Effects of para-substituted beta-adrenoceptor blocking agents and methyl-substituted phenoxypropanolamine derivatives on maximum upstroke velocity of action potential in guinea-pig papillary muscles

Author:

Ban T.,Sada S.,Takahashi Y.,Sada H.,Fujita T.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology,General Medicine

Reference31 articles.

1. Ban T, Sada H, Harada S (1983) Time dependent and independent depression of maximum upstroke velocity of guinea pig ventricular action potentials by ?-adrenoceptor blocking agents. J Mol Cell Cardiol (Suppl 1) 15:250

2. Barrett AM (1977) The pharmacology of atenolol. Postgrad Med J 53:58?64

3. Bean BP, Cohen CJ, Tsien RW (1982) Block of cardiac sodium channels by tetrodotoxin and lidocaine: sodium current andV max experiments. In: Paes de Carvalho A, Hoffman BF, Lieberman M (eds) Normal and abnormal conduction in the heart. Futura, New York, pp 189?209

4. Campbell TJ (1983) Importance of physico-chemical properties in determining the kinetics of the effects of Class I antiarrhythmic drugs on maximum rate of depolarization in guinea-pig ventricle. Br J Pharmacol 80:33?40

5. Carruthers SG (1978) Pamatolol: Phase I evaluation of the pharmacodynamics of a cardioselective beta adrenoceptor blocking drug. Clin Pharmacol Ther 24:168?174

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