The Effects of Human Chorionic Gonadotropin and Gonadotropin-Releasing Hormone Receptor Antagonist on Testicular Steroidogenesis in Normal and Obese Rats

Bull Exp Biol Med. 2024 Aug;177(4):436-441. doi: 10.1007/s10517-024-06204-x. Epub 2024 Sep 12.

Abstract

We studied the effect of a high-fat, high-carbohydrate diet (HFHCD) on basal testosterone levels in the blood and testosterone, its precursors, and expression of steroidogenic genes in the testes of rats treated with human chorionic gonadotropin (hCG, 10 IU/rat, subcutaneously, once), gonadotropin-releasing hormone receptor antagonist cetrorelix (75 μg/kg, subcutaneously, 3 days), and their combination. In HFHCD rats, no obvious signs of androgen deficiency were observed and the response of the testes to hCG stimulation was preserved. Unlike control rats (normal diet), the expression of the luteinizing hormone receptor gene in these rats did not change in response to hCG stimulation and cetrorelix administration; they also showed a paradoxical, more pronounced response to hCG administration under conditions of suppression of the gonadotropin secretion by cetrorelix. This suggests that the etiology and pathogenesis of obesity may have different effects on the hormonal status of the male reproductive system.

Keywords: gonadotropin; gonadotropin-releasing hormone receptor antagonist; obesity; steroidogenesis; testosterone.

MeSH terms

  • Animals
  • Chorionic Gonadotropin* / pharmacology
  • Diet, High-Fat / adverse effects
  • Gonadotropin-Releasing Hormone* / analogs & derivatives
  • Gonadotropin-Releasing Hormone* / metabolism
  • Hormone Antagonists / pharmacology
  • Humans
  • Male
  • Obesity* / drug therapy
  • Obesity* / metabolism
  • Rats
  • Rats, Wistar
  • Receptors, LHRH / antagonists & inhibitors
  • Receptors, LHRH / genetics
  • Receptors, LHRH / metabolism
  • Testis* / drug effects
  • Testis* / metabolism
  • Testosterone* / blood

Substances

  • Chorionic Gonadotropin
  • Testosterone
  • cetrorelix
  • Gonadotropin-Releasing Hormone
  • Receptors, LHRH
  • Hormone Antagonists