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Yiqihuoxue Formula Activates Autophagy and Offers Renoprotection in a Rat Model of Adenine-Induced Kidney Disease

Chronic kidney disease (CKD) is a worldwide health problem for which effective therapeutic methods are still lacking. Traditional Chinese medicine (TCM) has been indicated as an effective alternative treatment for kidney disease. In this study, a clinically effective therapy, yiqihuoxue (YQHX) formu...

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Autores principales: Xia, Chen Hui, Han, Xue Ting, Zhang, Xueqin, Zhu, Ze Bing, Guo, Jing, Cui, Hai Lan, Jiang, Han Xue, Huang, Wei Jun, Chen, Guo Zi, Liu, Yu Ning, Liu, Wei Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6948341/
https://www.ncbi.nlm.nih.gov/pubmed/31949466
http://dx.doi.org/10.1155/2019/3423981
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author Xia, Chen Hui
Han, Xue Ting
Zhang, Xueqin
Zhu, Ze Bing
Guo, Jing
Cui, Hai Lan
Jiang, Han Xue
Huang, Wei Jun
Chen, Guo Zi
Liu, Yu Ning
Liu, Wei Jing
author_facet Xia, Chen Hui
Han, Xue Ting
Zhang, Xueqin
Zhu, Ze Bing
Guo, Jing
Cui, Hai Lan
Jiang, Han Xue
Huang, Wei Jun
Chen, Guo Zi
Liu, Yu Ning
Liu, Wei Jing
author_sort Xia, Chen Hui
collection PubMed
description Chronic kidney disease (CKD) is a worldwide health problem for which effective therapeutic methods are still lacking. Traditional Chinese medicine (TCM) has been indicated as an effective alternative treatment for kidney disease. In this study, a clinically effective therapy, yiqihuoxue (YQHX) formula, was administrated to adenine-induced kidney disease rats for 6 weeks. We found that the adenine rats displayed a significant reduction in renal function as evidenced by the increased levels of serum creatinine (Scr), blood urea nitrogen (BUN), and 24-h urinary albumin level, which were attenuated by the YQHX treatment. The glomerulosclerosis, interstitial fibrosis, arteriolosclerosis, interstitial inflammation, and tubular dilatation were reversed by the YQHX treatment in the adenine rats. Furthermore, the hepatic damage characterized by increased levels of aspartate aminotransferase and alanine aminotransferase and inflammatory cell infiltration was improved by YQHX. In addition, the number of apoptotic cells in the adenine rats was obviously reduced by the YQHX treatment as manifested by the lower expression level of cleaved caspase-3 protein. Moreover, the YQHX treatment downregulated the expression levels of fibronectin, type I collagen, α-smooth muscle actin, and TGF-β1 in the adenine rats. Furthermore, autophagy was activated by the YQHX treatment, which manifested as an increased LC3-II and Beclin-1 expression levels and a decreased p62 level. In conclusion, the YQHX formula might retard the progression of kidney disease by activating autophagy.
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spelling pubmed-69483412020-01-16 Yiqihuoxue Formula Activates Autophagy and Offers Renoprotection in a Rat Model of Adenine-Induced Kidney Disease Xia, Chen Hui Han, Xue Ting Zhang, Xueqin Zhu, Ze Bing Guo, Jing Cui, Hai Lan Jiang, Han Xue Huang, Wei Jun Chen, Guo Zi Liu, Yu Ning Liu, Wei Jing Evid Based Complement Alternat Med Research Article Chronic kidney disease (CKD) is a worldwide health problem for which effective therapeutic methods are still lacking. Traditional Chinese medicine (TCM) has been indicated as an effective alternative treatment for kidney disease. In this study, a clinically effective therapy, yiqihuoxue (YQHX) formula, was administrated to adenine-induced kidney disease rats for 6 weeks. We found that the adenine rats displayed a significant reduction in renal function as evidenced by the increased levels of serum creatinine (Scr), blood urea nitrogen (BUN), and 24-h urinary albumin level, which were attenuated by the YQHX treatment. The glomerulosclerosis, interstitial fibrosis, arteriolosclerosis, interstitial inflammation, and tubular dilatation were reversed by the YQHX treatment in the adenine rats. Furthermore, the hepatic damage characterized by increased levels of aspartate aminotransferase and alanine aminotransferase and inflammatory cell infiltration was improved by YQHX. In addition, the number of apoptotic cells in the adenine rats was obviously reduced by the YQHX treatment as manifested by the lower expression level of cleaved caspase-3 protein. Moreover, the YQHX treatment downregulated the expression levels of fibronectin, type I collagen, α-smooth muscle actin, and TGF-β1 in the adenine rats. Furthermore, autophagy was activated by the YQHX treatment, which manifested as an increased LC3-II and Beclin-1 expression levels and a decreased p62 level. In conclusion, the YQHX formula might retard the progression of kidney disease by activating autophagy. Hindawi 2019-12-24 /pmc/articles/PMC6948341/ /pubmed/31949466 http://dx.doi.org/10.1155/2019/3423981 Text en Copyright © 2019 Chen Hui Xia 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
Xia, Chen Hui
Han, Xue Ting
Zhang, Xueqin
Zhu, Ze Bing
Guo, Jing
Cui, Hai Lan
Jiang, Han Xue
Huang, Wei Jun
Chen, Guo Zi
Liu, Yu Ning
Liu, Wei Jing
Yiqihuoxue Formula Activates Autophagy and Offers Renoprotection in a Rat Model of Adenine-Induced Kidney Disease
title Yiqihuoxue Formula Activates Autophagy and Offers Renoprotection in a Rat Model of Adenine-Induced Kidney Disease
title_full Yiqihuoxue Formula Activates Autophagy and Offers Renoprotection in a Rat Model of Adenine-Induced Kidney Disease
title_fullStr Yiqihuoxue Formula Activates Autophagy and Offers Renoprotection in a Rat Model of Adenine-Induced Kidney Disease
title_full_unstemmed Yiqihuoxue Formula Activates Autophagy and Offers Renoprotection in a Rat Model of Adenine-Induced Kidney Disease
title_short Yiqihuoxue Formula Activates Autophagy and Offers Renoprotection in a Rat Model of Adenine-Induced Kidney Disease
title_sort yiqihuoxue formula activates autophagy and offers renoprotection in a rat model of adenine-induced kidney disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6948341/
https://www.ncbi.nlm.nih.gov/pubmed/31949466
http://dx.doi.org/10.1155/2019/3423981
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