Kinetics of interaction of disopyramide with the cardiac sodium channel: Fast dissociation from open channels at normal rest potentials
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Physiology,Biophysics
Link
http://link.springer.com/content/pdf/10.1007/BF02505764.pdf
Reference59 articles.
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2. Anno, T., Hondeghem, L.M. 1990. Interaction of flecainide with guinea pig cardiac sodium channels. Importance of activation unblocking to the voltage dependence of recovery.Circ. Res. 66:789–803
3. Backx, P.H., Yue, D.T., Lawerence, J.H., Marban, E., Tomaselli, G.F. 1992. Molecular localization of an ion-binding site within the pore of mammalian sodium channels.Science 257:248–251
4. Benz, I., Kohlhardt, M. 1991. Responsiveness of cardiac Na+ channels to antiarrhythmic drugs: The role of inactivation.J. Membrane Biol. 122:267–278
5. Berman, M.F., Camarado, J.S., Robinson, R.B., Siegelbaum, S.A. 1987. Single sodium channels from canine ventricular myocytes: Voltage dependence and relative rate of activation and inactivation.J. Physiol. 415:503–531
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