Astragaloside IV regulates Snail1 lactylation and acetylation to mediate macrophage polarization and improve myocardial infarction.
- Author:
Shaopeng CHEN
1
,
2
;
Rudian KANG
3
;
Xinbao HONG
4
;
Yilong LIU
4
Author Information
1. Department of Cardiology, Second Affiliated Hospital of Fujian Medical University, Quanzhou 362000, China. *Corresponding author, E-mail: cshaopeng8812@
2. com.
3. Department of Nephrology, Quanzhou First Hospital, Quanzhou 362002, China.
4. Department of Cardiology, Second Affiliated Hospital of Fujian Medical University, Quanzhou 362000, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Myocardial Infarction/drug therapy*;
Rats;
Snail Family Transcription Factors/metabolism*;
Macrophages/cytology*;
Myocytes, Cardiac/metabolism*;
Triterpenes/pharmacology*;
Saponins/pharmacology*;
Acetylation/drug effects*;
Apoptosis/drug effects*;
Mice;
Cell Line;
RAW 264.7 Cells;
Transforming Growth Factor beta/metabolism*
- From:
Chinese Journal of Cellular and Molecular Immunology
2025;41(4):289-299
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the impact of Astragaloside-IV (AS-IV) on the progression of myocardial infarction (MI) through macrophage-dependent mechanisms by regulating Snail1 lactylation and acetylation, as well as the transforming growth factor β (TGF-β) pathway. Methods Oxygen glucose deprivation (OGD) was used to establish an in vitro myocardial ischemia model in rat cardiomyocytes (H9c2), which were then treated with AS-IV. Cell viability was assessed using CCK-8, apoptosis was evaluated by flow cytometry, and LDH levels were measured to assess cellular damage. RAW246.7 cells were treated with LPS, and lactate levels in the supernatant were measured using ELISA, while expression of macrophage phenotype markers was evaluated using Western blot. RAW246.7 cell-conditioned medium (CM) was co-cultured with H9c2 cells to assess the protective effects of AS-IV on macrophage CM-mediated H9c2 damage. RAW246.7 cells were induced to differentiate into M1-like macrophages using LPS (100 ng/mL) + IFN-γ (20 ng/mL), and Snail1 was overexpressed in M1 macrophages. Transfected M1 macrophage CM was co-cultured with H9c2 cells to validate the mechanisms of AS-IV in MI. An MI rat model was established by ligation of the left anterior descending coronary artery (LAD), and was treated with AS-IV. Cardiac function, myocardial cell apoptosis, and cardiac tissue pathology were studied using echocardiography, TUNEL, and HE staining, respectively. Results Compared to the OGD group, AS-IV treatment promoted cell viability, reduced apoptosis and decreased LDH release. LPS upregulated lactate levels in the supernatant of RAW246.7 cell cultures and induced polarization of RAW246.7 cells to the M1 phenotype. AS-IV attenuated the damaging effects of RAW246.7 cell CM on H9c2 cells . Overexpression of Snail1 in M1 macrophages weakened the protective effects of AS-IV on H9c2 cells . In vivo study, results showed that, compared to the MI group, AS-IV treatment reduced lactate levels in the hearts of MI rats, improved cardiac function and myocardial injury and attenuated myocardial cell apoptosis. Conclusion AS-IV inhibits TGF-β pathway activation through the suppression of Snail1 lactylation and acetylation in a macrophage-dependent manner, thereby mitigating myocardial cell damage following MI.
