Effect of adrenalectomy on the slimming activity of liposome-carried oleoyl-estrone in the rat

Int J Obes Relat Metab Disord. 1998 Dec;22(12):1225-30. doi: 10.1038/sj.ijo.0800751.

Abstract

Objective: To determine the extent of glucocorticoid counter-regulatory control in the slimming action of oleoylestrone.

Design: Control and adrenalectomized rats were subjected to a seven-day treatment with 3.5 micromol/kg/d oleoylestrone in liposomes injected i.v. continuously by implanted osmotic minipumps.

Subjects: Sham-operated control and adrenalectomized lean Zucker rats.

Measurements: Body weight and food intake; plasma glucose, urea, insulin, leptin and corticosterone; liver glycogen.

Results: Treatment with oleoyl-estrone resulted in decreases in body weight and in food intake, as well as in circulating glucose, insulin and leptin. Combined adrenalectomy and oleoyl-estrone treatment resulted in a loss of almost 15% body weight in only seven days, with a severe drop in circulating glucose and insulin, almost total disappearance of plasma leptin and liver glycogen and a 3-fold rise in circulating urea. Food intake decreased sharply, which resulted in the exhaustion of energy reserves.

Conclusion: The results presented here, strongly support the hypothesis that glucocorticoids play an important role in the modulation of oleoyl-estrone-induced imbalance of energy intake and expenditure. The large effect of oleoyl-estrone on glucose, glycogen- and protein-derived (urea levels) energy in adrenalectomized rats, provides more evidence for the assumed protective role of glucocorticoids against the oleoyl-estrone-induced net loss of energy reserves. The results also show the powerful destabilizing effects of unchecked oleoyl-estrone on energy balance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenalectomy*
  • Animals
  • Anti-Obesity Agents*
  • Corticosterone / blood
  • Eating
  • Energy Intake
  • Energy Metabolism
  • Estrone / administration & dosage
  • Estrone / analogs & derivatives*
  • Female
  • Insulin / blood
  • Leptin
  • Liposomes*
  • Oleic Acids / administration & dosage*
  • Proteins / metabolism
  • Rats
  • Rats, Zucker
  • Weight Loss*

Substances

  • Anti-Obesity Agents
  • Insulin
  • Leptin
  • Liposomes
  • Oleic Acids
  • Proteins
  • Estrone
  • oleoyl-estrone
  • Corticosterone