AI Article Synopsis

  • MAFLD is a common liver condition characterized by fat accumulation in the liver, linked to obesity and metabolic disorders, and currently lacks approved medications for treatment.
  • 20-Hydroxyecdysone (20E), a natural plant steroid, has shown potential to improve metabolic conditions, making it a candidate for MAFLD treatment.
  • In experiments with ovariectomized rats on a high-fat diet, 20E reduced liver fat and visceral fat, while also enhancing certain metabolic pathways related to fat metabolism, indicating its promising role in managing MAFLD.

Article Abstract

Metabolic dysfunction-associated fatty liver disease (MAFLD) is defined as hepatic steatosis in combination with overweight, diabetes, or other metabolic risk factors. MAFLD affects a significant number of the global population and imposes substantial clinical and economic burdens. With no approved pharmacotherapy, current treatment options are limited to diet and exercise. Therefore, the development of medicines for MAFLD treatment or prevention is necessary. 20-Hydroxyecdysone (20E) is a natural steroid found in edible plants and has been shown to improve metabolism and dyslipidemia. Therefore, it may be useful for MAFLD treatment. Here, we aimed to determine how dietary supplementation with 20E affects fat accumulation and lipogenesis in the liver and adipose tissue of ovariectomized rats fed a high-fat, high-fructose diet (OHFFD). We found that 20E reduced hepatic triglyceride content and visceral fat deposition. 20E increased the phosphorylation of AMP-activated protein kinase and acetyl CoA carboxylase while reducing the expression of fatty acid synthase in the liver and adipose tissue. Additionally, 20E increased hepatic expression of carnitine palmitoyltransferase-1 and reduced adipose expression of sterol regulatory element-binding protein-1. In conclusion, 20E demonstrated beneficial effects in rats with OHFFD-induced MAFLD. These findings suggest that 20E may represent a promising option for MAFLD prevention or treatment.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10377470PMC
http://dx.doi.org/10.3390/biomedicines11072071DOI Listing

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