The therapeutic effect of Qishen Huoxue Granule on myocardial injury in sepsis rats and its underlying mechanism via suppressing excessive autophagy
Open Access
- 1 September 2025
- journal article
- research article
- Published by Springer Nature in Scientific Reports
- Vol. 15 (1) , 1-15
Abstract
To determine therapeutic effect of Qishen Huoxue Granule (QHG) on the myocardial injury in sepsis and whether it is through the inhibition of excessive autophagy by using network pharmacological analysis and in vitro.120 SPF male Wistar rats were divided into 6 groups. Firstly, the function of the heart were evaluated through echocardiography, and pathological changes of myocardial tissue was observed by Hematoxylin-eosin (H&E) and Transmission electron microscopy (TEM). Subsequently, enzyme-linked immunosorbent assay (ELISA) was employed to measure the levels of myocardial injury markers (cTnT and BNP) and inflammatory cytokines (TNF-α and IL-1β). Finally, the expression of proteins associated with the MasR/PI3K-AKT-mTOR pathway and autophagy-related proteins was evaluated using immunohistochemistry, immunofluorescence, RT-qPCR, and Western blot analysis.The results demonstrated that QHG significantly improved systolic function in rats, reduced levels of myocardial injury markers and inflammatory cytokines, and downregulated autophagy-related genes (ATG5, LC3, and Beclin1). However, when QHG was combined with inhibitors of the MasR/PI3K-AKT-mTOR pathway, the mRNA and protein expression levels of pathway components were reduced. Concurrently, the mRNA and protein expressions of autophagy indicators were upregulated, counteracting the inhibitory effect of QHG on excessive autophagy.QHG ameliorated the myocardial injury in sepsis rats by inhibiting the excessive autophagy in myocardial cells via activating the MasR/PI3K-AKT-mTOR pathway.Keywords
Funding Information
- Grants from National Natural Science Foundation of China (No. 82374069, No. 82374069, No. 82374069, No. 82374069, No. 82374069)
- High-level Public Health Technical Personnel Project (Subject Leader-03-15, Subject Leader-03-15, Subject Leader-03-15, Subject Leader-03-15, Subject Leader-03-15)
This publication has 43 references indexed in Scilit:
- Mas receptor mediates cardioprotection of angiotensin‐(1‐7) against Angiotensin II‐induced cardiomyocyte autophagy and cardiac remodelling through inhibition of oxidative stressJournal of Cellular and Molecular Medicine, 2015
- Antagonism of angiotensin 1–7 prevents the therapeutic effects of recombinant human ACE2Journal of Molecular Medicine, 2015
- LC3- and p62-based biochemical methods for the analysis of autophagy progression in mammalian cellsMethods, 2015
- A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study of the Effects of Qili Qiangxin Capsules in Patients With Chronic Heart FailureJACC, 2013
- Kinetics and protective role of autophagy in a mouse cecal ligation and puncture-induced sepsisCritical Care, 2013
- Sirtinol attenuates trauma hemorrhage–induced hepatic injury through Akt-dependent pathway in ratsJournal of Trauma and Acute Care Surgery, 2013
- Rapamycin Inhibits the mTOR/p70S6K Pathway and Attenuates Cardiac Fibrosis in Adriamycin-induced Dilated CardiomyopathyThe Thoracic and Cardiovascular Surgeon, 2012
- Immunodesign of experimental sepsis by cecal ligation and punctureNature Protocols, 2008
- Molecular Mechanisms Involved in the Angiotensin-(1-7)/Mas Signaling Pathway in CardiomyocytesHypertension, 2008
- Cardiac autophagy is a maladaptive response to hemodynamic stressJournal of Clinical Investigation, 2007