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A multi-target protective effect of Danggui-Shaoyao-San on the vascular endothelium of atherosclerotic mice

BACKGROUND: Atherosclerosis (AS) is a chronic disease characterized by abnormal blood lipid metabolism, inflammation and vascular endothelial injury. Vascular endothelial injury is the initial stage during the occurrence of AS. However, the function and mechanism of anti-AS are not well characterize...

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Autores principales: Sun, Yuemeng, Gao, Yushan, Zhou, Lu, Lu, Yixing, Zong, Yulin, Zhu, Haoyu, Tang, Yang, Zheng, Fengjie, Sun, Yan, Li, Yuhang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9940384/
https://www.ncbi.nlm.nih.gov/pubmed/36803348
http://dx.doi.org/10.1186/s12906-023-03883-3
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author Sun, Yuemeng
Gao, Yushan
Zhou, Lu
Lu, Yixing
Zong, Yulin
Zhu, Haoyu
Tang, Yang
Zheng, Fengjie
Sun, Yan
Li, Yuhang
author_facet Sun, Yuemeng
Gao, Yushan
Zhou, Lu
Lu, Yixing
Zong, Yulin
Zhu, Haoyu
Tang, Yang
Zheng, Fengjie
Sun, Yan
Li, Yuhang
author_sort Sun, Yuemeng
collection PubMed
description BACKGROUND: Atherosclerosis (AS) is a chronic disease characterized by abnormal blood lipid metabolism, inflammation and vascular endothelial injury. Vascular endothelial injury is the initial stage during the occurrence of AS. However, the function and mechanism of anti-AS are not well characterized. Danggui-Shaoyao-San (DGSY) is a classic Traditional Chinese Medicine (TCM) prescription for the treatment of gynecological diseases, and has been widely used in the treatment of AS in recent years. METHODS: ApoE(−/−) atherosclerosis male mice were established by feeding with high-fat diet, and then randomly divided into three groups: Atherosclerosis group (AS), Danggui-Shaoyao-San group (DGSY), and Atorvastatin calcium group (X). The mice were administered with the drugs for 16 weeks. Pathological changes in aortic vessels were examined by staining with Oil red O, Masson and hematoxylin–eosin. In addition, blood lipids were analyzed. The level of IL-6 and IL-8 in aortic vessels were detected by ELISA and the expression of ICAM-1 and VCAM-1 in the aortic vascular endothelium were measured by Immunohistochemical. The mRNA expression of interα5β1/c-Abl/YAP in the aortic vessels were measured by Real-time quantitative PCR and location of expression was assessed by immunofluorescence. RESULTS: DGSY can significantly reduce the content of TC,TG and LDL-C and increase the level of HDL-C in the serum, reduce the plaque area and inhibit the concentration of IL-6 and IL-8, down-regulate the expression of IVAM-1,VCAM-1 and interα5β1/ c-Abl/YAP in the aortic vessels. CONCLUSIONS: Collectively, DGSY can alleviate vascular endothelium damage and delay the occurrence of AS, and the underlying mechanism may be related to the multi-target protective of DGSY.
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spelling pubmed-99403842023-02-21 A multi-target protective effect of Danggui-Shaoyao-San on the vascular endothelium of atherosclerotic mice Sun, Yuemeng Gao, Yushan Zhou, Lu Lu, Yixing Zong, Yulin Zhu, Haoyu Tang, Yang Zheng, Fengjie Sun, Yan Li, Yuhang BMC Complement Med Ther Research BACKGROUND: Atherosclerosis (AS) is a chronic disease characterized by abnormal blood lipid metabolism, inflammation and vascular endothelial injury. Vascular endothelial injury is the initial stage during the occurrence of AS. However, the function and mechanism of anti-AS are not well characterized. Danggui-Shaoyao-San (DGSY) is a classic Traditional Chinese Medicine (TCM) prescription for the treatment of gynecological diseases, and has been widely used in the treatment of AS in recent years. METHODS: ApoE(−/−) atherosclerosis male mice were established by feeding with high-fat diet, and then randomly divided into three groups: Atherosclerosis group (AS), Danggui-Shaoyao-San group (DGSY), and Atorvastatin calcium group (X). The mice were administered with the drugs for 16 weeks. Pathological changes in aortic vessels were examined by staining with Oil red O, Masson and hematoxylin–eosin. In addition, blood lipids were analyzed. The level of IL-6 and IL-8 in aortic vessels were detected by ELISA and the expression of ICAM-1 and VCAM-1 in the aortic vascular endothelium were measured by Immunohistochemical. The mRNA expression of interα5β1/c-Abl/YAP in the aortic vessels were measured by Real-time quantitative PCR and location of expression was assessed by immunofluorescence. RESULTS: DGSY can significantly reduce the content of TC,TG and LDL-C and increase the level of HDL-C in the serum, reduce the plaque area and inhibit the concentration of IL-6 and IL-8, down-regulate the expression of IVAM-1,VCAM-1 and interα5β1/ c-Abl/YAP in the aortic vessels. CONCLUSIONS: Collectively, DGSY can alleviate vascular endothelium damage and delay the occurrence of AS, and the underlying mechanism may be related to the multi-target protective of DGSY. BioMed Central 2023-02-20 /pmc/articles/PMC9940384/ /pubmed/36803348 http://dx.doi.org/10.1186/s12906-023-03883-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Sun, Yuemeng
Gao, Yushan
Zhou, Lu
Lu, Yixing
Zong, Yulin
Zhu, Haoyu
Tang, Yang
Zheng, Fengjie
Sun, Yan
Li, Yuhang
A multi-target protective effect of Danggui-Shaoyao-San on the vascular endothelium of atherosclerotic mice
title A multi-target protective effect of Danggui-Shaoyao-San on the vascular endothelium of atherosclerotic mice
title_full A multi-target protective effect of Danggui-Shaoyao-San on the vascular endothelium of atherosclerotic mice
title_fullStr A multi-target protective effect of Danggui-Shaoyao-San on the vascular endothelium of atherosclerotic mice
title_full_unstemmed A multi-target protective effect of Danggui-Shaoyao-San on the vascular endothelium of atherosclerotic mice
title_short A multi-target protective effect of Danggui-Shaoyao-San on the vascular endothelium of atherosclerotic mice
title_sort multi-target protective effect of danggui-shaoyao-san on the vascular endothelium of atherosclerotic mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9940384/
https://www.ncbi.nlm.nih.gov/pubmed/36803348
http://dx.doi.org/10.1186/s12906-023-03883-3
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