AJP - Heart Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Heart Circ Physiol 279: H466-H474, 2000;
0363-6135/00 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via ISI Web of Science (12)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Han, W.
Right arrow Articles by Nattel, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Han, W.
Right arrow Articles by Nattel, S.
Vol. 279, Issue 2, H466-H474, August 2000

A comparison of transient outward currents in canine cardiac Purkinje cells and ventricular myocytes

Wei Han1,3, Zhiguo Wang1,2, and Stanley Nattel1,2,3

1 Department of Medicine and Research Center, Montreal Heart Institute, Montreal, Quebec H1T 1C8; 2 Department of Medicine, University of Montreal, Montreal, Quebec H3C 3J7; and 3 Department of Pharmacology and Therapeutics, McGill University, Montreal, Quebec, Canada H3G 1Y6

Although abnormalities in Purkinje cell (PC) repolarization are important causes of cardiac arrhythmias, the detailed properties of repolarizing currents in PCs are incompletely understood. We compared transient outward K+ current (Ito) in single PCs from canine false tendons with midmyocardial ventricular myocytes (VMs). Ito reactivation was biexponential, with a similar rapid-phase time constant (30 ± 5 and 35 ± 4 ms for VM and PC, respectively) but a large, slow component in PCs with a much greater time constant than VM (1,427 ± 70 vs. 181 ± 24 ms, P < 0.001). Tetraethylammonium had no effect on VM Ito but reversibly inhibited PC Ito (IC50 = 2.4 ± 0.4 mM). PC Ito was also more sensitive to 4-aminopyridine (IC50 = 50 ± 7 vs. 526 ± 49 µM in VM, P < 0.0001). H2O2 slowed Ito inactivation in PCs but did not affect VM Ito. We conclude that PC Ito shows significant differences from VM Ito, with some features, such as tetraethylammonium sensitivity, that have been reported in neither cardiac Ito of atrial or ventricular myocytes nor cloned K+ channel subunits (Kv1.4, Kv4.2, or Kv4.3) known to participate in cardiac Ito.

potassium channels; molecular biology of cardiac ion channels; cardiac arrhythmias; action potentials; potassium channel blockers; antiarrhythmic drugs





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online