Affiliation:
1. From the Departments of Pharmacology (W.J.C., C.W.C.), Pediatrics (W.J.C.), and Surgery (J.D.P.), Tulane University School of Medicine, New Orleans, La.
Abstract
Abstract
Ion currents were examined in isolated human atrial myocytes by using the whole-cell patch-clamp technique. When currents were recorded with a K
+
-containing pipette solution, depolarizing voltage pulses elicited a rapidly activating outward current that decayed to an apparent steady state. Exposure of cells to 10 mmol/L 4-aminopyridine markedly reduced current amplitude; however, a rapidly activating current that was ≈30% of the steady state current amplitude remained. When pipette K
+
was replaced with Cs
+
, a similar rapidly activating current that reversed polarity at ≈0 mV was recorded. This current was seen in 100% of the cells tested from 17 different hearts (n=142), and its amplitude was ≈40% of the amplitude of the steady state current recorded in the presence of pipette K
+
. The current amplitude was not significantly different in cells isolated from adult (6.31±1.35 pA/pF, n=8) and pediatric (5.54±1.04 pA/pF, n=9) hearts. Studies designed to determine the charge-carrying species indicated that changes in bath Cl
−
concentration had no effect on either the amplitude or the reversal potential of this current, whereas removal of pipette Cs
+
and bath Na
+
dramatically reduced this current. In addition, this current was not modulated by either isoproterenol (1 μmol/L, 22°C) or cell swelling. This study provides the first description of a nonselective cation current in human atrial myocytes, which may play an important role in repolarization in human atria.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine,Physiology
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