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PMID: 3795082 Published · ppublish English Journal Article

Asymmetric charge movement in contracting muscle fibres in the rabbit.

The Journal of physiology ·Vol. 376 ·1986-07-00 ·Pages 63-83

Lamb GD

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.

MeSH Terms
Action Potentials/drug effects Animals In Vitro Techniques Membrane Potentials/drug effects Muscle Contraction Muscles/physiology Rabbits Sensory Thresholds/physiology Sucrose/pharmacology Time Factors
Chemicals
Sucrose
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Lamb G D
References (32)
32 references, click to expand
  1. Comparison between the delayed outward current in slow and fast twitch skeletal muscle in the rat.
    J Physiol. 1980 Oct;307:43-57 PMID: 7205672
  2. The membrane capacity of mammalian skeletal muscle fibres.
    J Muscle Res Cell Motil. 1984 Jun;5(3):315-32 PMID: 6746892
  3. Ionic currents in mammalian fast skeletal muscle.
    J Physiol. 1978 May;278:403-23 PMID: 671323
  4. Pharmacological separation of charge movement components in frog skeletal muscle.
    J Physiol. 1982 Mar;324:375-87 PMID: 6980275
  5. An improved vaseline gap voltage clamp for skeletal muscle fibers.
    J Gen Physiol. 1976 Mar;67(3):265-93 PMID: 1083424
  6. Pharmacological studies of charge movement in frog skeletal muscle.
    J Physiol. 1983 Apr;337:509-29 PMID: 6603512
  7. A comparative study of charge movement in rat and frog skeletal muscle fibres.
    J Physiol. 1981 Dec;321:583-602 PMID: 6978399
  8. T-tubule swelling in hypertonic solutions: a freeze substitution study.
    J Physiol. 1978 Oct;283:133-40 PMID: 309940
  9. Asymmetrical charge movement in slow- and fast-twitch mammalian muscle fibres in normal and paraplegic rats.
    J Physiol. 1983 Aug;341:213-31 PMID: 6620180
  10. A non-selective cation conductance in frog muscle membrane blocked by micromolar external calcium ions.
    J Physiol. 1984 Aug;353:565-83 PMID: 6090645
  11. Charge movement and membrane capacity in frog muscle.
    J Physiol. 1979 Apr;289:83-97 PMID: 458722
  12. Voltage clamp experiments in striated muscle fibres.
    J Physiol. 1970 Jul;208(3):607-44 PMID: 5499787
  13. Effects of glycerol treatment and maintained depolarization on charge movement in skeletal muscle.
    J Physiol. 1976 Jan;254(2):285-316 PMID: 1082507
  14. Calcium transients and intramembrane charge movement in skeletal muscle fibres.
    Nature. 1979 May 31;279(5712):391-6 PMID: 16068161
  15. The sarcoplasmic reticulum and T-system of rat extensor digitorum longus muscles exposed to hypertonic solutions.
    Aust J Exp Biol Med Sci. 1978 Aug;56(4):409-19 PMID: 727998
  16. Effects of membrane potential on the capacitance of skeletal muscle fibers.
    J Gen Physiol. 1976 Feb;67(2):125-63 PMID: 1082924
  17. The influence of transverse tubular delays on the kinetics of charge movement in mammalian skeletal muscle.
    J Gen Physiol. 1985 Jan;85(1):21-42 PMID: 3968532
  18. Excitation-contraction coupling and charge movement in denervated rat extensor digitorum longus and soleus muscles.
    J Physiol. 1985 Jan;358:75-89 PMID: 3981474
  19. A quantitative study of potassium channel kinetics in rat skeletal muscle from 1 to 37 degrees C.
    J Gen Physiol. 1983 Apr;81(4):485-512 PMID: 6304231
  20. Components of charge movement in rabbit skeletal muscle: the effect of tetracaine and nifedipine.
    J Physiol. 1986 Jul;376:85-100 PMID: 3795083
  21. Slow charge movement in mammalian skeletal muscle.
    J Gen Physiol. 1985 Jan;85(1):1-19 PMID: 3968530
  22. Sodium channel gating currents in frog skeletal muscle.
    J Gen Physiol. 1983 Nov;82(5):679-701 PMID: 6315862
  23. Membrane charge movement in contracting and non-contracting skeletal muscle fibres.
    J Physiol. 1981 May;314:565-93 PMID: 6975814
  24. Charge movements near the mechanical threshold in skeletal muscle of Rana temporaria.
    J Physiol. 1984 Apr;349:483-500 PMID: 6610742
  25. Voltage dependent charge movement of skeletal muscle: a possible step in excitation-contraction coupling.
    Nature. 1973 Mar 23;242(5395):244-6 PMID: 4540479
  26. Experimental analysis of the relationship between charge movement components in skeletal muscle of Rana temporaria.
    J Physiol. 1984 Aug;353:419-34 PMID: 6332900
  27. Effects of local anaesthetics on the relationship between charge movements and contractile thresholds in frog skeletal muscle.
    J Physiol. 1981 Nov;320:381-91 PMID: 6976433
  28. Membrane charge moved at contraction thresholds in skeletal muscle fibres.
    J Physiol. 1981 May;314:595-633 PMID: 6975815
  29. Effects of tetracaine on displacement currents and contraction of frog skeletal muscle.
    J Physiol. 1976 Nov;262(3):583-611 PMID: 1087641
  30. Charge movement and mechanical repriming in skeletal muscle.
    J Physiol. 1976 Jan;254(2):361-88 PMID: 1082510
  31. A non-linear voltage dependent charge movement in frog skeletal muscle.
    J Physiol. 1976 Jan;254(2):245-83 PMID: 1082506
  32. Charge movement in the membrane of striated muscle.
    J Physiol. 1976 Jan;254(2):339-60 PMID: 1082509
Article Info
Journal
The Journal of physiology
Abbr.
J Physiol
ISSN
0022-3751
Published
1986-07-00
Pages
63-83
Language
English
Region
England
NLM ID
0266262
PMCID
PMC1182787
Subset
IM
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