Low doses of insulin-like growth factor I improve insulin resistance, lipid metabolism, and oxidative damage in aging rats

Endocrinology. 2008 May;149(5):2433-42. doi: 10.1210/en.2007-1190. Epub 2008 Jan 10.

Abstract

GH and IGF-I concentrations decline with age. Age-related changes appear to be linked to decreases in the anabolic hormones, GH and IGF-I. The aim of this study was to investigate the antioxidant, anabolic, and metabolic effects of the IGF-I replacement therapy, at low doses, in aging rats. Three experimental groups were included in this protocol: young healthy controls (17 wk old); untreated old (O) rats (103 wk old); and aging rats (103 wk old) treated with IGF-I during 1 month (2.25 microg IGF-I/100 g body weight(-1).d(-1)). Compared with young controls, untreated aging rats showed a reduction of IGF-I and testosterone levels, and a decrease of serum total antioxidant status, which were corrected by IGF-I therapy. In addition, untreated O presented increased levels of serum glucose with hyperinsulinemia, cholesterol, and triglycerides, and a reduction of free fatty acid concentrations. IGF-I therapy was able to revert insulin resistance, and to reduce cholesterol and triglycerides levels increasing significantly free fatty acid concentrations. The O group showed higher oxidative damage in brain and liver tissues associated with alterations in antioxidant enzyme activities. IGF-I therapy reduced oxidative damage in brain and liver, normalizing antioxidant enzyme activities and mitochondrial dysfunction. In conclusion, low doses of IGF-I restore circulating IGF-I, improve glucose and lipid metabolism, increase testosterone levels and serum total antioxidant capability, and reduce oxidative damage in brain and liver associated with a normalization of antioxidant enzyme activities and mitochondrial function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / biosynthesis
  • Aging / blood
  • Aging / drug effects*
  • Aging / metabolism
  • Animals
  • Antioxidants / metabolism
  • Brain / drug effects
  • Brain / enzymology
  • Brain / metabolism
  • DNA Damage / drug effects
  • Dose-Response Relationship, Drug
  • Drug Evaluation, Preclinical
  • Insulin Resistance*
  • Insulin-Like Growth Factor I / pharmacology*
  • Lipid Metabolism / drug effects*
  • Liver / drug effects
  • Liver / enzymology
  • Liver / metabolism
  • Male
  • Matrix Metalloproteinases / metabolism
  • Mitochondria, Liver / drug effects
  • Mitochondria, Liver / metabolism
  • Models, Animal
  • Models, Biological
  • Oxidative Stress / drug effects*
  • Rats
  • Rats, Wistar

Substances

  • Antioxidants
  • Insulin-Like Growth Factor I
  • Adenosine Triphosphate
  • Matrix Metalloproteinases