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Effect of Qufengtongluo Decoction on PI3K/Akt Signaling Pathway in the Kidney of Type 2 Diabetes Mellitus Rat (GK Rat) with Diabetic Nephropathy

Qufengtongluo (QFTL) decoction is an effective treatment for diabetic nephropathy (DN). However, the underlying molecular mechanism is still unclear. In this study, we try to investigate whether QFTL decoction acts via inhibiting PI3K/Akt signaling pathway. Twenty-four GK rats were randomly divided...

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Autores principales: Huang, Wei-Jun, Fu, Qiang, Xiao, Yong-Hua, Gong, Qing, Wu, Wen-Jing, Shen, Zi-Long, Zhang, Hua, Jia, Xu, Huang, Xue-Min, Zhang, Ya-Xin, Zhao, Jin-Xi, Wang, Shi-Dong, Jia, Mian, Zhang, Yu-Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820584/
https://www.ncbi.nlm.nih.gov/pubmed/29552086
http://dx.doi.org/10.1155/2018/8421979
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author Huang, Wei-Jun
Fu, Qiang
Xiao, Yong-Hua
Gong, Qing
Wu, Wen-Jing
Shen, Zi-Long
Zhang, Hua
Jia, Xu
Huang, Xue-Min
Zhang, Ya-Xin
Zhao, Jin-Xi
Wang, Shi-Dong
Jia, Mian
Zhang, Yu-Ting
author_facet Huang, Wei-Jun
Fu, Qiang
Xiao, Yong-Hua
Gong, Qing
Wu, Wen-Jing
Shen, Zi-Long
Zhang, Hua
Jia, Xu
Huang, Xue-Min
Zhang, Ya-Xin
Zhao, Jin-Xi
Wang, Shi-Dong
Jia, Mian
Zhang, Yu-Ting
author_sort Huang, Wei-Jun
collection PubMed
description Qufengtongluo (QFTL) decoction is an effective treatment for diabetic nephropathy (DN). However, the underlying molecular mechanism is still unclear. In this study, we try to investigate whether QFTL decoction acts via inhibiting PI3K/Akt signaling pathway. Twenty-four GK rats were randomly divided into 3 groups: blank group, sham-operated group, and QFTL group. After model establishment, rats in QFTL group were given QFTL decoction by gavage, while the rest were given pure water. During the 8-week intervention, 24 hr urinal protein was measured every 2-3 weeks. After intervention, kidneys were removed for pathological smear, quantitative real-time PCR, and western blotting to detect expression levels of p-PI3K, p-Akt, PTEN, TGF-β, PI3K mRNA, Akt mRNA, PTEN mRNA, and TGF-β mRNA. QFTL group showed a slighter degree of renal fibrosis in Masson and PASM staining and a greater reduction of 24 hr urinal protein than blank group. Compared to blank group, expression levels of p-PI3K, p-Akt, PI3K mRNA, and Akt mRNA were lower in QFTL group, while expression levels of PTEN and PTEN mRNA were higher. Besides, TGF-β was downregulated by QFTL decoction. In conclusion, this study suggests that QFTL decoction might inhibit PI3K/Akt signaling pathway via activating PTEN and inhibiting TGF-β.
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spelling pubmed-58205842018-03-18 Effect of Qufengtongluo Decoction on PI3K/Akt Signaling Pathway in the Kidney of Type 2 Diabetes Mellitus Rat (GK Rat) with Diabetic Nephropathy Huang, Wei-Jun Fu, Qiang Xiao, Yong-Hua Gong, Qing Wu, Wen-Jing Shen, Zi-Long Zhang, Hua Jia, Xu Huang, Xue-Min Zhang, Ya-Xin Zhao, Jin-Xi Wang, Shi-Dong Jia, Mian Zhang, Yu-Ting Evid Based Complement Alternat Med Research Article Qufengtongluo (QFTL) decoction is an effective treatment for diabetic nephropathy (DN). However, the underlying molecular mechanism is still unclear. In this study, we try to investigate whether QFTL decoction acts via inhibiting PI3K/Akt signaling pathway. Twenty-four GK rats were randomly divided into 3 groups: blank group, sham-operated group, and QFTL group. After model establishment, rats in QFTL group were given QFTL decoction by gavage, while the rest were given pure water. During the 8-week intervention, 24 hr urinal protein was measured every 2-3 weeks. After intervention, kidneys were removed for pathological smear, quantitative real-time PCR, and western blotting to detect expression levels of p-PI3K, p-Akt, PTEN, TGF-β, PI3K mRNA, Akt mRNA, PTEN mRNA, and TGF-β mRNA. QFTL group showed a slighter degree of renal fibrosis in Masson and PASM staining and a greater reduction of 24 hr urinal protein than blank group. Compared to blank group, expression levels of p-PI3K, p-Akt, PI3K mRNA, and Akt mRNA were lower in QFTL group, while expression levels of PTEN and PTEN mRNA were higher. Besides, TGF-β was downregulated by QFTL decoction. In conclusion, this study suggests that QFTL decoction might inhibit PI3K/Akt signaling pathway via activating PTEN and inhibiting TGF-β. Hindawi 2018-01-14 /pmc/articles/PMC5820584/ /pubmed/29552086 http://dx.doi.org/10.1155/2018/8421979 Text en Copyright © 2018 Wei-Jun Huang et al. https://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
Huang, Wei-Jun
Fu, Qiang
Xiao, Yong-Hua
Gong, Qing
Wu, Wen-Jing
Shen, Zi-Long
Zhang, Hua
Jia, Xu
Huang, Xue-Min
Zhang, Ya-Xin
Zhao, Jin-Xi
Wang, Shi-Dong
Jia, Mian
Zhang, Yu-Ting
Effect of Qufengtongluo Decoction on PI3K/Akt Signaling Pathway in the Kidney of Type 2 Diabetes Mellitus Rat (GK Rat) with Diabetic Nephropathy
title Effect of Qufengtongluo Decoction on PI3K/Akt Signaling Pathway in the Kidney of Type 2 Diabetes Mellitus Rat (GK Rat) with Diabetic Nephropathy
title_full Effect of Qufengtongluo Decoction on PI3K/Akt Signaling Pathway in the Kidney of Type 2 Diabetes Mellitus Rat (GK Rat) with Diabetic Nephropathy
title_fullStr Effect of Qufengtongluo Decoction on PI3K/Akt Signaling Pathway in the Kidney of Type 2 Diabetes Mellitus Rat (GK Rat) with Diabetic Nephropathy
title_full_unstemmed Effect of Qufengtongluo Decoction on PI3K/Akt Signaling Pathway in the Kidney of Type 2 Diabetes Mellitus Rat (GK Rat) with Diabetic Nephropathy
title_short Effect of Qufengtongluo Decoction on PI3K/Akt Signaling Pathway in the Kidney of Type 2 Diabetes Mellitus Rat (GK Rat) with Diabetic Nephropathy
title_sort effect of qufengtongluo decoction on pi3k/akt signaling pathway in the kidney of type 2 diabetes mellitus rat (gk rat) with diabetic nephropathy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820584/
https://www.ncbi.nlm.nih.gov/pubmed/29552086
http://dx.doi.org/10.1155/2018/8421979
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