Effects of receptor blockers (methysergide, propranolol, phentolamine, yohimbine and prazosin) on desimipramine-induced pituitary hormone stimulation in humans--II. Prolactin

Psychoneuroendocrinology. 1986;11(4):463-74. doi: 10.1016/0306-4530(86)90007-7.

Abstract

In this report the effects of various receptor blockers on desimipramine (DMI)-induced prolactin (PRL) secretion in healthy male subjects are presented. Each trial consisted of two administrations: one of DMI i.v. alone and one of DMI i.v. in combination with the respective receptor blocker: methysergide (serotonin (5-HT) receptor blocker), propranolol (beta receptor blocker), phentolamine (alpha-1/alpha-2 receptor blocker), yohimbine (alpha-2 greater than alpha-1 receptor blocker), and prazosin (alpha-1 receptor blocker). Following administration of methysergide (12 mg p.o., n = 12), a significantly lower (p less than 0.01) DMI-induced PRL secretion compared to DMI alone in another group of subjects (n = 12) was observed. Combined administration with propranolol (15 mg i.v.) significantly enhanced the DMI-induced PRL secretion compared to DMI 50 mg i.v. alone (n = 18, incomplete block design) (p less than 0.01). Neither combined administration with phentolamine (60 mg i.v., n = 12), yohimbine (10 mg i.v., n = 6), nor prazosin (1 mg p.o., n = 12) significantly influenced the DMI-induced PRL secretion compared to DMI alone in the same subjects. The results of the present study, especially the inhibitory effect on DMI-induced PRL secretion of methysergide, indicate that the primarily noradrenaline (NA) and lesser serotonin (5-HT) reuptake inhibiting antidepressant DMI stimulates PRL secretion via 5-HT neurons. Furthermore, the significantly enhanced PRL release following combined administration of DMI and propranolol suggests that a noradrenergic inhibitory effect also may be involved in the transmission of the PRL stimulus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blood Glucose / metabolism
  • Blood Pressure / drug effects
  • Carrier Proteins*
  • Desipramine / pharmacology*
  • Drug Interactions
  • Heart Rate / drug effects
  • Humans
  • Male
  • Methysergide / pharmacology
  • Phentolamine / pharmacology
  • Pituitary Hormones / metabolism*
  • Prazosin / pharmacology
  • Prolactin / metabolism*
  • Propranolol / pharmacology
  • Receptors, Drug*
  • Receptors, Neurotransmitter / metabolism*
  • Time Factors
  • Yohimbine / pharmacology

Substances

  • Blood Glucose
  • Carrier Proteins
  • Pituitary Hormones
  • Receptors, Drug
  • Receptors, Neurotransmitter
  • desipramine receptor
  • Yohimbine
  • Prolactin
  • Propranolol
  • Desipramine
  • Prazosin
  • Methysergide
  • Phentolamine