Cargando…

Puerarin Attenuated Early Diabetic Kidney Injury through Down-Regulation of Matrix Metalloproteinase 9 in Streptozotocin-Induced Diabetic Rats

Radix puerariae, a traditional Chinese herbal medication, has been used successfully to treat patients with early stage of diabetic nephropathy. However, the underlined mechanism of this renal protective effect has not been determined. In the current study, we investigated the effects and the mechan...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhong, Yifei, Zhang, Xianwen, Cai, Xianfan, Wang, Ke, Chen, Yiping, Deng, Yueyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893265/
https://www.ncbi.nlm.nih.gov/pubmed/24454919
http://dx.doi.org/10.1371/journal.pone.0085690
_version_ 1782299654252134400
author Zhong, Yifei
Zhang, Xianwen
Cai, Xianfan
Wang, Ke
Chen, Yiping
Deng, Yueyi
author_facet Zhong, Yifei
Zhang, Xianwen
Cai, Xianfan
Wang, Ke
Chen, Yiping
Deng, Yueyi
author_sort Zhong, Yifei
collection PubMed
description Radix puerariae, a traditional Chinese herbal medication, has been used successfully to treat patients with early stage of diabetic nephropathy. However, the underlined mechanism of this renal protective effect has not been determined. In the current study, we investigated the effects and the mechanism of puerarin in Streptozotocin (STZ)-induced diabetic rats. We treated STZ-rats with either puerarin or losartan, an angiotensin II receptor blocker, as compared to those treated with vehicle. We found that both puerarin and losartan attenuated kidney hypertrophy, mesangial expansion, proteinuria, and podocyte foot process effacement in STZ rats. In addition, both puerarin and losartan increased expression of podocyte slit diaphragm proteins such as nephrin and podocin. Interestingly, we found that puerarin treatment induced a more pronounced suppression of oxidative stress production and S-nitrosylation of proteins in the diabetic kidneys as compared to losartan treatment. Furthermore, we found that matrix metalloproteinase-9 (MMP-9), which is known to be activated by oxidative stress and S-nitrosylation of proteins, was also suppressed more extensively by puerarin than losartan. In conclusion, these data provide for the first time the potential mechanism to support the use of puerarin in the treatment of early diabetic nephropathy.
format Online
Article
Text
id pubmed-3893265
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-38932652014-01-21 Puerarin Attenuated Early Diabetic Kidney Injury through Down-Regulation of Matrix Metalloproteinase 9 in Streptozotocin-Induced Diabetic Rats Zhong, Yifei Zhang, Xianwen Cai, Xianfan Wang, Ke Chen, Yiping Deng, Yueyi PLoS One Research Article Radix puerariae, a traditional Chinese herbal medication, has been used successfully to treat patients with early stage of diabetic nephropathy. However, the underlined mechanism of this renal protective effect has not been determined. In the current study, we investigated the effects and the mechanism of puerarin in Streptozotocin (STZ)-induced diabetic rats. We treated STZ-rats with either puerarin or losartan, an angiotensin II receptor blocker, as compared to those treated with vehicle. We found that both puerarin and losartan attenuated kidney hypertrophy, mesangial expansion, proteinuria, and podocyte foot process effacement in STZ rats. In addition, both puerarin and losartan increased expression of podocyte slit diaphragm proteins such as nephrin and podocin. Interestingly, we found that puerarin treatment induced a more pronounced suppression of oxidative stress production and S-nitrosylation of proteins in the diabetic kidneys as compared to losartan treatment. Furthermore, we found that matrix metalloproteinase-9 (MMP-9), which is known to be activated by oxidative stress and S-nitrosylation of proteins, was also suppressed more extensively by puerarin than losartan. In conclusion, these data provide for the first time the potential mechanism to support the use of puerarin in the treatment of early diabetic nephropathy. Public Library of Science 2014-01-15 /pmc/articles/PMC3893265/ /pubmed/24454919 http://dx.doi.org/10.1371/journal.pone.0085690 Text en © 2014 Zhong et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhong, Yifei
Zhang, Xianwen
Cai, Xianfan
Wang, Ke
Chen, Yiping
Deng, Yueyi
Puerarin Attenuated Early Diabetic Kidney Injury through Down-Regulation of Matrix Metalloproteinase 9 in Streptozotocin-Induced Diabetic Rats
title Puerarin Attenuated Early Diabetic Kidney Injury through Down-Regulation of Matrix Metalloproteinase 9 in Streptozotocin-Induced Diabetic Rats
title_full Puerarin Attenuated Early Diabetic Kidney Injury through Down-Regulation of Matrix Metalloproteinase 9 in Streptozotocin-Induced Diabetic Rats
title_fullStr Puerarin Attenuated Early Diabetic Kidney Injury through Down-Regulation of Matrix Metalloproteinase 9 in Streptozotocin-Induced Diabetic Rats
title_full_unstemmed Puerarin Attenuated Early Diabetic Kidney Injury through Down-Regulation of Matrix Metalloproteinase 9 in Streptozotocin-Induced Diabetic Rats
title_short Puerarin Attenuated Early Diabetic Kidney Injury through Down-Regulation of Matrix Metalloproteinase 9 in Streptozotocin-Induced Diabetic Rats
title_sort puerarin attenuated early diabetic kidney injury through down-regulation of matrix metalloproteinase 9 in streptozotocin-induced diabetic rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893265/
https://www.ncbi.nlm.nih.gov/pubmed/24454919
http://dx.doi.org/10.1371/journal.pone.0085690
work_keys_str_mv AT zhongyifei puerarinattenuatedearlydiabetickidneyinjurythroughdownregulationofmatrixmetalloproteinase9instreptozotocininduceddiabeticrats
AT zhangxianwen puerarinattenuatedearlydiabetickidneyinjurythroughdownregulationofmatrixmetalloproteinase9instreptozotocininduceddiabeticrats
AT caixianfan puerarinattenuatedearlydiabetickidneyinjurythroughdownregulationofmatrixmetalloproteinase9instreptozotocininduceddiabeticrats
AT wangke puerarinattenuatedearlydiabetickidneyinjurythroughdownregulationofmatrixmetalloproteinase9instreptozotocininduceddiabeticrats
AT chenyiping puerarinattenuatedearlydiabetickidneyinjurythroughdownregulationofmatrixmetalloproteinase9instreptozotocininduceddiabeticrats
AT dengyueyi puerarinattenuatedearlydiabetickidneyinjurythroughdownregulationofmatrixmetalloproteinase9instreptozotocininduceddiabeticrats