High-protein diets alters body composition and improves insulin resistance in a rat model of low birth weight

J Investig Med. 2012 Dec;60(8):1174-9. doi: 10.2310/JIM.0b013e3182746ce8.

Abstract

Objective: We aimed to investigate the effects of early high-protein supplementation on low birth weight (LBW)-associated adult metabolic disturbances.

Materials and methods: This study involved 32 LBW rat pups that were fed a normal protein (20% of energy intake) diet or high-protein (30% of energy intake) diet on their first 4 weeks of life. Sixteen rat pups with normal birth weight (NBW) fed the normal-protein diet were included as control. Biochemical measurements were performed at 4 and 12 weeks of age.

Results: Low birth weight offspring showed significantly (P < 0.05) increased fat mass percentage and adipocyte size and decreased lean mass percentage and muscle fiber size relative to NBW offspring. These LBW-related changes in body composition were corrected by high-protein diet intervention. At 12 weeks of age, the fasting insulin level (7.14 ± 0.83 vs 9.27 ± 0.67 mU/L) and homeostasis model of insulin resistance (1.71 ± 0.35 vs 2.30 ± 0.44) were significantly lower in high protein-fed LBW offspring than in normal protein-fed LBW offspring. Low birth weight rat pups showed a significant (P < 0.05) reduction in serum adiponectin concentrations, glucose transporter 4 mRNA abundance, and phosphorylation levels of AMP-activated protein kinase (AMPK) and mammalian target of rapamycin (mTOR) relative to NBW controls. These LBW-associated alterations in gene expression were reversed by early high-protein treatment.

Conclusions: Early postnatal high-protein intake alters the body composition and improves insulin resistance in adults with LBW, which is associated with activation of the AMPK and mTOR pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Birth Weight / physiology*
  • Body Composition / physiology*
  • Dietary Proteins / administration & dosage
  • Dietary Proteins / metabolism*
  • Female
  • Insulin Resistance / physiology*
  • Models, Animal*
  • Pregnancy
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Thinness / diet therapy
  • Thinness / metabolism*

Substances

  • Dietary Proteins