High and low (Gpp(NH)p-sensitive) affinity sites for β2-adrenergic blockers as antagonists of isoproterenol in the field-stimulated rat vas deferens

Author:

Lotti Victor J.,Kling Paul,Cerino Deborah

Publisher

Elsevier BV

Subject

Pharmacology

Reference18 articles.

1. Some quantitative uses of drug antagonists;Arunlakshana;Br. J. Pharmacol.,1959

2. Adrenergic neuron blocking properties of (±)-propranolo and (+)-propanolol;Barrett;J. Pharm. Pharmacol.,1970

3. Comparison of pharmacological and binding assays for ten β-adrenoceptor blocking agents and two β-adrenoceptor agonists;Bieth;Br. J. Pharmacol.,1980

4. The effects of β-adrenoceptor agonists and antagonists on responses of transmurally stimulated prostatic and epididymal portions of the isolated vas deferens of the rat;Brown;Br. J. Pharmacol.,1979

5. The subclassification of β-adrenoceptors: Evidence in support of the dual β-adrenoceptor hypothesis;Daly,1979

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