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Updated: Jul 6, 2026

In Vitro Modeling of Fat Deposition in Metabolic Dysfunction-Associated Steatotic Liver Disease
Published on: July 19, 2024
Ganoderic acid A alleviates metabolic dysfunction-associated fatty liver disease through attenuating steatosis and
Yang Yao1, Zhujun Liu2, Xujiao Wang3
1Chongqing Key Laboratory of Development and Utilization of Authentic Medicinal Materials in Three Gorges Reservoir Area, Chongqing Three Gorges Medical College, Wanzhou 404120, China; Department of Public Fundamentals, Chongqing Three Gorges Medical College, Wanzhou 404120, China; Department of Pharmacology, College of Pharmacy, Dalian Medical University, Dalian 116044, China.
Abstract:
Metabolic dysfunction-associated steatotic liver disease (MASLD) is a global metabolic epidemic with no specific effective therapy, characterized by hepatic steatosis and excessive hepatocyte apoptosis. This study explored the protective effects and mechanisms of Ganoderic acid A (GA-A) against MASLD. In high-fat diet (HFD)-fed mice and palmitic acid (PA)-stimulated HepG2 cells, GA-A notably relieved hepatic steatosis, liver injury, lipid metabolic disorders and hepatocyte apoptosis. Acetyl-CoA carboxylase (ACC) was identified as a direct target of GA-A via protein microarray, molecular docking, SPR, CETSA and Co-IP assays. Mechanistically, GA-A activated the AMPK-ACC pathway and suppressed ACC activity. Application of the ACC inhibitor ND646 and ACC silencing partially abrogated GA-A's therapeutic effects, confirming both ACC-dependent and independent actions. Collectively, GA-A directly targets ACC to ameliorate MASLD, indicating its potential as a promising candidate drug for this metabolic liver disease.
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