Article date: January 2000
By: C Ian Spencer, Wataru Uchida, Roland Z Kozlowski, in Volume 129, Issue 2, pages 235-238
Effects of extracellular anions were studied in electrophysiological experiments on freshly isolated rat ventricular myocytes. Under current‐clamp, action potential duration (APD) was prolonged by reducing the extracellular Cl− concentration and shortened by replacement of extracellular Cl− with I−. Under voltage‐clamp, membrane potential steps or ramps evoked an anionic background current (IAB) carried by either Cl−, Br−, I− or NO3−. Activation of IAB was Ca2+‐ and cyclic AMP‐independent, and was unaffected by cell shrinkage. IAB was insensitive to stilbene and fenamate anion transport blockers at concentrations that inhibit Ca2+‐, cyclic AMP‐ and swelling‐activated Cl− currents in ventricular cells of other mammals. These results suggest that IAB may be carried by a novel class of Cl− channel. Correlation of anion substitution experiments on membrane current and action potentials revealed that IAB could play a major role in controlling rat ventricular APD. These findings have important implications for those studying cardiac Cl− channels as potential targets for novel antiarrythmic agents.
British Journal of Pharmacology (2000) 129, 235–238; doi:10.1038/sj.bjp.0703074
DOI: 10.1038/sj.bjp.0703074
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