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Tanshinone IIA Protects Endothelial Cells from H(2)O(2)-Induced Injuries via PXR Activation

Tanshinone IIA (Tan IIA) is a pharmacologically active substance extracted from the rhizome of Salvia miltiorrhiza Bunge (also known as the Chinese herb Danshen), and is widely used to treat atherosclerosis. The pregnane X receptor (PXR) is a nuclear receptor that is a key regulator of xenobiotic an...

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Autores principales: Zhu, Haiyan, Chen, Zhiwu, Ma, Zengchun, Tan, Hongling, Xiao, Chengrong, Tang, Xianglin, Zhang, Boli, Wang, Yuguang, Gao, Yue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Applied Pharmacology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5685429/
https://www.ncbi.nlm.nih.gov/pubmed/28173640
http://dx.doi.org/10.4062/biomolther.2016.179
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author Zhu, Haiyan
Chen, Zhiwu
Ma, Zengchun
Tan, Hongling
Xiao, Chengrong
Tang, Xianglin
Zhang, Boli
Wang, Yuguang
Gao, Yue
author_facet Zhu, Haiyan
Chen, Zhiwu
Ma, Zengchun
Tan, Hongling
Xiao, Chengrong
Tang, Xianglin
Zhang, Boli
Wang, Yuguang
Gao, Yue
author_sort Zhu, Haiyan
collection PubMed
description Tanshinone IIA (Tan IIA) is a pharmacologically active substance extracted from the rhizome of Salvia miltiorrhiza Bunge (also known as the Chinese herb Danshen), and is widely used to treat atherosclerosis. The pregnane X receptor (PXR) is a nuclear receptor that is a key regulator of xenobiotic and endobiotic detoxification. Tan IIA is an efficacious PXR agonist that has a potential protective effect on endothelial injuries induced by xenobiotics and endobiotics via PXR activation. Previously numerous studies have demonstrated the possible effects of Tan IIA on human umbilical vein endothelial cells, but the further mechanism for its exerts the protective effect is not well established. To study the protective effects of Tan IIA against hydrogen peroxide (H(2)O(2)) in human umbilical vein endothelial cells (HUVECs), we pretreated cells with or without different concentrations of Tan IIA for 24 h, then exposed the cells to 400 μM H(2)O(2) for another 3 h. Therefore, our data strongly suggests that Tan IIA may lead to increased regeneration of glutathione (GSH) from the glutathione disulfide (GSSG) produced during the GSH peroxidase-catalyzed decomposition of H(2)O(2) in HUVECs, and the PXR plays a significant role in this process. Tan IIA may also exert protective effects against H(2)O(2)-induced apoptosis through the mitochondrial apoptosis pathway associated with the participation of PXR. Tan IIA protected HUVECs from inflammatory mediators triggered by H(2)O(2) via PXR activation. In conclusion, Tan IIA protected HUVECs against H(2)O(2)-induced cell injury through PXR-dependent mechanisms.
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spelling pubmed-56854292017-11-19 Tanshinone IIA Protects Endothelial Cells from H(2)O(2)-Induced Injuries via PXR Activation Zhu, Haiyan Chen, Zhiwu Ma, Zengchun Tan, Hongling Xiao, Chengrong Tang, Xianglin Zhang, Boli Wang, Yuguang Gao, Yue Biomol Ther (Seoul) Original Article Tanshinone IIA (Tan IIA) is a pharmacologically active substance extracted from the rhizome of Salvia miltiorrhiza Bunge (also known as the Chinese herb Danshen), and is widely used to treat atherosclerosis. The pregnane X receptor (PXR) is a nuclear receptor that is a key regulator of xenobiotic and endobiotic detoxification. Tan IIA is an efficacious PXR agonist that has a potential protective effect on endothelial injuries induced by xenobiotics and endobiotics via PXR activation. Previously numerous studies have demonstrated the possible effects of Tan IIA on human umbilical vein endothelial cells, but the further mechanism for its exerts the protective effect is not well established. To study the protective effects of Tan IIA against hydrogen peroxide (H(2)O(2)) in human umbilical vein endothelial cells (HUVECs), we pretreated cells with or without different concentrations of Tan IIA for 24 h, then exposed the cells to 400 μM H(2)O(2) for another 3 h. Therefore, our data strongly suggests that Tan IIA may lead to increased regeneration of glutathione (GSH) from the glutathione disulfide (GSSG) produced during the GSH peroxidase-catalyzed decomposition of H(2)O(2) in HUVECs, and the PXR plays a significant role in this process. Tan IIA may also exert protective effects against H(2)O(2)-induced apoptosis through the mitochondrial apoptosis pathway associated with the participation of PXR. Tan IIA protected HUVECs from inflammatory mediators triggered by H(2)O(2) via PXR activation. In conclusion, Tan IIA protected HUVECs against H(2)O(2)-induced cell injury through PXR-dependent mechanisms. The Korean Society of Applied Pharmacology 2017-11 2017-02-06 /pmc/articles/PMC5685429/ /pubmed/28173640 http://dx.doi.org/10.4062/biomolther.2016.179 Text en Copyright © 2017 The Korean Society of Applied Pharmacology http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Zhu, Haiyan
Chen, Zhiwu
Ma, Zengchun
Tan, Hongling
Xiao, Chengrong
Tang, Xianglin
Zhang, Boli
Wang, Yuguang
Gao, Yue
Tanshinone IIA Protects Endothelial Cells from H(2)O(2)-Induced Injuries via PXR Activation
title Tanshinone IIA Protects Endothelial Cells from H(2)O(2)-Induced Injuries via PXR Activation
title_full Tanshinone IIA Protects Endothelial Cells from H(2)O(2)-Induced Injuries via PXR Activation
title_fullStr Tanshinone IIA Protects Endothelial Cells from H(2)O(2)-Induced Injuries via PXR Activation
title_full_unstemmed Tanshinone IIA Protects Endothelial Cells from H(2)O(2)-Induced Injuries via PXR Activation
title_short Tanshinone IIA Protects Endothelial Cells from H(2)O(2)-Induced Injuries via PXR Activation
title_sort tanshinone iia protects endothelial cells from h(2)o(2)-induced injuries via pxr activation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5685429/
https://www.ncbi.nlm.nih.gov/pubmed/28173640
http://dx.doi.org/10.4062/biomolther.2016.179
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