Literature DB >> 3877737

Voltage dependence of membrane charge movement and calcium release in frog skeletal muscle fibres.

R F Rakowski, P M Best, M R James-Kracke.   

Abstract

Voltage dependent membrane charge movement (gating current) and the release of Ca2+ from intracellular stores have been measured simultaneously in intact frog skeletal muscle fibres. Charge movement was measured using the three microelectrode voltage clamp technique. Ca2+ release was measured using the metallochromic indicator dye arsenazo III. Fibres were bathed in 2.3 X hypertonic solutions to prevent contraction. Rb+, tetraethylammonium and tetrodotoxin (TTX) were used to eliminate voltage-dependent ionic currents. The maximum rate of Ca2+ release from the sarcoplasmic reticulum in response to voltage-clamp step depolarizations to 0 mV was calculated using the dye-related parameters of model 2 of Baylor et al. (1983) and a method described in the Appendix for calculating a scaling factor (1 + p) that accounts for the additional Ca2+ buffering power of the indicator dye. The estimates of the maximum rate of Ca2+ release at 5-6 degrees C ranged from 3 to 19 microM ms-1 in the 17 fibres examined. The mean value was 8.9 +/- 1.1 microM ms-1 (S.E.M.) The maximum rate of Ca2+ release was linearly related to the magnitude of the nonlinear membrane change moved during suprathreshold depolarizing steps. The voltage dependence of charge movement and the maximum rate of Ca2+ releases were nearly identical at 6 degrees C. The voltage-dependence of the delay between the test step and the onset of Ca2+ release could be adequately described by an equation having the same functional form as the voltage dependence of nonlinear charge movement. The relationship between the test pulse voltage and the delay was shifted to more negative voltages and to shorter delays as the temperature was raised from 6 degrees C to 15 degrees C. The inactivation of Ca2+ release was found to occur at more negative holding voltages and to be more steeply voltage dependent than the immobilization of nonlinear membrane charge movement. The above data are discussed using the 'hypothetical coupler' model of excitation-contraction coupling (Miledi et al., 1983b) applied to the specific case in which each mobile charge group controls the gating of one Ca2+ release site in the sarcoplasmic reticulum.

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Year:  1985        PMID: 3877737     DOI: 10.1007/bf00712580

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  40 in total

1.  Calcium transients in frog slow muscle fibres.

Authors:  R Miledi; I Parker; G Schalow
Journal:  Nature       Date:  1977-08-25       Impact factor: 49.962

2.  Charge movement and membrane capacity in frog muscle.

Authors:  R H Adrian; A Peres
Journal:  J Physiol       Date:  1979-04       Impact factor: 5.182

3.  Stoichiometries of arsenazo III-Ca complexes.

Authors:  P Palade; J Vergara
Journal:  Biophys J       Date:  1983-09       Impact factor: 4.033

4.  Activation heat and latency relaxation in relation to calcium movement in skeletal and cardiac muscle.

Authors:  L A Mulieri; N R Alpert
Journal:  Can J Physiol Pharmacol       Date:  1982-04       Impact factor: 2.273

5.  Time course of calcium release and removal in skeletal muscle fibers.

Authors:  W Melzer; E Rios; M F Schneider
Journal:  Biophys J       Date:  1984-03       Impact factor: 4.033

6.  Pharmacological dissection of charge movement in frog skeletal muscle fibers.

Authors:  C S Hui
Journal:  Biophys J       Date:  1982-07       Impact factor: 4.033

7.  Pharmacological separation of charge movement components in frog skeletal muscle.

Authors:  C L Huang
Journal:  J Physiol       Date:  1982-03       Impact factor: 5.182

8.  Optical measurements of intracellular pH and magnesium in frog skeletal muscle fibres.

Authors:  S M Baylor; W K Chandler; M W Marshall
Journal:  J Physiol       Date:  1982-10       Impact factor: 5.182

9.  Arsenazo III and antipyrylazo III calcium transients in single skeletal muscle fibers.

Authors:  P Palade; J Vergara
Journal:  J Gen Physiol       Date:  1982-04       Impact factor: 4.086

10.  Arsenazo III forms 2:1 complexes with Ca and 1:1 complexes with Mg under physiological conditions. Estimates of the apparent dissociation constants.

Authors:  M V Thomas
Journal:  Biophys J       Date:  1979-03       Impact factor: 4.033

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  23 in total

1.  A reconstruction of charge movement during the action potential in frog skeletal muscle.

Authors:  C L Huang; L D Peachey
Journal:  Biophys J       Date:  1992-05       Impact factor: 4.033

2.  Effects of conditioning depolarization and repetitive stimulation on Q beta and Q gamma charge components in frog cut twitch fibers.

Authors:  C S Hui; W Chen
Journal:  J Gen Physiol       Date:  1992-06       Impact factor: 4.086

3.  The relationship between Q gamma and Ca release from the sarcoplasmic reticulum in skeletal muscle.

Authors:  G Pizarro; L Csernoch; I Uribe; M Rodríguez; E Ríos
Journal:  J Gen Physiol       Date:  1991-05       Impact factor: 4.086

4.  Charge movement and depolarization-contraction coupling in arthropod vs. vertebrate skeletal muscle.

Authors:  T Scheuer; W F Gilly
Journal:  Proc Natl Acad Sci U S A       Date:  1986-11       Impact factor: 11.205

5.  Intramembrane charge movement in frog skeletal muscle fibres. Properties of charge 2.

Authors:  G Brum; E Rios
Journal:  J Physiol       Date:  1987-06       Impact factor: 5.182

6.  The effect of phenylglyoxal on contraction and intramembrane charge movement in frog skeletal muscle.

Authors:  E F Etter
Journal:  J Physiol       Date:  1990-02       Impact factor: 5.182

7.  Intramembrane charge movement and calcium release in frog skeletal muscle.

Authors:  W Melzer; M F Schneider; B J Simon; G Szucs
Journal:  J Physiol       Date:  1986-04       Impact factor: 5.182

8.  Voltage sensors of the frog skeletal muscle membrane require calcium to function in excitation-contraction coupling.

Authors:  G Brum; R Fitts; G Pizarro; E Ríos
Journal:  J Physiol       Date:  1988-04       Impact factor: 5.182

9.  Potassium contractures and asymmetric charge movement in extensor digitorum longus and soleus muscles from thyrotoxic rats.

Authors:  A F Dulhunty; P W Gage; G D Lamb
Journal:  J Muscle Res Cell Motil       Date:  1987-08       Impact factor: 2.698

10.  Intracellular Ca2+ changes and Ca2+-activated K+ channel activation induced by acetylcholine at the endplate of mouse skeletal muscle fibres.

Authors:  B Allard; J C Bernengo; O Rougier; V Jacquemond
Journal:  J Physiol       Date:  1996-07-15       Impact factor: 5.182

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