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. 1995 Jul 1;486(Pt 1):105–112. doi: 10.1113/jphysiol.1995.sp020794

Involvement of dihydropyridine receptors in terminating Ca2+ release in rat skeletal myotubes.

N Suda 1
PMCID: PMC1156500  PMID: 7562626

Abstract

1. Combined patch-clamp and fura-2 measurements were performed in order to investigate the effect of dihydropyridine (DHP) antagonists on termination of sarcoplasmic reticulum (SR) Ca2+ release in cultured rat skeletal myoballs. 2. Ca2+ transients induced by 10 mM caffeine were curtailed by depolarization (e.g. +20 mV for 1 s) and subsequent repolarization (-70 mV). This phenomenon is termed RISC (repolarization-induced stop of caffeine-induced Ca2+ release). 3. At 0.5 to 1 microM, DHP antagonists (nifedipine or (+)PN200-110) strongly inhibited RISC and also slowed the decay of intracellular Ca2+ concentration ([Ca2+]i) following repolarization after depolarization-induced Ca2+ release (-20 or -10 mV for 5 s). 4. The activation time course of the Ca2+ channel associated with the DHP receptor (DHPR) was investigated by measuring DHP-sensitive Ca2+ channel tail currents, while varying the duration of depolarizing pulses. The tail currents increased with pulse duration and peaked around 0.7, 0.9 and 1.1 s for depolarizations to +70, +40 and +20 mV, respectively. These values are compatible with the activation time course of RISC (0.5-1 s to maximally activate RISC at +20 to +60 mV). 5. These results suggest that the DHPR in T-tubular membranes regulates closing of the ryanodine receptor (RyR)-Ca2+ release channel complex through membrane potential change.

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Selected References

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  1. Adams B. A., Tanabe T., Mikami A., Numa S., Beam K. G. Intramembrane charge movement restored in dysgenic skeletal muscle by injection of dihydropyridine receptor cDNAs. Nature. 1990 Aug 9;346(6284):569–572. doi: 10.1038/346569a0. [DOI] [PubMed] [Google Scholar]
  2. Beam K. G., Knudson C. M. Effect of postnatal development on calcium currents and slow charge movement in mammalian skeletal muscle. J Gen Physiol. 1988 Jun;91(6):799–815. doi: 10.1085/jgp.91.6.799. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Caputo C., Fernandez de Bolaños P. Membrane potential, contractile activation and relaxation rates in voltage clamped short muscle fibres of the frog. J Physiol. 1979 Apr;289:175–189. doi: 10.1113/jphysiol.1979.sp012731. [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. Feldmeyer D., Melzer W., Pohl B., Zöllner P. Modulation of calcium current gating in frog skeletal muscle by conditioning depolarization. J Physiol. 1992 Nov;457:639–653. doi: 10.1113/jphysiol.1992.sp019399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. García J., Beam K. G. Measurement of calcium transients and slow calcium current in myotubes. J Gen Physiol. 1994 Jan;103(1):107–123. doi: 10.1085/jgp.103.1.107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. García J., Tanabe T., Beam K. G. Relationship of calcium transients to calcium currents and charge movements in myotubes expressing skeletal and cardiac dihydropyridine receptors. J Gen Physiol. 1994 Jan;103(1):125–147. doi: 10.1085/jgp.103.1.125. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Huang C. L. Voltage-dependent block of charge movement components by nifedipine in frog skeletal muscle. J Gen Physiol. 1990 Sep;96(3):535–557. doi: 10.1085/jgp.96.3.535. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Jong D. S., Pape P. C., Chandler W. K., Baylor S. M. Reduction of calcium inactivation of sarcoplasmic reticulum calcium release by fura-2 in voltage-clamped cut twitch fibers from frog muscle. J Gen Physiol. 1993 Aug;102(2):333–370. doi: 10.1085/jgp.102.2.333. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Kass R. S., Arena J. P., Chin S. Block of L-type calcium channels by charged dihydropyridines. Sensitivity to side of application and calcium. J Gen Physiol. 1991 Jul;98(1):63–75. doi: 10.1085/jgp.98.1.63. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Lamb G. D. Components of charge movement in rabbit skeletal muscle: the effect of tetracaine and nifedipine. J Physiol. 1986 Jul;376:85–100. doi: 10.1113/jphysiol.1986.sp016143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Lamb G. D., Stephenson D. G. Control of calcium release and the effect of ryanodine in skinned muscle fibres of the toad. J Physiol. 1990 Apr;423:519–542. doi: 10.1113/jphysiol.1990.sp018037. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Lamb G. D., Stephenson D. G. Effect of Mg2+ on the control of Ca2+ release in skeletal muscle fibres of the toad. J Physiol. 1991 Mar;434:507–528. doi: 10.1113/jphysiol.1991.sp018483. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Marks A. R., Taubman M. B., Saito A., Dai Y., Fleischer S. The ryanodine receptor/junctional channel complex is regulated by growth factors in a myogenic cell line. J Cell Biol. 1991 Jul;114(2):303–312. doi: 10.1083/jcb.114.2.303. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Melzer W., Rios E., Schneider M. F. A general procedure for determining the rate of calcium release from the sarcoplasmic reticulum in skeletal muscle fibers. Biophys J. 1987 Jun;51(6):849–863. doi: 10.1016/S0006-3495(87)83413-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. 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]
  17. Rousseau E., Ladine J., Liu Q. Y., Meissner G. Activation of the Ca2+ release channel of skeletal muscle sarcoplasmic reticulum by caffeine and related compounds. Arch Biochem Biophys. 1988 Nov 15;267(1):75–86. doi: 10.1016/0003-9861(88)90010-0. [DOI] [PubMed] [Google Scholar]
  18. Ríos E., Pizarro G. Voltage sensor of excitation-contraction coupling in skeletal muscle. Physiol Rev. 1991 Jul;71(3):849–908. doi: 10.1152/physrev.1991.71.3.849. [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. Inactivation of calcium release from the sarcoplasmic reticulum in frog skeletal muscle. J Physiol. 1988 Nov;405:727–745. doi: 10.1113/jphysiol.1988.sp017358. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Suda N., Penner R. Membrane repolarization stops caffeine-induced Ca2+ release in skeletal muscle cells. Proc Natl Acad Sci U S A. 1994 Jun 7;91(12):5725–5729. doi: 10.1073/pnas.91.12.5725. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Takeshima H., Iino M., Takekura H., Nishi M., Kuno J., Minowa O., Takano H., Noda T. Excitation-contraction uncoupling and muscular degeneration in mice lacking functional skeletal muscle ryanodine-receptor gene. Nature. 1994 Jun 16;369(6481):556–559. doi: 10.1038/369556a0. [DOI] [PubMed] [Google Scholar]
  23. Tanabe T., Beam K. G., Powell J. A., Numa S. Restoration of excitation-contraction coupling and slow calcium current in dysgenic muscle by dihydropyridine receptor complementary DNA. Nature. 1988 Nov 10;336(6195):134–139. doi: 10.1038/336134a0. [DOI] [PubMed] [Google Scholar]
  24. Tang S., Yatani A., Bahinski A., Mori Y., Schwartz A. Molecular localization of regions in the L-type calcium channel critical for dihydropyridine action. Neuron. 1993 Dec;11(6):1013–1021. doi: 10.1016/0896-6273(93)90215-d. [DOI] [PubMed] [Google Scholar]

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