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AJP - Heart and Circulatory Physiology, Vol 273, Issue 2 511-H525, Copyright © 1997 by American Physiological Society
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D. M. Roden and A. L. George Jr
Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-6602, USA.
The application of patch-clamp and molecular approaches has resulted in an increasingly refined understanding of the molecular entities underlying cardiac sodium and potassium currents. The sodium current results from expression of a single large alpha-subunit, whereas multiple potassium currents and potassium channel alpha-subunits have been identified. Recapitulation of some ion currents in heterologous expression systems requires not only expression of alpha-subunits but also ancillary (beta) subunits. Domains common to functions such as activation, inactivation, and drug block are now being identified in alpha- and beta-gene products. Variability in the expression or function of individual ion-channel genes is an increasingly recognized source of variability in the ion currents recorded in heart cells under physiological conditions (e.g. during development) as well as in disease.
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