Different Ability of Clenbuterol and Salbutamol to Block Sodium Channels Predicts Their Therapeutic Use in Muscle Excitability Disorders-Reference-Cited by-同舟云学术

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Different Ability of Clenbuterol and Salbutamol to Block Sodium Channels Predicts Their Therapeutic Use in Muscle Excitability Disorders

Published:2003-03-01 Issue:3 Volume:63 Page:659-670
ISSN:0026-895X
Container-title:Molecular Pharmacology
language:en
Short-container-title:Mol Pharmacol

Author:

Desaphy Jean-François,Pierno Sabata,De Luca Annamaria,Didonna Paola,Camerino Diana Conte

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference38 articles.

1. 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

2. Lidocaine block of cardiac sodium channels.

3. Serine-1321-independent regulation of the mu 1 adult skeletal muscle Na+ channel by protein kinase C.

4. Actions of sympathomimetic amines and their antagonists on skeletal muscle.;Bowman;Pharmacol Rev,1969

5. Voltage-gated ion channelopathies of the nervous system

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