AI Article Synopsis

  • Metabolic dysfunction-associated steatotic liver disease (MASLD) is a serious health issue linked to insulin resistance, involving conditions from simple fat accumulation in the liver to liver cancer.
  • A study explored the effects of a traditional herbal remedy used in East Asia and its active ingredient, atractylodin, on treating MASLD in mice, showing reductions in body weight, liver fat, and blood sugar levels after 8 weeks on a high-fat diet.
  • The findings revealed that atractylodin activated a key protein (AMPK), leading to improvements in obesity, fatty liver, and glucose metabolism, indicating its potential as a treatment option for MASLD.

Article Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD), which encompasses a spectrum of conditions ranging from simple steatosis to hepatocellular carcinoma, is a growing global health concern associated with insulin resistance. Since there are limited treatment options for MASLD, this study investigated the therapeutic potential of , a traditional herbal remedy for digestive disorders in East Asia, and its principal component, atractylodin, in treating MASLD. Following 8 weeks of high-fat diet (HFD) feeding, mice received oral doses of 30, 60, or 120 mg/kg of . In HFD-fed mice, treatment reduced the body weight; serum triglyceride, total cholesterol, and alanine aminotransferase levels; and hepatic lipid content. Furthermore, significantly ameliorated fasting serum glucose, fasting serum insulin, and homeostatic model assessment of insulin resistance levels in response to HFD. Additionally, a glucose tolerance test demonstrated improved glucose homeostasis. Treatment with 5 or 10 mg/kg atractylodin also resulted in anti-obesity, anti-steatosis, and glucose-lowering effects. Atractylodin treatment resulted in the downregulation of key lipogenic genes (, , , and ) and the upregulation of genes regulated by peroxisome proliferator-activated receptor-α. Notably, the molecular docking model suggested a robust binding affinity between atractylodin and AMP-activated protein kinase (AMPK). Atractylodin activated AMPK, which contributed to SREBP1c regulation. In conclusion, our results revealed that and atractylodin activated the AMPK signaling pathway, leading to improvements in HFD-induced obesity, fatty liver, and glucose intolerance. This study suggests that the phytochemical, atractylodin, can be a treatment option for MASLD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11535289PMC
http://dx.doi.org/10.4062/biomolther.2024.083DOI Listing

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