H1-histaminergic activation stimulates inositol-1-phosphate accumulation in chromaffin cells.

Abstract:

:Adrenal medullary chromaffin cells maintained in vitro were prelabeled with [3H]inositol and the accumulation of [3H]inositol-1-phosphate, was determined following stimulation with a variety of pharmacological agents. Carbachol, bradykinin, and histamine produced significantly greater accumulation of [3H] inositol-1-phosphate over basal levels, with histamine producing the greatest effect. H1-histamine receptor antagonists, mepyramine, pyrilamine, tripelennamine and clemastine were all able to reduce or completely block the histamine response. The two specific H2-histamine receptor antagonists, cimetidine and ranitidine, had no effect on this response. Histamine dose-response characteristics in the presence of mepyramine and clemastine suggest the H1 antagonism to be competitive in nature.

authors

Noble EP,Bommer M,Sincini E,Costa T,Herz A

doi

10.1016/0006-291x(86)90031-8

subject

Has Abstract

pub_date

1986-03-13 00:00:00

pages

566-73

issue

2

eissn

0006-291X

issn

1090-2104

pii

0006-291X(86)90031-8

journal_volume

135

pub_type

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