Liver mRNA expression of IGF-I and IGFBPs in adult undernourished diabetic rats

Life Sci. 1999;64(24):2255-71. doi: 10.1016/s0024-3205(99)00177-0.

Abstract

To investigate the role played by factors other than GH, such as nutrients and insulin, on IGF-I secretion, adult male rats of 200 g.b.w. were food-restricted for 7 days and then made diabetic by streptozotocin administration (UD). Different groups of UD rats were submitted to the following four day treatments: left untreated (UD), refed (UD+R), treated with insulin (UD+I), or a combination of both refeeding and insulin (UD+R+I). Serum concentration of IGF-I and liver mRNA expression of IGF-I, IGF-binding proteins and GH receptor were measured. Insulin treatment alone partially recovered liver IGF-I and IGFBPs mRNA expression, while refeeding alone had no effect. Only a combination of both insulin and refeeding recovered both parameters. Contrary to the results obtained with a longer period of recovery, these experiments show that serum and mRNA expression of IGF-I and IGFBPs in adult undernourished diabetic rats can be restored by insulin and nutrients administration with no prior restoration of serum and pituitary GH to control values and no compensatory changes in GH receptor gene expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose / metabolism
  • Body Weight
  • Diabetes Mellitus, Experimental / complications
  • Diabetes Mellitus, Experimental / genetics*
  • Diabetes Mellitus, Experimental / metabolism*
  • Food Deprivation
  • Gene Expression / drug effects
  • Growth Hormone / blood
  • Growth Hormone / metabolism
  • Insulin / blood
  • Insulin / pharmacology
  • Insulin-Like Growth Factor Binding Proteins / genetics*
  • Insulin-Like Growth Factor I / metabolism*
  • Liver / drug effects
  • Liver / metabolism*
  • Male
  • Nutrition Disorders / complications
  • Nutrition Disorders / genetics*
  • Nutrition Disorders / metabolism*
  • Pituitary Gland / metabolism
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism*
  • Rats
  • Rats, Wistar
  • Receptors, Somatotropin / genetics

Substances

  • Blood Glucose
  • Insulin
  • Insulin-Like Growth Factor Binding Proteins
  • RNA, Messenger
  • Receptors, Somatotropin
  • Insulin-Like Growth Factor I
  • Growth Hormone