Oligostilbenes extracts from Iris lactea Pall. var. chinensis (Fisch.) Koidz improve lipid metabolism in HFD/STZ-induced diabetic mice and inhibit adipogenesis in 3T3-L1 cells

Biomed Pharmacother. 2020 Nov:131:110800. doi: 10.1016/j.biopha.2020.110800. Epub 2020 Sep 29.

Abstract

The present study investigated the anti-diabetic effects of Oligostilbenes extracts (Olie) from Iris lactea Pall. var. chinensis (Fisch.) Koidz (I. lactea) and the potential mechanisms, in high-fat-diet (HFD)-induced diabetic mice and 3T3-L1 adipocytes. Olie are a group of major active extracts from I. lactea that have been used as nutraceutical because of their antioxidant activity. Six-week Olie treatment improved fasting blood glucose levels, as well as blood lipid profiles in HFD/streptozocin (STZ)-induced diabetic mice, compared with non-treated mice. Olie treatment upregulated the levels of phosphorylated of AMPK and lipolysis-related proteins, while the hepatic expression of ACC and FAS in diabetic mice was inhibited. In cultured 3T3-L1 cells, Olie (2-15 μg/mL) treatment dose-dependently suppressed the differentiation into mature adipocytes and lowered cellular lipid accumulation. Consistently, Olie reduced expression of adipogenic transcription factors including CCAAT/enhancer-binding protein β (C/EBPβ) and peroxisome proliferator-activated receptor γ (PPARγ). In addition, mitochondrial function in 3T3-L1 adipocytes was improved after Olie treatment. Taken together, our findings indicate that a lipid-lowering effect of Olie in HFD/STZ-induced diabetic mice and adipogenesis/ lipogenesis suppressing effect in 3T3-L1 cells, via regulating the expression of lipid metabolism-related proteins.

Keywords: 3T3-L1 cells; Anti-adipogenesis; Lipid metabolism; Oligostilbenes extracts; Type 2 diabetes.

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / drug effects
  • Adipogenesis / drug effects
  • Animals
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diet, High-Fat
  • Dose-Response Relationship, Drug
  • Hypolipidemic Agents / administration & dosage
  • Hypolipidemic Agents / isolation & purification
  • Hypolipidemic Agents / pharmacology
  • Iris / chemistry*
  • Lipid Metabolism / drug effects
  • Lipogenesis / drug effects
  • Male
  • Mice
  • Mice, Inbred ICR
  • Plant Extracts / administration & dosage
  • Plant Extracts / pharmacology*
  • Stilbenes / administration & dosage
  • Stilbenes / isolation & purification
  • Stilbenes / pharmacology*
  • Streptozocin

Substances

  • Hypolipidemic Agents
  • Plant Extracts
  • Stilbenes
  • Streptozocin