Effects of growth hormone and insulin-like growth factor 1 (IGF-1) treatments on the nitrogen metabolism and hepatic IGF-1-messenger RNA expression in postoperative parenterally fed rats

JPEN J Parenter Enteral Nutr. 1996 Sep-Oct;20(5):325-31. doi: 10.1177/0148607196020005325.

Abstract

Background: Few studies have made direct comparisons of the metabolic effects of growth hormone (GH) and insulin-like growth factor 1 (IGF-1). We have assessed the dose-dependent effects of GH and IGF-1 treatments on nitrogen metabolism, intestinal structure, and hepatic IGF-1-messenger RNA (mRNA) expression in postoperative parenterally fed rats.

Methods: Rats were maintained on total parenteral nutrition (TPN) for 3 days after gastrectomy. GH (0.4 or 0.8 IU/kg/d) or IGF-1 (1,2, or 4 mg/kg/d) was infused throughout the experimental period. Anabolic effects of GH and IGF-1 were assessed by body weight change, nitrogen excretion, and whole-body protein turnover. Organ weights, intestinal structure, plasma IGF-1 levels and hepatic IGF-1-mRNA contents were also determined.

Results: Both GH and IGF-1 attenuated body weight loss and nitrogen excretion and increased whole-body protein synthesis and spleen weight. These observations suggest that the anabolic effects of 1 mg/kg/d of IGF-1 were equivalent to those of 0.66 IU/kg/d of GH. IGF-1, but not GH, reduced atrophy of the intestinal mucosa. GH treatment increased hepatic IGF-1-mRNA and the plasma IGF-1 level, whereas IGF-1 treatment increased the plasma IGF-1 level with no change in the hepatic IGF-1-mRNA content.

Conclusions: Administration of GH or IGF-1 attenuates catabolism after surgery. The anabolic effects of 1 mg/kg/d of IGF-1 are equivalent to those of 0.66 IU/kg/d of GH. IGF-1 reduces intestinal mucosal atrophy. GH increases hepatic IGF-1-mRNA and the plasma IGF-1 level.

MeSH terms

  • Animals
  • Blotting, Northern
  • Body Weight / drug effects
  • Body Weight / physiology
  • Cohort Studies
  • Dose-Response Relationship, Drug
  • Glycine / analysis
  • Glycine / metabolism
  • Human Growth Hormone / administration & dosage*
  • Insulin-Like Growth Factor I / administration & dosage*
  • Insulin-Like Growth Factor I / drug effects
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / metabolism
  • Liver / drug effects
  • Liver / metabolism*
  • Male
  • Nitrogen / metabolism*
  • Nitrogen / urine
  • Nitrogen Radioisotopes
  • Organ Size / drug effects
  • Organ Size / physiology
  • Parenteral Nutrition*
  • Postoperative Period
  • Proteins / metabolism
  • RNA, Messenger / analysis
  • RNA, Messenger / genetics
  • Rats
  • Rats, Wistar
  • Recombinant Proteins / administration & dosage

Substances

  • Nitrogen Radioisotopes
  • Proteins
  • RNA, Messenger
  • Recombinant Proteins
  • Human Growth Hormone
  • Insulin-Like Growth Factor I
  • Nitrogen
  • Glycine