Anti-Obesity and Anti-Diabetic Effects of Ostericum koreanum (Ganghwal) Extract

Int J Mol Sci. 2024 Apr 30;25(9):4908. doi: 10.3390/ijms25094908.

Abstract

"Ganghwal" is a widely used herbal medicine in Republic of Korea, but it has not been reported as a treatment strategy for obesity and diabetes within adipocytes. In this study, we determined that Ostericum koreanum extract (OKE) exerts an anti-obesity effect by inhibiting adipogenesis and an anti-diabetic effect by increasing the expression of genes related to glucose uptake in adipocytes and inhibiting α-glucosidase activity. 3T3-L1 preadipocytes were differentiated for 8 days in methylisobutylxanthine, dexamethasone, and insulin medium, and the effect of OKE was confirmed by the addition of 50 and 100 µg/mL of OKE during the differentiation process. This resulted in a reduction in lipid accumulation and the expression of PPARγ (Peroxisome proliferator-activated receptor γ) and C/EBPα (CCAAT enhancer binding protein α). Significant activation of AMPK (AMP-activated protein kinase), increased expression of GLUT4 (Glucose Transporter Type 4), and inhibition of α-glucosidase activity were also observed. These findings provide the basis for the anti-obesity and anti-diabetic effects of OKE. In addition, OKE has a significant antioxidant effect. This study presents OKE as a potential natural product-derived material for the treatment of patients with metabolic diseases such as obesity- and obesity-induced diabetes.

Keywords: Ganghwal; Ostericum koreanum; anti-diabetes; anti-obesity; antioxidant effect.

MeSH terms

  • 3T3-L1 Cells*
  • AMP-Activated Protein Kinases / metabolism
  • Adipocytes* / drug effects
  • Adipocytes* / metabolism
  • Adipogenesis* / drug effects
  • Animals
  • Anti-Obesity Agents* / pharmacology
  • Antioxidants / pharmacology
  • CCAAT-Enhancer-Binding Protein-alpha / genetics
  • CCAAT-Enhancer-Binding Protein-alpha / metabolism
  • Cell Differentiation / drug effects
  • Crassulaceae / chemistry
  • Glucose Transporter Type 4 / genetics
  • Glucose Transporter Type 4 / metabolism
  • Glycoside Hydrolase Inhibitors / pharmacology
  • Hypoglycemic Agents* / pharmacology
  • Hypoglycemic Agents* / therapeutic use
  • Lipid Metabolism / drug effects
  • Mice
  • Obesity / drug therapy
  • Obesity / metabolism
  • PPAR gamma* / genetics
  • PPAR gamma* / metabolism
  • Plant Extracts* / chemistry
  • Plant Extracts* / pharmacology
  • alpha-Glucosidases / metabolism

Substances

  • Plant Extracts
  • Hypoglycemic Agents
  • PPAR gamma
  • Anti-Obesity Agents
  • Glucose Transporter Type 4
  • CCAAT-Enhancer-Binding Protein-alpha
  • alpha-Glucosidases
  • AMP-Activated Protein Kinases
  • Antioxidants
  • Glycoside Hydrolase Inhibitors

Grants and funding

This study was supported by the National Research Foundation of Korea (NRF) funded by the Korean government (RS-2023-00278650).