Pulsatile growth hormone secretion decreases S-adenosylmethionine synthetase in rat liver

Am J Physiol Endocrinol Metab. 2001 Feb;280(2):E280-6. doi: 10.1152/ajpendo.2001.280.2.E280.

Abstract

S-adenosylmethionine synthetase (AdoMet synthetase) is responsible for the synthesis of the major methyl donor S-adenosylmethionine. The AdoMet synthetase gene was identified by subtractive suppressive hybridization as being expressed at higher levels in the liver of rats continuously exposed to growth hormone (GH) than in rats intermittently exposed to the hormone. Further studies on the regulation of AdoMet synthetase showed that the activity and mRNA levels were higher in female than in male rats. Hypophysectomy increased AdoMet synthetase mRNA in both male and female rats. Combined thyroxine and cortisol treatment of hypophysectomized rats had no effect on AdoMet synthetase mRNA levels. Two daily injections of GH for 7 days, mimicking the male secretory pattern of GH, decreased AdoMet synthetase activity and mRNA levels. A continuous infusion of GH, mimicking the female secretory pattern of GH, had small or no effects on AdoMet synthetase activity and decreased the mRNA levels to a lesser degree than two daily injections. It is concluded that the lower AdoMet synthetase activity in male rats is due to an inhibitory effect of the male characteristic pulsatile secretory pattern of GH on AdoMet synthetase mRNA expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Drug Administration Schedule
  • Drug Combinations
  • Female
  • Growth Hormone / administration & dosage
  • Growth Hormone / metabolism*
  • Growth Hormone / pharmacology
  • Hydrocortisone / pharmacology
  • Hypophysectomy
  • Injections, Subcutaneous
  • Liver / metabolism*
  • Male
  • Methionine Adenosyltransferase / antagonists & inhibitors
  • Methionine Adenosyltransferase / genetics
  • Methionine Adenosyltransferase / metabolism*
  • Pulsatile Flow
  • RNA, Messenger / antagonists & inhibitors
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Sex Characteristics
  • Thyroxine / pharmacology

Substances

  • Drug Combinations
  • RNA, Messenger
  • Growth Hormone
  • Methionine Adenosyltransferase
  • Thyroxine
  • Hydrocortisone