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Effect of Pitavastatin on Vascular Reactivity in Hypercholesterolemic Rabbits
BACKGROUND: Pitavastatin is the newest statin available in Brazil and likely the one with fewer side effects. Thus, pitavastatin was evaluated in hypercholesterolemic rabbits in relation to its action on vascular reactivity. OBJECTIVE: To assess the lowest dose of pitavastatin necessary to reduce pl...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Cardiologia
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4126755/ https://www.ncbi.nlm.nih.gov/pubmed/25014056 http://dx.doi.org/10.5935/abc.20140090 |
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author | de Almeida, Eros Antonio Ozaki, Michiko Regina |
author_facet | de Almeida, Eros Antonio Ozaki, Michiko Regina |
author_sort | de Almeida, Eros Antonio |
collection | PubMed |
description | BACKGROUND: Pitavastatin is the newest statin available in Brazil and likely the one with fewer side effects. Thus, pitavastatin was evaluated in hypercholesterolemic rabbits in relation to its action on vascular reactivity. OBJECTIVE: To assess the lowest dose of pitavastatin necessary to reduce plasma lipids, cholesterol and tissue lipid peroxidation, as well as endothelial function in hypercholesterolemic rabbits. METHODS: Thirty rabbits divided into six groups (n = 5): G1 - standard chow diet; G2 - hypercholesterolemic diet for 30 days; G3 - hypercholesterolemic diet and after the 16(th) day, diet supplemented with pitavastatin (0.1 mg); G4 - hypercholesterolemic diet supplemented with pitavastatin (0.25 mg); G5 - hypercholesterolemic diet supplemented with pitavastatin (0.5 mg); G6 - hypercholesterolemic diet supplemented with pitavastatin (1.0 mg). After 30 days, total cholesterol, HDL, triglycerides, glucose, creatine kinase (CK), aspartate aminotransferase (AST), alanine aminotransferase (ALT) were measured and LDL was calculated. In-depth anesthesia was performed with sodium thiopental and aortic segments were removed to study endothelial function, cholesterol and tissue lipid peroxidation. The significance level for statistical tests was 5%. RESULTS: Total cholesterol and LDL were significantly elevated in relation to G1. HDL was significantly reduced in G4, G5 and G6 when compared to G2. Triglycerides, CK, AST, ALT, cholesterol and tissue lipid peroxidation showed no statistical difference between G2 and G3-G6. Significantly endothelial dysfunction reversion was observed in G5 and G6 when compared to G2. CONCLUSION: Pitavastatin starting at a 0.5 mg dose was effective in reverting endothelial dysfunction in hypercholesterolemic rabbits. |
format | Online Article Text |
id | pubmed-4126755 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Sociedade Brasileira de Cardiologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-41267552014-08-11 Effect of Pitavastatin on Vascular Reactivity in Hypercholesterolemic Rabbits de Almeida, Eros Antonio Ozaki, Michiko Regina Arq Bras Cardiol Original Articles BACKGROUND: Pitavastatin is the newest statin available in Brazil and likely the one with fewer side effects. Thus, pitavastatin was evaluated in hypercholesterolemic rabbits in relation to its action on vascular reactivity. OBJECTIVE: To assess the lowest dose of pitavastatin necessary to reduce plasma lipids, cholesterol and tissue lipid peroxidation, as well as endothelial function in hypercholesterolemic rabbits. METHODS: Thirty rabbits divided into six groups (n = 5): G1 - standard chow diet; G2 - hypercholesterolemic diet for 30 days; G3 - hypercholesterolemic diet and after the 16(th) day, diet supplemented with pitavastatin (0.1 mg); G4 - hypercholesterolemic diet supplemented with pitavastatin (0.25 mg); G5 - hypercholesterolemic diet supplemented with pitavastatin (0.5 mg); G6 - hypercholesterolemic diet supplemented with pitavastatin (1.0 mg). After 30 days, total cholesterol, HDL, triglycerides, glucose, creatine kinase (CK), aspartate aminotransferase (AST), alanine aminotransferase (ALT) were measured and LDL was calculated. In-depth anesthesia was performed with sodium thiopental and aortic segments were removed to study endothelial function, cholesterol and tissue lipid peroxidation. The significance level for statistical tests was 5%. RESULTS: Total cholesterol and LDL were significantly elevated in relation to G1. HDL was significantly reduced in G4, G5 and G6 when compared to G2. Triglycerides, CK, AST, ALT, cholesterol and tissue lipid peroxidation showed no statistical difference between G2 and G3-G6. Significantly endothelial dysfunction reversion was observed in G5 and G6 when compared to G2. CONCLUSION: Pitavastatin starting at a 0.5 mg dose was effective in reverting endothelial dysfunction in hypercholesterolemic rabbits. Sociedade Brasileira de Cardiologia 2014-07 /pmc/articles/PMC4126755/ /pubmed/25014056 http://dx.doi.org/10.5935/abc.20140090 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles de Almeida, Eros Antonio Ozaki, Michiko Regina Effect of Pitavastatin on Vascular Reactivity in Hypercholesterolemic Rabbits |
title | Effect of Pitavastatin on Vascular Reactivity in Hypercholesterolemic
Rabbits |
title_full | Effect of Pitavastatin on Vascular Reactivity in Hypercholesterolemic
Rabbits |
title_fullStr | Effect of Pitavastatin on Vascular Reactivity in Hypercholesterolemic
Rabbits |
title_full_unstemmed | Effect of Pitavastatin on Vascular Reactivity in Hypercholesterolemic
Rabbits |
title_short | Effect of Pitavastatin on Vascular Reactivity in Hypercholesterolemic
Rabbits |
title_sort | effect of pitavastatin on vascular reactivity in hypercholesterolemic
rabbits |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4126755/ https://www.ncbi.nlm.nih.gov/pubmed/25014056 http://dx.doi.org/10.5935/abc.20140090 |
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