Literature DB >> 3795082

Asymmetric charge movement in contracting muscle fibres in the rabbit.

G D Lamb.   

Abstract

The Vaseline-gap technique was used to record asymmetric charge movement in small segments of muscle fibres from the white sternomastoid or the soleus muscle of the rabbit. At 22 degrees C, non-linear ionic currents (Na+, K+, Cl-, Ca2+) were virtually eliminated for potential steps to 0 mV or below by specific blocking agents or ion substitution. A Boltzmann fit of charge movement (Q) vs. potential (V) produced the mean values Qmax = 15.2 nC/microF, V = -26.8 mV and k = 15.3 mV for twenty-three sternomastoid fibres, and 4.8 nC/microF, -32 mV and 13.7 mV for seven soleus fibres. Qmax for the sternomastoid fibres was similar to that for other fast-twitch fibres when normalized by surface area rather than capacitance. Using a 55 ms step, the mean threshold potential (Vth) for contraction in twenty-eight fibres was -25.9 (+/- 2.9) mV (+/- S.E. of mean), and the mean amount of charge moved (qth) at the threshold potential was 8.5 (+/- 0.4) nC/microF. In some contracting fibres, a component of charge movement was observed which was analogous to q gamma in amphibian muscle in its time course and potential dependence. Addition of 80 mM-sucrose to the external solution increased the speed of both the asymmetric charge movement and the charging of the linear capacitance of each fibre. The effect was reversible. A clear relation between the time course of these two parameters was established, and this strongly indicated that the majority of the asymmetric charge was located in the transverse tubular system or beyond. Moreover, it was shown that at 22 degrees C nearly all asymmetric charge moved in less than 0.5 ms after depolarization of the T-system. Sucrose in the external solution affected the Q vs. V relation, steepening the curve and shifting it to more negative potentials, as well as slightly increasing Qmax. The actions of sucrose strongly suggest that it effectively dilates and/or shortens the transverse tubular system, probably by osmotic effects.

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Year:  1986        PMID: 3795082      PMCID: PMC1182787          DOI: 10.1113/jphysiol.1986.sp016142

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  32 in total

1.  An improved vaseline gap voltage clamp for skeletal muscle fibers.

Authors:  B Hille; D T Campbell
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2.  T-tubule swelling in hypertonic solutions: a freeze substitution study.

Authors:  C Franzini-Armstrong; J E Heuser; T S Reese; A P Somlyo; A V Somlyo
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3.  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

4.  A comparative study of charge movement in rat and frog skeletal muscle fibres.

Authors:  S Hollingworth; M W Marshall
Journal:  J Physiol       Date:  1981-12       Impact factor: 5.182

5.  The membrane capacity of mammalian skeletal muscle fibres.

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6.  Ionic currents in mammalian fast skeletal muscle.

Authors:  A Duval; C Léoty
Journal:  J Physiol       Date:  1978-05       Impact factor: 5.182

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.  Comparison between the delayed outward current in slow and fast twitch skeletal muscle in the rat.

Authors:  A Duval; C Léoty
Journal:  J Physiol       Date:  1980-10       Impact factor: 5.182

9.  A non-selective cation conductance in frog muscle membrane blocked by micromolar external calcium ions.

Authors:  W Almers; E W McCleskey; P T Palade
Journal:  J Physiol       Date:  1984-08       Impact factor: 5.182

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

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

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  26 in total

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Journal:  J Physiol       Date:  1992-08       Impact factor: 5.182

Review 2.  Voltage clamp methods for the study of membrane currents and SR Ca(2+) release in adult skeletal muscle fibres.

Authors:  Erick O Hernández-Ochoa; Martin F Schneider
Journal:  Prog Biophys Mol Biol       Date:  2012-01-26       Impact factor: 3.667

3.  Excitation-contraction coupling in skeletal muscle fibres of rat and toad in the presence of GTP gamma S.

Authors:  G D Lamb; D G Stephenson
Journal:  J Physiol       Date:  1991-12       Impact factor: 5.182

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

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Journal:  J Gen Physiol       Date:  1991-05       Impact factor: 4.086

5.  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

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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

7.  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

8.  Transient and persistent sodium currents in normal and denervated mammalian skeletal muscle.

Authors:  P W Gage; G D Lamb; B T Wakefield
Journal:  J Physiol       Date:  1989-11       Impact factor: 5.182

9.  The action of ryanodine on rat fast and slow intact skeletal muscles.

Authors:  M W Fryer; G D Lamb; I R Neering
Journal:  J Physiol       Date:  1989-07       Impact factor: 5.182

10.  Components of charge movement in rabbit skeletal muscle: the effect of tetracaine and nifedipine.

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

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