Affiliation:
1. From the Department of Molecular Biology and Pharmacology (W.G., H.L., J.M.N.), Washington University School of Medicine, St. Louis, Mo, and Cardiovascular Institute (B.L.), University of Pittsburgh Medical Center, Pittsburgh, Pa.
Abstract
Abstract
—It was recently reported that the slow transient outward K
+
current,
I
to, s
, that is evident in mouse left ventricular septal cells is eliminated in mice with a targeted deletion of the Kv1.4 gene (Kv1.4
−/−
). The rapidly inactivating transient outward K
+
current,
I
to, f
, in contrast, is selectively eliminated in ventricular myocytes isolated from transgenic mice expressing a dominant-negative Kv4 α subunit, Kv4.2W362F. Expression of Kv4.2W362F results in marked prolongation of action potentials and QT intervals. In addition, a slow transient outward K
+
current, that is similar to
I
to, s
in wild-type mouse left ventricular septal cells, is evident in all Kv4.2W362F-expressing (left and right) ventricular cells. To test directly the hypothesis that upregulation of Kv1.4 α subunit underlies the appearance of this slow transient outward K
+
current in Kv4.2W362F-expressing ventricular cells and to explore the functional consequences of elimination of
I
to, f
and
I
to, s
, mice expressing Kv4.2W362F in the Kv1.4
−/−
background (Kv4.2W362F×Kv1.4
−/−
) were generated. Histological and echocardiographic studies revealed no evidence of structural abnormalities or contractile dysfunction in Kv4.2W362F×Kv1.4
−/−
mouse hearts. Electrophysiological recordings from the majority (≈80%) of cells isolated from the right ventricle and left ventricular apex of Kv4.2W362F×Kv1.4
−/−
animals demonstrated that both
I
to, f
and
I
to, s
are eliminated; action potentials are prolonged significantly; and, in some cells, early afterdepolarizations were observed. In addition, in vivo telemetric ECG recordings from Kv4.2W362F×Kv1.4
−/−
animals revealed marked QT prolongation, atrioventricular block, and ventricular tachycardia. These observations demonstrate that upregulation of Kv1.4 contributes to the electrical remodeling evident in the ventricles of Kv4.2W362F-expressing mice and that elimination of both
I
to, f
and
I
to, s
has dramatic functional consequences. (
Circ Res. 2000;87:73-79.)
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine,Physiology
Cited by
155 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献