PMID: 6145292Apr 1, 1984

Characterization of the beta-adrenergic receptor on the human platelet: a beta 2-subtype

Acta Pharmacologica Et Toxicologica
R KlysnerK Winther

Abstract

The human platelet beta-adrenergic receptor was characterized by using the ability of different drugs to stimulate the adenylate cyclase activity and the effects of various beta-antagonists to block the isoprenaline-stimulated adenylate cyclase activity. Isoprenaline was found 10 times more potent than adrenaline and 1000 times more potent than noradrenaline in stimulating the adenylate cyclase activity in these cells. Isoprenaline-stimulated activity was blocked by the non-selective beta-antagonists propranolol and alprenolol and by the beta 2-selective antagonist IPS 339 and prenalterol. Metoprolol, a beta 1-selective blocker, was without effect on the isoprenaline-stimulated adenylate cyclase activity. We conclude from our findings that the beta-adrenergic receptor type on the human platelet is mainly of the beta 2-subtype.

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Citations

Jan 1, 1986·European Journal of Clinical Pharmacology·K WintherJ Jensen
Jan 5, 2014·Circulation Research·Brandon M Williams, Julie C Williams
Jun 1, 1988·Stroke; a Journal of Cerebral Circulation·R JosephF Clifford Rose
Sep 1, 2012·Medicine and Science in Sports and Exercise·Joshua P WhittakerVernon G Coffey

Related Concepts

Cyclic AMP, (R)-Isomer
Adenylate Cyclase
Adrenergic beta-Agonists
Adrenergic beta-Antagonists
Blood Platelets
Enzyme Activation
Beta-adrenergic receptor

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