A selective role for brain histamine in prolactin release induced by opiates

Agents Actions. 1990 Apr;30(1-2):223-5. doi: 10.1007/BF01969044.

Abstract

We studied the effects of histamine (HA) antagonists on the facilitatory action of morphine (M) and beta-endorphin (beta E) on prolactin (PRL) release and the effect of alpha-fluoromethylhistidine (alpha-FMH, inhibitor of HA synthesis) on beta E-induced PRL secretion. Male rats were injected intracerebroventricularly (i.c.v.) with mepyramine (MEP, H1-antagonist, 0.8 mumol/rat) or ranitidine (RAN, H2-antagonist, 0.4 mumol/rat) 10 min before M (6 mg/kg, intracarotid, i.a.) or beta E (0.25 micrograms/rat, i.c.v.). alpha-FMH (200 micrograms/rat, i.c.v.) was administered 3 h before beta E. Plasma PRL levels were measured at various times before and after drug treatment. RAN but not MEP significantly reduced PRL release induced by M whereas neither HA-antagonists nor alpha-FMH modified beta E-induced PRL release. The results obtained show that brain HA contributes through activation of H2-receptors to the PRL facilitatory action of M but not of beta E.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain Chemistry / drug effects*
  • Histamine / physiology*
  • Injections, Intraventricular
  • Male
  • Methylhistidines / pharmacology
  • Prolactin / metabolism*
  • Pyrilamine / pharmacology
  • Ranitidine / pharmacology
  • Rats
  • Rats, Inbred Strains
  • beta-Endorphin / pharmacology*

Substances

  • Methylhistidines
  • beta-Endorphin
  • alpha-fluoromethylhistidine
  • Histamine
  • Ranitidine
  • Prolactin
  • Pyrilamine