fig05m">Figura 5</xref>).</p>
    <p content-type="asset">
      <fig id="a06fig05m">
        <graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf07.jpg"/></fig>
    </p>
    <p>
      <bold>Discuss&#227;o</bold>
    </p>
    <p>Empreendemos os melhores esfor&#231;os para criar um ambiente interno quase-natural, no qual a v&#225;lvula mitral se encontra e que &#233; mediado pelo sistema nervoso aut&#244;nomo (SNA). Os principais achados desse estudo s&#227;o que, sob condi&#231;&#245;es fisiol&#243;gicas, os nervos aut&#244;nomos (simp&#225;tico e vago) modulam de forma significante as propriedades mec&#226;nicas das c&#250;spides mitrais porcinas, atrav&#233;s de neurotransmissores liberados pelas extremidades nervosas. A rigidez das v&#225;lvulas mitrais era significantemente diminu&#237;da em resposta ao aumento das concentra&#231;&#245;es de ACH de forma concentra&#231;&#227;o-dependente, e ao contr&#225;rio, elevada pela NE de forma dose-dependente. Ao mesmo tempo observamos que o endot&#233;lio valvar, &#945;/&#946; adrenoceptor e receptor colin&#233;rgico tinham um papel fundamental na regula&#231;&#227;o das propriedades mec&#226;nicas. </p>
    <p>Tem sido proposto que disfun&#231;&#245;es do sistema nervoso aut&#244;nomo prevalecem na grande maioria dos pacientes com doen&#231;as card&#237;acas. Essa proposta &#233; baseada, em sua maior parte, nos resultados de diversos estudos de variabilidade de frequ&#234;ncia card&#237;aca e alguns sintomas de disautonomia, tais como s&#237;ncope reflexa, ansiedade, sofrimento psicol&#243;gico, palpita&#231;&#245;es, e assim por diante. Foi observado que as v&#225;lvulas mitrais s&#227;o moduladas pelo SNA em rela&#231;&#227;o &#224; fun&#231;&#227;o e responderam ativamente, diferentemente dos folhetos passivos propelidos apenas pela press&#227;o transvalvar.</p>
    <p>Entretanto, poucos detalhes do processo s&#227;o conhecidos, de forma que esse estudo foi realizado com o objetivo de identificar o papel dos nervos aut&#244;nomos na regula&#231;&#227;o das propriedades mec&#226;nicas da v&#225;lvula mitral porcina. </p>
    <p>A extremidade nervosa auton&#244;mica libera v&#225;rias subst&#226;ncias bioativas <italic>in vivo</italic>, especialmente NE e ACH, exercendo rea&#231;&#245;es muito complicadas no tecido e &#243;rg&#227;o alvo. Al&#233;m disso, a ACH &#233; um relaxante celular de m&#250;sculo liso espec&#237;fico em tecido valvar e os receptores muscar&#237;nicos da ACH (M2) tem sido considerados como sendo funcionais, enquanto os outros subtipos aparentemente n&#227;o tem um efeito fisiol&#243;gico<sup>5</sup>. Foi demonstrado que a ACH induz relaxamento do tecido valvar a&#243;rtico em um modelo <italic>ex vivo</italic><sup>4</sup>. Em nosso estudo, o uso de ACH ex&#243;gena serviu para demonstrar o efeito desse pept&#237;deo na avalia&#231;&#227;o de sua capacidade sobre a rigidez valvar mitral. Observou-se que sob as presentes condi&#231;&#245;es experimentais, a ACH diminuiu a rigidez de forma concentra&#231;&#227;o-dependente, como esperado. Al&#233;m disso, parece que a ACH pode induzir relaxamento do tecido da v&#225;lvula mitral, resultando em rigidez diminu&#237;da atrav&#233;s do M2, como demonstrado ap&#243;s a adi&#231;&#227;o de Atrop, quando as respostas da ACH foram completamente revogadas. Para entender especificamente o efeito da estimula&#231;&#227;o da ACH nas v&#225;lvulas, Ohashi e cols.<sup>6</sup> mostraram que a ACH produzia transit&#243;ria e ent&#227;o sustentada hiperpolariza&#231;&#227;o da membrana em endot&#233;lio valvar de aorta de coelho; e a descontinua&#231;&#227;o da ACH causou uma despolariza&#231;&#227;o transit&#243;ria. Esses mecanismos contribuem para a libera&#231;&#227;o de fatores vasoativos endot&#233;lio-dependentes, tais como NO<sup>7,8</sup> em v&#225;lvulas mitrais caninas e porcinas. Esse pode ser um dos mecanismos da ACH para mediar a rigidez. A NE pode causar uma potente contra&#231;&#227;o de c&#233;lulas de m&#250;sculo liso, atrav&#233;s da estimula&#231;&#227;o espec&#237;fica de subtipos de receptor em v&#225;lvula a&#243;rtica equina<sup>9,10</sup>. H&#225; mais subtipos de adrenoceptores conhecidos, que tem sido encontrados em tecido valvar de cora&#231;&#227;o humano: adrenoceptores &#945;1, &#945;2, &#946;1 e &#946;2<sup>10,11</sup>. Williams TH e cols.<sup>3</sup> relataram que v&#225;lvulas mitrais de ratos tinham mostrado movimentos espont&#226;neos similares &#224; contra&#231;&#245;es, localizados no folheto em si, imediatamente ap&#243;s ser dissecado do cora&#231;&#227;o, e que foram aumentados com a adi&#231;&#227;o de NE de forma dose-dependente. De outra forma, a fim de examinar as respostas das c&#250;spides aos neuromoduladores <italic>ex vivo </italic>e determinar os receptores espec&#237;ficos envolvidos na media&#231;&#227;o desses efeitos, c&#250;spides de v&#225;lvulas a&#243;rticas porcinas, montadas axialmente em uma c&#226;mara de &#243;rg&#227;os, contra&#237;ram de forma significante em resposta ao aumento das concentra&#231;&#245;es de &#945;-adrenoreceptores agonistas, como indicado pela aus&#234;ncia de qualquer resposta ap&#243;s a adi&#231;&#227;o de ioimbina, um &#945;2-adrenoreceptor antagonista, mas n&#227;o ap&#243;s a adi&#231;&#227;o de prazosina, um inibidor de &#945;1-adrenoreceptores em v&#225;lvulas a&#243;rticas equina<sup>9</sup>. Em nosso experimenta, observamos a resposta valvar &#224; NE na rigidez, que pode ser mitigada pelo inibidor n&#227;o-seletivo &#945;-adrenoceptor FENT, n&#227;o pela prazosina. Esses resultados confirmaram os relatos anteriores e sugeriram que o adrenoceptor &#946;1 pode ter tido um papel na modula&#231;&#227;o da rigidez. Parece que as altera&#231;&#245;es na rigidez consistentemente se correlacionaram com a resposta de relaxamento ou contra&#231;&#227;o do tecido porcino aos mediadores. Sendo assim, obviamente, &#233; prov&#225;vel que o estado do SNA influencie a fun&#231;&#227;o de longo prazo e a flexibilidade das v&#225;lvulas devido &#224; rapidez da abertura e fechamento valvar e disautonomia, particularmente doen&#231;a card&#237;aca valvar concomitante, parece ser n&#227;o-insignificante. </p>
    <p>Estudos recentes tem indicado que as c&#233;lulas endoteliais de v&#225;lvulas a&#243;rticas porcinas apresentam caracter&#237;sticas celulares e moleculares espec&#237;ficas que tem um papel fundamental na regula&#231;&#227;o do t&#244;nus valvar card&#237;aco<sup>12,13</sup>. Foi relatado que o endot&#233;lio valvar exercia seu efeito atrav&#233;s da modula&#231;&#227;o da rigidez da c&#250;spide valvar a&#243;rtica humana &#224; diferentes mediadores: ON e ET-1<sup>14</sup>. Apesar disso, o papel fisiol&#243;gico do SNA no endot&#233;lio valvar card&#237;aco ainda n&#227;o tinha sido adequadamente definido. Com base nos desfechos do presente estudo, foi aparentemente observado que a rigidez alterada pela ACH foi completamente dependente do endot&#233;lio valvar, enquanto a rigidez alterada pela NE foi parcialmente dependente do endot&#233;lio valvar e outros mecanismos podem estar envolvidos. Essas respostas podem ser obtidas pela distribui&#231;&#227;o dos respectivos receptores. Os achados de Pompilio e cols.<sup>4</sup> em v&#225;lvulas pulmonares e a&#243;rticas porcinas podem ajudar a apreciar essa rea&#231;&#227;o. O efeito da ACH, induzindo relaxamento do tecido da v&#225;lvula a&#243;rtica, estava ausente quando endot&#233;lio foi removido mecanicamente, enfatizando o papel essencial do endot&#233;lio e receptores M2 (mencionados anteriormente). As altera&#231;&#245;es nas propriedades mec&#226;nicas do tecido valvar em resposta &#224; diferentes mediadores podem ser explicadas pela presen&#231;a de miofibroblastos e c&#233;lulas de m&#250;sculo liso nas v&#225;lvulas humanas<sup>15</sup>. O endot&#233;lio valvar porcino sozinho n&#227;o pode facilitar anatomicamente as popula&#231;&#245;es de c&#233;lulas intersticiais na rigidez, como demonstrado pela aus&#234;ncia de altera&#231;&#227;o na rigidez valvar ap&#243;s o desnudamento endotelial por meio mec&#226;nico. Entretanto, a rea&#231;&#227;o cruzada entre os miofibroblastos intersticiais e endoteliais e as c&#233;lulas de m&#250;sculo liso foi sugerida por esse estudo, atrav&#233;s da observa&#231;&#227;o que o desnudamento endotelial diminuiu a capacidade da NE em aumentar a rigidez, somente mantendo a NE de alta dose (10<sup>-5</sup>) significante quando comparada aos grupos de menor dose. Esse pode ser o meio atrav&#233;s do qual o endot&#233;lio da v&#225;lvula mitral regula as propriedades mec&#226;nicas das c&#250;spides de v&#225;lvulas porcinas. Sendo assim, a estrutura e fun&#231;&#227;o &#250;nicas das c&#233;lulas endoteliais valvares deveriam ser enfatizadas. </p>
    <p>Esse &#233; um estudo <italic>ex vivo</italic>, e os valores reais do meio-ambiente geral, os sinais neur&#243;crinos, end&#243;crinos, par&#225;crinos podem diferir daqueles <italic>in vivo</italic>. A configura&#231;&#227;o experimental aguda n&#227;o leva em considera&#231;&#227;o os efeitos tr&#243;ficos de longo prazo desses neurotransmissores ou sua capacidade de modular a matriz extracelular em seres humanos<sup>16</sup>. Estudos adicionais s&#227;o necess&#225;rios para avaliar quaisquer outros par&#226;metros biol&#243;gicos envolvidos na resposta &#224; est&#237;mulos nervosos auton&#244;mos, bem como as diferen&#231;as responsivas entre popula&#231;&#245;es de c&#233;lulas endoteliais e intersticiais. </p>
    <p>
      <bold>Implica&#231;&#227;o cl&#237;nica</bold>
    </p>
    <p>&#201; prov&#225;vel que altera&#231;&#245;es nas respostas mec&#226;nicas das v&#225;lvulas card&#237;acas com vias auton&#244;micas nervo-dependentes sejam significantes na patofisiologia da doen&#231;a valvar. Tem sido demonstrado que os arcos reflexos parassimp&#225;ticos e simp&#225;ticos diferiam com o envelhecimento, incluindo aumento nos n&#237;veis de NE circulante na linha basal e em resposta &#224; estresse, diminui&#231;&#227;o na concentra&#231;&#227;o de catecolamina em cora&#231;&#227;o de rato senescente, aumento na s&#237;ntese e na degrada&#231;&#227;o de enzimas para catecolaminas<sup>17</sup>. Houve um aumento na preval&#234;ncia de disfun&#231;&#227;o valvar card&#237;aca com o envelhecimento e est&#227;o geralmente associadas a mudan&#231;as no SNA nas estruturas valvares e sistema circulat&#243;rio. De forma similar, biov&#225;lvulas card&#237;acas, consideradas superiores &#224; mec&#226;nicas em rela&#231;&#227;o ao desempenho hemodin&#226;mico e biocompatibilidade (complica&#231;&#245;es tromboemb&#243;licas m&#237;nimas, sem necessidade de anti-coagula&#231;&#227;o), apresentam, entretanto, durabilidade limitada, resultante de deteriora&#231;&#227;o e disfun&#231;&#227;o valvar desconhecida. De acordo com esse estudo, o aumento da preval&#234;ncia de disfun&#231;&#227;o valvar com o envelhecimento e a limitada longevidade da biov&#225;lvula pode ter uma correla&#231;&#227;o &#237;ntima e significante com o desequil&#237;brio ou falta de modula&#231;&#227;o nervosa aut&#244;noma. Finalmente, novas estrat&#233;gias diagn&#243;sticas e terap&#234;uticas podem emergir como liga&#231;&#245;es de vias anteriormente desconhecidas e revelar novos alvos de interven&#231;&#227;o ao longo desses circuitos biol&#243;gicos emergentes. </p>
    <p>
      <bold>Conclus&#245;es</bold>
    </p>
    <p>Em conclus&#227;o, esse estudo demonstrou que as propriedades mec&#226;nicas das c&#250;spides da v&#225;lvula mitral s&#227;o ativamente reguladas atrav&#233;s de vias auton&#244;micas nervo-dependentes. Os nervos aut&#244;nomos (simp&#225;tico e vago) exercem seus efeito atrav&#233;s da modula&#231;&#227;o da rigidez das c&#250;spides atrav&#233;s dos receptores &#945;2, &#946;1 e M2 na endot&#233;lio da v&#225;lvula, al&#233;m das c&#233;lulas intersticiais. Estamos gratos por esses achados ajudarem na compreens&#227;o da patofisiologia valvar e estabelecer um mapa das respostas adaptativas das propriedades mec&#226;nicas das v&#225;lvulas para futuras v&#225;lvulas card&#237;acas biol&#243;gicas.</p>
    <p>
      <bold>Potencial Conflito de Interesses</bold>
    </p>
    <p>Declaro n&#227;o haver conflito de interesses pertinentes.</p>
    <p>
      <bold>Fontes de Financiamento</bold>
    </p>
    <p>O presente estudo n&#227;o teve fontes de financiamento externas.</p>
    <p>
      <bold>Vincula&#231;&#227;o Acad&#234;mica</bold>
    </p>
    <p>N&#227;o h&#225; vincula&#231;&#227;o deste estudo a programas de p&#243;s-gradua&#231;&#227;o.</p>
    <p>
      <fn id="end" fn-type="corresp">
        <label>
          <bold>Correspond&#234;ncia:</bold>
        </label>
        <p> Qiang Zhao </p>
        <p> Department of Cardiac Surgery, Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine </p>
        <p> Shanghai, 200025, PRC </p>
        <p> E-mail: </p>
        <p>
          <email xlink:href="zq11607@rjh.com.cn">zq11607@rjh.com.cn</email>
        </p>
      </fn>
    </p>
    <p> Artigo recebido em 01/09/10; revisado recebido em 01/11/10; aceito em 23/11/10.</p>
  </body>
  <back>
    <ref-list>
      <ref id="B1">
        <mixed-citation>1. Voloshchenko AA. Afferent innervation of atrioventricular valve. Fed Proc Transl Suppl. 1965;24(4):571-4.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Afferent innervation of atrioventricular valve</article-title>
          <source>Fed Proc Transl Suppl</source>
          <date>
            <year>1965</year>
          </date>
          <fpage>571</fpage>
          <lpage>4</lpage>
          <issue>4</issue>
          <volume>24</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Voloshchenko</surname>
              <given-names>AA</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B2">
        <mixed-citation>2. Williams TH. Mitral and tricuspid valve innervation. Br Heart J. 1964;26:105-15.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Mitral and tricuspid valve innervation</article-title>
          <source>Br Heart J</source>
          <date>
            <year>1964</year>
          </date>
          <fpage>105</fpage>
          <lpage>15</lpage>
          <volume>26</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Williams</surname>
              <given-names>TH</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B3">
        <mixed-citation>3. Williams TH, Jew JY. Is the mitral valve passive flap theory overstated? An active valve is hypothesized. Med Hypotheses. 2004;62(4):605-11.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Is the mitral valve passive flap theory overstated: An active valve is hypothesized</article-title>
          <source>Med Hypotheses</source>
          <date>
            <year>2004</year>
          </date>
          <fpage>605</fpage>
          <lpage>11</lpage>
          <issue>4</issue>
          <volume>62</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Williams</surname>
              <given-names>TH</given-names>
            </name>
            <name>
              <surname>Jew</surname>
              <given-names>JY</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B4">
        <mixed-citation>4. Pompilio G, Rossoni G, Sala A, Polvani GL, Berti F, Dainese L, et al. Endothelial-dependent dynamic and antithrombotic properties of porcine aortic and pulmonary valves. Ann Thorac Surg. 1998;65(4):986-92.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Endothelial-dependent dynamic and antithrombotic properties of porcine aortic and pulmonary valves</article-title>
          <source>Ann Thorac Surg</source>
          <date>
            <year>1998</year>
          </date>
          <fpage>986</fpage>
          <lpage>92</lpage>
          <issue>4</issue>
          <volume>65</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Pompilio</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Rossoni</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Sala</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Polvani</surname>
              <given-names>GL</given-names>
            </name>
            <name>
              <surname>Berti</surname>
              <given-names>F</given-names>
            </name>
            <name>
              <surname>Dainese</surname>
              <given-names>L</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B5">
        <mixed-citation>5. van Zwieten PA, Doods HN. Muscarinic receptors and drugs in cardiovascular medicine. Cardiovasc Drugs Ther. 1995;9(1):159-67.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Muscarinic receptors and drugs in cardiovascular medicine</article-title>
          <source>Cardiovasc Drugs Ther</source>
          <date>
            <year>1995</year>
          </date>
          <fpage>159</fpage>
          <lpage>67</lpage>
          <issue>1</issue>
          <volume>9</volume>
          <person-group person-group-type="author">
            <name>
              <surname>van Zwieten</surname>
              <given-names>PA</given-names>
            </name>
            <name>
              <surname>Doods</surname>
              <given-names>HN</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B6">
        <mixed-citation>6. Ohashi M, Satoh K, Itoh T. Acetylcholine-induced membrane potential changes in endothelial cells of rabbit aortic valve. Br J Pharmacol. 1999;126(1):19-26.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Acetylcholine-induced membrane potential changes in endothelial cells of rabbit aortic valve</article-title>
          <source>Br J Pharmacol</source>
          <date>
            <year>1999</year>
          </date>
          <fpage>19</fpage>
          <lpage>26</lpage>
          <issue>1</issue>
          <volume>126</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Ohashi</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Satoh</surname>
              <given-names>K</given-names>
            </name>
            <name>
              <surname>Itoh</surname>
              <given-names>T</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B7">
        <mixed-citation>7. Ku DD, Nelson JM, Caulfield JB, Winn MJ. Release of endothelium-derived relaxing factors from canine cardiac valves. J Cardiovasc Pharmacol. 1990;16(2):212-8.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Release of endothelium-derived relaxing factors from canine cardiac valves</article-title>
          <source>J Cardiovasc Pharmacol</source>
          <date>
            <year>1990</year>
          </date>
          <fpage>212</fpage>
          <lpage>8</lpage>
          <issue>2</issue>
          <volume>16</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Ku</surname>
              <given-names>DD</given-names>
            </name>
            <name>
              <surname>Nelson</surname>
              <given-names>JM</given-names>
            </name>
            <name>
              <surname>Caulfield</surname>
              <given-names>JB</given-names>
            </name>
            <name>
              <surname>Winn</surname>
              <given-names>MJ</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B8">
        <mixed-citation>8. Siney L, Lewis MJ. Nitric oxide release from porcine mitral valves. Cardiovasc Res. 1993;27(9):1657-61.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Nitric oxide release from porcine mitral valves</article-title>
          <source>Cardiovasc Res</source>
          <date>
            <year>1993</year>
          </date>
          <fpage>1657</fpage>
          <lpage>61</lpage>
          <issue>9</issue>
          <volume>27</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Siney</surname>
              <given-names>L</given-names>
            </name>
            <name>
              <surname>Lewis</surname>
              <given-names>MJ</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B9">
        <mixed-citation>9. Bowen IM, Marr CM, Chester AH, Wheeler-Jones CP, Elliott J. In vitro contraction of the equine aortic valve. J Heart Valve Dis. 2004;13(4):593-9.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>In vitro contraction of the equine aortic valve</article-title>
          <source>J Heart Valve Dis</source>
          <date>
            <year>2004</year>
          </date>
          <fpage>593</fpage>
          <lpage>9</lpage>
          <issue>4</issue>
          <volume>13</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Bowen</surname>
              <given-names>IM</given-names>
            </name>
            <name>
              <surname>Marr</surname>
              <given-names>CM</given-names>
            </name>
            <name>
              <surname>Chester</surname>
              <given-names>AH</given-names>
            </name>
            <name>
              <surname>Wheeler-Jones</surname>
              <given-names>CP</given-names>
            </name>
            <name>
              <surname>Elliott</surname>
              <given-names>J</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B10">
        <mixed-citation>10. Chester AH, Misfeld M, Yacoub MH. Receptor-mediated contraction of aortic valve leaflets. J Heart Valve Dis. 2000;9(2):250-4.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Receptor-mediated contraction of aortic valve leaflets</article-title>
          <source>J Heart Valve Dis</source>
          <date>
            <year>2000</year>
          </date>
          <fpage>250</fpage>
          <lpage>4</lpage>
          <issue>2</issue>
          <volume>9</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Chester</surname>
              <given-names>AH</given-names>
            </name>
            <name>
              <surname>Misfeld</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Yacoub</surname>
              <given-names>MH</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B11">
        <mixed-citation>11. Osman L, Chester AH, Sarathchandra P, Latif N, Meng W, Taylor PM, et al. A novel role of the sympatho-adrenergic system in regulating valve calcification. Circulation. 2007;116(11 Suppl):I282-7.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>A novel role of the sympatho-adrenergic system in regulating valve calcification</article-title>
          <source>Circulation</source>
          <date>
            <year>2007</year>
          </date>
          <fpage>I282</fpage>
          <lpage>7</lpage>
          <volume>116</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Osman</surname>
              <given-names>L</given-names>
            </name>
            <name>
              <surname>Chester</surname>
              <given-names>AH</given-names>
            </name>
            <name>
              <surname>Sarathchandra</surname>
              <given-names>P</given-names>
            </name>
            <name>
              <surname>Latif</surname>
              <given-names>N</given-names>
            </name>
            <name>
              <surname>Meng</surname>
              <given-names>W</given-names>
            </name>
            <name>
              <surname>Taylor</surname>
              <given-names>PM</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B12">
        <mixed-citation>12. Butcher JT, Penrod AM, Garcia AJ, Nerem RM. Unique morphology and focal adhesion development of valvular endothelial cells in static and fluid flow environments. Arterioscler Thromb Vasc Biol. 2004;24(8):1429-34.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Unique morphology and focal adhesion development of valvular endothelial cells in static and fluid flow environments</article-title>
          <source>Arterioscler Thromb Vasc Biol</source>
          <date>
            <year>2004</year>
          </date>
          <fpage>1429</fpage>
          <lpage>34</lpage>
          <issue>8</issue>
          <volume>24</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Butcher</surname>
              <given-names>JT</given-names>
            </name>
            <name>
              <surname>Penrod</surname>
              <given-names>AM</given-names>
            </name>
            <name>
              <surname>Garcia</surname>
              <given-names>AJ</given-names>
            </name>
            <name>
              <surname>Nerem</surname>
              <given-names>RM</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B13">
        <mixed-citation>13. Butcher JT, Tressel S, Johnson T, Turner D, Sorescu G, Jo H, et al. Transcriptional profiles of valvular and vascular endothelial cells reveal phenotypic differences: influence of shear stress. Arterioscler Thromb Vasc Biol. 2006;26(1):69-77.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Transcriptional profiles of valvular and vascular endothelial cells reveal phenotypic differences: influence of shear stress</article-title>
          <source>Arterioscler Thromb Vasc Biol</source>
          <date>
            <year>2006</year>
          </date>
          <fpage>69</fpage>
          <lpage>77</lpage>
          <issue>1</issue>
          <volume>26</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Butcher</surname>
              <given-names>JT</given-names>
            </name>
            <name>
              <surname>Tressel</surname>
              <given-names>S</given-names>
            </name>
            <name>
              <surname>Johnson</surname>
              <given-names>T</given-names>
            </name>
            <name>
              <surname>Turner</surname>
              <given-names>D</given-names>
            </name>
            <name>
              <surname>Sorescu</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Jo</surname>
              <given-names>H</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B14">
        <mixed-citation>14. El-Hamamsy I, Balachandran K, Yacoub MH, Stevens LM, Sarathchandra P, Taylor PM, et al. Endothelium-dependent regulation of the mechanical properties of aortic valve cusps. J Am Coll Cardiol. 2009;53(16):1448-55.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Endothelium-dependent regulation of the mechanical properties of aortic valve cusps</article-title>
          <source>J Am Coll Cardiol</source>
          <date>
            <year>2009</year>
          </date>
          <fpage>1448</fpage>
          <lpage>55</lpage>
          <issue>16</issue>
          <volume>53</volume>
          <person-group person-group-type="author">
            <name>
              <surname>El-Hamamsy</surname>
              <given-names>I</given-names>
            </name>
            <name>
              <surname>Balachandran</surname>
              <given-names>K</given-names>
            </name>
            <name>
              <surname>Yacoub</surname>
              <given-names>MH</given-names>
            </name>
            <name>
              <surname>Stevens</surname>
              <given-names>LM</given-names>
            </name>
            <name>
              <surname>Sarathchandra</surname>
              <given-names>P</given-names>
            </name>
            <name>
              <surname>Taylor</surname>
              <given-names>PM</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B15">
        <mixed-citation>15. Roy A, Brand NJ, Yacoub MH. Molecular characterization of interstitial cells isolated from human heart valves. J Heart Valve Dis. 2000;9(3):459-64.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Molecular characterization of interstitial cells isolated from human heart valves</article-title>
          <source>J Heart Valve Dis</source>
          <date>
            <year>2000</year>
          </date>
          <fpage>459</fpage>
          <lpage>64</lpage>
          <issue>3</issue>
          <volume>9</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Roy</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Brand</surname>
              <given-names>NJ</given-names>
            </name>
            <name>
              <surname>Yacoub</surname>
              <given-names>MH</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B16">
        <mixed-citation>16. Hafizi S, Taylor PM, Chester AH, Allen SP, Yacoub MH. Mitogenic and secretory responses of human valve interstitial cells to vasoactive agents. J Heart Valve Dis. 2000;9(3):454-8.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Mitogenic and secretory responses of human valve interstitial cells to vasoactive agents</article-title>
          <source>J Heart Valve Dis</source>
          <date>
            <year>2000</year>
          </date>
          <fpage>454</fpage>
          <lpage>8</lpage>
          <issue>3</issue>
          <volume>9</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Hafizi</surname>
              <given-names>S</given-names>
            </name>
            <name>
              <surname>Taylor</surname>
              <given-names>PM</given-names>
            </name>
            <name>
              <surname>Chester</surname>
              <given-names>AH</given-names>
            </name>
            <name>
              <surname>Allen</surname>
              <given-names>SP</given-names>
            </name>
            <name>
              <surname>Yacoub</surname>
              <given-names>MH</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B17">
        <mixed-citation>17. Jew JY, Williams TH. Innervation of the mitral valve is strikingly depleted with age. Anat Rec. 1999;255(3):252-60.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Innervation of the mitral valve is strikingly depleted with age</article-title>
          <source>Anat Rec</source>
          <date>
            <year>1999</year>
          </date>
          <fpage>252</fpage>
          <lpage>60</lpage>
          <issue>3</issue>
          <volume>255</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Jew</surname>
              <given-names>JY</given-names>
            </name>
            <name>
              <surname>Williams</surname>
              <given-names>TH</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
    </ref-list>
  </back>
  <sub-article article-type="translation" id="TRes" xml:lang="es">
    <front-stub>
      <article-categories/>
      <title-group>
        <article-title xml:lang="es">Regulaci&#243;n auton&#243;mica de las propiedades mec&#225;nicas en biopr&#243;tesis valvular porcina</article-title>
      </title-group>
      <abstract xml:lang="es">
        <p>FUNDAMENTO: La presencia de nervios en las v&#225;lvulas card&#237;acas qued&#243; demostrada por primera vez hace algunas d&#233;cadas e identificadas en sub-poblaciones: simp&#225;ticas y parasimp&#225;ticas y por lo tanto, lo que se espera es que las v&#225;lvulas reciban una gran afectaci&#243;n de los nervios aut&#243;nomos. Sin embargo, pocos estudios se han concentrado en la regulaci&#243;n de v&#225;lvulas card&#237;acas a trav&#233;s del sistema nervioso aut&#243;nomo. OBJETIVO: Buscamos identificar el papel del sistema nervioso aut&#243;nomo en la regulaci&#243;n de las propiedades mec&#225;nicas de los tejidos de las v&#225;lvulas mitrales porcinas. M&#201;TODOS: Las propiedades mec&#225;nicas de las capas de v&#225;lvulas mitrales porcinas fueron evaluadas en respuesta a la norepinefrina (NE) y a la acetilcolina (ACH), los principales neurotransmisores. Igualmente, la fentolamina (FENT), el metoprolol (Metop), la atropina (Atrop) y la denudaci&#243;n endotelial tambi&#233;n se a&#241;adieron al sistema reactivo. RESULTADOS: Bajo condiciones fisiol&#243;gicas, la rigidez no se afect&#243; por el denudaci&#243;n endotelial (p &gt; 0,05). La NE aument&#243; significativamente la rigidez valvular con un aumento de 10 veces en la concentraci&#243;n (10-6 vs 10-7, p &lt; 0,05; 10-5 vs 10-6, p &lt; 0,05). Esa respuesta fue amenizada por FENT, Metop o denudaci&#243;n endotelial (p &lt; 0,05); pero se mantuvo aumentada de manera significativa cuando se le compar&#243; con los Controles (p &lt; 0,05). La ACH caus&#243; una disminuci&#243;n en la rigidez acompa&#241;ada por un aumento en su concentraci&#243;n (alteraci&#243;n significativa en la rigidez por el aumento en 10 veces de la concentraci&#243;n de ACH, 10-6 vs Control, p &lt; 0,05; 10-5 vs 10-6, p &lt; 0,05), que fue revertida por la denudaci&#243;n endotelial y Atrop (p &gt; 0,05 vs Control). CONCLUSI&#211;N: Esos hallazgos destacan el rol del sistema nervioso aut&#243;nomo en la regulaci&#243;n de las propiedades mec&#225;nicas de las c&#250;spides de la v&#225;lvula mitral porcina, lo que refuerza la importancia del estado nervioso aut&#243;nomo en el funcionamiento ideal de la v&#225;lvula.</p>
      </abstract>
      <kwd-group xml:lang="es">
        <kwd>V&#225;lvula mitral</kwd>
        <kwd>v&#237;as aut&#243;nomas</kwd>
        <kwd>biopr&#243;tesis</kwd>
        <kwd>sistema nervioso aut&#243;nomo</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <bold>ART&#205;CULO ORIGINAL</bold>
      </p>
      <p>
        <fn id="enda-body2">
          <label>
            <bold>Regulaci&#243;n auton&#243;mica de las propiedades mec&#225;nicas en biopr&#243;tesis valvular porcina</bold>
          </label>
          <p>
            <bold>Xiang Hu; Qiang Zhao; Xiaofeng Ye</bold>
          </p>
        </fn>
      </p>
      <p> Department of Cardiac Surgery, Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, PRC</p>
      <p>Correspondencia</p>
      <p>
        <bold>RESUMEN</bold>
      </p>
      <p><bold>FUNDAMENTO:</bold> La presencia de nervios en las v&#225;lvulas card&#237;acas qued&#243; demostrada por primera vez hace algunas d&#233;cadas e identificadas en sub-poblaciones: simp&#225;ticas y parasimp&#225;ticas y por lo tanto, lo que se espera es que las v&#225;lvulas reciban una gran afectaci&#243;n de los nervios aut&#243;nomos. Sin embargo, pocos estudios se han concentrado en la regulaci&#243;n de v&#225;lvulas card&#237;acas a trav&#233;s del sistema nervioso aut&#243;nomo.</p>
      <p><bold>OBJETIVO:</bold> Buscamos identificar el papel del sistema nervioso aut&#243;nomo en la regulaci&#243;n de las propiedades mec&#225;nicas de los tejidos de las v&#225;lvulas mitrales porcinas.</p>
      <p><bold>M&#201;TODOS:</bold> Las propiedades mec&#225;nicas de las capas de v&#225;lvulas mitrales porcinas fueron evaluadas en respuesta a la norepinefrina (NE) y a la acetilcolina (ACH), los principales neurotransmisores. Igualmente, la fentolamina (FENT), el metoprolol (Metop), la atropina (Atrop) y la denudaci&#243;n endotelial tambi&#233;n se a&#241;adieron al sistema reactivo.</p>
      <p><bold>RESULTADOS:</bold> Bajo condiciones fisiol&#243;gicas, la rigidez no se afect&#243; por el denudaci&#243;n endotelial (p &gt; 0,05). La NE aument&#243; significativamente la rigidez valvular con un aumento de 10 veces en la concentraci&#243;n (10<sup>-6</sup><italic>vs</italic> 10<sup>-7</sup>, p &lt; 0,05; 10<sup>-5</sup><italic>vs</italic> 10<sup>-6</sup>, p &lt; 0,05). Esa respuesta fue amenizada por FENT, Metop o denudaci&#243;n endotelial (p &lt; 0,05); pero se mantuvo aumentada de manera significativa cuando se le compar&#243; con los Controles (p &lt; 0,05). La ACH caus&#243; una disminuci&#243;n en la rigidez acompa&#241;ada por un aumento en su concentraci&#243;n (alteraci&#243;n significativa en la rigidez por el aumento en 10 veces de la concentraci&#243;n de ACH, 10<sup>-6</sup><italic>vs</italic> Control, p &lt; 0,05; 10<sup>-5</sup><italic>vs</italic> 10<sup>-6</sup>, p &lt; 0,05), que fue revertida por la denudaci&#243;n endotelial y Atrop (p &gt; 0,05 <italic>vs</italic> Control).</p>
      <p><bold>CONCLUSI&#211;N:</bold> Esos hallazgos destacan el rol del sistema nervioso aut&#243;nomo en la regulaci&#243;n de las propiedades mec&#225;nicas de las c&#250;spides de la v&#225;lvula mitral porcina, lo que refuerza la importancia del estado nervioso aut&#243;nomo en el funcionamiento ideal de la v&#225;lvula. </p>
      <p><bold>Palabras clave:</bold> V&#225;lvula mitral, v&#237;as aut&#243;nomas, biopr&#243;tesis, sistema nervioso aut&#243;nomo.</p>
      <p>
        <bold>Introducci&#243;n</bold>
      </p>
      <p>La funci&#243;n de las v&#225;lvulas card&#237;acas es bastante complicada, porque los movimientos pasivos de la v&#225;lvula no tienen en cuenta su capacidad de adaptarse al ambiente hemodin&#225;mico y humoral. Eso se comprueba en la presencia de nervios en las v&#225;lvulas card&#237;acas, demostrada por primera vez hace d&#233;cadas e identificadas en subpoblaciones: simp&#225;ticas, parasimp&#225;ticas, sensoriales y marcadores colin&#233;rgicos nerviosos<sup>1,2</sup>. La arritmia card&#237;aca es frecuentemente detectada en pacientes con enfermedades card&#237;acas, incluyendo las coronarias y valvulares. El tono aut&#243;nomo inadecuado as&#237; como la supuesta etiolog&#237;a, se consideran prevalentes para la mayor&#237;a de las enfermedades card&#237;acas. Se espera por lo tanto, que las v&#225;lvulas est&#233;n muy afectadas por los nervios aut&#243;nomos. Sin embargo, pocas investigaciones se han concentrado en la regulaci&#243;n de las v&#225;lvulas card&#237;acas por el sistema nervioso aut&#243;nomo. Los recientes estudios mostraron que la adici&#243;n de norepinefrina (NE) y acetilcolina (ACH), produjo aumentos dosis dependientes en la contractilidad de la v&#225;lvula mitral y en el relajamiento del tejido de la v&#225;lvula a&#243;rtica, en un modelo <italic>ex vivo</italic>, respectivamente<sup>3,4</sup>. El papel funcional de los neurotransmisores sobre las propiedades mec&#225;nicas del tejido de las c&#250;spides permanece indeterminado. Eso podr&#237;a ser vital, considerando que la v&#225;lvula se somete a elevados esfuerzos mec&#225;nicos en cada ciclo card&#237;aco. La compresi&#243;n de las propiedades mec&#225;nicas valvulares es crucial para el abordaje de una enfermedad valvular card&#237;aca cada vez m&#225;s prevalente, principalmente cuando se considera el aumento de la expectativa de vida en la poblaci&#243;n en general y la mejor&#237;a en la supervivencia a largo plazo de pacientes con enfermedad valvular card&#237;aca, sometidos a la cirug&#237;a de sustituci&#243;n de v&#225;lvula card&#237;aca alog&#233;nica. Este estudio se centr&#243;, principalmente, en las v&#225;lvulas mitrales, porque de las cuatro v&#225;lvulas card&#237;acas, la mitral es la que m&#225;s a menudo sufre afectaci&#243;n en los procesos patol&#243;gicos que requieren intervenci&#243;n quir&#250;rgica. </p>
      <p>Nuestra hip&#243;tesis se basa en que, bajo condiciones fisiol&#243;gicas, la rigidez del tejido de la v&#225;lvula mitral (m&#243;dulo de elasticidad), var&#237;a en respuesta a agentes nerviosos aut&#243;nomos a trav&#233;s del endotelio valvular y respectivos receptores, por ende, el tono de la capa y la funci&#243;n de la v&#225;lvula se modulan. Los objetivos del estudio son evaluar las alteraciones neurotransmisoras dependientes en las propiedades mec&#225;nicas de la v&#225;lvula mitral. </p>
      <p>
        <bold>M&#233;todos</bold>
      </p>
      <p>
        <bold>Aislamiento del tejido</bold>
      </p>
      <p>Corazones porcinos (20 a 24 meses de edad) que fueron obtenidos de un matadero (FuXing Meats, Xangai, China). Las c&#250;spides mitrales (capa anterior o posterior, randomicamente), sin evidencias visible de lesiones, fueron colocadas inmediatamente en una soluci&#243;n tamp&#243;n fr&#237;o de Krebs y analizadas en un m&#225;ximo de 24 horas despu&#233;s del sacrificio de los animales. Las muestras fueron inicialmente preparadas, eliminado todas las cuerdas tend&#237;neas y divididas en tiras rectangulares id&#233;nticas de 15 x 10 mm del vientre de cada c&#250;spide en direcci&#243;n radial y circunferencial. La direcci&#243;n circunferencial se defini&#243; como siendo la paralela al borde libre, y la direcci&#243;n radial, como la del borde libre a la membrana basal de la v&#225;lvula mitral. Las tiras radiales y circunferenciales se analizaron por separado. Los cortes fueron designados para diferentes grupos de acuerdo con los neurotransmisores utilizados al acaso: norepinefrina (NE) (10<sup>-7</sup>-10<sup>-4 </sup>M; n = 10; SIGMA), acetilcolina (ACH) (10<sup>-6</sup>-10<sup>-4 </sup>M; n = 10; SIGMA) y Controles normales (n = 10). Para identificar la localizaci&#243;n y el mecanismo de los neuroagentes involucrados en la rigidez, se usaron tiras sometidas a la denudaci&#243;n endotelial obtenidas mec&#225;nicamente con la utilizaci&#243;n de un raspador celular, (grupo con denudaci&#243;n endotelial, n = 10). Cada corte de tejido se expuso solamente a un solo neurotransmisor para evitar interacciones entre los diversos agentes y la soluci&#243;n seriada fue sustituida por una nueva cada vez, con el fin de garantizar la concentraci&#243;n. Los procedimientos con animales y su cuidado fueron aprobados por el Comit&#233; de Cuidados y Uso de Animales de la Facultad de Medicina de Shanghai Jiao Tong University. </p>
      <p>
        <bold>Papel de los receptores de los neurotransmisores</bold>
      </p>
      <p>Con el fin de evaluar el aporte de los receptores de los neurotransmisores en los cambios de las propiedades mec&#225;nicas de los tejidos, las tiras se preincubaron durante 1 hora con fentolamina (FENT, un inhibidor no selectivo &#945;-adrenoceptor, SIGMA), prazosina (Praz, un inhibidor selectivo &#945;1-adrenoceptor, SIGMA), metoprolol (Metop, un inhibidor selectivo &#946;1-adrenoceptor, SIGMA), propranolol (Propr, un inhibidor no selectivo &#946;-adrenoceptor, SIGMA) y atropina (Atrop, un inhibidor del receptor colin&#233;rgico M, SIGMA) antes del test.</p>
      <p>
        <bold>Protocolo experimental</bold>
      </p>
      <p>Despu&#233;s de ser presellados en las dos extremidades con grapas de acero inoxidable y forrados con papel abrasivo, las muestras se pusieron encima de un dispositivo de test mec&#225;nico modificado (modelo 8511; Instron, Canton, Mass) en un ba&#241;o de soluci&#243;n de Krebs a 37&#186; C siendo continuamente sometidas a un 95% O<sub>2</sub> y a un 5% de CO<sub>2</sub>. El pH de las soluciones se estabiliz&#243; entre 7,35 y 7,45. Los transductores de fuerza para la medida de la tensi&#243;n se conectaron a lo largo de los ejes para monitorizar, en tiempo real, las alteraciones de la tensi&#243;n en las direcciones radial y circunferencial, respectivamente.</p>
      <p>
        <bold>Medidas de rigidez tisular (m&#243;dulo de elasticidad) </bold>
      </p>
      <p>Las presillas se colocaron inicialmente 1 a 2 cm m&#225;s pr&#243;ximas para arrugar ligeramente el tejido y asegurar la ausencia de la precarga. Las muestras fueron preacondicionadas por carga y descarga continuas a 4 mm/s a una carga predeterminada (entre 200 y 400 g), a 20 ciclos para permitir que la respuesta de tensi&#243;n-deformaci&#243;n de la v&#225;lvula pudiese repetirse. Otros tres ciclos de medidas de tensi&#243;n deformaci&#243;n se registraron para los ejes radial y circunferencial (grupo basal). El tejido se someti&#243; a concentraciones progresivamente m&#225;s altas de neurotransmisores y sus respectivos bloqueantes de receptor. Tres ciclos adicionales de tensi&#243;n versus deformaci&#243;n fueron registrados (grupo de tratamiento). Cada muestra sirvi&#243; como su propio control y fue utilizada solamente una vez. La rigidez de las muestras se calcul&#243; a partir del gradiente de la porci&#243;n lineal de la curva de tensi&#243;n-deformaci&#243;n (<xref ref-type="fig" rid="es_a06fig01m-body2">Fig.1</xref>). En ese manuscrito, los t&#233;rminos rigidez, m&#243;dulo y m&#243;dulo de elasticidad, se usan de forma intercambiable. </p>
      <p content-type="asset">
        <fig id="es_a06fig01m-body2">
          <graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf01-es.jpg"/></fig>
      </p>
      <p>
        <bold>An&#225;lisis de los datos</bold>
      </p>
      <p>Los datos se expresan en promedio &#177; DP. Las comparaciones de las propiedades mec&#225;nicas entre tejidos normales y tratados se hicieron a trav&#233;s del test <italic>t</italic> de Student bilateral para dos muestras independientes o test ANOVA one-way para grupos m&#250;ltiples. Todos los valores de p &lt; 0,05 se consideraron significativos. Los an&#225;lisis estad&#237;sticos se hicieron mediante el <italic>software</italic> SPSS versi&#243;n 13.0 (SPSS Institute).</p>
      <p>
        <bold>Resultados</bold>
      </p>
      <p>
        <bold>Datos basales de rigidez en los dos ejes.</bold>
      </p>
      <p>La rigidez basal fue evaluada en los grupos iniciales: controles normales y capas despu&#233;s de la denudaci&#243;n endotelial. La rigidez en los controles no se vio afectada por la denudaci&#243;n (Control <italic>vs</italic> Denudaci&#243;n; Circunferencial: 5,08 &#177; 0,41 <italic>vs</italic> 4,71 &#177; 0,64, p &gt; 0,05; Radial: 2,40 &#177; 0,10 <italic>vs</italic> 2,18 &#177; 0,41, p &gt; 0,05). Adem&#225;s, no hubo diferencia significativa entre los ejes radial y circunferencial dentro del grupo de acuerdo con la anisotrop&#237;a de ese tejido (Circunferencial <italic>vs</italic> Radial; Control: 5,08 &#177; 0,41 <italic>vs</italic> 2,40 &#177; 0,10, p &lt; 0,05; Denudaci&#243;n: 4.71 &#177; 0.64 <italic>vs</italic> 2.18 &#177; 0.41, p &lt; 0.05). Ver <xref ref-type="table" rid="tab01-body2">Tabla 1</xref>.</p>
      <table-wrap id="tab01-body2">
        <graphic xlink:href="1678-4170-abc-98-04-0321-00006-gt01-es.jpg"/></table-wrap>
      <p>
        <bold>Regulaci&#243;n simp&#225;tica de la alteraci&#243;n en la rigidez tisular</bold>
      </p>
      <p>Cuando se sometieron a la NE en una concentraci&#243;n de gradiente, las v&#225;lvulas presentaron un aumento en la rigidez de forma concentraci&#243;n dependiente (<xref ref-type="fig" rid="es_a06fig02-body2">Fig. 2A</xref>). La NE aument&#243; la rigidez valvular con un aumento de 10 veces en la concentraci&#243;n (10<sup>-6</sup><italic>vs</italic> 10<sup>-7</sup>: Circunferencial: 6,15 &#177; 0,78 <italic>vs</italic> 5,34 &#177; 0,23, Radial: 3,28 &#177; 0,74 <italic>vs</italic> 2,64 &#177; 0,39, p &lt; 0,05; 10<sup>-5</sup><italic>vs</italic> 10<sup>-6</sup>: Circunferencial: 7.03 &#177; 0.51 <italic>vs</italic> 6.15 &#177; 0.78, Radial: 4.32 &#177; 0.99 <italic>vs</italic> 3.28 &#177; 0.74, p &lt; 0,05), alcanzando la meseta y concentraci&#243;n efecto al final (10<sup>-4</sup><italic>vs</italic> 10<sup>-5</sup>, p &gt; 0,05).</p>
      <p content-type="html"><fig id="es_a06fig02-body2"><graphic xlink:href="https://minio.scielo.br/documentstore/1678-4170/frqNCdKgppcwkZ5LsHNXMyw/efb7e9a9a334632c8b50c8e0bfede1a532a0406f.jpg"/><graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf02-es.jpg"/></fig>&#13;
&#160;&#13;
</p>
      <p>Pero la denudaci&#243;n endotelial redujo la capacidad de la NE al aumentar la rigidez (<xref ref-type="fig" rid="en_a06fig02-body2">Fig. 2B</xref>), manteniendo la NE de alta dosis (10<sup>-5</sup>) significativa, cuando fue comparada con los grupos de menor dosis (10<sup>-5</sup><italic>vs</italic> 10<sup>-6</sup>: Circunferencial: 6,20 &#177; 0,67 <italic>vs</italic> 5,37 &#177; 0,35, Radial: 3,24 &#177; 0,66 <italic>vs</italic> 2,59 &#177; 0,55, p &lt; 0,05) con el efecto meseta sin alteraciones. </p>
      <p content-type="html"><fig id="en_a06fig02-body2"><graphic xlink:href="https://minio.scielo.br/documentstore/1678-4170/frqNCdKgppcwkZ5LsHNXMyw/745d3698bd87b76d36c4c7bf2ae100f197196cf6.jpg"/><graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf03-es.jpg"/></fig>&#13;
&#160;&#13;
</p>
      <p>A semejanza de lo anterior, cuando la FENT estaba presente en el ba&#241;o del &#243;rgano, hab&#237;a una tendencia a la disminuci&#243;n de la rigidez de la c&#250;spide despu&#233;s de la adici&#243;n de NE de respuesta m&#225;xima (FENT <italic>vs</italic> 10<sup>-5</sup>; Circunferencial: 5,96 &#177; 1,06 <italic>vs</italic> 7,03 &#177; 0,51, Radial: 3,14 &#177; 0,64 <italic>vs</italic> 4,32 &#177; 0,99, p &lt; 0,05), que era significativa en comparaci&#243;n con los Controles (FENT <italic>vs</italic> control; Circunferencial: 5,96 &#177; 1,06 <italic>vs</italic> 5,08 &#177; 0,41, Radial: 3,14 &#177; 0,64 <italic>vs</italic> 2,40 &#177; 0,10, p &lt; 0,05), ver <xref ref-type="fig" rid="es_a06fig03-body2">Figura 3A</xref>. Pero esa respuesta no se dio en presencia de Praz o FENT, aisladamente. </p>
      <p content-type="html"><fig id="es_a06fig03-body2"><graphic xlink:href="https://minio.scielo.br/documentstore/1678-4170/frqNCdKgppcwkZ5LsHNXMyw/26c91ed40f4503044435484689b9d92c0c4901c2.jpg"/><graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf04-es.jpg"/></fig>&#13;
&#160;&#13;
</p>
      <p>Finalmente, y despu&#233;s de la incubaci&#243;n de las c&#250;spides con Metop, la adici&#243;n de NE trajo una diferencia significativa para la rigidez de la c&#250;spide en comparaci&#243;n con NE aisladamente (Metop <italic>vs</italic> NE; Circunferencial: 5,67 &#177; 0,73 <italic>vs</italic> 7,03 &#177; 0,51, Radial: 3,09 &#177; 0,68 <italic>vs</italic> 4,32 &#177; 0,99, p &lt; 0,05). Sin embargo, comparaciones directas de alteraciones posteriores a Metop y NE <italic>versus</italic> controles, todav&#237;a permanec&#237;an estad&#237;sticamente significativas (p &lt; 0,05). Ver <xref ref-type="fig" rid="es_a06fig03-body2">Figura 3B</xref>. La rigidez no se afect&#243; por la adici&#243;n aislada de Propr o Metop. </p>
      <p>
        <bold>Aporte vagal para rigidez tisular</bold>
      </p>
      <p>La rigidez de las c&#250;spides mitrales disminuy&#243; significativamente en respuesta al aumento de las concentraciones de ACH (significativa alteraci&#243;n en rigidez por aumento de 10 veces en la concentraci&#243;n de ACH, 10<sup>-5</sup><italic>vs</italic> 10<sup>-6</sup>; Circunferencial: 3,40 &#177; 1,10 <italic>vs</italic> 4,35 &#177; 0,76, Radial: 1,05 &#177; 0,38 <italic>vs</italic> 1,80 &#177; 0,79, p &lt; 0,05). El grupo con la escala m&#225;s baja (10<sup>-6</sup> mol/l), todav&#237;a mostraba un efecto significativo en la disminuci&#243;n del m&#243;dulo cuando se le compar&#243; con los Controles (Circunferencial: 4,35 &#177; 0,76 <italic>vs</italic> 5,08 &#177; 0,41, Radial: 1,80 &#177; 0,79 <italic>vs</italic> 2,40 &#177; 0,10, p &lt; 0,05 <italic>vs</italic> control), con el efecto meseta en la concentraci&#243;n de 10<sup>-5 </sup>mol/l (10<sup>-5</sup><italic>vs</italic> 10<sup>-4</sup>, p &gt; 0,05). Ver <xref ref-type="fig" rid="es_a06fig04m-body2">Figura 4</xref>. </p>
      <p content-type="asset">
        <fig id="es_a06fig04m-body2">
          <graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf05-es.jpg"/></fig>
      </p>
      <p>Cuando las muestras de las v&#225;lvulas se preincubaron en Atrop o sufrieron una denudaci&#243;n endotelial por medios mec&#225;nicos, la respuesta a la ACHO fue completamente revocada (p &gt; 0,05 <italic>vs</italic> control) (<xref ref-type="fig" rid="es_a06fig05m-body2">Figura 5</xref>).</p>
      <p content-type="asset">
        <fig id="es_a06fig05m-body2">
          <graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf06-es.jpg"/></fig>
      </p>
      <p>
        <bold>Discusi&#243;n</bold>
      </p>
      <p>Nos esforzamos al m&#225;ximo para crear un ambiente interno casi natural, en el cual se encuentra la v&#225;lvula mitral, y que est&#225; intermediado por el sistema nervioso aut&#243;nomo (SNA). Los principales hallazgos de este estudio son los siguientes: bajo condiciones fisiol&#243;gicas, los nervios aut&#243;nomos (simp&#225;tico y vago), modulan de forma significativa las propiedades mec&#225;nicas de las c&#250;spides mitrales porcinas, a trav&#233;s de neurotransmisores liberados por las extremidades nerviosas. La rigidez de las v&#225;lvulas mitrales estaba significativamente reducida como respuesta al aumento de las concentraciones de ACH de forma concentraci&#243;n dependiente y al contrario, elevada por la NE de forma dosis dependiente. Al mismo tiempo, observamos que el endotelio valvular, &#945;/&#946; adrenoceptor y el receptor colin&#233;rgico, ten&#237;an un papel fundamental en la regulaci&#243;n de las propiedades mec&#225;nicas.</p>
      <p>Se ha propuesto que las disfunciones del sistema nervioso aut&#243;nomo prevalecen en su gran mayor&#237;a en los pacientes con enfermedades card&#237;acas. Esa propuesta se basa, de manera general, en los resultados de diversos estudios de variabilidad de frecuencia card&#237;aca y en algunos s&#237;ntomas de disautonom&#237;a, tales como s&#237;ncope reflejo, ansiedad, sufrimiento psicol&#243;gico, palpitaciones y otros. Foi observado que as v&#225;lvulas mitrales s&#227;o moduladas pelo SNA em relaci&#243;n &#224; funci&#243;n e responderam ativamente, diferentemente de los folhetos passivos propelidos apenas pela press&#227;o transvalvular.</p>
      <p>Sin embargo, se conocen pocos detalles del proceso, por tanto, ese estudio fue realizado con el objetivo de identificar el papel de los nervios aut&#243;nomos en la regulaci&#243;n de las propiedades mec&#225;nicas de la v&#225;lvula mitral porcina. </p>
      <p>La extremidad nerviosa auton&#243;mica libera varias sustancias bioactivas <italic>in vivo</italic>, especialmente NE y ACH, ejerciendo reacciones muy complicadas en el tejido y el &#243;rgano objetivo. Adem&#225;s, la ACH es un relajante celular del m&#250;sculo liso espec&#237;fico en tejido valvular y los receptores muscar&#237;nicos de la ACH (M2) han sido considerados como funcionales, mientras que los otros subtipos aparentemente no tienen un efecto fisiol&#243;gico<sup>5</sup>. Se ha demostrado que la ACH induce al relajamiento del tejido valvular a&#243;rtico en un modelo <italic>ex vivo</italic><sup>4</sup>. En nuestro estudio, el uso de ACH ex&#243;gena sirvi&#243; para demostrar el efecto de ese p&#233;ptido en la evaluaci&#243;n de su capacidad sobre la rigidez valvular mitral. Se observ&#243; que bajo las presentes condiciones experimentales, la ACH reduce la rigidez de forma concentraci&#243;n dependiente como se esperaba. Adem&#225;s, parece que la ACH puede inducir al relajamiento del tejido de la v&#225;lvula mitral, resultando en una rigidez disminuida a trav&#233;s del M2, como qued&#243; demostrado despu&#233;s de la adici&#243;n de Atrop, cuando las respuestas de la ACH fueron completamente revocadas. Para entender espec&#237;ficamente el efecto de la estimulaci&#243;n de la ACH en las v&#225;lvulas, Ohashi et al<sup>6</sup> mostraron que la ACH produc&#237;a una transitoria y sostenible hiperpolarizaci&#243;n de la membrana en el endotelio valvular de la aorta de conejo, y la no continuaci&#243;n de la ACH caus&#243; una despolarizaci&#243;n transitoria. Esos mecanismos contribuyen para la liberaci&#243;n de factores vasoactivos endotelio-dependientes, tales como NO<sup>7,8</sup> en v&#225;lvulas mitrales caninas y porcinas. Ese puede ser uno de los mecanismos de la ACH para mediar la rigidez. La NE puede causar una potente contracci&#243;n de las c&#233;lulas del m&#250;sculo liso, a trav&#233;s de la estimulaci&#243;n espec&#237;fica de subtipos de receptor en la v&#225;lvula a&#243;rtica equina<sup>9,10</sup>. Hay m&#225;s subtipos de adrenoceptores conocidos, que se han encontrados en tejido valvular de coraz&#243;n humano: adrenoceptores &#945;1, &#945;2, &#946;1 and &#946;2<sup>10,11</sup>. Williams TH et al<sup>3 </sup>relataron que v&#225;lvulas mitrales de ratones hab&#237;an mostrado movimientos espont&#225;neos similares a las contracciones, localizados en la capa en s&#237;, e inmediatamente despu&#233;s de haber sido disecado el coraz&#243;n, y que fueron aumentados con la adici&#243;n de NE de forma dosis dependiente. De otra forma, y para examinar las respuestas de las c&#250;spides a los neuromoduladores <italic>ex vivo </italic>y poder determinar los receptores espec&#237;ficos involucrados en la mediaci&#243;n de esos efectos, c&#250;spides de v&#225;lvulas a&#243;rticas porcinas, montadas axialmente en una c&#225;mara de &#243;rganos, se contrajeron de forma significativa en respuesta al aumento de las concentraciones de &#945;-adrenoreceptores agonistas, como lo indica la ausencia de cualquier respuesta despu&#233;s de la adici&#243;n de ioimbina, un &#945;2-adrenoreceptor antagonista. Lo mismo no sucedi&#243; despu&#233;s de la adici&#243;n de la prazosina, un inhibidor de &#945;1-adrenoreceptores en v&#225;lvulas a&#243;rticas equinas<sup>9</sup>. En nuestro experimento, observamos la respuesta valvular a la NE en la rigidez, que puede ser mitigada por el inhibidor no selectivo &#945;-adrenoceptor FENT, no por la prazosina. Esos resultados confirmaron los relatos anteriores y nos sugirieron que el adrenoceptor &#946;1 puede haber tenido un papel en la modulaci&#243;n de la rigidez. Parece que las alteraciones en la rigidez se correlacionaron consistentemente con la respuesta de relajamiento o contracci&#243;n del tejido porcino a los mediadores. De esa forma, obviamente, es probable que el estado del SNA influya en la funci&#243;n a largo plazo y en la flexibilidad de las v&#225;lvulas debido a la rapidez de la abertura y del cierre valvular y disautonom&#237;a, particularmente doen&#231;a card&#237;aca valvular concomitante, parece ser n&#227;o-insignificativa.</p>
      <p>Estudios recientes han indicado que las c&#233;lulas endoteliales de las v&#225;lvulas a&#243;rticas porcinas presentan caracter&#237;sticas celulares y moleculares espec&#237;ficas, que poseen un papel fundamental en la regulaci&#243;n del tono valvular card&#237;aco<sup>12,13</sup>. Ya ha sido relatado que el endotelio valvular ejerc&#237;a su efecto a trav&#233;s de la modulaci&#243;n de la rigidez de la c&#250;spide valvular a&#243;rtica humana respecto de diferentes mediadores: ON y ET-1<sup>14</sup>. A pesar de eso, el papel fisiol&#243;gico del SNA en el endotelio valvular card&#237;aco todav&#237;a no hab&#237;a sido adecuadamente definido. En base a los desenlaces del presente estudio, se observ&#243; aparentemente, que la rigidez alterada por la ACH fue completamente dependiente del endotelio valvular, mientras que la rigidez alterada por la NE fue parcialmente dependiente del endotelio valvular y otros mecanismos pueden estar involucrados. Esas respuestas pueden ser obtenidas por la distribuci&#243;n de los respectivos receptores. Los hallazgos de Pompilio et al<sup>4</sup> en v&#225;lvulas pulmonares y a&#243;rticas porcinas pueden ayudar a apreciar esa reacci&#243;n. El efecto de la ACH, induciendo al relajamiento del tejido de la v&#225;lvula a&#243;rtica, no apareci&#243; cuando el endotelio fue removido mec&#225;nicamente, destacando el papel esencial del endotelio y de los receptores M2 (mencionados anteriormente). Las alteraciones en las propiedades mec&#225;nicas del tejido valvular en respuesta a los diferentes mediadores pueden ser explicados por la presencia de miofibroblastos y c&#233;lulas de m&#250;sculo liso en las v&#225;lvulas humanas<sup>15</sup>. El endotelio valvular porcino por s&#237; mismo, no puede facilitar anat&#243;micamente las poblaciones de c&#233;lulas intersticiales en la rigidez, como queda demostrado por la ausencia de la alteraci&#243;n en la rigidez valvular despu&#233;s de la denudaci&#243;n endotelial por medio mec&#225;nico. Sin embargo, la reacci&#243;n cruzada entre los miofibroblastos intersticiales y endoteliales, y las c&#233;lulas del m&#250;sculo liso fue sugerida por este estudio, cuando observamos que la denudaci&#243;n endotelial redujo la capacidad de la NE en aumentar la rigidez, solamente manteniendo la NE de alta dosis (10<sup>-5</sup>) significativa cuando fue comparada con los grupos de menor dosis. &#201;se puede ser el elemento por medio del cual el endotelio de la v&#225;lvula mitral regula las propiedades mec&#225;nicas de las c&#250;spides de v&#225;lvulas porcinas. Siendo as&#237;, la estructura y la funci&#243;n &#250;nicas de las c&#233;lulas endoteliales valvulares deber&#237;an ser enfatizadas. </p>
      <p>Este es un estudio <italic>ex vivo</italic>, y los valores reales del medio ambiente general, las se&#241;ales neur&#243;crinas, endocrinas y paracrinas pueden diferir de los datos <italic>in vivo</italic>. La configuraci&#243;n experimental aguda no conlleva a una consideraci&#243;n sobre los efectos tr&#243;ficos a largo plazo de esos neurotransmisores, o sobre su capacidad de modular la matriz extracelular en seres humanos<sup>16</sup>. Se hace necesario, por tanto, estudios adicionales para evaluar otros par&#225;metros biol&#243;gicos que est&#233;n involucrados en la respuesta a est&#237;mulos nerviosos aut&#243;nomos, como tambi&#233;n las diferencias de respuesta entre las poblaciones de c&#233;lulas endoteliales e intersticiales. </p>
      <p>
        <bold>Implicaci&#243;n cl&#237;nica </bold>
      </p>
      <p>Es probable que alteraciones en las respuestas mec&#225;nicas de las v&#225;lvulas card&#237;acas con v&#237;as auton&#243;micas nervio dependientes sean significativas para al patofisiolog&#237;a de la enfermedad valvular. Se ha demostrado que los arcos reflejos parasimp&#225;ticos y simp&#225;ticos eran diferentes al envejecer, incluyendo el aumento en los niveles de NE circulante en la l&#237;nea basal y en respuesta al estr&#233;s, disminuci&#243;n en la concentraci&#243;n de catecolamina en el coraz&#243;n de rata envejecido, aumento en la s&#237;ntesis y en la degradaci&#243;n de enzimas para catecolaminas<sup>17</sup>. Hubo un aumento en la prevalencia de la disfunci&#243;n valvular card&#237;aca con el envejecimiento y est&#225;n generalmente asociadas a los cambios en el SNA en las estructuras valvulares y en el sistema circulatorio. Igualmente, biov&#225;lvulas card&#237;acas, consideradas superiores a las mec&#225;nicas con relaci&#243;n al desempe&#241;o hemodin&#225;mico y a la biocompatibilidad (complicaciones tromboemb&#243;licas m&#237;nimas, sin necesidad de anticoagulaci&#243;n), presentan, sin embargo, una durabilidad limitada, resultante de la deterioraci&#243;n y de la disfunci&#243;n valvular desconocidas. De acuerdo con este estudio, el aumento de la prevalencia de disfunci&#243;n valvular con el envejecimiento y la limitada longevidad de la biov&#225;lvula, puede tener una correlaci&#243;n &#237;ntima y significativa con el desequilibrio o con la falta de modulaci&#243;n nerviosa aut&#243;noma. Finalmente, nuevas estrategias diagn&#243;sticas y terap&#233;uticas pueden aparecer como conexiones de v&#237;as anteriormente desconocidas y revelar nuevos objetos de intervenci&#243;n a lo largo de esos circuitos biol&#243;gicos emergentes. </p>
      <p>
        <bold>Conclusiones</bold>
      </p>
      <p>Como conclusi&#243;n, este estudio demostr&#243; que las propiedades mec&#225;nicas de las c&#250;spides de la v&#225;lvula mitral son activamente reguladas a trav&#233;s de v&#237;as auton&#243;micas nervio-dependientes. Los nervios aut&#243;nomos (simp&#225;tico y vago), ejercen sus efectos a trav&#233;s de la modulaci&#243;n de la rigidez de las c&#250;spides por medio de los receptores &#945;2, &#946;1 y M2 en el endotelio de la v&#225;lvula, adem&#225;s de las c&#233;lulas intersticiales. </p>
      <p>Nos satisface saber que esos hallazgos ayudar&#225;n a comprender la patofisiolog&#237;a valvular y a establecer un mapa de las respuestas de adaptaci&#243;n de las propiedades mec&#225;nicas de las v&#225;lvulas para futuras v&#225;lvulas card&#237;acas biol&#243;gicas.</p>
      <p>
        <bold>Potencial Conflicto de Intereses</bold>
      </p>
      <p>Declaro no haber conflicto de intereses pertinentes.</p>
      <p>
        <bold>Fuentes de Financiaci&#243;n</bold>
      </p>
      <p>El presente estudio no tuve fuentes de financiaci&#243;n externas.</p>
      <p>
        <bold>Vinculaci&#243;n Acad&#233;mica</bold>
      </p>
      <p>No hay vinculaci&#243;n de este estudio a programas de postgrado.</p>
      <p>
        <bold>Referencias</bold>
      </p>
    </body>
  </sub-article>
  <sub-article article-type="translation" id="TRen" xml:lang="en">
    <front-stub>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Original Articles</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title xml:lang="en">Autonomic regulation of mechanical properties in porcine mitral valve cusps</article-title>
      </title-group>
      <abstract xml:lang="en">
        <p>BACKGROUND: The presence of nerves in heart valves was first depicted decades ago and identified into subpopulations: sympathetic, parasympathetic. So valves are expected to be greatly affected by the autonomic nerves. However, few studies have focused on the regulation of heart valves by the autonomic nervous system. OBJECTIVE: We sought to identify the role of the autonomic nervous system in the regulation of the mechanical properties of porcine mitral valve tissues. METHODS: Mechanical properties of porcine mitral valve leaflets were evaluated in response to norepinephrine (NE) and acetylcholine (ACH), the main neurotransmitters. At the same time, phentolamine (Phent), metoprolol (Metop), atropine (Atrop) and endothelial denudation were added to the reactive system. RESULTS: Under physiological conditions, the stiffness was not affected by endothelial denudation (p &gt; 0.05). NE elevated the valve stiffness significantly per 10-fold increase in concentration (10-6 vs 10-7, p &lt; 0.05; 10-5 vs 10-6, p &lt; 0.05). This response was mitigated by Phent, Metop or endothelial denudation (p &lt; 0.05), however, it was still increased significantly when compared to Controls (p &lt; 0.05). ACH caused a decrease in stiffness accompanied by an increase in its concentration (significant change in stiffness per 10-fold increase in ACH concentration, 10-6 vs Control, p &lt; 0.05; 10-5 vs 10-6, p &lt; 0.05), which were reversed by endothelial denudation and Atrop (p &gt; 0.05 vs Control). CONCLUSION: These findings highlight the role of the autonomic nervous system in the regulation of the mechanical properties of porcine mitral valve cusps, which underline the importance of autonomic nervous status for optimal valve function.</p>
      </abstract>
      <kwd-group xml:lang="en">
        <kwd>Mitral valve</kwd>
        <kwd>autonomic pathways</kwd>
        <kwd>bioprosthesis</kwd>
        <kwd>autonomic nervous system</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <bold>ORIGINAL ARTICLE</bold>
      </p>
      <p>
        <fn id="enda-body3">
          <label>
            <bold>Autonomic regulation of mechanical properties in porcine mitral valve cusps</bold>
          </label>
          <p>
            <bold>Xiang Hu; Qiang Zhao; Xiaofeng Ye</bold>
          </p>
        </fn>
      </p>
      <p>Department of Cardiac Surgery, Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, PRC</p>
      <p>Mailing Address</p>
      <p>
        <bold>ABSTRACT</bold>
      </p>
      <p><bold>Background:</bold> The presence of nerves in heart valves was first depicted decades ago and identified into subpopulations: sympathetic, parasympathetic. The autonomic nerve is expected to greatly affect heart valves. However, regarding the aspect of mechanical properties regulated by nerves, very little focus has been placed on that.</p>
      <p><bold>OBJECTIVE:</bold> We sought to identify the role of the autonomic nervous system in the regulation of the mechanical properties of porcine mitral valve tissues.</p>
      <p><bold>METHODS:</bold> Mechanical properties of porcine mitral valve leaflets were evaluated in response to norepinephrine (NE) and acetylcholine (ACH), the main neurotransmitters. At the same time, phentolamine (Phent), metoprolol (Metop), atropine (Atrop) and endothelial denudation were added to the reactive system.</p>
      <p><bold>RESULTS:</bold> Under physiological conditions, the stiffness was not affected by endothelial denudation (p &gt; 0.05). NE elevated the valve stiffness significantly per 10-fold increase in concentration (10<sup>-6</sup><italic>vs</italic> 10<sup>-7</sup>, p &lt; 0.05; 10<sup>-5</sup><italic>vs</italic> 10<sup>-6</sup>, p &lt; 0.05). The stiffness elevated by NE was mitigated by Phent and Metop addition or endothelial denudation (p &lt; 0.05). However, the stiffness remained significant when compared to Control (p &lt; 0.05). ACH caused a decrease in stiffness accompanied by an increase in its concentration (significant change in stiffness per 10-fold increase in ACH concentration, 10<sup>-6</sup><italic>vs</italic> Control, p &lt; 0.05; 10<sup>-5</sup><italic>vs</italic> 10<sup>-6</sup>, p &lt; 0.05), which were reversed by endothelial denudation and Atrop (p &gt; 0.05 <italic>vs</italic> Control).</p>
      <p><bold>CONCLUSION:</bold> These findings highlight the role of the autonomic nervous system in the regulation of the mechanical properties of porcine mitral valve cusps, which underline the importance of autonomic nervous status for optimal valve function. </p>
      <p><bold>Keywords:</bold> Mitral valve; autonomic pathways; bioprosthesis; autonomic nervous system.</p>
      <p>
        <bold>Introduction</bold>
      </p>
      <p>Heart valve function is quite complicated, as the passive movements of valve do not account for its ability to adapt to the hemodynamic and humoral milieu. This is exemplified by the presence of nerves in heart valves, which was first depicted decades ago and identified into subpopulations: sympathetic, parasympathetic, sensory and cholinergic nerve markers<sup>1,2</sup>. Cardiac arrhythmia is frequently detected in patients with heart diseases, including the coronary-derived and valve-derived ones. Improper autonomic tone, the supposed etiology, is considered prevalent in majority of heart diseases, so valves are expected to be greatly affected by the autonomic nerves. However, very little focus has been given to the regulation of heart valves by the autonomic nervous system. Recent studies have indicated that the addition of norepinephrine (NE) and acetylcholine (ACH) produced dose-dependent increases in mitral valve contractility and aortic valve tissue relaxation in an ex vivo model, respectively<sup>3,4</sup>. The functional role of neurotransmitters in the mechanical properties of cusp tissue remains undetermined. This could be vital, as the valve is subjected to high mechanical forces at each cardiac cycle. Understanding valvular mechanical properties is crucial to address an increasingly prevalent heart valve disease entity, even more so considering the increase in life expectancy of the general population and the improvement in long-term survival of patients with heart valve disease undergoing allogenic valve replacement surgery. This study will focus mainly on mitral valves, considering that, of all four heart valves, the mitral valve is the most commonly affected in disease processes requiring surgical intervention.</p>
      <p>We hypothesize that under physiological conditions, mitral valve tissue stiffness (elastic modulus) varies in response to autonomic nervous agents through the valve endothelium and concerning receptors and accordingly, leaflet tone and valve function are modulated. The aims of the study are to evaluate the neurotransmitter dependent changes in mitral valve mechanical properties.</p>
      <p>
        <bold>Methods</bold>
      </p>
      <p>
        <bold>Tissue isolation</bold>
      </p>
      <p>Porcine hearts (20 to 24 months old) were harvested from a slaughterhouse (FuXing Meats, Shanghai, China). Mitral cusps (anterior or posterior leaflet, randomly), with no visible evidence of lesion, were immersed immediately in ice-cold Krebs buffer and used within 24 hours of the animal's sacrifice. Specimens were prepared by first trimming away all chordae and were divided into identical 15 x 10 mm rectangular strips from the "belly" of each cusp in radial and circumferential directions. The circumferential direction was defined as parallel to the free edge and the radial direction went from the free edge to the basement of mitral valves. Radial and circumferential strips were analyzed separately. Sections were assigned to different groups, according to the neurotransmitters used at random: norepinephrine (NE) (10<sup>-7</sup> - 10<sup>-4 </sup>M; n = 10; SIGMA), acetylcholine (ACH) (10<sup>-6</sup> - 10<sup>-4 </sup>M; n = 10; SIGMA) and normal Controls (n = 10). In order to identify the location and mechanism of the neuroagents involved in stiffness, endothelial-denuded strips, which were mechanically accomplished with a cell scraper, were also employed (denuded group, n = 10). Each tissue section was only exposed to a single neurotransmitter to avoid interactions between various agents and the serial solution was replaced by a new one every time, ensuring the concentration. Procedures involving animals and their care were approved by Animal Care and Use Committee of the Shanghai Jiao Tong University School of Medicine.</p>
      <p>
        <bold>Role of the neurotransmitter receptors</bold>
      </p>
      <p>To evaluate the contribution of the neurotransmitter receptors to changes in tissue mechanical properties, strips were preincubated for 1 hour with phentolamine (Phent, a nonselective &#945; adrenoceptor inhibitor, SIGMA), prazosin (Praz, a selective &#945;1 adrenoceptor inhibitor, SIGMA), metoprolol (Metop, a selective &#946;1 adrenoceptor inhibitor, SIGMA), propranolol (Propr, a nonselective &#946;-adrenoceptor inhibitor, SIGMA), and atropine (Atrop, a M cholinergic receptor inhibitor, SIGMA), before testing.</p>
      <p>
        <bold>Experimental protocol</bold>
      </p>
      <p>Gripped at both ends with 2-piece stainless clamps lined with sandpaper, the specimens were mounted in a modified mechanical testing device (model 8511; Instron, Canton, Mass) in a Krebs bath heated at 37&#186; C and continuously gassed with 95% O<sub>2</sub> and 5% CO<sub>2</sub>. The pH of solutions was stabilized between 7.35 and 7.45. Strain gauge force transducers were attached along long axes to real-time monitor the changes of tension in the radial and circumferential orientations respectively.</p>
      <p>
        <bold>Tissue stiffness (modulus) measurements</bold>
      </p>
      <p>The grips were first placed 1 to 2 mm closer together to slightly wrinkle the tissue and to ensure no preload. The specimens were then preconditioned by continuously loading and unloading at 4 mm/s to a predetermined load (between 200 and 400 g) for 20 cycles, to allow the tension-strain response of the valve to become repeatable. Another three cycles of tension-strain measurements were then recorded for radial and circumferential axes (baseline group). The tissue was then challenged with increasing concentrations of neurotransmitters and some respective receptor blockers. Three more cycles of tension <italic>versus</italic> strain were recorded (treatment group). Each sample served as its own control and was used only once. The stiffness of the specimens was calculated from the gradient of the linear portion of this tension-strain curve (<xref ref-type="fig" rid="en_a06fig01m-body3">Figure 1</xref>). In this manuscript, the terms stiffness, modulus, and elastic modulus are used interchangeably.</p>
      <p content-type="asset">
        <fig id="en_a06fig01m-body3">
          <graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf01-en.jpg"/></fig>
      </p>
      <p>
        <bold>Data analysis</bold>
      </p>
      <p>Data are expressed as mean &#177; SD. Comparisons of mechanical properties between normal and treated tissues were performed by means of a 2-sided Student t test for two independent samples or One-way ANOVA test for multiple groups. All values of p &lt; 0.05 were considered statistically significant. The statistical analyses were performed using SPSS version 13.0 (SPSS Institute).</p>
      <p>
        <bold>Results</bold>
      </p>
      <p>
        <bold>Baseline of stiffness in both axes</bold>
      </p>
      <p>Baseline stiffness was assessed for the initial groups: normal Control and endothelial-denuded leaflets. Endothelial denudation did not affect valve stiffness (Control vs. Denudation; Circumferential: 5.08 &#177; 0.41 <italic>vs</italic> 4.71 &#177; 0.64, p &gt; 0.05; Radial: 2.40 &#177; 0.10 <italic>vs</italic> 2.18 &#177; 0.41, p &gt; 0.05). In addition, there was a significant difference between radial and circumferential axes within group in compliance with with the anisotropy of this tissue (Circumferential <italic>vs</italic> Radial; Control: 5.08 &#177; 0.41 <italic>vs</italic> 2.40 &#177; 0.10, p &lt; 0.05; Denudation: 4.71 &#177; 0.64 <italic>vs</italic> 2.18 &#177; 0.41, p &lt; 0.05). See <xref ref-type="table" rid="tab01-body3">Table 1</xref>.</p>
      <table-wrap id="tab01-body3">
        <graphic xlink:href="1678-4170-abc-98-04-0321-00006-gt01-en.jpg"/></table-wrap>
      <p>
        <bold>Sympathetic regulation of change in tissue stiffness</bold>
      </p>
      <p>When challenged with NE in gradient concentration, the valves presented increasing stiffness in a concentration-dependent manner (<xref ref-type="fig" rid="en_a06fig02-body3">Fig 2A</xref>). NE elevated the valve stiffness statistically per 10-fold increase in concentration (10<sup>-6</sup><italic>vs</italic> 10<sup>-7</sup>: Circumferential: 6.15 &#177; 0.78 <italic>vs</italic> 5.34 &#177; 0.23, Radial: 3.28 &#177; 0.74 <italic>vs</italic> 2.64 &#177; 0.39, p &lt; 0.05; 10<sup>-5</sup><italic>vs</italic> 10<sup>-6</sup>: Circumferential: 7.03 &#177; 0.51 <italic>vs</italic> 6.15 &#177; 0.78, Radial: 4.32 &#177; 0.99 <italic>vs</italic> 3.28 &#177; 0.74, p &lt; 0.05), reaching the concentration-effect plateau in the end (10<sup>-4</sup><italic>vs</italic> 10<sup>-5</sup>, p&gt;0.05).</p>
      <p content-type="html"><fig id="en_a06fig02-body3"><graphic xlink:href="https://minio.scielo.br/documentstore/1678-4170/frqNCdKgppcwkZ5LsHNXMyw/745d3698bd87b76d36c4c7bf2ae100f197196cf6.jpg"/><graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf02-en.jpg"/></fig>&#13;
&#160;&#13;
</p>
      <p>However, endothelium-denudation blunted the ability of NE in increasing stiffness (<xref ref-type="fig" rid="en_a06fig02-body3">Fig 2B</xref>), only maintaining the high-dose NE (10<sup>-5</sup>) significant compared to lower-dose groups (10<sup>-5</sup><italic>vs</italic> 10<sup>-6</sup>: Circumferential: 6.20 &#177; 0.67 <italic>vs</italic> 5.37 &#177; 0.35, Radial: 3.24 &#177; 0.66 <italic>vs</italic> 2.59 &#177; 0.55, p &lt; 0.05) with the plateau effect unchangeable.</p>
      <p>Similarly, when Phent was present in the organ bath, there was a diminishing trend in cusp stiffness after addition of maximal responsive NE (Phent <italic>vs</italic> 10<sup>-5</sup>; Circumferential: 5.96 &#177; 1.06 <italic>vs</italic> 7.03 &#177; 0.51, Radial: 3.14 &#177; 0.64 <italic>vs</italic> 4.32 &#177; 0.99, p &lt; 0.05), still significant compared with Control (Phent <italic>vs</italic> control; Circumferential: 5.96 &#177; 1.06 <italic>vs</italic> 5.08 &#177; 0.41, Radial: 3.14 &#177; 0.64 <italic>vs</italic> 2.40 &#177; 0.10, p &lt; 0.05), see <xref ref-type="fig" rid="en_a06fig03-body3">Fig 3A</xref>. However, this response did not occur in the presence of Praz or Phent alone.</p>
      <p content-type="html"><fig id="en_a06fig03-body3"><graphic xlink:href="https://minio.scielo.br/documentstore/1678-4170/frqNCdKgppcwkZ5LsHNXMyw/65b08b53e712e6d8fcdf987223f18b43c1c99567.jpg"/><graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf03-en.jpg"/></fig>&#13;
&#160;&#13;
</p>
      <p>At last, after incubation of cusps in Metop, addition of NE resulted in a significant difference in cusp stiffness compared to NE alone (Metop <italic>vs</italic> NE; Circumferential: 5.67 &#177; 0.73 <italic>vs</italic> 7.03 &#177; 0.51, Radial: 3.09 &#177; 0.68 <italic>vs</italic> 4.32 &#177; 0.99, p &lt; 0.05). However, direct comparison of changes after Metop and NE versus control was still statistically significant (p &lt; 0.05). See <xref ref-type="fig" rid="en_a06fig03-body3">Fig 3B</xref>. The stiffness was not affected by addition of Propr or Metop alone.</p>
      <p>
        <bold>Vagal contribution to tissue stiffness</bold>
      </p>
      <p>The stiffness of mitral cusps was significantly decreased in response to increasing concentrations of ACH (significant change in stiffness per 10-fold increase in ACH concentration, 10<sup>-5</sup><italic>vs</italic> 10<sup>-6</sup>; Circumferential: 3.40 &#177; 1.10 <italic>vs</italic> 4.35 &#177; 0.76, Radial: 1.05 &#177; 0.38 <italic>vs</italic> 1.80 &#177; 0.79, p &lt; 0.05). The lowest scale group (10<sup>-6</sup> mol/l) still exhibited significant effects in diminishing modulus when compared with Controls (Circumferential: 4.35 &#177; 0.76 <italic>vs</italic> 5.08 &#177; 0.41, Radial: 1.80 &#177; 0.79 <italic>vs</italic> 2.40 &#177; 0.10, p &lt; 0.05 <italic>vs</italic> control), with the plateau effect occurring at the concentration of 10<sup>-5 </sup>mol/l (10<sup>-5</sup><italic>vs</italic> 10<sup>-4</sup>, p &gt; 0.05). See <xref ref-type="fig" rid="en_a06fig04m-body3">Fig 4</xref>.</p>
      <p content-type="asset">
        <fig id="en_a06fig04m-body3">
          <graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf04-en.jpg"/></fig>
      </p>
      <p>When valve specimens were preincubated in Atrop or denuded with mechanical means, the response to ACH was abrogated completely (p &gt; 0.05 <italic>vs</italic> control). See <xref ref-type="fig" rid="en_a06fig05m-body3">Fig 5</xref>.</p>
      <p content-type="asset">
        <fig id="en_a06fig05m-body3">
          <graphic xlink:href="1678-4170-abc-98-04-0321-00006-gf05-en.jpg"/></fig>
      </p>
      <p>
        <bold>Discussion</bold>
      </p>
      <p>We strove to create a near-natural internal environment, in which the mitral valve lies and is mediated by the autonomic nervous system. The main findings from this article are, under physiological conditions, the autonomic nerve (sympathetic and vagus) significantly modulates the mechanical properties of porcine mitral cusps through the neurotransmitters released by nervous ends. Stiffness of mitral valves was significantly decreased in response to increasing concentrations of ACH in a concentration-dependent fashion, and diversely, elevated by NE in a dose-effect manner. At the same time, we observed that valvular endothelium, &#945;/&#946;-adrenoceptor and cholinergic receptor played a fundamental role in regulating mechanical properties.</p>
      <p>It has been proposed that autonomic nervous system dysfunction prevails in the vast majority of patients with heart diseases. This proposal is based mostly on the results of diverse heart rate variability studies and some dysautonomic symptoms, such as reflex syncope, anxiety, psychological distress, palpitation and so on. Mitral valves, which are far more than passive leaflets by transvalvular pressure, have been considered to be also regulated by the autonomic nervous system. However, little is known about the details of such process, so this study was performed aiming to identify the role of autonomic nerve in the regulation of porcine mitral valve mechanical properties.</p>
      <p>The autonomic nervous end releases a number of bioactive substances <italic>in vivo</italic>, notably NE and ACH, exerting very complicated reactions on the target tissue and organ. Moreover, ACH is a smooth muscle cell relaxant specific in valve tissue, and muscarinic 2 acetylcholine receptors (M2) have been found to be functional, whereas the other subtypes have no apparent physiological effect<sup>5</sup>. ACH was shown to induce aortic valve tissue relaxation in an <italic>ex vivo</italic> model<sup>4</sup>. In our study, the use of exogenous ACH demonstrated the effect of this peptide by evaluating its effect on the mitral valvular stiffness. It turned out that under the present experimental conditions, ACH decreased the stiffness in a concentration-dependent manner, as expected. In addition, it appears that ACH may induce mitral valve tissue relaxation resulting in stiffness diminished through M2, as evidenced after the addition of Atrop, when responses to ACH were abrogated thoroughly. In order to specifically understand the effect of ACH stimulation on valves, Ohashi et al<sup>6</sup> showed that ACH produced transient and then sustained membrane hyperpolarizations on rabbit aortic valvular endothelium; and ACH withdrawal evoked a transient depolarization. These mechanisms contribute to release of endothelium-dependent vasoactive factors such as NO<sup>7,8</sup> in canine and porcine mitral valves. This may be one of the ACH mechanisms that mediate stiffness. NE can cause a potent contraction of smooth muscle cells through the stimulation of specific receptor subtypes in equine aortic valve<sup>9,10</sup>. There are more known adrenoceptor subtypes, a number of which have been found in human heart valve tissue: &#945;1, &#945;2, &#946;1 and &#946;2 adrenoceptors<sup>10,11</sup>. Williams TH et al<sup>3 </sup>reported that rat mitral valves had been shown to display spontaneous contraction-like movements localized to the leaflet itself, immediately after being dissected from the heart, which was enhanced by addition of norepinephrine (NE) in a dose-dependent fashion. Otherwisely, in an effort to examine valve cusps' responses to neuromodulators <italic>ex vivo</italic> and determine the specific receptors involved in mediating these effects, porcine aortic valve cusps, mounted uniaxially in an organ chamber, contracted significantly in response to increasing concentrations of &#945; adrenoreceptor agonists, including norepinephrine. These contractions were specifically mediated by &#945;2-adrenoreceptors as indicated by the absence of any response following the addition of yohimbine, an &#945;2-adrenoreceptor antagonist, but not after addition of prazosin, an inhibitor of &#945;1-adrenoreceptors in equine aortic valves<sup>9</sup>. In our experiment, we observed the valvular response to NE in stiffness, which could be mitigated by the nonselective &#945; adrenoceptor inhibitor Phent, not prazosin. These results all confirmed the reports before and suggested &#946;1 adrenoceptor might take part in the modulation of stiffness. It seemed that changes in elastic modulus consistently correlated with relaxation or contraction responses of the porcine tissue to the mediators. Therefore, obviously the status of the autonomic nervous system is more likely to influence the long-term function and pliability of the valves due to the rapidity of valve opening and closing, and dysautonomia, particularly in concurrent heart valve disease, appears non-negligible.</p>
      <p>Recent studies have indicated that porcine aortic valve endothelial cells have specific cellular and molecular characteristics that play a fundamental role in regulating heart valve tone<sup>12,13</sup>. It was reported that the valve endothelium exerted its effects by modulating human aortic valve cusp stiffness to different mediators: ON and ET-1<sup>14</sup>. Nevertheless, the physiological role of the autonomic nervous system in heart valve endothelium has not been adequately defined. Based on the outcomes of this study, it was apparently observed that the stiffness altered by ACH was completely dependent on the valvular endothelium, whereas the stiffness altered by NE was partially dependent on the valvular endothelium and other mechanisms might be involved. These responses may be elicited by the distribution of the respective receptors. The findings by Pompilio et al<sup>4</sup> on porcine aortic and pulmonary valves may help appreciate this reaction. The effect of ACH, inducing aortic valve tissue relaxation, was absent when the endothelium was mechanically removed, underlining the essential role of the endothelium and M2 receptors (above mentioned). The changes in the mechanical properties of valve tissue in response to different mediators can be explained by the presence of myofibroblasts and smooth muscle cells in the human valves<sup>15</sup>. The porcine valvular endothelium alone cannot anatomically facilitate the interstitial cell populations in modulus, as evidenced by the absence of change in valve stiffness after mechanical denudation of the endothelium. However, the cross-talk between endothelial and interstitial myofibroblasts and smooth muscle cells was suggested by this study, seen from the observation that endothelium-denudation blunted the ability of NE in increasing modulus, only preserving the high-dose NE (10<sup>-5</sup>) significant compared to lower-dose groups. This may be the means by which the mitral valve endothelium regulates the mechanical properties of porcine valve cusps. Therefore, the unique structure and function of valve endothelial cells should be highlighted.</p>
      <p>This is an <italic>ex vivo</italic> study, and actual values of the overall environment: endocrine, paracrine and neurocrine signals may differ from those <italic>in vivo</italic>. The acute experimental setup does not account for the long-term trophic effects of these neurotransmitters or their ability to modulate the extracellular matrix in human beings<sup>16</sup>. Further studies are required to evaluate any other biological parameters involved in response to autonomic nervous stimuli, as well as the responsive differences between endothelial cells from interstitial cell populations.</p>
      <p>
        <bold>Clinical implication</bold>
      </p>
      <p>Changes in heart valves mechanical responses with autonomic nervous-dependent pathways are likely to be significant in the pathophysiology of valve disease. It has been shown that parasympathetic and sympathetic reflex arcs differed with aging, including increased circulating norepinephrine levels at baseline and in response to stress, decreased catecholamine concentration in senescent rat heart, increased synthesizing and degrading enzymes for catecholamines<sup>17</sup>. Heart valve dysfunctions show increased prevalence with age and are generally supposed to accompany autonomic nervous changes both in valve structures and circulation system. Similarly, tissue-engineered heart valves, considered to be superior to mechanical valve with regard to hemodynamic performance and biocompatibility (minimal thromboembolic complications, no anticoagulation required), have limited durability, however, resulting from degeneration and unknown valve dysfunction. According to this study, the increasing prevalence of valve dysfunction with age and the limited longevity of tissue-engineered valves may have a close and significant correlation with imbalance or lack of autonomic nervous modulation. At last, novel diagnostic and therapeutic strategies may emerge as previously unrecognized pathway links unmasking new targets of intervention along these emerging biologic circuits.</p>
      <p>
        <bold>Conclusions</bold>
      </p>
      <p>In conclusion, this study has shown that the mechanical properties of mitral valve cusps are actively regulated through autonomic nervous-dependent pathways. The autonomic nerve (sympathetic and vagus) exerts its effects by modulating the stiffness of the cusps through &#945;2, &#946;1 and M2 receptors in the valve endothelium, in addition to interstitial cells. We are grateful that these findings will help to understand valve pathophysiology and establish a blueprint of adaptive responses of valve mechanical properties for future tissue-engineered heart valves.</p>
      <p>
        <bold>Potential Conflict of Interest</bold>
      </p>
      <p>No potential conflict of interest relevant to this article was reported.</p>
      <p>
        <bold>Sources of Funding</bold>
      </p>
      <p>There were no external funding sources for this study.</p>
      <p>
        <bold>Study Association</bold>
      </p>
      <p>This study is not associated with any post-graduation program.</p>
      <p>
        <bold>References</bold>
      </p>
    </body>
  </sub-article>
</article>
