Effect of naloxone on gonadotropin secretion before and after testosterone in Klinefelter's syndrome

Psychoneuroendocrinology. 1985;10(3):337-44. doi: 10.1016/0306-4530(85)90010-1.

Abstract

A study was performed on eight subjects with Klinefelter's syndrome to assess the relation between gonadal hormones and opioid inhibition of gonadotropin secretion through comparison of their gonadotropin response to naloxone (NAL) (0.3 mg/kg; 1/3 bolus iv. at time 0 and 2/3 iv. for 120 min) before and after testosterone propionate (TP) 100 mg/day im. for 5 days. Under basal conditions, NAL failed to induce a significant change in LH levels. After TP, however, despite unchanged basal LH levels (mean +/- S.E.M.: 27.0 +/- 3.4 vs 21.2 +/- 3.21 microU/ml), LH significantly increased in response to NAL. FSH did not respond to NAL either before or after TP administration, though FSH levels were significantly reduced by TP. These findings suggest that in man, as in animals, gonadal hormones regulate opioid inhibition of LH secretion. The negative feedback of testosterone and its ability to activate opioid inhibiting tone may be dissociated, in keeping with the view that gonadal hormones control gonadotropin secretion through the activation of distinct, albeit concomitant, mechanisms.

MeSH terms

  • Adolescent
  • Adult
  • Endorphins / physiology*
  • Estradiol / blood
  • Follicle Stimulating Hormone / metabolism*
  • Humans
  • Klinefelter Syndrome / drug therapy*
  • Klinefelter Syndrome / physiopathology
  • Luteinizing Hormone / metabolism*
  • Male
  • Naloxone*
  • Pituitary Gland, Anterior / metabolism
  • Testosterone / blood
  • Testosterone / therapeutic use*

Substances

  • Endorphins
  • Naloxone
  • Testosterone
  • Estradiol
  • Luteinizing Hormone
  • Follicle Stimulating Hormone