Curcumin attenuates insulin resistance and hepatic lipid accumulation in a rat model of intra-uterine growth restriction through insulin signalling pathway and sterol regulatory element binding proteins

Br J Nutr. 2019 Sep 28;122(6):616-624. doi: 10.1017/S0007114519001508. Epub 2019 Jun 25.

Abstract

The objective of the present study was to investigate the effect of curcumin on insulin resistance (IR) and hepatic lipid accumulation in intra-uterine growth restriction (IUGR). Rats with a normal birth weight (NBW) or IUGR were fed basic diets (NBW and IUGR groups) or basic diets supplemented with curcumin (NBW-C and IUGR-C groups) from 6 to 12 weeks. Rats in the IUGR group showed higher levels of glucose and homeostasis model assessment for insulin resistance index (HOMA-IR) (P < 0·05) than in the NBW group. The livers of IUGR rats exhibited higher (P < 0·05) concentration of TAG and lower (P < 0·05) activities of lipolysis enzymes compared with the normal rats. In response to dietary curcumin supplementation, concentrations of serum insulin, glucose and HOMA-IR, pyruvate, TAG, total cholesterol and NEFA in the liver were decreased (P < 0·05). The concentrations of glycogen and activities of lipolysis enzymes in the liver were increased (P < 0·05) in the IUGR-C group compared with the IUGR group. These results were associated with lower (P < 0·05) phosphorylated insulin receptor substrate 1, protein kinase B or Akt, glycogen synthase kinase 3β and expressions of sterol regulatory element binding protein 1 and fatty acid synthase (FASN); decreased expressions for Cd36, sterol regulatory element binding protein 1c (Srebf1) and Fasn; increased (P < 0·05) expression of PPARα; and expressions for Ppara and hormone-sensitive lipase in the liver of IUGR-C rats than the IUGR rats. Maternal malnutrition caused IR and lipid accumulation in the liver. Curcumin supplementation prevented IR by regulating insulin signalling pathways and attenuated hepatic lipid accumulation.

Keywords: Curcumin; Insulin resistance; Intra-uterine growth restriction; Lipid metabolism; Rats.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Curcumin / pharmacology*
  • Disease Models, Animal
  • Female
  • Fetal Growth Retardation / metabolism*
  • Gene Expression / drug effects
  • Insulin / blood*
  • Insulin Resistance*
  • Lipid Metabolism / drug effects*
  • Lipolysis
  • Liver / drug effects*
  • Liver / metabolism
  • Liver Glycogen / metabolism
  • Pregnancy
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction / drug effects*
  • Sterol Regulatory Element Binding Proteins / metabolism*

Substances

  • Insulin
  • Liver Glycogen
  • Sterol Regulatory Element Binding Proteins
  • Curcumin