Literature DB >> 3968530

Slow charge movement in mammalian skeletal muscle.

B J Simon, K G Beam.   

Abstract

Voltage-dependent charge movements were measured in the rat omohyoid muscle with the three-microelectrode voltage-clamp technique. Contraction was abolished with hypertonic sucrose. The standard (ON-OFF) protocol for eliciting charge movements was to depolarize the fiber from -90 mV to a variable test potential (V) and then repolarize the fiber to -90 mV. The quantity of charge moved saturated at test potentials of approximately 0 mV. The steady state dependence of the amount of charge that moves as a function of test potential could be well fitted by the Boltzmann relation: Q = Qmax/(1 + exp[-(V - V)/k]), where Qmax is the maximum charge that can be moved, V is the potential at which half the charge moves, and k is a constant. At 15 degrees C, these values were Qmax = 28.5 nC/microF, V = -34.2 mV, and k = 8.7 mV. Qmax, k, and V exhibited little temperature dependence over the range 7-25 degrees C. "Stepped OFF" charge movements were elicited by depolarizing the fiber from -90 mV to a fixed conditioning level that moved nearly all the mobile charge (0 mV), and then repolarizing the fiber to varying test potentials. The sum of the charge that moved when the fiber was depolarized directly from -90 mV to a given test potential and the stepped OFF charge that moved when the fiber was repolarized to the same test potential had at all test potentials a value close to Qmax for that fiber. In nearly all cases, the decay phase of ON, OFF, and stepped OFF charge movements could be well fitted with a single exponential. The time constant, tau decay, for an ON charge movement at a given test potential was comparable to tau decay for a stepped OFF charge movement at the same test potential. Tau decay had a bell-shaped dependence on membrane potential: it was slowest at a potential near V (the midpoint of the steady state charge distribution) and became symmetrically faster on either side of this potential. Raising the temperature from 7 to 15 degrees C caused tau decay to become faster by about the same proportion at all potentials, with a Q10 averaging 2.16. Raising the temperature from 15 to 25 degrees C caused tau decay to become faster at potentials near V, but not at potentials farther away.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1985        PMID: 3968530      PMCID: PMC2215813          DOI: 10.1085/jgp.85.1.1

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  24 in total

1.  Observations on intramembrane charge movements in skeletal muscle.

Authors:  W Almers
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1975-06-10       Impact factor: 6.237

2.  Voltage dependent charge movement of skeletal muscle: a possible step in excitation-contraction coupling.

Authors:  M F Schneider; W K Chandler
Journal:  Nature       Date:  1973-03-23       Impact factor: 49.962

3.  The effect o f calcium on contraction and conductance thresholds in frog skeletal muscle.

Authors:  L L Costantin
Journal:  J Physiol       Date:  1968-03       Impact factor: 5.182

4.  Asymmetrical charge movement in slow- and fast-twitch mammalian muscle fibres in normal and paraplegic rats.

Authors:  A F Dulhunty; P W Gage
Journal:  J Physiol       Date:  1983-08       Impact factor: 5.182

5.  Differential properties of two charge components in frog skeletal muscle.

Authors:  C S Hui
Journal:  J Physiol       Date:  1983-04       Impact factor: 5.182

6.  Voltage clamp experiments in striated muscle fibres.

Authors:  R H Adrian; W K Chandler; A L Hodgkin
Journal:  J Physiol       Date:  1970-07       Impact factor: 5.182

7.  Pharmacological studies of charge movement in frog skeletal muscle.

Authors:  C S Hui
Journal:  J Physiol       Date:  1983-04       Impact factor: 5.182

8.  Calcium currents in a fast-twitch skeletal muscle of the rat.

Authors:  P L Donaldson; K G Beam
Journal:  J Gen Physiol       Date:  1983-10       Impact factor: 4.086

9.  The influence of transverse tubular delays on the kinetics of charge movement in mammalian skeletal muscle.

Authors:  B J Simon; K G Beam
Journal:  J Gen Physiol       Date:  1985-01       Impact factor: 4.086

10.  A quantitative study of potassium channel kinetics in rat skeletal muscle from 1 to 37 degrees C.

Authors:  K G Beam; P L Donaldson
Journal:  J Gen Physiol       Date:  1983-04       Impact factor: 4.086

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  25 in total

1.  Separation of charge movement components in mammalian skeletal muscle fibres.

Authors:  F Francini; C Bencini; C Piperio; R Squecco
Journal:  J Physiol       Date:  2001-11-15       Impact factor: 5.182

2.  Ca2+ current and charge movement in adult single human skeletal muscle fibres.

Authors:  J García; K McKinley; S H Appel; E Stefani
Journal:  J Physiol       Date:  1992-08       Impact factor: 5.182

3.  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

4.  The Qgamma component of intra-membrane charge movement is present in mammalian muscle fibres, but suppressed in the absence of S100A1.

Authors:  Benjamin L Prosser; Erick O Hernández-Ochoa; Danna B Zimmer; Martin F Schneider
Journal:  J Physiol       Date:  2009-08-03       Impact factor: 5.182

5.  Intramembrane charge movement and sarcoplasmic calcium release in enzymatically isolated mammalian skeletal muscle fibres.

Authors:  P Szentesi; V Jacquemond; L Kovács; L Csernoch
Journal:  J Physiol       Date:  1997-12-01       Impact factor: 5.182

6.  Calcium current and charge movement of mammalian muscle: action of amyotrophic lateral sclerosis immunoglobulins.

Authors:  O Delbono; J García; S H Appel; E Stefani
Journal:  J Physiol       Date:  1991-12       Impact factor: 5.182

7.  Ca channels in adrenal glomerulosa cells: K+ and angiotensin II increase T-type Ca channel current.

Authors:  C J Cohen; R T McCarthy; P Q Barrett; H Rasmussen
Journal:  Proc Natl Acad Sci U S A       Date:  1988-04       Impact factor: 11.205

8.  Intramembrane charge movement in guinea-pig and rat ventricular myocytes.

Authors:  R W Hadley; W J Lederer
Journal:  J Physiol       Date:  1989-08       Impact factor: 5.182

9.  Asymmetric charge movement in contracting muscle fibres in the rabbit.

Authors:  G D Lamb
Journal:  J Physiol       Date:  1986-07       Impact factor: 5.182

10.  Nifedipine-sensitive intramembrane charge movement in Purkinje cells from mouse cerebellum.

Authors:  K Melliti; R Bournaud; B Bastide; T Shimahara
Journal:  J Physiol       Date:  1996-01-15       Impact factor: 5.182

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