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Erzhi Pill(®) Protected Experimental Liver Injury Against Apoptosis via the PI3K/Akt/Raptor/Rictor Pathway

Erzhi Pill (EZP) is one of the basic prescriptions for treating liver diseases in traditional Chinese medicine. However, its mechanism of action is still undefined. The PI3K/AKT/Raptor/Rictor signaling pathway is closely related to apoptosis and plays a significant role in the pathogenesis of liver...

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Autores principales: Zhao, Hai-Mei, Zhang, Xiao-Yun, Lu, Xiu-Yun, Yu, Song-Ren, Wang, Xin, Zou, Yong, Zuo, Zheng-Yun, Liu, Duan-Yong, Zhou, Bu-Gao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880944/
https://www.ncbi.nlm.nih.gov/pubmed/29636693
http://dx.doi.org/10.3389/fphar.2018.00283
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author Zhao, Hai-Mei
Zhang, Xiao-Yun
Lu, Xiu-Yun
Yu, Song-Ren
Wang, Xin
Zou, Yong
Zuo, Zheng-Yun
Liu, Duan-Yong
Zhou, Bu-Gao
author_facet Zhao, Hai-Mei
Zhang, Xiao-Yun
Lu, Xiu-Yun
Yu, Song-Ren
Wang, Xin
Zou, Yong
Zuo, Zheng-Yun
Liu, Duan-Yong
Zhou, Bu-Gao
author_sort Zhao, Hai-Mei
collection PubMed
description Erzhi Pill (EZP) is one of the basic prescriptions for treating liver diseases in traditional Chinese medicine. However, its mechanism of action is still undefined. The PI3K/AKT/Raptor/Rictor signaling pathway is closely related to apoptosis and plays a significant role in the pathogenesis of liver disease. To define the mechanism of the hepatoprotective effect of EZP in the treatment of liver disease, hepatic injury induced by 2-acetylaminofluorene/partial hepatectomy was treated by EZP for 14 days. The therapeutic effect of EZP was confirmed by the decreased production of aspartate aminotransferase and alanine aminotransferase, recovery of pathological liver injury, followed by inhibition of pro-inflammatory cytokines and transforming growth factor-β1. Bromodeoxyuridine assay and TUNEL staining indicated that apoptosis was suppressed and the numbers of cells in S phase and G0/G1phase were decreased. The crucial proteins in the PI3K/AKT/Raptor/Rictor signaling pathway were deactivated in rats with experimental liver injury treated by EZP. These results indicated that the hepatoprotective effect of EZP via inhibition of hepatocyte apoptosis was closely related to repression of the PI3K/Akt/Raptor/Rictor signaling pathway.
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spelling pubmed-58809442018-04-10 Erzhi Pill(®) Protected Experimental Liver Injury Against Apoptosis via the PI3K/Akt/Raptor/Rictor Pathway Zhao, Hai-Mei Zhang, Xiao-Yun Lu, Xiu-Yun Yu, Song-Ren Wang, Xin Zou, Yong Zuo, Zheng-Yun Liu, Duan-Yong Zhou, Bu-Gao Front Pharmacol Pharmacology Erzhi Pill (EZP) is one of the basic prescriptions for treating liver diseases in traditional Chinese medicine. However, its mechanism of action is still undefined. The PI3K/AKT/Raptor/Rictor signaling pathway is closely related to apoptosis and plays a significant role in the pathogenesis of liver disease. To define the mechanism of the hepatoprotective effect of EZP in the treatment of liver disease, hepatic injury induced by 2-acetylaminofluorene/partial hepatectomy was treated by EZP for 14 days. The therapeutic effect of EZP was confirmed by the decreased production of aspartate aminotransferase and alanine aminotransferase, recovery of pathological liver injury, followed by inhibition of pro-inflammatory cytokines and transforming growth factor-β1. Bromodeoxyuridine assay and TUNEL staining indicated that apoptosis was suppressed and the numbers of cells in S phase and G0/G1phase were decreased. The crucial proteins in the PI3K/AKT/Raptor/Rictor signaling pathway were deactivated in rats with experimental liver injury treated by EZP. These results indicated that the hepatoprotective effect of EZP via inhibition of hepatocyte apoptosis was closely related to repression of the PI3K/Akt/Raptor/Rictor signaling pathway. Frontiers Media S.A. 2018-03-27 /pmc/articles/PMC5880944/ /pubmed/29636693 http://dx.doi.org/10.3389/fphar.2018.00283 Text en Copyright © 2018 Zhao, Zhang, Lu, Yu, Wang, Zou, Zuo, Liu and Zhou. 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 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 Pharmacology
Zhao, Hai-Mei
Zhang, Xiao-Yun
Lu, Xiu-Yun
Yu, Song-Ren
Wang, Xin
Zou, Yong
Zuo, Zheng-Yun
Liu, Duan-Yong
Zhou, Bu-Gao
Erzhi Pill(®) Protected Experimental Liver Injury Against Apoptosis via the PI3K/Akt/Raptor/Rictor Pathway
title Erzhi Pill(®) Protected Experimental Liver Injury Against Apoptosis via the PI3K/Akt/Raptor/Rictor Pathway
title_full Erzhi Pill(®) Protected Experimental Liver Injury Against Apoptosis via the PI3K/Akt/Raptor/Rictor Pathway
title_fullStr Erzhi Pill(®) Protected Experimental Liver Injury Against Apoptosis via the PI3K/Akt/Raptor/Rictor Pathway
title_full_unstemmed Erzhi Pill(®) Protected Experimental Liver Injury Against Apoptosis via the PI3K/Akt/Raptor/Rictor Pathway
title_short Erzhi Pill(®) Protected Experimental Liver Injury Against Apoptosis via the PI3K/Akt/Raptor/Rictor Pathway
title_sort erzhi pill(®) protected experimental liver injury against apoptosis via the pi3k/akt/raptor/rictor pathway
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880944/
https://www.ncbi.nlm.nih.gov/pubmed/29636693
http://dx.doi.org/10.3389/fphar.2018.00283
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