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HuangqiGuizhiWuwu Decoction Prevents Vascular Dysfunction in Diabetes via Inhibition of Endothelial Arginase 1
Hyperglycemia induces vascular endothelial dysfunction, which contributes to the development of vascular complication of diabetes. A classic prescription of traditional medicine, HuangqiGuizhiWuwu Decoction (HGWWD) has been used for the treatment of various cardiovascular and cerebrovascular disease...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7109290/ https://www.ncbi.nlm.nih.gov/pubmed/32269530 http://dx.doi.org/10.3389/fphys.2020.00201 |
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author | Cheng, Hong Lu, Tian Wang, Jingya Xia, Yucen Chai, Xiaoshu Zhang, Minyi Yao, Yutong Zhou, Na Zhou, Sisi Chen, Xinyi Su, Weiwei Liu, Cunzhi Yi, Wei Chen, Yongjun Yao, Lin |
author_facet | Cheng, Hong Lu, Tian Wang, Jingya Xia, Yucen Chai, Xiaoshu Zhang, Minyi Yao, Yutong Zhou, Na Zhou, Sisi Chen, Xinyi Su, Weiwei Liu, Cunzhi Yi, Wei Chen, Yongjun Yao, Lin |
author_sort | Cheng, Hong |
collection | PubMed |
description | Hyperglycemia induces vascular endothelial dysfunction, which contributes to the development of vascular complication of diabetes. A classic prescription of traditional medicine, HuangqiGuizhiWuwu Decoction (HGWWD) has been used for the treatment of various cardiovascular and cerebrovascular diseases, which all are related with vascular pathology. The present study investigated the effect of HGWWD treatment in streptozocin (STZ)-induced vascular dysfunction in mouse models. In vivo studies were performed using wild type mice as well as arginase 1 knockout specific in endothelial cells (EC-A1(–/–)) of control mice, diabetes mice and diabetes mice treated with HGWWD (60 g crude drugs/kg/d) for 2 weeks. For in vitro studies, aortic tissues were treated with mice serum containing HGWWD with or without adenoviral arginase 1 (Ad-A1) transduction in high glucose (HG) medium. We found that HGWWD treatment restored STZ-induced impaired mean velocity and pulsatility index of mouse left femoral arteries, aortic pulse wave velocity and vascular endothelial relaxation accompanied by elevated NO production in the aorta and plasma, as well as reduced endothelial arginase activity and aortic arginase 1 expression. The protective effect of HGWWD is reversed by an inhibitor of nitric oxide synthesis. Meanwhile, the preventive effect of serum containing HGWWD in endothelial vascular dysfunction is completely blocked by Ad-A1 transduction in HG incubated aortas. HGWWD treatment further improved endothelial vascular dysfunction in STZ induced EC-A1(–/–) mice. This study demonstrates that HGWWD improved STZ-induced vascular dysfunction through arginase 1 – NO signaling, specifically targeting endothelial arginase 1. |
format | Online Article Text |
id | pubmed-7109290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71092902020-04-08 HuangqiGuizhiWuwu Decoction Prevents Vascular Dysfunction in Diabetes via Inhibition of Endothelial Arginase 1 Cheng, Hong Lu, Tian Wang, Jingya Xia, Yucen Chai, Xiaoshu Zhang, Minyi Yao, Yutong Zhou, Na Zhou, Sisi Chen, Xinyi Su, Weiwei Liu, Cunzhi Yi, Wei Chen, Yongjun Yao, Lin Front Physiol Physiology Hyperglycemia induces vascular endothelial dysfunction, which contributes to the development of vascular complication of diabetes. A classic prescription of traditional medicine, HuangqiGuizhiWuwu Decoction (HGWWD) has been used for the treatment of various cardiovascular and cerebrovascular diseases, which all are related with vascular pathology. The present study investigated the effect of HGWWD treatment in streptozocin (STZ)-induced vascular dysfunction in mouse models. In vivo studies were performed using wild type mice as well as arginase 1 knockout specific in endothelial cells (EC-A1(–/–)) of control mice, diabetes mice and diabetes mice treated with HGWWD (60 g crude drugs/kg/d) for 2 weeks. For in vitro studies, aortic tissues were treated with mice serum containing HGWWD with or without adenoviral arginase 1 (Ad-A1) transduction in high glucose (HG) medium. We found that HGWWD treatment restored STZ-induced impaired mean velocity and pulsatility index of mouse left femoral arteries, aortic pulse wave velocity and vascular endothelial relaxation accompanied by elevated NO production in the aorta and plasma, as well as reduced endothelial arginase activity and aortic arginase 1 expression. The protective effect of HGWWD is reversed by an inhibitor of nitric oxide synthesis. Meanwhile, the preventive effect of serum containing HGWWD in endothelial vascular dysfunction is completely blocked by Ad-A1 transduction in HG incubated aortas. HGWWD treatment further improved endothelial vascular dysfunction in STZ induced EC-A1(–/–) mice. This study demonstrates that HGWWD improved STZ-induced vascular dysfunction through arginase 1 – NO signaling, specifically targeting endothelial arginase 1. Frontiers Media S.A. 2020-03-25 /pmc/articles/PMC7109290/ /pubmed/32269530 http://dx.doi.org/10.3389/fphys.2020.00201 Text en Copyright © 2020 Cheng, Lu, Wang, Xia, Chai, Zhang, Yao, Zhou, Zhou, Chen, Su, Liu, Yi, Chen and Yao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Cheng, Hong Lu, Tian Wang, Jingya Xia, Yucen Chai, Xiaoshu Zhang, Minyi Yao, Yutong Zhou, Na Zhou, Sisi Chen, Xinyi Su, Weiwei Liu, Cunzhi Yi, Wei Chen, Yongjun Yao, Lin HuangqiGuizhiWuwu Decoction Prevents Vascular Dysfunction in Diabetes via Inhibition of Endothelial Arginase 1 |
title | HuangqiGuizhiWuwu Decoction Prevents Vascular Dysfunction in Diabetes via Inhibition of Endothelial Arginase 1 |
title_full | HuangqiGuizhiWuwu Decoction Prevents Vascular Dysfunction in Diabetes via Inhibition of Endothelial Arginase 1 |
title_fullStr | HuangqiGuizhiWuwu Decoction Prevents Vascular Dysfunction in Diabetes via Inhibition of Endothelial Arginase 1 |
title_full_unstemmed | HuangqiGuizhiWuwu Decoction Prevents Vascular Dysfunction in Diabetes via Inhibition of Endothelial Arginase 1 |
title_short | HuangqiGuizhiWuwu Decoction Prevents Vascular Dysfunction in Diabetes via Inhibition of Endothelial Arginase 1 |
title_sort | huangqiguizhiwuwu decoction prevents vascular dysfunction in diabetes via inhibition of endothelial arginase 1 |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7109290/ https://www.ncbi.nlm.nih.gov/pubmed/32269530 http://dx.doi.org/10.3389/fphys.2020.00201 |
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