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Possible role of histamine (H 1 ‐ and H 2 ‐) receptors in the regulation of meningeal blood flow
Author(s) -
Dux Mária,
Schwenger Nina,
Messlinger Karl
Publication year - 2002
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0704946
Subject(s) - cimetidine , histamine , histamine h2 receptor , endocrinology , medicine , histamine h1 receptor , chemistry , histamine h3 receptor , antagonist , blood flow , pharmacology , anesthesia , receptor
Vasodilatation in the dura mater has been suggested to play an important role in the pathophysiology of vascular headaches. Histamine may contribute to these vascular changes. The aim of the present study was to examine the role of different histamine receptors in histamine‐induced meningeal hyperperfusion using laser Doppler flowmetry. The blood flow in the medial meningeal artery was monitored in the exposed parietal dura mater encephali of barbiturate anaesthetized rats. Local application of histamine (10 −5 and 10 −4 M ) onto the dura caused increases in flow to 114.2±9.6 and 135.1±19.1%, respectively, of the basal flow. Flow increases induced by topical application of histamine (10 −4 M ) were reduced by local pretreatment with the H 2 ‐receptor antagonist cimetidine (0.4 and 4 m M ) to 63.4±17 and 37.8±18.8%, respectively. Systemic pre‐administration of cimetidine (5 mg kg −1 i.v.) did not change histamine‐induced flow increases. Local pretreatment with the H 1 ‐receptor antagonist cetirizine (2 μ M ) further increased the flow evoked by topical histamine administration (10 −4 M ) to 123.5±14.7% of the histamine control. Increases in blood flow induced by i.v. administration of histamine (10 μg kg −1 ) were reduced by i.v. pre‐injection of cetirizine (50 μg kg −1 ) to 31.9±9% but not by i.v. cimetidine (5 mg kg −1 ). We conclude that histamine‐induced relaxation of dural arterial vessels is mediated by H 2 ‐receptors, most likely located on vascular smooth muscle cells, and by endothelial H 1 ‐receptors. In addition, H 1 ‐receptors on smooth muscle cells may mediate vasoconstriction.British Journal of Pharmacology (2002) 137 , 874–880. doi: 10.1038/sj.bjp.0704946

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