Sodium modulation of 3H-agonist and 3H-antagonist binding to α2-adrenoceptor subtypes

Author:

MacKinnon A.C.,Spedding M.,Brown C.M.

Publisher

Wiley

Subject

Pharmacology

Reference33 articles.

1. The pharmacology of RS-15385-197, a potent and selective alpha2-adrenoceptor antagonist;BROWN;Br. J. Pharmacol.,1993

2. Heterogeneity of alpha2-adrenergic receptors;BYLUND;Pharmacol. Biochem. Behav.,1985

3. Alpha2A- and alpha2B-adrenergic receptors: antagonist binding in tissues and cell lines containing only one subtype;BYLUND;J. Pharmacol. Exp. Ther.,1988

4. Relationship between the inhibition constant (Ki) and the concentration of inhibitor which caused 50 per cent inhibition (I50) of an enzymic reaction;CHENG;Biochem. Pharmacol.,1973

5. [3H]-Rauwolscine and [3H]-yohimbine binding to rat cerebral and human platelet membranes: possible heterogeneity of alpha2-adrenoceptors;CHEUNG;Eur. J. Pharmacol.,1982

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