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

Biophysical Journal 61: 1109-1116 (1992)
© 1992 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 Simon, B J
Right arrow Articles by Hill, D A
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Simon, B J
Right arrow Articles by Hill, D A

Charge movement and SR calcium release in frog skeletal muscle can be related by a Hodgkin-Huxley model with four gating particles.

B J Simon and D A Hill

Department of Physiology and Biophysics, University of Texas Medical Branch, Galveston 77550.

ABSTRACT

Charge movement currents (IQ) and calcium transients (delta[Ca2+]) were measured simultaneously in frog skeletal muscle fibers, voltage clamped in a double vaseline gap chamber, using Antipyrylazo III as the calcium indicator. The rate of release of calcium from the SR (Rrel) was calculated from the calcium transients using the removal model of Melzer, W., E. Rios, and M. F. Schneider (1987. Biophys. J. 51:849-863.). IQ and delta [Ca2+] were calculated for 100 ms depolarizing test pulses to membrane potentials from -30 to +20 mV. To eliminate an inactivating component of Rrel, each test pulse was preceded by a large, fixed prepulse to +20 mV. The resulting Rrel records, which represent the noninactivating component of Rrel, were compared with integral of IQdt.(Q), the total charge that moves. The voltage dependence of the steady state Rrel was steeper then that of Q and shifted to the right. During depolarization, the Rrel waveform was similar to that of Q but was delayed by several ms, while, during repolarization, Rrel preceded Q. All of these results could be explained with a Hodgkin-Huxley type model for E-C coupling in which four voltage sensors in the t-tubule membrane which give rise to IQ must all be in their activating positions for the calcium release channel in the SR membrane to open.(ABSTRACT TRUNCATED AT 250 WORDS)




This article has been cited by other articles:


Home page
Biophys. JHome page
C. S. Hui
Association of the I{gamma} and I{delta} Charge Movement with Calcium Release in Frog Skeletal Muscle
Biophys. J., February 1, 2005; 88(2): 1030 - 1045.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
D. C. Sheridan, W. Cheng, C. A. Ahern, L. Mortenson, D. Alsammarae, P. Vallejo, and R. Coronado
Truncation of the Carboxyl Terminus of the DihydropyridineReceptor {beta}1a Subunit Promotes Ca2+ Dependent Excitation-Contraction Coupling in Skeletal Myotubes
Biophys. J., January 1, 2003; 84(1): 220 - 237.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. Yano, R. El-Hayek, and N. Ikemoto
Role of Calcium Feedback in Excitation-Contraction Coupling in Isolated Triads
J. Biol. Chem., August 25, 1995; 270(34): 19936 - 19942.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1992 by the Biophysical Society.