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Daming capsule restores endothelial dysfunction induced by high-fat diet
BACKGROUND: Daming capsule (DMC), a traditional Chinese formula, has a lipid-modulating action with reduced adverse side effects as compared with other lipid lowering compounds. Since endothelial dysfunction often accompanies the hyperlipidemic state, we hypothesize that DMC might restore endothelia...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3383478/ https://www.ncbi.nlm.nih.gov/pubmed/22443680 http://dx.doi.org/10.1186/1472-6882-12-21 |
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author | Zhang, Rong Niu, Huifang Wang, Ning Sun, Lihua Xu, Yi Zhao, Ruibo Ban, Xiang Yu, Yao Yang, Baofeng Ai, Jing |
author_facet | Zhang, Rong Niu, Huifang Wang, Ning Sun, Lihua Xu, Yi Zhao, Ruibo Ban, Xiang Yu, Yao Yang, Baofeng Ai, Jing |
author_sort | Zhang, Rong |
collection | PubMed |
description | BACKGROUND: Daming capsule (DMC), a traditional Chinese formula, has a lipid-modulating action with reduced adverse side effects as compared with other lipid lowering compounds. Since endothelial dysfunction often accompanies the hyperlipidemic state, we hypothesize that DMC might restore endothelial dysfunction produced by a high-fat (HF) diet. Importantly, we also investigate possible mechanisms involved in mediating the effects of DMC on vascular reactivity. METHODS: Rats were divided into four groups: control, HF diet, HF mixed DMC diet, HF mixed atorvastatin (ATV) diet. After 30 days, the thoracic cavity was exposed to remove the thoracic aorta for (i) histological examination; (ii) measurement of endothelial nitric oxide synthase (eNOS) by western blot; and (iii) tension study of thoracic aortic ring. RESULTS: HF diet induced significant attenuation in the contraction and relaxation of rat aortic rings. Treatment with DMC significantly improved the relaxation of the aortic rings as compared with those from HF rats (P < 0.05), which was abolished by a nonspecific NOS inhibitor L-NAME. Moreover DMC significantly restored the decrease in eNOS expression induced by HF diet. Similar results were found in histopathologic changes. DMC failed to restore the loss of vasocontraction of aorta explained by an impairment of ATP-sensitive K(+ )channels (K(ATP)) on the structure and/or function. DMC exerted the same protective effect as ATV, a positive control drug, on vascular injury produced by HF diet. CONCLUSION: DMC partially protects the aorta from HF-induced endothelial dysfunction via upregulation of the expression of eNOS. |
format | Online Article Text |
id | pubmed-3383478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33834782012-06-27 Daming capsule restores endothelial dysfunction induced by high-fat diet Zhang, Rong Niu, Huifang Wang, Ning Sun, Lihua Xu, Yi Zhao, Ruibo Ban, Xiang Yu, Yao Yang, Baofeng Ai, Jing BMC Complement Altern Med Research Article BACKGROUND: Daming capsule (DMC), a traditional Chinese formula, has a lipid-modulating action with reduced adverse side effects as compared with other lipid lowering compounds. Since endothelial dysfunction often accompanies the hyperlipidemic state, we hypothesize that DMC might restore endothelial dysfunction produced by a high-fat (HF) diet. Importantly, we also investigate possible mechanisms involved in mediating the effects of DMC on vascular reactivity. METHODS: Rats were divided into four groups: control, HF diet, HF mixed DMC diet, HF mixed atorvastatin (ATV) diet. After 30 days, the thoracic cavity was exposed to remove the thoracic aorta for (i) histological examination; (ii) measurement of endothelial nitric oxide synthase (eNOS) by western blot; and (iii) tension study of thoracic aortic ring. RESULTS: HF diet induced significant attenuation in the contraction and relaxation of rat aortic rings. Treatment with DMC significantly improved the relaxation of the aortic rings as compared with those from HF rats (P < 0.05), which was abolished by a nonspecific NOS inhibitor L-NAME. Moreover DMC significantly restored the decrease in eNOS expression induced by HF diet. Similar results were found in histopathologic changes. DMC failed to restore the loss of vasocontraction of aorta explained by an impairment of ATP-sensitive K(+ )channels (K(ATP)) on the structure and/or function. DMC exerted the same protective effect as ATV, a positive control drug, on vascular injury produced by HF diet. CONCLUSION: DMC partially protects the aorta from HF-induced endothelial dysfunction via upregulation of the expression of eNOS. BioMed Central 2012-03-24 /pmc/articles/PMC3383478/ /pubmed/22443680 http://dx.doi.org/10.1186/1472-6882-12-21 Text en Copyright ©2012 Zhang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zhang, Rong Niu, Huifang Wang, Ning Sun, Lihua Xu, Yi Zhao, Ruibo Ban, Xiang Yu, Yao Yang, Baofeng Ai, Jing Daming capsule restores endothelial dysfunction induced by high-fat diet |
title | Daming capsule restores endothelial dysfunction induced by high-fat diet |
title_full | Daming capsule restores endothelial dysfunction induced by high-fat diet |
title_fullStr | Daming capsule restores endothelial dysfunction induced by high-fat diet |
title_full_unstemmed | Daming capsule restores endothelial dysfunction induced by high-fat diet |
title_short | Daming capsule restores endothelial dysfunction induced by high-fat diet |
title_sort | daming capsule restores endothelial dysfunction induced by high-fat diet |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3383478/ https://www.ncbi.nlm.nih.gov/pubmed/22443680 http://dx.doi.org/10.1186/1472-6882-12-21 |
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