Is there a role for glucagon-like peptide-1 receptor agonists in the treatment of male infertility?

Andrology. 2021 Sep;9(5):1499-1503. doi: 10.1111/andr.13015. Epub 2021 May 5.

Abstract

Glucagon-like peptide-1 receptor agonists (GLP1-RAs) are novel anti-hyperglycemic drugs efficacious on glucose control, weight loss, and cardiovascular prevention. These drugs may also be effective in modulating testicular function. In fact, they increase serum testosterone levels in diabetic and/or obese patients with functional hypogonadism on a dysmetabolic basis. Although part of this effect can be ascribed to weight loss, some evidence suggests that there is a direct effect at the testicular level. Indeed, human Leydig, Sertoli, and germ cells express GLP1 receptors. GLP1-RAs improve sperm metabolism, motility, and insulin secretion in vitro. Likewise, GLP1-RAs exert positive effects on the metabolism of human Sertoli cells in vitro. Finally, GLP1 is secreted by mouse Leydig cells and this suggests the presence of a paracrine mechanism by which these cells could support the metabolism of Sertoli cells. Therefore, the widespread use of GLP1-RAs in clinical practice may reveal an important role in the management of male infertility in obese and/or diabetic patients given the negative impact of these diseases on testicular steroidogenesis and spermatogenesis. This should suggest the design of randomized controlled studies aimed at evaluating the effects of these drugs on testicular function.

Keywords: GLP1-RA; hypogonadism; infertility; spermatozoa.

MeSH terms

  • Animals
  • Diabetes Complications / drug therapy
  • Diabetes Complications / metabolism
  • Diabetes Mellitus / metabolism
  • Glucagon-Like Peptide-1 Receptor / agonists*
  • Humans
  • Hypoglycemic Agents / pharmacology*
  • Infertility, Male / drug therapy*
  • Infertility, Male / etiology
  • Infertility, Male / metabolism
  • Leydig Cells / drug effects
  • Male
  • Mice
  • Obesity / complications
  • Obesity / metabolism
  • Sertoli Cells / drug effects
  • Spermatogenesis / drug effects
  • Spermatozoa / metabolism
  • Testis / metabolism
  • Testosterone / blood

Substances

  • Glucagon-Like Peptide-1 Receptor
  • Hypoglycemic Agents
  • Testosterone