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Buyang Huanwu Decoction Promotes Angiogenesis after Cerebral Ischemia by Inhibiting the Nox4/ROS Pathway

BACKGROUND: Buyang Huanwu decoction (BYHWD), an important traditional Chinese medicine (TCM), has been used clinically for centuries for the treatment of various diseases. The study aims to explore the BYHWD effects on angiogenesis and neuroprotection after cerebral ischemia/reperfusion (CI/R) injur...

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Autores principales: Shen, Jian, Huang, Kaiyuan, Zhu, Yu, Xu, Kangli, Zhan, Renya, Pan, Jianwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7415092/
https://www.ncbi.nlm.nih.gov/pubmed/32802129
http://dx.doi.org/10.1155/2020/5264205
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author Shen, Jian
Huang, Kaiyuan
Zhu, Yu
Xu, Kangli
Zhan, Renya
Pan, Jianwei
author_facet Shen, Jian
Huang, Kaiyuan
Zhu, Yu
Xu, Kangli
Zhan, Renya
Pan, Jianwei
author_sort Shen, Jian
collection PubMed
description BACKGROUND: Buyang Huanwu decoction (BYHWD), an important traditional Chinese medicine (TCM), has been used clinically for centuries for the treatment of various diseases. The study aims to explore the BYHWD effects on angiogenesis and neuroprotection after cerebral ischemia/reperfusion (CI/R) injury in rats and to explore the underlying angiogenic roles and mechanisms of BYHWD in hydrogen peroxide (H(2)O(2)) induced oxidative stress in human umbilical vein endothelial cells (HUVECs) model. METHODS: The effects of BYHWD on neurological function were screened by measuring neurological deficits, spatial memory function, and angiogenesis (by microvascular density (MVD) and cerebral blood flow (CBF)) after CI/R injury in middle cerebral artery occlusion (MCAO) in vivo in rats. In vitro, we examined the angiogenic roles and mechanisms of action of BYHWD in an H(2)O(2)-induced oxidative stress HUVECs model by measuring cell viability, apoptosis, vascular tube formation, intracellular ROS generation, NADPH oxidase (Nox) activity, and Nox4 protein expression. RESULTS: BYHWD significantly improved neurological function, including neurological deficits and spatial learning and memory, and significantly increased MVD and CBF in the ischemic penumbra after CI/R injury in rats. BYHWD significantly increased cell viability, inhibited apoptosis, induced vascular tube formation, decreased intracellular ROS generation, and reduced Nox activity and Nox4 protein expression in H(2)O(2)-treated HUVECs in a dose-dependent manner. CONCLUSIONS: Our study demonstrates that BYHWD promotes neurological function recovery and increases angiogenesis. BYHWD exerts angiogenic effects against cerebral ischemic injury through the downregulation of Nox4, which results in the reduction of ROS generation.
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spelling pubmed-74150922020-08-14 Buyang Huanwu Decoction Promotes Angiogenesis after Cerebral Ischemia by Inhibiting the Nox4/ROS Pathway Shen, Jian Huang, Kaiyuan Zhu, Yu Xu, Kangli Zhan, Renya Pan, Jianwei Evid Based Complement Alternat Med Research Article BACKGROUND: Buyang Huanwu decoction (BYHWD), an important traditional Chinese medicine (TCM), has been used clinically for centuries for the treatment of various diseases. The study aims to explore the BYHWD effects on angiogenesis and neuroprotection after cerebral ischemia/reperfusion (CI/R) injury in rats and to explore the underlying angiogenic roles and mechanisms of BYHWD in hydrogen peroxide (H(2)O(2)) induced oxidative stress in human umbilical vein endothelial cells (HUVECs) model. METHODS: The effects of BYHWD on neurological function were screened by measuring neurological deficits, spatial memory function, and angiogenesis (by microvascular density (MVD) and cerebral blood flow (CBF)) after CI/R injury in middle cerebral artery occlusion (MCAO) in vivo in rats. In vitro, we examined the angiogenic roles and mechanisms of action of BYHWD in an H(2)O(2)-induced oxidative stress HUVECs model by measuring cell viability, apoptosis, vascular tube formation, intracellular ROS generation, NADPH oxidase (Nox) activity, and Nox4 protein expression. RESULTS: BYHWD significantly improved neurological function, including neurological deficits and spatial learning and memory, and significantly increased MVD and CBF in the ischemic penumbra after CI/R injury in rats. BYHWD significantly increased cell viability, inhibited apoptosis, induced vascular tube formation, decreased intracellular ROS generation, and reduced Nox activity and Nox4 protein expression in H(2)O(2)-treated HUVECs in a dose-dependent manner. CONCLUSIONS: Our study demonstrates that BYHWD promotes neurological function recovery and increases angiogenesis. BYHWD exerts angiogenic effects against cerebral ischemic injury through the downregulation of Nox4, which results in the reduction of ROS generation. Hindawi 2020-07-31 /pmc/articles/PMC7415092/ /pubmed/32802129 http://dx.doi.org/10.1155/2020/5264205 Text en Copyright © 2020 Jian Shen et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Shen, Jian
Huang, Kaiyuan
Zhu, Yu
Xu, Kangli
Zhan, Renya
Pan, Jianwei
Buyang Huanwu Decoction Promotes Angiogenesis after Cerebral Ischemia by Inhibiting the Nox4/ROS Pathway
title Buyang Huanwu Decoction Promotes Angiogenesis after Cerebral Ischemia by Inhibiting the Nox4/ROS Pathway
title_full Buyang Huanwu Decoction Promotes Angiogenesis after Cerebral Ischemia by Inhibiting the Nox4/ROS Pathway
title_fullStr Buyang Huanwu Decoction Promotes Angiogenesis after Cerebral Ischemia by Inhibiting the Nox4/ROS Pathway
title_full_unstemmed Buyang Huanwu Decoction Promotes Angiogenesis after Cerebral Ischemia by Inhibiting the Nox4/ROS Pathway
title_short Buyang Huanwu Decoction Promotes Angiogenesis after Cerebral Ischemia by Inhibiting the Nox4/ROS Pathway
title_sort buyang huanwu decoction promotes angiogenesis after cerebral ischemia by inhibiting the nox4/ros pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7415092/
https://www.ncbi.nlm.nih.gov/pubmed/32802129
http://dx.doi.org/10.1155/2020/5264205
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