Skip to main content
Biophysical Journal logoLink to Biophysical Journal
. 1989 Jul;56(1):1–14. doi: 10.1016/S0006-3495(89)82647-5

Effects of cobalt, magnesium, and cadmium on contraction of rat soleus muscle.

A F Dulhunty 1, P W Gage 1
PMCID: PMC1280447  PMID: 2752079

Abstract

The effects on isometric tension of three divalent ions that block calcium channels, magnesium, cobalt, and cadmium, were tested in small bundles of rat soleus fibers. Cobalt, at a concentration of 2 or 6 mM, reversibly depressed twitch and tetanic tension and the depression was much greater in solutions containing no added calcium ions. Magnesium caused much less depression of tension than cobalt. The depression of tension was not accompanied by membrane depolarization or a reduction in the amplitude of action potentials. A reduction caused by 6 mM cobalt in the amplitude of 40 or 80 mM potassium contractures was not accompanied by a comparable reduction in tension during 200 mM potassium contractures, and could be explained by a shift in the potassium contracture tension-voltage curve to more positive potentials (by +7 mV on average). Similar effects were not seen with 2 or 6 mM magnesium. At a concentration of 20 mM, both cobalt and magnesium depressed twitch and tetanic tension, cobalt having greater effect than magnesium. Both ions shifted the potassium contracture tension-voltage curve to the right by +5 to +10 mV, caused a small depression of maximum tension, and slowed the time course of potassium contractures. Cadmium (3 mM) depressed twitch, tetanic, and potassium contracture tension by more than 6 mM cobalt, but experiments were complicated by the gradual appearance of large contractures that became even larger, and sometimes oscillatory, when the solution containing cadmium was washed out. It was concluded that divalent cations affect both activation and inactivation of tension in a manner that cannot be completely explained by a change in surface charge.

Full text

PDF
1

Selected References

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

  1. Adrian R. H., Peachey L. D. Reconstruction of the action potential of frog sartorius muscle. J Physiol. 1973 Nov;235(1):103–131. doi: 10.1113/jphysiol.1973.sp010380. [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. Armstrong C. M., Bezanilla F. M., Horowicz P. Twitches in the presence of ethylene glycol bis( -aminoethyl ether)-N,N'-tetracetic acid. Biochim Biophys Acta. 1972 Jun 23;267(3):605–608. doi: 10.1016/0005-2728(72)90194-6. [DOI] [PubMed] [Google Scholar]
  4. Avila-Sakar A. J., Cota G., Gamboa-Aldeco R., Garcia J., Huerta M., Muñiz J., Stefani E. Skeletal muscle Ca2+ channels. J Muscle Res Cell Motil. 1986 Aug;7(4):291–298. doi: 10.1007/BF01753649. [DOI] [PubMed] [Google Scholar]
  5. Bolaños P., Caputo C., Velaz L. Effects of calcium, barium and lanthanum on depolarization-contraction coupling in skeletal muscle fibres of Rana pipiens. J Physiol. 1986 Jan;370:39–60. doi: 10.1113/jphysiol.1986.sp015921. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. 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]
  7. Caputo C., Gimenez M. Effects of external calcium deprivation on single muscle fibers. J Gen Physiol. 1967 Oct;50(9):2177–2195. doi: 10.1085/jgp.50.9.2177. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Caputo C. Nickel substitution for calcium and the time course of potassium contractures of single muscle fibres. J Muscle Res Cell Motil. 1981 Jun;2(2):167–182. doi: 10.1007/BF00711867. [DOI] [PubMed] [Google Scholar]
  9. 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]
  10. 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]
  11. Dulhunty A. F. Distribution of potassium and chloride permeability over the surface and T-tubule membranes of mammalian skeletal muscle. J Membr Biol. 1979 Apr 9;45(3-4):293–310. doi: 10.1007/BF01869290. [DOI] [PubMed] [Google Scholar]
  12. Dulhunty A. F., Gage P. W. Effects of extracellular calcium concentration and dihydropyridines on contraction in mammalian skeletal muscle. J Physiol. 1988 May;399:63–80. doi: 10.1113/jphysiol.1988.sp017068. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Dulhunty A. F., Gage P. W. Excitation-contraction coupling and charge movement in denervated rat extensor digitorum longus and soleus muscles. J Physiol. 1985 Jan;358:75–89. doi: 10.1113/jphysiol.1985.sp015541. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Dörrscheidt-Käfer M. The action of Ca2+ , Mg2+ and H+ on the contraction threshold of frog skeletal muscle: Evidence for surface charges controlling electro-mechanical coupling. Pflugers Arch. 1976 Mar 11;362(1):33–41. doi: 10.1007/BF00588678. [DOI] [PubMed] [Google Scholar]
  15. Eisenberg R. S., McCarthy R. T., Milton R. L. Paralysis of frog skeletal muscle fibres by the calcium antagonist D-600. J Physiol. 1983 Aug;341:495–505. doi: 10.1113/jphysiol.1983.sp014819. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Flockerzi V., Oeken H. J., Hofmann F., Pelzer D., Cavalié A., Trautwein W. Purified dihydropyridine-binding site from skeletal muscle t-tubules is a functional calcium channel. Nature. 1986 Sep 4;323(6083):66–68. doi: 10.1038/323066a0. [DOI] [PubMed] [Google Scholar]
  17. Fryer M. W., Gage P. W., Neering I. R., Dulhunty A. F., Lamb G. D. Paralysis of skeletal muscle by butanedione monoxime, a chemical phosphatase. Pflugers Arch. 1988 Jan;411(1):76–79. doi: 10.1007/BF00581649. [DOI] [PubMed] [Google Scholar]
  18. Gallant E. M., Goettl V. M. Effects of calcium antagonists on mechanical responses of mammalian skeletal muscles. Eur J Pharmacol. 1985 Nov 5;117(2):259–265. doi: 10.1016/0014-2999(85)90611-9. [DOI] [PubMed] [Google Scholar]
  19. 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]
  20. Hui C. S., Milton R. L., Eisenberg R. S. Charge movement in skeletal muscle fibers paralyzed by the calcium-entry blocker D600. Proc Natl Acad Sci U S A. 1984 Apr;81(8):2582–2585. doi: 10.1073/pnas.81.8.2582. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Jaimovich E., Venosa R. A., Shrager P., Horowicz P. Density and distribution of tetrodotoxin receptors in normal and detubulated frog sartorius muscle. J Gen Physiol. 1976 Apr;67(4):399–416. doi: 10.1085/jgp.67.4.399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Kotsias B. A., Muchnik S., Obejero Paz C. A. Co2+, low Ca2+, and verapamil reduce mechanical activity in rat skeletal muscles. Am J Physiol. 1986 Jan;250(1 Pt 1):C40–C46. doi: 10.1152/ajpcell.1986.250.1.C40. [DOI] [PubMed] [Google Scholar]
  23. 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]
  24. Lamb G. D., Walsh T. Calcium currents, charge movement and dihydropyridine binding in fast- and slow-twitch muscles of rat and rabbit. J Physiol. 1987 Dec;393:595–617. doi: 10.1113/jphysiol.1987.sp016843. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Lorković H., Rüdel R. Influence of divalent cations on potassium contracture duration in frog muscle fibres. Pflugers Arch. 1983 Jul;398(2):114–119. doi: 10.1007/BF00581057. [DOI] [PubMed] [Google Scholar]
  26. Lüttgau H. C., Gottschalk G., Berwe D. The effect of calcium and Ca antagonists upon excitation-contraction coupling. Can J Physiol Pharmacol. 1987 Apr;65(4):717–723. doi: 10.1139/y87-118. [DOI] [PubMed] [Google Scholar]
  27. 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]
  28. McCleskey E. W. Calcium channels and intracellular calcium release are pharmacologically different in frog skeletal muscle. J Physiol. 1985 Apr;361:231–249. doi: 10.1113/jphysiol.1985.sp015643. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Miledi R., Parker I., Zhu P. H. Extracellular ions and excitation-contraction coupling in frog twitch muscle fibres. J Physiol. 1984 Jun;351:687–710. doi: 10.1113/jphysiol.1984.sp015271. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. 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]
  31. 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]
  32. Schwartz L. M., McCleskey E. W., Almers W. Dihydropyridine receptors in muscle are voltage-dependent but most are not functional calcium channels. 1985 Apr 25-May 1Nature. 314(6013):747–751. doi: 10.1038/314747a0. [DOI] [PubMed] [Google Scholar]
  33. Stephenson D. G., Thieleczek R. Activation of the contractile apparatus of skinned fibres of frog by the divalent cations barium, cadmium and nickel. J Physiol. 1986 Nov;380:75–92. doi: 10.1113/jphysiol.1986.sp016273. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Storey D. J., Shears S. B., Kirk C. J., Michell R. H. Stepwise enzymatic dephosphorylation of inositol 1,4,5-trisphosphate to inositol in liver. Nature. 1984 Nov 22;312(5992):374–376. doi: 10.1038/312374a0. [DOI] [PubMed] [Google Scholar]
  35. 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]
  36. Vergara J., Tsien R. Y., Delay M. Inositol 1,4,5-trisphosphate: a possible chemical link in excitation-contraction coupling in muscle. Proc Natl Acad Sci U S A. 1985 Sep;82(18):6352–6356. doi: 10.1073/pnas.82.18.6352. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Biophysical Journal are provided here courtesy of The Biophysical Society

RESOURCES