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  2. Keyword: Models, Animal
ABCIC
Original Article

Standard Echocardiography, Strain and Strain Rate by Two-Dimensional Speckle Tracking in Capuchin Monkey (Cebus Apella, Linnaeus, 1758)

Laecio da Silva Moura et al. Renan Paraguassú de Sá Rodrigues Andrezza Braga Soares da Silva Gerson Tavares Pessoa … Francisco das Chagas Araújo Sousa Jacyara de Jesus Rosa Pereira Alves Luiz Bezerra Neto Kassio Vieira Macedo Marcelo Campos Vieira Flávio Ribeiro Alves

Abstract

Introduction

The capuchin monkey is a type of nonhuman primate that has shown great potential for preclinical studies because of its anatomical and physiological similarities to humans.

Objective

To study the indices of myocardial deformation in anesthetized capuchin monkeys using speckle tracking.

Methods

Sixteen animals from the Zoobotanical Park, Teresina, Piauí, Brazil, were used and chemically restrained using a combination of ketamine and midazolam. Echocardiography recordings were obtained in B, M and Doppler modes, and strain and strain rate were measured using speckle tracking.

Results

The variables that showed statistically significant correlation coefficients in relation to weight were LVFWd, LVIDd, LVIDs, E wave, A’RV, MAM and TAPSE. HR showed a positive correlation with the E wave and A wave and a negative correlation with IVRT. FS presented a positive correlation with the E/A wave relationship (r = 0.61). TAPSE showed positive correlations with E’RV and A’RV. The values obtained for circumferential (-18.17 ± 4.68%), radial (47.13 ± 5.24%) and longitudinal (- 26.46 ± 5.15%) strain for the capuchin monkeys were within the normal ranges for males and females.

Conclusion

The present study provides the first reference values for echocardiographic measurements in B, M and Doppler modes for capuchin monkeys anesthetized with ketamine and midazolam. The strain and strain rate values obtained using speckle tracking showed similarities with those obtained in humans, suggesting that this tool has the potential to be exploited in preclinical studies using the capuchin monkey model. (Arq Bras Cardiol: Imagem cardiovasc. 2018;31(1):4-13)

  • Echocardiography/standards
  • Models, Animal
  • Myocardial Contraction
  • Myocardial/abnormalities
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Creative Commons Attribution (CC BY) Creative Commons license
20/01/2022 DOI: 10.5935/2318-8219.20180004 Views 1
Figure 1
ABC
Original Article

Atorvastatin Reduces Accumulation of Vascular Smooth Muscle Cells to Inhibit Intimal Hyperplasia via p38 MAPK Pathway Inhibition in a Rat Model of Vein Graft

Tianshu Chu et al. Molin Huang Zhiwei Zhao Fei Ling … Jing Cao Jianjun Ge

Abstract

Background:

The rate of saphenous vein graft failure one year after coronary artery bypass grafting ranges from 10% to 25%. The aim of this study was to explore whether atorvastatin can reduce accumulation of vascular smooth muscle cells to inhibit intimal hyperplasia via p38 MAPK pathway inhibition.

Methods:

Forty-five Sprague-Dawley rats were randomized to three groups. Thirty rats received a vein graft operation, and they were randomized to be treated with vehicle or atorvastatin; fifteen rats received a sham operation. We detected intimal hyperplasia by hematoxylin-eosin staining and related protein expression by immunohistochemical and Western blot analysis. Comparisons were analyzed by single-factor analysis of variance and Fisher’s least significant difference test, with p < 0.05 considered significant.

Results:

The intima analyzed by hematoxylin-eosin staining was dramatically thicker in the control group than in the atorvastatin group and sham group (p < 0.01). The outcomes of immunohistochemical staining of α-SMA demonstrated that the percentage of α-SMA-positive cells in the control group was higher than in the atorvastatin group (p < 0.01). We also evaluated α-SMA, PCNA, p38 MAPK, and phosphorylation of p38 MAPK after statin treatment by Western blot analysis, and the results indicated that atorvastatin did not lead to p38 MAPK reduction (p < 0.05); it did, however, result in inhibition of p38 MAPK phosphorylation (p < 0.01), and it significantly reduced α-SMA and PCNA levels, in comparison with the control group (p < 0.01).

Conclusion:

We have demonstrated that atorvastatin can inhibit accumulation of vascular smooth muscle cells by inhibiting the p38 MAPK pathway, and it is capable of inhibiting intimal hyperplasia in a rat vein graft model.

  • Atorvastatin
  • Hyperplasia
  • Mitogen Activated Protein Kinases
  • Models, Animal
  • Myocardial Revascularization, Rats
  • Myocytes Smooth Muscle
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Creative Commons Attribution (CC BY) Creative Commons license
23/10/2020 DOI: 10.36660/abc.20190231 Views 1
ABC
Editorial

Influence of Atorvastatin on Intimal Hyperplasia in the Experimental Model

Mariana Gatto et al. Luana Urbano Pagan Gustavo Augusto Ferreira Mota

Despite the significant advance in cardiovascular biomedicine in recent years, which provided a better understanding of the pathophysiology of coronary artery disease (CAD) as well as its prevention and treatment, this disease is still responsible for considerable mortality.

The CAD results from the pathological accumulation of atherosclerotic plaques in the coronary arteries that can lead to their occlusion and ischemia of the cardiac tissue. Among the treatments used for CAD, stands out the venous graft (VG), a type of surgical intervention for coronary artery bypass grafting. However, in the long term, there is a high rate of obstruction of VG, with expansive remodeling and increased deposition of low-density lipoprotein (LDL), which can cause intimal hyperplasia (IH), atherosclerosis and thrombosis., The IH is closely related to restenosis of the VG and begins in response to certain stress, which triggers inflammatory process and consequent endothelial dysfunction with proliferation and migration of vascular smooth muscle cells (VSMC).,

[…]

  • Atorvastatin/prevention and control
  • Coronary Artery Dsease/physiopathology
  • Hyperplasia, Rats
  • Models, Animal
  • Muscle, Smooth, Vascular
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Creative Commons Attribution (CC BY) Creative Commons license
23/10/2020 DOI: 10.36660/abc.20200518
Experimental cardiac arrest treatment with adrenaline, vasopressin, or placebo
ABC
Artigo Original

Experimental cardiac arrest treatment with adrenaline, vasopressin, or placebo

Manoel Ângelo Gomes Palácio et al. Edison Ferreira de Paiva Luciano Cesar Pontes de Azevedo Ari Timerman

BACKGROUND: The effect of vasoconstrictors in prolonged cardiopulmonary resuscitation (CPR) has not been fully clarified. OBJECTIVES: To evaluate adrenaline and vasopressin pressure effect, and observe the return of spontaneous circulation (ROSC). METHODS: A prospective, randomized, blinded, and placebo-controlled study. After seven minutes of untreated ventricular fibrillation, pigs received two minutes cycles of CPR. Defibrillation was attempted (4 J/kg) once at 9 minutes, and after every cycle if a shockable rhythm was present, after what CPR was immediately resumed. At 9 minutes and every five minutes intervals, 0.02 mg/kg (n = 12 pigs) adrenaline, or 0.4 U/kg (n = 12) vasopressin, or 0.2 mL/kg (n = 8) 0.9% saline solution was administered. CPR continued for 30 minutes or until the ROSC. RESULTS: Coronary perfusion pressure increased to about 20 mmHg in the three groups. Following vasoconstrictors doses, pressure level reached 35 mmHg versus 15 mmHg with placebo (p < 0.001). Vasopressin effect remained at 15-20 mmHg after three doses versus zero with adrenaline or placebo. ROSC rate differed (p = 0.031) among adrenaline (10/12), vasopressin (6/12), and placebo (2/8). Time-to-ROSC did not differ (16 minutes), nor the number of doses previously received (one or two). There was no difference between vasoconstrictors, but against placebo, only adrenaline significantly increased the ROSC rate (p = 0.019). CONCLUSION: The vasoconstrictors initial pressure effect was equivalent and vasopressin maintained a late effect at prolonged resuscitation. Nevertheless, when compared with placebo, only adrenaline significantly increased the ROSC rate.

  • Arginine vasopressin
  • Cardiopulmonary Resuscitation
  • Epinephrine
  • Models, Animal
  • Ventricular Fibrillation
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Creative Commons Attribution (CC BY) Creative Commons license
01/11/2013 DOI: 10.5935/abc.20130213 Views 1

How to cite this article

EndNote RIS

Electronic Document Format (Vancouver)

Moura LS, Rodrigues RPS, Silva ABS, Pessoa GT, Sousa FCA, Alves JJRP, Bezerra Neto L, et al. Standard Echocardiography, Strain and Strain Rate by Two-Dimensional Speckle Tracking in Capuchin Monkey (Cebus Apella, Linnaeus, 1758). Arquivos Brasileiros de Cardiologia Imagem cardiovascular 2022;31(1):4-10.

Electronic Document Format (ABNT)

Moura, Laecio da Silva; Rodrigues, Renan Paraguassú de Sá; Silva, Andrezza Braga Soares da; Pessoa, Gerson Tavares; Sousa, Francisco das Chagas Araújo; Alves, Jacyara de Jesus Rosa Pereira; Bezerra Neto, Luiz; Macedo, Kassio Vieira; Vieira, Marcelo Campos; Alves, Flávio Ribeiro. Standard Echocardiography, Strain and Strain Rate by Two-Dimensional Speckle Tracking in Capuchin Monkey (Cebus Apella, Linnaeus, 1758). Arquivos Brasileiros de Cardiologia Imagem cardiovascular, v. 31, n. 1, p. 4-10, Jan. 2022.

Electronic Document Format (APA)

Moura, L. S., Rodrigues, R. P. S., Silva, A. B. S. , Pessoa, G. T., Sousa, F. C. A., Alves, J. J. R. P., Bezerra Neto, L., Macedo, K. V., Vieira, M. C., & Alves, F. R. (2022). Standard Echocardiography, Strain and Strain Rate by Two-Dimensional Speckle Tracking in Capuchin Monkey (Cebus Apella, Linnaeus, 1758). Arquivos Brasileiros de Cardiologia Imagem cardiovascular, 31(1), 4-10.

Electronic Document Format (ISO)

Moura, Laecio da Silva and Rodrigues, Renan Paraguassú de Sá and Silva, Andrezza Braga Soares da and Pessoa, Gerson Tavares and Sousa, Francisco das Chagas Araújo and Alves, Jacyara de Jesus Rosa Pereira and Bezerra Neto, Luiz and Macedo, Kassio Vieira and Vieira, Marcelo Campos and Alves, Flávio Ribeiro. Standard Echocardiography, Strain and Strain Rate by Two-Dimensional Speckle Tracking in Capuchin Monkey (Cebus Apella, Linnaeus, 1758). Arquivos Brasileiros de Cardiologia Imagem cardiovascular [online]. 2022, vol. 31, n. 1, [cited 2026-10-14], pp. 4-10. Available from: <https://journals.cardiol.br/en/article/standard-echocardiography-strain-and-strain-rate-by-two-dimensional-speckle-tracking-in-capuchin-monkey-cebus-apella-linnaeus-1758/>. ISSN 2318-8219

EndNote RIS

Electronic Document Format (Vancouver)

Chu T, Huang M, Zhao Z, Ling F, Cao J, Ge J. Atorvastatin Reduces Accumulation of Vascular Smooth Muscle Cells to Inhibit Intimal Hyperplasia via p38 MAPK Pathway Inhibition in a Rat Model of Vein Graft. Arquivos Brasileiros de Cardiologia 2020;115(4):630-6.

Electronic Document Format (ABNT)

Chu, Tianshu; Huang, Molin; Zhao, Zhiwei; Ling, Fei; Cao, Jing; Ge, Jianjun. Atorvastatin Reduces Accumulation of Vascular Smooth Muscle Cells to Inhibit Intimal Hyperplasia via p38 MAPK Pathway Inhibition in a Rat Model of Vein Graft. Arquivos Brasileiros de Cardiologia, v. 115, n. 4, p. 630-636, Oct. 2020.

Electronic Document Format (APA)

Chu, T., Huang, M., Zhao, Z., Ling, F., Cao, J., & Ge, J. (2020). Atorvastatin Reduces Accumulation of Vascular Smooth Muscle Cells to Inhibit Intimal Hyperplasia via p38 MAPK Pathway Inhibition in a Rat Model of Vein Graft. Arquivos Brasileiros de Cardiologia, 115(4), 630-636.

Electronic Document Format (ISO)

Chu, Tianshu and Huang, Molin and Zhao, Zhiwei and Ling, Fei and Cao, Jing and Ge, Jianjun. Atorvastatin Reduces Accumulation of Vascular Smooth Muscle Cells to Inhibit Intimal Hyperplasia via p38 MAPK Pathway Inhibition in a Rat Model of Vein Graft. Arquivos Brasileiros de Cardiologia [online]. 2020, vol. 115, n. 4, [cited 2026-10-14], pp. 630-636. Available from: <https://journals.cardiol.br/en/article/atorvastatin-reduces-accumulation-of-vascular-smooth-muscle-cells-to-inhibit-intimal-hyperplasia-via-p38-mapk-pathway-inhibition-in-a-rat-model-of-vein-graft/>. ISSN 0066-782X

EndNote RIS

Electronic Document Format (Vancouver)

Gatto M, Pagan LU, Mota GAF. Influence of Atorvastatin on Intimal Hyperplasia in the Experimental Model. Arquivos Brasileiros de Cardiologia 2020;115(4):637-8.

Electronic Document Format (ABNT)

Gatto, Mariana; Pagan, Luana Urbano; Mota, Gustavo Augusto Ferreira. Influence of Atorvastatin on Intimal Hyperplasia in the Experimental Model. Arquivos Brasileiros de Cardiologia, v. 115, n. 4, p. 637-638, Oct. 2020.

Electronic Document Format (APA)

Gatto, M., Pagan, L. U., & Mota, G. A. F. (2020). Influence of Atorvastatin on Intimal Hyperplasia in the Experimental Model. Arquivos Brasileiros de Cardiologia, 115(4), 637-638.

Electronic Document Format (ISO)

Gatto, Mariana and Pagan, Luana Urbano and Mota, Gustavo Augusto Ferreira. Influence of Atorvastatin on Intimal Hyperplasia in the Experimental Model. Arquivos Brasileiros de Cardiologia [online]. 2020, vol. 115, n. 4, [cited 2026-10-14], pp. 637-638. Available from: <https://journals.cardiol.br/en/article/influence-of-atorvastatin-on-intimal-hyperplasia-in-the-experimental-model/>. ISSN 0066-782X

EndNote RIS

Electronic Document Format (Vancouver)

Palácio MG, Paiva EF, Azevedo LCP, Timerman A. Experimental cardiac arrest treatment with adrenaline, vasopressin, or placebo. Arquivos Brasileiros de Cardiologia 2013;101(6):536-44.

Electronic Document Format (ABNT)

Palácio, Manoel Ângelo Gomes; Paiva, Edison Ferreira de; Azevedo, Luciano Cesar Pontes de; Timerman, Ari. Experimental cardiac arrest treatment with adrenaline, vasopressin, or placebo. Arquivos Brasileiros de Cardiologia, v. 101, n. 6, p. 536-544, Oct. 2013.

Electronic Document Format (APA)

Palácio, M. G., Paiva, E. F. , Azevedo, L. C. P. , & Timerman, A. (2013). Experimental cardiac arrest treatment with adrenaline, vasopressin, or placebo. Arquivos Brasileiros de Cardiologia, 101(6), 536-544.

Electronic Document Format (ISO)

Palácio, Manoel Ângelo Gomes and Paiva, Edison Ferreira de and Azevedo, Luciano Cesar Pontes de and Timerman, Ari. Experimental cardiac arrest treatment with adrenaline, vasopressin, or placebo. Arquivos Brasileiros de Cardiologia [online]. 2013, vol. 101, n. 6, [cited 2026-10-14], pp. 536-544. Available from: <https://journals.cardiol.br/en/article/experimental-cardiac-arrest-treatment-with-adrenaline-vasopressin-or-placebo/>. ISSN 0066-782X

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