Why do some drugs preferentially block open sodium channels?
- 1 June 1988
- journal article
- research article
- Published by Elsevier in Journal of Molecular and Cellular Cardiology
- Vol. 20 (6) , 461-464
- https://doi.org/10.1016/s0022-2828(88)80073-7
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Block of activated and inactivated sodium channels by class-I antiarrhythmic drugs studied by using the maximum upstroke velocity (V̇max) of action potential in guinea-pig cardiac musclesJournal of Molecular and Cellular Cardiology, 1987
- Mechanisms of use-dependent block of sodium channels in excitable membranes by local anestheticsBiophysical Journal, 1984
- Time- and voltage-dependent interactions of antiarrhythmic drugs with cardiac sodium channelsBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1977
- Local anesthetics: hydrophilic and hydrophobic pathways for the drug-receptor reaction.The Journal of general physiology, 1977