Anti-Autophagy Mechanism of Zhi Gan Prescription Based on Network Pharmacology in Nonalcoholic Steatohepatitis Rats

Zhi Gan prescription (ZGP) has been clinically proven to exert a favorable therapeutic effect on nonalcoholic steatohepatitis (NASH). This study purpose to reveal the underlying molecular mechanisms of ZGP action in NASH. Systematic network pharmacology was used to identify bioactive components, pot...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in pharmacology Vol. 12; p. 708479
Main Authors Qin, Chufeng, Luo, Lichuan, Cui, Yusheng, Jiang, Li, Li, Beilei, Lou, Yijie, Weng, Zhuofan, Lou, Jingwen, Liu, Chenxin, Weng, Cuiting, Wang, Zhaojun, Ji, Yunxi
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 19.07.2021
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Zhi Gan prescription (ZGP) has been clinically proven to exert a favorable therapeutic effect on nonalcoholic steatohepatitis (NASH). This study purpose to reveal the underlying molecular mechanisms of ZGP action in NASH. Systematic network pharmacology was used to identify bioactive components, potential targets, and the underlying mechanism of ZGP action in NASH. High fat (HF)-induced NASH model rats were used to assess the effect of ZGP against NASH, and to verify the possible molecular mechanisms as predicted by network pharmacology. A total of 138 active components and 366 potential targets were acquired in ZGP. In addition, 823 targets of NASH were also screened. experiments showed that ZGP significantly improved the symptoms in HF-induced NASH rats. qRT-PCR and western blot analyses showed that ZGP could regulate the hub genes, PTEN, IL-6 and TNF in NASH model rats. In addition, ZGP suppressed mitochondrial autophagy through mitochondrial fusion and fission via the PINK/Parkin pathway. ZGP exerts its effects on NASH through mitochondrial autophagy. These findings provide novel insights into the mechanisms of ZGP in NASH.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
This article was submitted to Gastrointestinal and Hepatic Pharmacology, a section of the journal Frontiers in Pharmacology
Edited by: Jiang-Jiang Qin, Institute of Cancer and Basic Medicine (CAS), China
Zuodong Qin, Hunan University of Science and Engineering, China
These authors have contributed equally to this work
Reviewed by: Hongwei Guo, Guangxi Medical University, China
ISSN:1663-9812
1663-9812
DOI:10.3389/fphar.2021.708479