Mechanism of hypothyroidism action on insulin-like growth factor-I and -II from neonatal to adult rats: insulin mediates thyroid hormone effects in the neonatal period

Endocrinology. 1998 Dec;139(12):4782-92. doi: 10.1210/endo.139.12.6355.

Abstract

The effects of thyroid hormone deficiency on serum levels and liver messenger RNA (mRNA) expression of insulin-like growth factors (IGFs) were studied in neonatal (until 20 days of life), weaned (22-37 days), and adult (72-87 days) rats, short periods (5, 10, and 15 days) after thyroidectomy (T). Serum levels and liver mRNA expression of IGF-I, plasma and pituitary GH, plasma insulin, and glycemia were measured in all populations; and serum levels and liver mRNA expression of IGF-II were measured only in the neonatal populations. Surprisingly, plasma insulin and GH and serum and liver mRNA expression of IGF-I were found elevated in T neonatal rats, and they decreased in weaned and adult rats and in neonatal rats rendered hypothyroid by mercapto-1-methylimidazole (MMI) treatment (MMI-hypothyroid). T and MMI-treatment of neonatal rats disturbed the normal pattern of progressive decrease of IGF-II with age. A positive correlation between insulin and IGF-I and a poor correlation between GH and IGF-I were found in both hypothyroid neonates (T and MMI-hypothyroid). On the contrary, a positive correlation between GH and IGF-I and a poor correlation between insulin and IGF-I were found for control and T adult rats. Because plasma insulin and GH changed in the same direction in all groups, insulin secretion in T neonatal was suppressed by streptozotocin, and insulin was given to T adult rats. The combined results of these experiments support the idea that the effects of thyroid hormones on IGF-I secretion are age-dependent, and they are mediated mainly by insulin during the neonatal period and by GH during adulthood.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / blood*
  • Animals
  • Animals, Newborn / blood*
  • Animals, Newborn / growth & development
  • Female
  • Humans
  • Hypothyroidism / blood*
  • Hypothyroidism / chemically induced
  • Hypothyroidism / physiopathology
  • Imidazoles
  • Insulin / pharmacology
  • Insulin / physiology
  • Insulin Antagonists / pharmacology
  • Insulin-Like Growth Factor I / analysis*
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor II / analysis*
  • Insulin-Like Growth Factor II / genetics
  • Liver / metabolism
  • Male
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Streptozocin / pharmacology
  • Thyroid Hormones / physiology
  • Thyroidectomy
  • Weaning

Substances

  • Imidazoles
  • Insulin
  • Insulin Antagonists
  • RNA, Messenger
  • Thyroid Hormones
  • Streptozocin
  • Insulin-Like Growth Factor I
  • Insulin-Like Growth Factor II
  • 1-methylimidazole