Regulation of metabolic water and protein compartments by insulin-like growth factor-I and testosterone in growth hormone-deficient lit/lit mice

J Endocrinol. 1993 Dec;139(3):431-9. doi: 10.1677/joe.0.1390431.

Abstract

Insulin-like growth factor-I (IGF-I) and testosterone are major hormonal regulators of protein metabolism. We chose genetically GH-deficient little (lit/lit) mice to test whether these anabolic hormones act independently or in concert with each other to stimulate protein metabolism. Hormones were administered for 14 days at constant rates to 14-week-old lit/lit female mice, IGF-I was infused via mini-osmotic pumps at 30 micrograms/day and testosterone was administered using 30 mg pellets. Food consumption was measured during the experimental period, and at the end we measured: (a) serum IGF-I, IGF-I-binding proteins (IGFBPs) and blood urea nitrogen (BUN); (b) body and musculo-skeletal carcass weights; (c) musculo-skeletal carcass water, fat, protein and mineral; and (d) selected organ weights plus protein and DNA contents. We found that both of these growth-stimulatory hormones, IGF-I and testosterone, alone and in combination, had anabolic effects on different metabolic compartments in specific target organs. The most unexpected finding in this study was that the IGF-I-induced increase in musculo-skeletal carcass weight arose solely from increased water, revealing the importance of this compartment as an early target of IGF-I action. Other effects caused specifically by IGF-I, but not testosterone, included increases in serum IGFBP-3, body weight and spleen weight. The specific effect of testosterone, but not IGF-I, was to increase serum IGFBP-2. Independent effects were induced by each hormone alone for kidney and spleen weight, kidney and spleen protein content and BUN.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Body Weight / drug effects
  • Carrier Proteins / analysis
  • Drug Synergism
  • Female
  • Growth Hormone / deficiency*
  • Insulin-Like Growth Factor Binding Protein 2
  • Insulin-Like Growth Factor Binding Proteins
  • Insulin-Like Growth Factor I / analysis
  • Insulin-Like Growth Factor I / pharmacology*
  • Kidney / anatomy & histology
  • Kidney / metabolism
  • Liver / metabolism
  • Mice
  • Mice, Mutant Strains
  • Muscles / drug effects
  • Muscles / metabolism
  • Organ Size / drug effects
  • Proteins / metabolism*
  • Somatomedins / analysis
  • Spleen / anatomy & histology
  • Spleen / metabolism
  • Testosterone / pharmacology*
  • Water / metabolism*

Substances

  • Carrier Proteins
  • Insulin-Like Growth Factor Binding Protein 2
  • Insulin-Like Growth Factor Binding Proteins
  • Proteins
  • Somatomedins
  • Water
  • Testosterone
  • Insulin-Like Growth Factor I
  • Growth Hormone