Artesunate inhibits adipogeneis in 3T3-L1 preadipocytes by reducing the expression and/or phosphorylation levels of C/EBP-α, PPAR-γ, FAS, perilipin A, and STAT-3

Biochem Biophys Res Commun. 2016 May 20;474(1):220-225. doi: 10.1016/j.bbrc.2016.04.109. Epub 2016 Apr 22.

Abstract

Differentiation of preadipocyte, also called adipogenesis, leads to the phenotype of mature adipocyte. However, excessive adipogenesis is closely linked to the development of obesity. Artesunate, one of artemisinin-type sesquiterpene lactones from Artemisia annua L., is known for anti-malarial and anti-cancerous activities. In this study, we investigated the effect of artesunate on adipogenesis in 3T3-L1 preadipocytes. Artesunate strongly inhibited lipid accumulation and triglyceride (TG) synthesis during the differentiation of 3T3-L1 preadipocytes into adipocytes at 5 μM concentration. Artesunate at 5 μM also reduced not only the expressions of CCAAT/enhancer-binding protein-α (C/EBP-α), peroxisome proliferator-activated receptor-γ (PPAR-γ), fatty acid synthase (FAS), and perilipin A but also the phosphorylation levels of signal transducer and activator of transcription-3 (STAT-3) during adipocyte differentiation. Moreover, artesunate at 5 μM reduced leptin, but not adiponectin, mRNA expression during adipocyte differentiation. Taken together, these findings demonstrate that artesunate inhibits adipogenesis in 3T3-L1 preadipoytes through the reduced expression and/or phosphorylation levels of C/EBP-α, PPAR-γ, FAS, perilipin A, and STAT-3.

Keywords: Adipogenesis; Artesunate; C/EBP-α; FAS; PPAR-γ; STAT-3.

MeSH terms

  • 3T3 Cells
  • Adipogenesis / drug effects
  • Adipogenesis / physiology*
  • Animals
  • Artemisinins / administration & dosage*
  • Artesunate
  • CCAAT-Enhancer-Binding Protein-alpha / metabolism*
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology
  • Mice
  • PPAR gamma / metabolism*
  • Perilipin-1 / metabolism*
  • Phosphorylation / drug effects
  • STAT3 Transcription Factor / metabolism*
  • fas Receptor / metabolism*

Substances

  • Artemisinins
  • CCAAT-Enhancer-Binding Protein-alpha
  • Fas protein, mouse
  • PPAR gamma
  • Perilipin-1
  • STAT3 Transcription Factor
  • Stat3 protein, mouse
  • fas Receptor
  • Artesunate