Histamine H3-receptors modulate nonadrenergic noncholinergic neural bronchoconstriction in guinea-pig in vivo

Masakazu Ichinose, Peter J. Barnes

Research output: Contribution to journalArticle

69 Citations (Scopus)

Abstract

We have investigated whether the histamine H3-receptors influence nonadrenergic noncholinergic (NANC) bronchoconstriction in guinea-pig in vivo. Atropine, propranolol, mepyramine and cimetidine were administered to block the effects of β-adrenoceptor-, acetylcholine, H1- and H2-receptor-mediated responses, respectively. Vagal stimulation evoked a NANC bronchoconstrictor response. The selective H3-agonist, α-methylhistamine (α-MeHA, 1-10 mg/kg i.v.) did not alter basal respiratory insufflation pressure, but reduced the NANC bronchoconstrictor response to vagal stimulation in dose-dependent manner (with a maximal inhibition of 46.0 ± 10.3%; mean ± S.E. at 10 mg/kg) (P < 0.02). Histamine itself also had a significant inhibitory effect on NANC responses with H1- and H2-blockade. The α-adrenoceptor antagonist phentolamine had no effect on the inhibitory response produced by α-MeHA, but the H3-receptor antagonist thioperamide blocked the inhibitory effect of α-MeHA. α-MeHA had no inhibitory effect on bronchoconstriction induced by exogenous substance P (5-25 μg/kg i.v.). We conclude that H3-receptors inhibit the release of transmitter from NANC nerves and that H3-receptors might play a role in regulation of neurogenic inflammatory responses in the airways.

Original languageEnglish
Pages (from-to)49-55
Number of pages7
JournalEuropean Journal of Pharmacology
Volume174
Issue number1
DOIs
Publication statusPublished - 1989 Dec 12
Externally publishedYes

Keywords

  • (R)-α-Methylhistamine
  • Neuropeptides
  • Thioperamide
  • Vagal stimulation

ASJC Scopus subject areas

  • Pharmacology

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