Effects of alpha-fluoromethylhistidine (FMH), an irreversible inhibitor of histidine decarboxylase, on development of brain histamine and catecholamine systems in the neonatal rat

Life Sci. 1983 Jun 20;32(25):2897-903. doi: 10.1016/0024-3205(83)90326-0.

Abstract

Daily administration of FMH to neonatal rats produced long-lasting inhibition of histidine decarboxylase in hypothalamus and cerebral cortex and led to depletion of histamine in both brain regions. The onset of depletion was more rapid in cerebral cortex, a region in which non-neurotransmitter pools of histamine predominate in early postnatal life, appearing as early as postnatal day 3; depletion in the hypothalamus, a region rich in histaminergic neuronal projections, appeared later. No effects were seen on body or brain growth, nor was development of other biogenic amine systems affected. FMH thus provides a selective probe for examining the role of histamine in brain development.

Publication types

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

MeSH terms

  • Aging
  • Animals
  • Animals, Newborn
  • Carboxy-Lyases / antagonists & inhibitors*
  • Catecholamines / metabolism*
  • Cerebral Cortex / drug effects
  • Cerebral Cortex / enzymology
  • Cerebral Cortex / growth & development*
  • Dopamine / metabolism
  • Histamine / metabolism*
  • Histidine / analogs & derivatives*
  • Histidine Decarboxylase / antagonists & inhibitors*
  • Hypothalamus / drug effects
  • Hypothalamus / enzymology
  • Hypothalamus / growth & development*
  • Methylhistidines / pharmacology*
  • Norepinephrine / metabolism
  • Rats
  • Rats, Inbred Strains

Substances

  • Catecholamines
  • Methylhistidines
  • Histidine
  • alpha-fluoromethylhistidine
  • Histamine
  • Carboxy-Lyases
  • Histidine Decarboxylase
  • Dopamine
  • Norepinephrine