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. 1983 Aug;341:495–505. doi: 10.1113/jphysiol.1983.sp014819

Paralysis of frog skeletal muscle fibres by the calcium antagonist D-600.

R S Eisenberg, R T McCarthy, R L Milton
PMCID: PMC1195346  PMID: 6604805

Abstract

The Ca2+ channel blocker D-600 (methoxyverapamil) paralyses single muscle fibres of the frog: fibres exposed to the drug at 7 degrees C give a single K+ contracture after which they are paralysed, unable to contract in response to electrical stimulation or further applications of K+. Paralysed fibres contract in response to caffeine and have normal resting potentials and action potentials. Fibres treated with D-600 at 22 degrees C are not paralysed. Paralysed fibres warmed to 22 degrees C recover contractile properties: they twitch and give K+ contractures. Other workers have shown that D-600 blocks a Ca2+ channel at room temperature; thus, the paralytic action of D-600 is probably mediated by a different membrane protein, perhaps a different Ca2+ channel from that blocked at room temperature. These results suggest that the binding of D-600 can disrupt the mechanism coupling electrical potential changes across the T membrane to Ca2+ release from the sarcoplasmic reticulum.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Almers W., Fink R., Palade P. T. Calcium depletion in frog muscle tubules: the decline of calcium current under maintained depolarization. J Physiol. 1981 Mar;312:177–207. doi: 10.1113/jphysiol.1981.sp013623. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Almers W., Palade P. T. Slow calcium and potassium currents across frog muscle membrane: measurements with a vaseline-gap technique. J Physiol. 1981 Mar;312:159–176. doi: 10.1113/jphysiol.1981.sp013622. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bianchi C. P. Some historical aspects of excitation--contraction coupling. Can J Physiol Pharmacol. 1982 Apr;60(4):415–416. doi: 10.1139/y82-061. [DOI] [PubMed] [Google Scholar]
  4. Caputo C. Excitation and contraction processes in muscle. Annu Rev Biophys Bioeng. 1978;7:63–83. doi: 10.1146/annurev.bb.07.060178.000431. [DOI] [PubMed] [Google Scholar]
  5. Caputo C. The time course of potassium contractures of single muscle fibres. J Physiol. 1972 Jun;223(2):483–505. doi: 10.1113/jphysiol.1972.sp009859. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. 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]
  7. Cota G., Stefani E. Effects of external calcium reduction on the kinetics of potassium contractures in frog twitch muscle fibres. J Physiol. 1981 Aug;317:303–316. doi: 10.1113/jphysiol.1981.sp013826. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Dörrscheidt-Käfer M. The action of D600 on frog skeletal muscle: facilitation of excitation-contraction coupling. Pflugers Arch. 1977 Jul 19;369(3):259–267. doi: 10.1007/BF00582193. [DOI] [PubMed] [Google Scholar]
  9. Eisenberg B. R., Eisenberg R. S. The T-SR junction in contracting single skeletal muscle fibers. J Gen Physiol. 1982 Jan;79(1):1–19. doi: 10.1085/jgp.79.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Eisenberg B. R., Mathias R. T., Gilai A. Intracellular localization of markers within injected or cut frog muscle fibers. Am J Physiol. 1979 Jul;237(1):C50–C55. doi: 10.1152/ajpcell.1979.237.1.C50. [DOI] [PubMed] [Google Scholar]
  11. Eisenberg R. S., Mathias R. T. Structural analysis of electrical properties of cells and tissues. Crit Rev Bioeng. 1980;4(3):203–232. [PubMed] [Google Scholar]
  12. Endo M. Calcium release from the sarcoplasmic reticulum. Physiol Rev. 1977 Jan;57(1):71–108. doi: 10.1152/physrev.1977.57.1.71. [DOI] [PubMed] [Google Scholar]
  13. Gonzalez-Serratos H., Valle-Aguilera R., Lathrop D. A., Garcia M. C. Slow inward calcium currents have no obvious role in muscle excitation-contraction coupling. Nature. 1982 Jul 15;298(5871):292–294. doi: 10.1038/298292a0. [DOI] [PubMed] [Google Scholar]
  14. HODGKIN A. L., HOROWICZ P. Potassium contractures in single muscle fibres. J Physiol. 1960 Sep;153:386–403. doi: 10.1113/jphysiol.1960.sp006541. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. HODGKIN A. L., HOROWICZ P. The effect of sudden changes in ionic concentrations on the membrane potential of single muscle fibres. J Physiol. 1960 Sep;153:370–385. doi: 10.1113/jphysiol.1960.sp006540. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. HODGKIN A. L., HOROWICZ P. The influence of potassium and chloride ions on the membrane potential of single muscle fibres. J Physiol. 1959 Oct;148:127–160. doi: 10.1113/jphysiol.1959.sp006278. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Hescheler J., Pelzer D., Trube G., Trautwein W. Does the organic calcium channel blocker D600 act from inside or outside on the cardiac cell membrane? Pflugers Arch. 1982 Jun;393(4):287–291. doi: 10.1007/BF00581411. [DOI] [PubMed] [Google Scholar]
  18. 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]
  19. Huang C. L. Pharmacological separation of charge movement components in frog skeletal muscle. J Physiol. 1982 Mar;324:375–387. doi: 10.1113/jphysiol.1982.sp014118. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Huerta M., Stefani E. Potassium and caffeine contractures in fast and slow muscles of the chicken. J Physiol. 1981 Sep;318:181–189. doi: 10.1113/jphysiol.1981.sp013857. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Hui C. S. Pharmacological dissection of charge movement in frog skeletal muscle fibers. Biophys J. 1982 Jul;39(1):119–122. doi: 10.1016/S0006-3495(82)84498-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Kaumann A. J., Uchitel O. D. Reversible Inhibition of Potassium Contractures by optical isomers of verapamil and D 600 on slow muscle fibres of the frog. Naunyn Schmiedebergs Arch Pharmacol. 1976;292(1):21–27. doi: 10.1007/BF00506485. [DOI] [PubMed] [Google Scholar]
  23. 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]
  24. Mathias R. T., Levis R. A., Eisenberg R. S. Electrical models of excitation-contraction coupling and charge movement in skeletal muscle. J Gen Physiol. 1980 Jul;76(1):1–31. doi: 10.1085/jgp.76.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Mathias R. T., Rae J. L., Eisenberg R. S. Electrical properties of structural components of the crystalline lens. Biophys J. 1979 Jan;25(1):181–201. doi: 10.1016/S0006-3495(79)85284-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Miledi R., Parker I. Blocking of acetylcholine-induced channels by extracellular or intracellular application of D600. Proc R Soc Lond B Biol Sci. 1980 Dec 31;211(1182):143–150. doi: 10.1098/rspb.1980.0162. [DOI] [PubMed] [Google Scholar]
  27. Miyamoto H., Racker E. Mechanism of calcium release from skeletal sarcoplasmic reticulum. J Membr Biol. 1982;66(3):193–201. doi: 10.1007/BF01868494. [DOI] [PubMed] [Google Scholar]
  28. Pelzer D., Trautwein W., McDonald T. F. Calcium channel block and recovery from block in mammalian ventricular muscle treated with organic channel inhibitors. Pflugers Arch. 1982 Aug;394(2):97–105. doi: 10.1007/BF00582909. [DOI] [PubMed] [Google Scholar]
  29. Sanchez J. A., Stefani E. Inward calcium current in twitch muscle fibres of the frog. J Physiol. 1978 Oct;283:197–209. doi: 10.1113/jphysiol.1978.sp012496. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Sandow A. Excitation-contraction coupling in skeletal muscle. Pharmacol Rev. 1965 Sep;17(3):265–320. [PubMed] [Google Scholar]
  31. 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]
  32. Somlyo A. V. Bridging structures spanning the junctioning gap at the triad of skeletal muscle. J Cell Biol. 1979 Mar;80(3):743–750. doi: 10.1083/jcb.80.3.743. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Taylor S. R., Lopez J. R., Griffiths P. J., Trube G., Cecchi G. Calcium in excitation--contraction coupling of frog skeletal muscle. Can J Physiol Pharmacol. 1982 Apr;60(4):489–502. doi: 10.1139/y82-068. [DOI] [PubMed] [Google Scholar]

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