help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Biophysical Journal 69: 873-882 (1995)
© 1995 the Biophysical Society

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Böhle, T
Right arrow Articles by Benndorf, K
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Böhle, T
Right arrow Articles by Benndorf, K

Voltage-dependent properties of three different gating modes in single cardiac Na+ channels.

T Böhle and K Benndorf

Department of Physiology, University of Cologne, Germany.

ABSTRACT

Three different modes of Na+ channel action, the F mode (fast inactivating), the S mode (slowly inactivating), and the P mode (persistent), were studied at different potentials in exceptionally small cell-attached patches containing one and only one channel. Switching between the modes was independent of voltage. In the F mode, the mean open time (tau o) at -30 and -40 mV was 0.14 and 0.16 ms, respectively, which was significantly larger than at -60 and 0 mV, where the values were 0.07 and 0.08 ms, respectively. The time before which half of the first channel openings occurred (t 0.5), decreased from 0.58 ms at -60 mV to 0.14 ms at 0 mV. The fit of steady-state activation with a Boltzmann function yielded a half-maximum value (V 0.5) at -48.1 mV and a slope (k) of 5.6 mV. The mean open time in the S mode increased steadily from 0.12 ms at -80 mV to 1.09 ms at -30 mV, but was not prolonged further at -20 mV (1.07 ms). Concomitantly, t 0.5 decreased from 1.61 ms at -80 mV to 0.22 ms at -20mV. Here the midpoint of steady-state activation was found at -61.2 mV, and the slope was 8.7 mV. The mean open time in the P mode increased from 0.07 ms at -60 mV to 0.45 ms at 0 mV and t 0.5 declined from 2.14 ms at -60 mV to 0.19 ms at +20 mV. Steady-state activation had its midpoint at -14.7 mV, and the slope was 10.9 mV. It is concluded that a single Na+ channel may switch among the F, S, and P mode and that the three modes differ by a characteristic pattern of voltage dependence of tau 0, t 0.5, and steady-state activation.




This article has been cited by other articles:


Home page
Circ. Res.Home page
T. Bohle, M. C. Brandt, M. Lindner, and D. J. Beuckelmann
Identification of Gating Modes in Single Native Na+ Channels From Human Atrium and Ventricle
Circ. Res., September 6, 2002; 91(5): 421 - 426.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
V. A. Maltsev, H. N. Sabbah, R. S. D. Higgins, N. Silverman, M. Lesch, and A. I. Undrovinas
Novel, Ultraslow Inactivating Sodium Current in Human Ventricular Cardiomyocytes
Circulation, December 8, 1998; 98(23): 2545 - 2552.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
R. Dumaine and G. E. Kirsch
Mechanism of lidocaine block of late current in long Q-T mutant Na+ channels
Am J Physiol Heart Circ Physiol, February 1, 1998; 274(2): H477 - H487.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1995 by the Biophysical Society.