Effects of yeast hydrolysate on hepatic lipid metabolism in high-fat-diet-induced obese mice: yeast hydrolysate suppresses body fat accumulation by attenuating fatty acid synthesis

Ann Nutr Metab. 2012;61(2):89-94. doi: 10.1159/000338441.

Abstract

Aims: We observed whether the anti-obesity activity of yeast hydrolysate (YH) was due to the alteration of lipid-regulating enzyme activities.

Methods: Male ICR mice were divided into four groups: a normal diet group (ND; 4.2% fat), a high-fat diet group (HF; 27.7% fat), an HF group treated orally with 0.5% or 1% YH in the drinking water (HF+YH0.5; 27.7% fat and HF+YH1; 27.7% fat).

Results: After 5 weeks, the YH groups (HF+YH0.5=3.92±0.17 g/100 g BW and HF+YH1=3.76±0.13 g/100 g BW) had significantly lower levels of epididymal fats compared to the HF group (4.91±0.29 g/100 g BW; p<0.05). YH supplementation produced a decrease in serum triglycerides and low-density lipoprotein cholesterol concentrations and body weight gain, and produced a dose-dependent significant increase in serum ghrelin compared with the HF group (p<0.05). Hepatic glucose-6-phosphate dehydrogenase (G6PD) activity was inhibited by YH supplementation compared with the HF group, and mice treated orally with 1% YH exhibited a significant decrease in hepatic malic enzyme (ME) activity compared to obese mice treated with the vehicle (HF=10.44±2.74 nmol/min/mg protein vs. HF+YH1=6.68±2.23 nmol/min/mg protein; p<0.05).

Conclusions: YH supplementation suppressed body fat accumulation by attenuating fatty acid synthesis through the downregulation of hepatic G6PD and ME activities.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / drug effects*
  • Adipose Tissue / metabolism
  • Animals
  • Anti-Obesity Agents / pharmacology
  • Cholesterol, LDL / blood
  • Diet, High-Fat
  • Down-Regulation
  • Ghrelin / blood
  • Glucosephosphate Dehydrogenase / antagonists & inhibitors
  • Glucosephosphate Dehydrogenase / genetics
  • Glucosephosphate Dehydrogenase / metabolism
  • Leptin / blood
  • Lipid Metabolism / drug effects*
  • Lipogenesis / drug effects*
  • Liver / drug effects*
  • Liver / enzymology
  • Malate Dehydrogenase / antagonists & inhibitors
  • Malate Dehydrogenase / genetics
  • Malate Dehydrogenase / metabolism
  • Male
  • Mice
  • Mice, Inbred ICR
  • Protein Hydrolysates / pharmacology*
  • Triglycerides / blood
  • Weight Gain / drug effects
  • Yeasts / enzymology*

Substances

  • Anti-Obesity Agents
  • Cholesterol, LDL
  • Ghrelin
  • Leptin
  • Protein Hydrolysates
  • Triglycerides
  • Malate Dehydrogenase
  • Glucosephosphate Dehydrogenase