Gigantol Ameliorates Metabolic Dysfunction-Associated Steatohepatitis by Promoting TFEB-Mediated Lipophagy and Fatty Acid Oxidation

  • J Agric Food Chem. 2026 Feb 11;74(5):4389-4406. doi: 10.1021/acs.jafc.5c09366.
Cong Zhang  1  2 Yingxi Luo  3 Yangkun Xiong  1 Liang Chen  4 Haixia Zhao  1  2 Zhenpeng Qiu  4  5  6  7 Yuan Yang  8
Affiliations
  • 1. College of Basic Medical Science, China Three Gorges University, Yichang 443002, China.
  • 2. Hubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges University, Yichang 443002, China.
  • 3. College of Biological & Pharmaceutical Sciences, China Three Gorges University, Yichang 443002, China.
  • 4. School of Pharmacy, Hubei University of Chinese Medicine, Wuhan 430065, China.
  • 5. Hubei Key Laboratory of Resources and Chemistry of Chinese Medicine, Hubei University of Chinese Medicine, Wuhan 430065, China.
  • 6. Center of Traditional Chinese Medicine Modernization for Liver Diseases, School of Pharmacy, Hubei University of Chinese Medicine, Wuhan 430065, China.
  • 7. Hubei Shizhen Laboratory, Wuhan 430061, China.
  • 8. Institute of Maternal and Child Health, Wuhan Children's Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430016, China.
Abstract

Gigantol, a naturally active molecule derived from the edible plant Dendrobium, has been demonstrated to have hepatoprotective potential, but its effect in the treatment of metabolic dysfunction-associated steatohepatitis (MASH) remains unclear. Here, we found that gigantol treatment greatly corrected dyslipidemia, hepatic dysfunction, and hepatic histological changes that arrested MASH occurrence in high-fat and high-fructose-diet (HFFD)-fed mice. Mechanistically, gigantol promoted the nuclear translocation of the transcription factor EB (TFEB) to regulate the key factors of lipophagy and fatty acid oxidation to maintain hepatic lipid metabolism homeostasis. Consistent results were observed in palmitic acid-induced cell models. Notably, silencing TFEB reversed the effect of gigantol in enhancing lipophagy and fatty acid oxidation in vivo and in vitro. In summary, this study provides strong evidence to demonstrate that gigantol attenuates HFFD-induced MASH by promoting TFEB-dependent lipophagy and fatty acid oxidation, suggesting that gigantol, an edible plant-derived compound, is promising to be developed as a therapeutic drug for MASH in the future.

Keywords
TFEB; fatty acid oxidation; gigantol; lipophagy; metabolic dysfunction-associated steatohepatitis.
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