Anti-Obesity Effect of 6,8-Diprenylgenistein, an Isoflavonoid of Cudrania tricuspidata Fruits in High-Fat Diet-Induced Obese Mice

Nutrients. 2015 Dec 15;7(12):10480-90. doi: 10.3390/nu7125544.

Abstract

Obesity, which is characterized by excessive fat accumulation, is associated with several pathological disorders, including metabolic diseases. In this study, the anti-obesity effect of 6,8-diprenylgenistein (DPG), a major isoflavonoid of Cudrania tricuspidata fruits was investigated using high fat-diet (HFD)-induced obese mice at the doses of 10 and 30 mg/kg for six week. The body weight of the DPG-treated groups was significantly lower compared to the HFD-treated group. In addition, fat accumulation in epididymal adipose tissue and liver was dramatically decreased in the HFD + DPG groups. The food efficiency ratios of the HFD + DPG groups were also lower compared to the HFD group with the same food intake. Metabolic parameters that had increased in the HFD group were decreased in the HFD + DPG groups. Further studies demonstrate that DPG efficiently reduces lipogenic genes by regulation of transcription factors, such as peroxisome proliferator-activated receptor γ (PPARγ) and CCAAT/enhancer-binding protein α (C/EBPα), and hormones, such as leptin and adiponection. DPG also regulates acetyl-CoA carboxylase (ACC) and hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR) by AMP-activated protein kinase (AMPK) activation. Taken together, DPG is beneficial for the regulation of obesity, especially resulting from high fat intake.

Keywords: 6,8-Diprenylgenistein (DPG); AMPK; Cudrania tricuspidata; high-fat diet-induced obesity; lipid profile.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / genetics
  • AMP-Activated Protein Kinases / metabolism
  • Acetyl-CoA Carboxylase / genetics
  • Acetyl-CoA Carboxylase / metabolism
  • Adiponectin / metabolism
  • Adipose Tissue / drug effects
  • Adipose Tissue / metabolism
  • Animals
  • Anti-Obesity Agents / pharmacology*
  • CCAAT-Enhancer-Binding Protein-alpha / genetics
  • CCAAT-Enhancer-Binding Protein-alpha / metabolism
  • Diet, High-Fat
  • Fruit / chemistry*
  • Gene Expression Regulation
  • Genistein / analogs & derivatives*
  • Genistein / pharmacology
  • Hydroxymethylglutaryl CoA Reductases / genetics
  • Hydroxymethylglutaryl CoA Reductases / metabolism
  • Isoflavones / pharmacology*
  • Leptin / metabolism
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Obese
  • Moraceae / chemistry*
  • Obesity / drug therapy*
  • PPAR gamma / genetics
  • PPAR gamma / metabolism
  • Plant Extracts / pharmacology

Substances

  • 6,8-diprenylgenistein
  • Adiponectin
  • Anti-Obesity Agents
  • CCAAT-Enhancer-Binding Protein-alpha
  • Isoflavones
  • Leptin
  • PPAR gamma
  • Plant Extracts
  • Genistein
  • Hydroxymethylglutaryl CoA Reductases
  • AMP-Activated Protein Kinases
  • Acetyl-CoA Carboxylase