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Metformin enhances nitric oxide production and diminishes Rho kinase activity in rats with hyperlipidemia

BACKGROUND: Rho kinase over-activation is associated with nitric oxide (NO) reduction and atherosclerosis. Metformin is favorable for endothelial function improvement and cardiovascular outcomes. Whether cardio-protective effect of metformin is associated with Rho kinase activity is unknown. METHODS...

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Autores principales: Liu, Yan, Huang, Congwu, Ceng, Chuan, Zhan, Haiyong, Zheng, Dongdan, Han, Weixing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109376/
https://www.ncbi.nlm.nih.gov/pubmed/25028180
http://dx.doi.org/10.1186/1476-511X-13-115
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author Liu, Yan
Huang, Congwu
Ceng, Chuan
Zhan, Haiyong
Zheng, Dongdan
Han, Weixing
author_facet Liu, Yan
Huang, Congwu
Ceng, Chuan
Zhan, Haiyong
Zheng, Dongdan
Han, Weixing
author_sort Liu, Yan
collection PubMed
description BACKGROUND: Rho kinase over-activation is associated with nitric oxide (NO) reduction and atherosclerosis. Metformin is favorable for endothelial function improvement and cardiovascular outcomes. Whether cardio-protective effect of metformin is associated with Rho kinase activity is unknown. METHODS: Hyperlipidemia model of rats were established accordingly. Thereafter, medical interventions in terms of atorvastatin, metformin or combined therapy were administered for 4 weeks. Laboratory parameters were compared among each groups at initial, 6 weeks of high-fat and high-cholesterol diet administration, and 4 weeks of medical intervention. Lineal regression analyses were performed. RESULTS: No significant difference of laboratory parameters was observed initially. Six weeks of high-fat and high-cholesterol diet administration, serum levels of cholesterol, C-reactive protein (CRP) level, and Rho kinase activity were significantly increased while NO production was concomitantly reduced in comparison to the sham group. After 4 weeks of medical intervention, CRP level and Rho kinase activity were profoundly diminished while NO production was significantly enhanced in the atorvastatin and metformin groups, and these benefits were further enhanced with combined therapy. Lineal regression analyses showed that Rho kinase activity was negatively correlated with NO production but positively correlated with CRP level. CONCLUSION: In rats with hyperlipidemia, metformin and atorvastatin therapy is favorable for NO production and CRP reduction, which might be associated with Rho kinase activity decrease.
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spelling pubmed-41093762014-07-25 Metformin enhances nitric oxide production and diminishes Rho kinase activity in rats with hyperlipidemia Liu, Yan Huang, Congwu Ceng, Chuan Zhan, Haiyong Zheng, Dongdan Han, Weixing Lipids Health Dis Research BACKGROUND: Rho kinase over-activation is associated with nitric oxide (NO) reduction and atherosclerosis. Metformin is favorable for endothelial function improvement and cardiovascular outcomes. Whether cardio-protective effect of metformin is associated with Rho kinase activity is unknown. METHODS: Hyperlipidemia model of rats were established accordingly. Thereafter, medical interventions in terms of atorvastatin, metformin or combined therapy were administered for 4 weeks. Laboratory parameters were compared among each groups at initial, 6 weeks of high-fat and high-cholesterol diet administration, and 4 weeks of medical intervention. Lineal regression analyses were performed. RESULTS: No significant difference of laboratory parameters was observed initially. Six weeks of high-fat and high-cholesterol diet administration, serum levels of cholesterol, C-reactive protein (CRP) level, and Rho kinase activity were significantly increased while NO production was concomitantly reduced in comparison to the sham group. After 4 weeks of medical intervention, CRP level and Rho kinase activity were profoundly diminished while NO production was significantly enhanced in the atorvastatin and metformin groups, and these benefits were further enhanced with combined therapy. Lineal regression analyses showed that Rho kinase activity was negatively correlated with NO production but positively correlated with CRP level. CONCLUSION: In rats with hyperlipidemia, metformin and atorvastatin therapy is favorable for NO production and CRP reduction, which might be associated with Rho kinase activity decrease. BioMed Central 2014-07-15 /pmc/articles/PMC4109376/ /pubmed/25028180 http://dx.doi.org/10.1186/1476-511X-13-115 Text en Copyright © 2014 Liu 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
Liu, Yan
Huang, Congwu
Ceng, Chuan
Zhan, Haiyong
Zheng, Dongdan
Han, Weixing
Metformin enhances nitric oxide production and diminishes Rho kinase activity in rats with hyperlipidemia
title Metformin enhances nitric oxide production and diminishes Rho kinase activity in rats with hyperlipidemia
title_full Metformin enhances nitric oxide production and diminishes Rho kinase activity in rats with hyperlipidemia
title_fullStr Metformin enhances nitric oxide production and diminishes Rho kinase activity in rats with hyperlipidemia
title_full_unstemmed Metformin enhances nitric oxide production and diminishes Rho kinase activity in rats with hyperlipidemia
title_short Metformin enhances nitric oxide production and diminishes Rho kinase activity in rats with hyperlipidemia
title_sort metformin enhances nitric oxide production and diminishes rho kinase activity in rats with hyperlipidemia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109376/
https://www.ncbi.nlm.nih.gov/pubmed/25028180
http://dx.doi.org/10.1186/1476-511X-13-115
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