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Yindanxinnaotong, a Chinese compound medicine, synergistically attenuates atherosclerosis progress

Yindanxinnaotong (YD), a traditional Chinese medicine, has been introduced to clinical medicine for more than a decade, while its pharmacological properties are still not to be well addressed. This report aimed to explore the anti-atherosclerosis properties and underlying mechanisms of YD. We initia...

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Autores principales: Cheng, Long, Pan, Guo-feng, Zhang, Xiao-dong, Wang, Jian-lu, Wang, Wan-dan, Zhang, Jian-yong, Wang, Hui, Liang, Ri-xin, Sun, Xiao-bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508829/
https://www.ncbi.nlm.nih.gov/pubmed/26196108
http://dx.doi.org/10.1038/srep12333
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author Cheng, Long
Pan, Guo-feng
Zhang, Xiao-dong
Wang, Jian-lu
Wang, Wan-dan
Zhang, Jian-yong
Wang, Hui
Liang, Ri-xin
Sun, Xiao-bo
author_facet Cheng, Long
Pan, Guo-feng
Zhang, Xiao-dong
Wang, Jian-lu
Wang, Wan-dan
Zhang, Jian-yong
Wang, Hui
Liang, Ri-xin
Sun, Xiao-bo
author_sort Cheng, Long
collection PubMed
description Yindanxinnaotong (YD), a traditional Chinese medicine, has been introduced to clinical medicine for more than a decade, while its pharmacological properties are still not to be well addressed. This report aimed to explore the anti-atherosclerosis properties and underlying mechanisms of YD. We initially performed a computational prediction based on a network pharmacology simulation, which clued YD exerted synergistically anti-atherosclerosis properties by vascular endothelium protection, lipid-lowering, anti-inflammation, and anti-oxidation. These outcomes were then validated in atherosclerosis rats. The experiments provided evidences indicating YD’s contribution in this study included, (1) significantly reduced the severity of atherosclerosis, inhibited reconstruction of the artery wall and regulated the lipid profile; (2) enhanced antioxidant power, strengthened the activity of antioxidant enzymes, and decreased malondialdhyde levels; (3) significantly increased the viability of umbilical vein endothelial cells exposed to oxidative stress due to pretreatment with YD; (4) significantly reduced the level of pro-inflammatory cytokines; (5) significantly down-regulated NF-kB/p65 and up-regulated IkB in the YD-treated groups. Overall, these results demonstrated that YD intervention relieves atherosclerosis through regulating lipids, reducing lipid particle deposition in the endothelial layer of artery, enhancing antioxidant power, and repressing inflammation activity by inhibiting the nuclear factor-kappa B signal pathway.
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spelling pubmed-45088292015-07-28 Yindanxinnaotong, a Chinese compound medicine, synergistically attenuates atherosclerosis progress Cheng, Long Pan, Guo-feng Zhang, Xiao-dong Wang, Jian-lu Wang, Wan-dan Zhang, Jian-yong Wang, Hui Liang, Ri-xin Sun, Xiao-bo Sci Rep Article Yindanxinnaotong (YD), a traditional Chinese medicine, has been introduced to clinical medicine for more than a decade, while its pharmacological properties are still not to be well addressed. This report aimed to explore the anti-atherosclerosis properties and underlying mechanisms of YD. We initially performed a computational prediction based on a network pharmacology simulation, which clued YD exerted synergistically anti-atherosclerosis properties by vascular endothelium protection, lipid-lowering, anti-inflammation, and anti-oxidation. These outcomes were then validated in atherosclerosis rats. The experiments provided evidences indicating YD’s contribution in this study included, (1) significantly reduced the severity of atherosclerosis, inhibited reconstruction of the artery wall and regulated the lipid profile; (2) enhanced antioxidant power, strengthened the activity of antioxidant enzymes, and decreased malondialdhyde levels; (3) significantly increased the viability of umbilical vein endothelial cells exposed to oxidative stress due to pretreatment with YD; (4) significantly reduced the level of pro-inflammatory cytokines; (5) significantly down-regulated NF-kB/p65 and up-regulated IkB in the YD-treated groups. Overall, these results demonstrated that YD intervention relieves atherosclerosis through regulating lipids, reducing lipid particle deposition in the endothelial layer of artery, enhancing antioxidant power, and repressing inflammation activity by inhibiting the nuclear factor-kappa B signal pathway. Nature Publishing Group 2015-07-21 /pmc/articles/PMC4508829/ /pubmed/26196108 http://dx.doi.org/10.1038/srep12333 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Cheng, Long
Pan, Guo-feng
Zhang, Xiao-dong
Wang, Jian-lu
Wang, Wan-dan
Zhang, Jian-yong
Wang, Hui
Liang, Ri-xin
Sun, Xiao-bo
Yindanxinnaotong, a Chinese compound medicine, synergistically attenuates atherosclerosis progress
title Yindanxinnaotong, a Chinese compound medicine, synergistically attenuates atherosclerosis progress
title_full Yindanxinnaotong, a Chinese compound medicine, synergistically attenuates atherosclerosis progress
title_fullStr Yindanxinnaotong, a Chinese compound medicine, synergistically attenuates atherosclerosis progress
title_full_unstemmed Yindanxinnaotong, a Chinese compound medicine, synergistically attenuates atherosclerosis progress
title_short Yindanxinnaotong, a Chinese compound medicine, synergistically attenuates atherosclerosis progress
title_sort yindanxinnaotong, a chinese compound medicine, synergistically attenuates atherosclerosis progress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508829/
https://www.ncbi.nlm.nih.gov/pubmed/26196108
http://dx.doi.org/10.1038/srep12333
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