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Synergistic effects of colchicine combined with atorvastatin in rats with hyperlipidemia

BACKGROUND: Inflammation and endothelial dysfunction is implicated in the atherosclerosis initiation and progression in the setting of hyperlipidemia. Colchicine is a potent anti-inflammatory agent and whether colchicine combined with atorvastatin has synergistic effects on inflammation amelioration...

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Autores principales: Huang, Congwu, Cen, Chuan, Wang, ChengXu, Zhan, Haiyong, Ding, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005013/
https://www.ncbi.nlm.nih.gov/pubmed/24742015
http://dx.doi.org/10.1186/1476-511X-13-67
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author Huang, Congwu
Cen, Chuan
Wang, ChengXu
Zhan, Haiyong
Ding, Xin
author_facet Huang, Congwu
Cen, Chuan
Wang, ChengXu
Zhan, Haiyong
Ding, Xin
author_sort Huang, Congwu
collection PubMed
description BACKGROUND: Inflammation and endothelial dysfunction is implicated in the atherosclerosis initiation and progression in the setting of hyperlipidemia. Colchicine is a potent anti-inflammatory agent and whether colchicine combined with atorvastatin has synergistic effects on inflammation amelioration and endothelial function improvement is unknown. METHODS: Hyperlipidemic rat model was produced by high-fat and high-cholesterol diet for 6 weeks. Rats with normal diet were served as shame group. In hyperlipidemic group, normal saline, atorvastatin (10 mg/kg body weight/day), colchicines (0.5 mg/kg body weight/day), or atorvastatin combined with colchicines (same dosages) were prescribed for 2 weeks. Serum levels of lipid profile, C-reactive protein (CRP), liver enzyme, lipoprotein associated phospholipase A2 (Lp-PLA2) and nitric oxide (NO) production were serially assessed. RESULTS: Before the beginning of the study, all laboratory variables were comparable among each group. After 6 weeks of hyperlipidemic model production, serum levels of cholesterols, CRP and Lp-PLA2 were significantly increased when compared to sham group, whereas NO production was reduced. With 2 weeks of colchicine therapy, serum levels of CRP and Lp-PLA2 were decreased and NO production was enhanced in the colchicine group in a lipid-lowering independent manner. Added colchicine into atorvastatin therapy further improved NO production and decreased CRP and Lp-PLA2 levels, indicating a potential synergism of colchicine and atorvastatin. CONCLUSION: Colchicine combined with atorvastatin may have stronger protective effects on improving endothelial function and ameliorating inflammation in rats with hyperlipidemia.
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spelling pubmed-40050132014-05-01 Synergistic effects of colchicine combined with atorvastatin in rats with hyperlipidemia Huang, Congwu Cen, Chuan Wang, ChengXu Zhan, Haiyong Ding, Xin Lipids Health Dis Research BACKGROUND: Inflammation and endothelial dysfunction is implicated in the atherosclerosis initiation and progression in the setting of hyperlipidemia. Colchicine is a potent anti-inflammatory agent and whether colchicine combined with atorvastatin has synergistic effects on inflammation amelioration and endothelial function improvement is unknown. METHODS: Hyperlipidemic rat model was produced by high-fat and high-cholesterol diet for 6 weeks. Rats with normal diet were served as shame group. In hyperlipidemic group, normal saline, atorvastatin (10 mg/kg body weight/day), colchicines (0.5 mg/kg body weight/day), or atorvastatin combined with colchicines (same dosages) were prescribed for 2 weeks. Serum levels of lipid profile, C-reactive protein (CRP), liver enzyme, lipoprotein associated phospholipase A2 (Lp-PLA2) and nitric oxide (NO) production were serially assessed. RESULTS: Before the beginning of the study, all laboratory variables were comparable among each group. After 6 weeks of hyperlipidemic model production, serum levels of cholesterols, CRP and Lp-PLA2 were significantly increased when compared to sham group, whereas NO production was reduced. With 2 weeks of colchicine therapy, serum levels of CRP and Lp-PLA2 were decreased and NO production was enhanced in the colchicine group in a lipid-lowering independent manner. Added colchicine into atorvastatin therapy further improved NO production and decreased CRP and Lp-PLA2 levels, indicating a potential synergism of colchicine and atorvastatin. CONCLUSION: Colchicine combined with atorvastatin may have stronger protective effects on improving endothelial function and ameliorating inflammation in rats with hyperlipidemia. BioMed Central 2014-04-17 /pmc/articles/PMC4005013/ /pubmed/24742015 http://dx.doi.org/10.1186/1476-511X-13-67 Text en Copyright © 2014 Huang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Huang, Congwu
Cen, Chuan
Wang, ChengXu
Zhan, Haiyong
Ding, Xin
Synergistic effects of colchicine combined with atorvastatin in rats with hyperlipidemia
title Synergistic effects of colchicine combined with atorvastatin in rats with hyperlipidemia
title_full Synergistic effects of colchicine combined with atorvastatin in rats with hyperlipidemia
title_fullStr Synergistic effects of colchicine combined with atorvastatin in rats with hyperlipidemia
title_full_unstemmed Synergistic effects of colchicine combined with atorvastatin in rats with hyperlipidemia
title_short Synergistic effects of colchicine combined with atorvastatin in rats with hyperlipidemia
title_sort synergistic effects of colchicine combined with atorvastatin in rats with hyperlipidemia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005013/
https://www.ncbi.nlm.nih.gov/pubmed/24742015
http://dx.doi.org/10.1186/1476-511X-13-67
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