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Combined use of probucol and cilostazol with atorvastatin attenuates atherosclerosis in moderately hypercholesterolemic rabbits

BACKGROUND: Atherosclerotic cardiovascular disease is one of the major diseases that seriously impacts human health. Combined drug therapy may be efficacious in delaying the occurrence of cardiovascular events. AIM: The current study was designed to investigate whether combined use of probucol (an a...

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Autores principales: Wang, Yanli, Bai, Liang, Lin, Yan, Chen, Yulong, Guan, Hua, Zhu, Ninghong, Li, Yafeng, Gao, Shoucui, Sun, Lijing, Zhao, Sihai, Fan, Jianglin, Liu, Enqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517357/
https://www.ncbi.nlm.nih.gov/pubmed/26220196
http://dx.doi.org/10.1186/s12944-015-0083-5
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author Wang, Yanli
Bai, Liang
Lin, Yan
Chen, Yulong
Guan, Hua
Zhu, Ninghong
Li, Yafeng
Gao, Shoucui
Sun, Lijing
Zhao, Sihai
Fan, Jianglin
Liu, Enqi
author_facet Wang, Yanli
Bai, Liang
Lin, Yan
Chen, Yulong
Guan, Hua
Zhu, Ninghong
Li, Yafeng
Gao, Shoucui
Sun, Lijing
Zhao, Sihai
Fan, Jianglin
Liu, Enqi
author_sort Wang, Yanli
collection PubMed
description BACKGROUND: Atherosclerotic cardiovascular disease is one of the major diseases that seriously impacts human health. Combined drug therapy may be efficacious in delaying the occurrence of cardiovascular events. AIM: The current study was designed to investigate whether combined use of probucol (an anti-oxidant agent) with cilostazol (a platelet aggregation inhibitor) would increase the inhibitory effect of statins (a lipid-lowering agent) on atherosclerosis in moderately hypercholesterolemic rabbits. METHODS AND RESULTS: Thirty Japanese white rabbits were fed with a high cholesterol diet for 12 weeks, which was supplemented with either 0.005 % atorvastatin alone or 0.005 % atorvastatin plus 0.3 % probucol and 0.3 % cilostazol. Except for high-density lipoprotein cholesterol, no difference was found in plasma lipids among vehicle, statin, and the combined treatment group. However, atherosclerotic lesions were significantly reduced by statin treatment compared with vehicle. Moreover, we found that the anti-atherogenic effect of statin was further enhanced by the combined treatment, which was due to increased anti-inflammatory and anti-oxidant properties. CONCLUSIONS: These data demonstrated that combined drug treatment exhibits potent athero-protective effects via pleiotropic functions, such as anti-inflammatory and anti-oxidative stress, which is independent of the lipid-lowering effect.
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spelling pubmed-45173572015-07-29 Combined use of probucol and cilostazol with atorvastatin attenuates atherosclerosis in moderately hypercholesterolemic rabbits Wang, Yanli Bai, Liang Lin, Yan Chen, Yulong Guan, Hua Zhu, Ninghong Li, Yafeng Gao, Shoucui Sun, Lijing Zhao, Sihai Fan, Jianglin Liu, Enqi Lipids Health Dis Research BACKGROUND: Atherosclerotic cardiovascular disease is one of the major diseases that seriously impacts human health. Combined drug therapy may be efficacious in delaying the occurrence of cardiovascular events. AIM: The current study was designed to investigate whether combined use of probucol (an anti-oxidant agent) with cilostazol (a platelet aggregation inhibitor) would increase the inhibitory effect of statins (a lipid-lowering agent) on atherosclerosis in moderately hypercholesterolemic rabbits. METHODS AND RESULTS: Thirty Japanese white rabbits were fed with a high cholesterol diet for 12 weeks, which was supplemented with either 0.005 % atorvastatin alone or 0.005 % atorvastatin plus 0.3 % probucol and 0.3 % cilostazol. Except for high-density lipoprotein cholesterol, no difference was found in plasma lipids among vehicle, statin, and the combined treatment group. However, atherosclerotic lesions were significantly reduced by statin treatment compared with vehicle. Moreover, we found that the anti-atherogenic effect of statin was further enhanced by the combined treatment, which was due to increased anti-inflammatory and anti-oxidant properties. CONCLUSIONS: These data demonstrated that combined drug treatment exhibits potent athero-protective effects via pleiotropic functions, such as anti-inflammatory and anti-oxidative stress, which is independent of the lipid-lowering effect. BioMed Central 2015-07-29 /pmc/articles/PMC4517357/ /pubmed/26220196 http://dx.doi.org/10.1186/s12944-015-0083-5 Text en © Wang et al. 2015 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
Wang, Yanli
Bai, Liang
Lin, Yan
Chen, Yulong
Guan, Hua
Zhu, Ninghong
Li, Yafeng
Gao, Shoucui
Sun, Lijing
Zhao, Sihai
Fan, Jianglin
Liu, Enqi
Combined use of probucol and cilostazol with atorvastatin attenuates atherosclerosis in moderately hypercholesterolemic rabbits
title Combined use of probucol and cilostazol with atorvastatin attenuates atherosclerosis in moderately hypercholesterolemic rabbits
title_full Combined use of probucol and cilostazol with atorvastatin attenuates atherosclerosis in moderately hypercholesterolemic rabbits
title_fullStr Combined use of probucol and cilostazol with atorvastatin attenuates atherosclerosis in moderately hypercholesterolemic rabbits
title_full_unstemmed Combined use of probucol and cilostazol with atorvastatin attenuates atherosclerosis in moderately hypercholesterolemic rabbits
title_short Combined use of probucol and cilostazol with atorvastatin attenuates atherosclerosis in moderately hypercholesterolemic rabbits
title_sort combined use of probucol and cilostazol with atorvastatin attenuates atherosclerosis in moderately hypercholesterolemic rabbits
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517357/
https://www.ncbi.nlm.nih.gov/pubmed/26220196
http://dx.doi.org/10.1186/s12944-015-0083-5
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