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  2. Keyword: lipid peroxidation
Effects of atorvastatin, fluvastatin, pravastatin, and simvastatin on endothelial function, lipid peroxidation, and aortic atherosclerosis in hypercholesterolemic rabbits
ABC
Artigo Original

Effects of atorvastatin, fluvastatin, pravastatin, and simvastatin on endothelial function, lipid peroxidation, and aortic atherosclerosis in hypercholesterolemic rabbits

Paulo Afonso Ribeiro Jorge et al. Eros Antonio de Almeida Michiko R. Ozaki Mariana Jorge Adriano Carneiro

OBJECTIVE: To compare the effects of atorvastatin, fluvastatin, pravastatin, and simvastatin on endothelial function, aortic atherosclerosis, and the content of malondialdehyde (MDA) in native and oxidized LDL and in the arterial wall of hypercholesterolemic rabbits after adjusting the dosages of those statins to reduce total serum cholesterol levels to similar values. METHODS: Male rabbits were divided into the following 6 groups of 10 animals (n=10): 1) GH (control) – hypercholesterolemic animals; 2) GA – atorvastatin; 3) GF – fluvastatin; 4) GP – pravastatin; 5) GS – simvastatin; and 6) GN – normal. The animals were fed a standard food preparation enriched with 0.5% cholesterol and 2% coconut oil for 45 days. Fifteen days after beginning the experiment, atorvastatin, fluvastatin, pravastatin and simvastatin were administered for 15 days through gavage, and the dosages were adjusted to obtain similar cholesterol values in each group. At the end of the experiment, a blood sample was withdrawn for determining total cholesterol and separating the lipoproteins, and a segment of the thoracic aorta was removed to be used for studying endothelial function and lipid peroxidation, and for measuring aortic atherosclerosis in histological sections. RESULTS: The statins significantly reduced total serum cholesterol levels, LDL-cholesterol levels, and aortic atherosclerosis. The MDA content was also significantly reduced in native and oxidized LDL, as well as in the arterial wall. Endothelium-dependent relaxation was significantly greater in the treated group compared with that in the hypercholesterolemic group. CONCLUSION: The statins, at dosages adjusted, had a significant and similar effect in reducing lipid peroxidation in native and oxidized LDL-C and in arterial walls, in decreasing aortic atherosclerosis, and in reverting endothelial dysfunction.

  • aortic atherosclerosis
  • HMG-CoA reductase inhibitors
  • lipid peroxidation
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Creative Commons Attribution (CC BY) Creative Commons license
03/05/2005 DOI: 10.1590/S0066-782X2005000400008
Lipid peroxidation and nitric oxide inactivation in postmenopausal women
ABC
Original Article

Lipid peroxidation and nitric oxide inactivation in postmenopausal women

Isabela Rosier Olimpio Pereira et al. Marcelo Chiara Bertolami André Arpad Faludi Maria Fernanda Campos … Simone Ferderbar Emersom Silva Lima José Mendes Aldrighi Dulcineia Saes Parra Abdalla

OBJECTIVE: To assess the effect of endogenous estrogens on the bioavailability of nitric oxide (·NO) and in the formation of lipid peroxidation products in pre- and postmenopausal women. METHODS: NOx and S-nitrosothiols were determined by gaseous phase chemiluminescence, nitrotyrosine was determined by ELISA, COx (cholesterol oxides) by gas chromatography, and cholesteryl linoleate hydroperoxides (CE18:2-OOH), trilinolein (TG18:2-OOH), and phospholipids (PC-OOH) by HPLC in samples of plasma. RESULTS: The concentrations of NOx, nitrotyrosine, COx, CE18:2-OOH, and PC-OOH were higher in the postmenopausal period (33.8±22.3 mM; 230±130 nM; 55±19 ng/mL; 17±8.7 nM; 2775±460 nM, respectively) as compared with those in the premenopausal period (21.1±7.3 mM; 114±41 nM; 31±13 ng/mL; 6±1.4 nM; 1635±373 nM). In contrast, the concentration of S-nitrosothiols was lower in the postmenopausal period (91±55 nM) as compared with that in the premenopausal p in the premenopausal period (237±197 nM). CONCLUSION: In the postmenopausal period, an increase in nitrotyrosine and a reduction of S-nitrosothiol formation, as well as an increase of COx, CE18:2-OOH and PC-OOH formation occurs. Therefore, •NO inactivation and the increase in lipid peroxidation may contribute to endothelial dysfunction and to the greater risk for atherosclerosis in postmenopausal women.

  • lipid peroxidation
  • Menopause
  • Nitric Oxide
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Creative Commons Attribution (CC BY) Creative Commons license
19/05/2003 DOI: 10.1590/S0066-782X2003000400005

How to cite this article

EndNote RIS

Electronic Document Format (Vancouver)

Jorge PAR, Almeida EA, Ozaki MR, Jorge M, Carneiro A. Effects of atorvastatin, fluvastatin, pravastatin, and simvastatin on endothelial function, lipid peroxidation, and aortic atherosclerosis in hypercholesterolemic rabbits. Arquivos Brasileiros de Cardiologia 2005;84(4):314-9.

Electronic Document Format (ABNT)

Jorge, Paulo Afonso Ribeiro; Almeida, Eros Antonio de; Ozaki, Michiko R.; Jorge, Mariana; Carneiro, Adriano. Effects of atorvastatin, fluvastatin, pravastatin, and simvastatin on endothelial function, lipid peroxidation, and aortic atherosclerosis in hypercholesterolemic rabbits. Arquivos Brasileiros de Cardiologia, v. 84, n. 4, p. 314-319, May. 2005.

Electronic Document Format (APA)

Jorge, P. A. R., Almeida, E. A. , Ozaki, M. R., Jorge, M., & Carneiro, A. (2005). Effects of atorvastatin, fluvastatin, pravastatin, and simvastatin on endothelial function, lipid peroxidation, and aortic atherosclerosis in hypercholesterolemic rabbits. Arquivos Brasileiros de Cardiologia, 84(4), 314-319.

Electronic Document Format (ISO)

Jorge, Paulo Afonso Ribeiro and Almeida, Eros Antonio de and Ozaki, Michiko R. and Jorge, Mariana and Carneiro, Adriano. Effects of atorvastatin, fluvastatin, pravastatin, and simvastatin on endothelial function, lipid peroxidation, and aortic atherosclerosis in hypercholesterolemic rabbits. Arquivos Brasileiros de Cardiologia [online]. 2005, vol. 84, n. 4, [cited 2026-10-14], pp. 314-319. Available from: <https://journals.cardiol.br/en/article/effects-of-atorvastatin-fluvastatin-pravastatin-and-simvastatin-on-endothelial-function-lipid-peroxidation-and-aortic-atherosclerosis-in-hypercholesterolemic-rabbits/>. ISSN 0066-782X

EndNote RIS

Electronic Document Format (Vancouver)

Pereira IRO, Bertolami MC, Faludi AA, Campos MF, Ferderbar S, Lima ES, Aldrighi JM, et al. Lipid peroxidation and nitric oxide inactivation in postmenopausal women. Arquivos Brasileiros de Cardiologia 2003;80(4):415-23.

Electronic Document Format (ABNT)

Pereira, Isabela Rosier Olimpio; Bertolami, Marcelo Chiara; Faludi, André Arpad; Campos, Maria Fernanda; Ferderbar, Simone; Lima, Emersom Silva; Aldrighi, José Mendes; Abdalla, Dulcineia Saes Parra. Lipid peroxidation and nitric oxide inactivation in postmenopausal women. Arquivos Brasileiros de Cardiologia, v. 80, n. 4, p. 415-423, May. 2003.

Electronic Document Format (APA)

Pereira, I. R. O., Bertolami, M. C., Faludi, A. A., Campos, M. F., Ferderbar, S., Lima, E. S., Aldrighi, J. M., & Abdalla, D. S. P. (2003). Lipid peroxidation and nitric oxide inactivation in postmenopausal women. Arquivos Brasileiros de Cardiologia, 80(4), 415-423.

Electronic Document Format (ISO)

Pereira, Isabela Rosier Olimpio and Bertolami, Marcelo Chiara and Faludi, André Arpad and Campos, Maria Fernanda and Ferderbar, Simone and Lima, Emersom Silva and Aldrighi, José Mendes and Abdalla, Dulcineia Saes Parra. Lipid peroxidation and nitric oxide inactivation in postmenopausal women. Arquivos Brasileiros de Cardiologia [online]. 2003, vol. 80, n. 4, [cited 2026-10-14], pp. 415-423. Available from: <https://journals.cardiol.br/en/article/lipid-peroxidation-and-nitric-oxide-inactivation-in-postmenopausal-women/>. ISSN 0066-782X

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