Protective effect of Shenfu Injection on regulation of autophagy in rats with chronic heart failure based on PI3K/Akt/mTOR pathway.
10.19540/j.cnki.cjcmm.20230619.502
- Author:
Xiao-Qian LIAO
1
;
Shu-Min HUANG
2
;
Xing-Yu FAN
1
;
Zi-Yi WANG
1
;
Qian ZHANG
1
;
Zhi-Xi HU
1
Author Information
1. School of Traditional Chinese Medicine, Hunan University of Chinese Medicine Changsha 410208, China.
2. School of Traditional Chinese Medicine, Hunan University of Chinese Medicine Changsha 410208, China the Second People's Hospital Affiliated to Fujian University of Traditional Chinese Medicine Fuzhou 350003, China.
- Publication Type:Journal Article
- Keywords:
PI3K/Akt/mTOR signaling pathway;
Shenfu Injection;
autophagy;
chronic heart failure
- MeSH:
Rats;
Animals;
Proto-Oncogene Proteins c-akt/metabolism*;
Phosphatidylinositol 3-Kinases/metabolism*;
Rats, Sprague-Dawley;
TOR Serine-Threonine Kinases/metabolism*;
Heart Failure/drug therapy*;
Autophagy;
Fibrosis
- From:
China Journal of Chinese Materia Medica
2023;48(21):5908-5914
- CountryChina
- Language:Chinese
-
Abstract:
This study aimed to investigate the mechanism and target sites of Shenfu Injection in the intervention of chronic heart fai-lure based on the PI3K/Akt/mTOR autophagy signaling pathway. The chronic heart failure model was induced in rats by subcutaneous injection of isoproterenol. The model rats were randomly divided into model group, Shenfu Injection group, and 3-methyladenine autophagy inhibitor(3-MA) group. A normal group was also set up. After 15 days of administration, cardiac function indexes of the rats were detected by echocardiography. The serum N-terminal pro-B-type natriuretic peptide(NT-proBNP) levels were measured using the ELISA. HE and Masson staining was performed to observe the morphological changes in myocardial tissues, and electron microscopy was used to observe the autophagosomes in myocardial tissues. Western blot was conducted to measure the changes in autophagy-related proteins(LC3 Ⅱ/Ⅰ and p62), PI3K, Akt, mTOR, and phosphorylation levels. The results showed that compared with normal group, model group in rats led to reduced cardiac function, significant activation of cardiac autophagy, increased fibrotic lesions in myocardial tissues, structural disorder of the myocardium, increased autophagosomes, and cytoplasmic vacuolization. Compared with model group, Shenfu Injection group in rats led to cardiac function significantly improved, myocardial fibrosis decreased, and the number of autophagosomes and cytoplasmic vacuolization decreased. The phosphorylation levels of PI3K, Akt, and mTOR were significantly increased(P<0.01). In the 3-MA group, autophagy was inhibited through the activation of the PI3K/Akt/mTOR signaling pathway, resulting in improved cardiac function, reduced myocardial fibrosis, and no significant cytoplasmic vacuolization. The findings suggest that Shenfu Injection can activate the PI3K/Akt/mTOR signaling pathway and inhibit autophagy, thereby improving cardiac function.
