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. 1991 May 1;97(5):885–896. doi: 10.1085/jgp.97.5.885

Effect of the calcium buffer EGTA on the "hump" component of charge movement in skeletal muscle

PMCID: PMC2216504  PMID: 1650811

Abstract

Three manifestations of excitation-contraction (E-C) coupling were measured in cut skeletal muscle fibers of the frog, voltage clamped in a double Vaseline gap: intramembrane charge movements, myoplasmic Ca2+ transients, and changes in optical transparency. Pulsing patterns in the presence of high [EGTA] intracellularly, shown by Garcia et al. (1989. J. Gen. Physiol. 94:973-986) to deplete Ca2+ in the sarcoplasmic reticulum, were found to change the above manifestations. With an intracellular solution containing 15 mM EGTA and 0 Ca, 10-15 pulses (100 ms) to -20 mV at a frequency of 2 min-1 reduced the "hump" component of charge movement current. This effect was reversible by 5 min of rest. The same effect was obtained in 62.5 mM EGTA and 0 Ca by pulsing at 0.2 min-1. This effect was reversible by adding calcium to the EGTA solution, for a nominal [Ca2+]i of 200 nM, and was prevented by adding calcium to the EGTA solution before pulsing. The suppression of the hump was accompanied by elimination of the optical manifestations of E-C coupling. The current suppressed was found by subtraction and had the following properties: delayed onset, a peak at a variable interval (10-20 ms) into the pulse, a negative phase (inward current) after the peak, and a variable OFF transient that could be multi-phasic and carried less charge than the ON transient. In the previous paper (Csernoch et al., 1991. J. Gen. Physiol. 97:845-884) it was shown that several interventions suppress a similar component of charge movement current, identified with the "hump" or Q gamma current (I gamma). Based on the similarity to that component, the charge movement suppressed by the depletion protocols can also be identified with I gamma. The fact that I gamma is suppressed by Ca2+ depletion and the kinetic properties of the charge suppressed is inconsistent with the existence of separate sets of voltage sensors underlying the two components of charge movement, Q beta and Q gamma. This is explicable if Q gamma is a consequence of calcium release from the sarcoplasmic reticulum.

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Selected References

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  1. Barry W. H., Carnay L. D. Changes in light scattered by striated muscle during excitation-contraction coupling. Am J Physiol. 1969 Nov;217(5):1425–1430. doi: 10.1152/ajplegacy.1969.217.5.1425. [DOI] [PubMed] [Google Scholar]
  2. Brum G., Fitts R., Pizarro G., Ríos E. Voltage sensors of the frog skeletal muscle membrane require calcium to function in excitation-contraction coupling. J Physiol. 1988 Apr;398:475–505. doi: 10.1113/jphysiol.1988.sp017053. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Brum G., Ríos E., Stéfani E. Effects of extracellular calcium on calcium movements of excitation-contraction coupling in frog skeletal muscle fibres. J Physiol. 1988 Apr;398:441–473. doi: 10.1113/jphysiol.1988.sp017052. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chandler W. K., Rakowski R. F., Schneider M. F. Effects of glycerol treatment and maintained depolarization on charge movement in skeletal muscle. J Physiol. 1976 Jan;254(2):285–316. doi: 10.1113/jphysiol.1976.sp011233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Csernoch L., Pizarro G., Uribe I., Rodríguez M., Ríos E. Interfering with calcium release suppresses I gamma, the "hump" component of intramembranous charge movement in skeletal muscle. J Gen Physiol. 1991 May;97(5):845–884. doi: 10.1085/jgp.97.5.845. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Feldmeyer D., Melzer W., Pohl B. Effects of gallopamil on calcium release and intramembrane charge movements in frog skeletal muscle fibres. J Physiol. 1990 Feb;421:343–362. doi: 10.1113/jphysiol.1990.sp017948. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Francini F., Stefani E. Decay of the slow calcium current in twitch muscle fibers of the frog is influenced by intracellular EGTA. J Gen Physiol. 1989 Nov;94(5):953–969. doi: 10.1085/jgp.94.5.953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. García J., Amador M., Stefani E. Relationship between myoplasmic calcium transients and calcium currents in frog skeletal muscle. J Gen Physiol. 1989 Dec;94(6):973–986. doi: 10.1085/jgp.94.6.973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. HILL D. K. Changes in transparency of muscle during a twitch. J Physiol. 1949 May;108(3):292–302. [PubMed] [Google Scholar]
  10. Horowicz P., Schneider M. F. Membrane charge moved at contraction thresholds in skeletal muscle fibres. J Physiol. 1981 May;314:595–633. doi: 10.1113/jphysiol.1981.sp013726. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Horowicz P., Schneider M. F. Membrane charge movement in contracting and non-contracting skeletal muscle fibres. J Physiol. 1981 May;314:565–593. doi: 10.1113/jphysiol.1981.sp013725. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hui C. S. Differential properties of two charge components in frog skeletal muscle. J Physiol. 1983 Apr;337:531–552. doi: 10.1113/jphysiol.1983.sp014640. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Kovacs L., Rios E., Schneider M. F. Measurement and modification of free calcium transients in frog skeletal muscle fibres by a metallochromic indicator dye. J Physiol. 1983 Oct;343:161–196. doi: 10.1113/jphysiol.1983.sp014887. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kovács L., Ríos E., Schneider M. F. Calcium transients and intramembrane charge movement in skeletal muscle fibres. Nature. 1979 May 31;279(5712):391–396. doi: 10.1038/279391a0. [DOI] [PubMed] [Google Scholar]
  15. Kovács L., Schneider M. F. Increased optical transparency associated with excitation--contraction coupling in voltage-clamped cut skeletal muscle fibres. Nature. 1977 Feb 10;265(5594):556–560. doi: 10.1038/265556a0. [DOI] [PubMed] [Google Scholar]
  16. Lüttgau H. C., Spiecker W. The effects of calcium deprivation upon mechanical and electrophysiological parameters in skeletal muscle fibres of the frog. J Physiol. 1979 Nov;296:411–429. doi: 10.1113/jphysiol.1979.sp013013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Pizarro G., Csernoch L., Uribe I., Rodríguez M., Ríos E. The relationship between Q gamma and Ca release from the sarcoplasmic reticulum in skeletal muscle. J Gen Physiol. 1991 May;97(5):913–947. doi: 10.1085/jgp.97.5.913. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Rios E., Brum G. Involvement of dihydropyridine receptors in excitation-contraction coupling in skeletal muscle. Nature. 1987 Feb 19;325(6106):717–720. doi: 10.1038/325717a0. [DOI] [PubMed] [Google Scholar]
  19. Schneider M. F., Chandler W. K. Voltage dependent charge movement of skeletal muscle: a possible step in excitation-contraction coupling. Nature. 1973 Mar 23;242(5395):244–246. doi: 10.1038/242244a0. [DOI] [PubMed] [Google Scholar]
  20. Schneider M. F., Simon B. J., Szucs G. Depletion of calcium from the sarcoplasmic reticulum during calcium release in frog skeletal muscle. J Physiol. 1987 Nov;392:167–192. doi: 10.1113/jphysiol.1987.sp016775. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Szücs G., Csernoch L., Magyar J., Kovács L. Contraction threshold and the "hump" component of charge movement in frog skeletal muscle. J Gen Physiol. 1991 May;97(5):897–911. doi: 10.1085/jgp.97.5.897. [DOI] [PMC free article] [PubMed] [Google Scholar]

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