Luteal phase defects induced by an agonist of luteinizing hormone-releasing factor: a model for fertility control

Science. 1982 Jan 8;215(4529):170-2. doi: 10.1126/science.6797068.

Abstract

Subcutaneous injection of 50 micrograms of a luteinizing hormone-releasing factor agonist (LRF agonist) for three successive days at the time of menstruation in normal cycling women induces a shortened luteal phase with suboptimal concentrations of circulating estradiol and progesterone. This luteal phase defect follows a reduced concentration of follicle-stimulating hormone during the follicular phase and a resulting inadequate follicular maturation. Since a short luteal phase is associated with an endometrium not conductive to implantation, administration of the LRF agonist at the onset of menstrual cycle may prove to be a practical and novel approach to fertility control.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Contraception*
  • Estradiol / blood
  • Female
  • Follicle Stimulating Hormone / blood
  • Follicle Stimulating Hormone / metabolism
  • Gonadotropin-Releasing Hormone / analogs & derivatives*
  • Gonadotropin-Releasing Hormone / pharmacology
  • Humans
  • Luteinizing Hormone / blood
  • Menstruation / drug effects
  • Progesterone / blood
  • Triptorelin Pamoate* / analogs & derivatives*

Substances

  • Triptorelin Pamoate
  • Gonadotropin-Releasing Hormone
  • Progesterone
  • Estradiol
  • Tryptal
  • Luteinizing Hormone
  • Follicle Stimulating Hormone