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. 1975 Apr 1;65(4):459–482. doi: 10.1085/jgp.65.4.459

Effects of sudden changes in external sodium concentration on twitch tension in isolated muscle fibers

PMCID: PMC2214928  PMID: 1080184

Abstract

When [Na] was suddenly introduced to single muscle fibers (Xenopus or frog), which had been pretreated with Na-free solution (Tris- substituted), the time-course of twitch recovery was very variable, half-time ranging from less than 1 S to 5 S. The [Na] vs. twitch height relationship was also variable. In small Xenopus fibers, decreases of [Na] to 50% increased the twitch, while in large Xenopus fibers twitch height remained constant or decreased as [Na] was decreased to 50%. The apparent diffusion constant (D') of Na+ or K+, calculated from the time- course of twitch recovery and the [Na] vs. twitch relation, and from the time-course of the slow repolarization upon sudden reduction of [K] was about 1-1.5 X 10(-6) cm2/S. This is one order of magnitude smaller than the diffusion constants in an aqueous solution. Even if the tortuosity factor of the T system is taken into account, there remains a substantial discrepancy. Although our value of D' is subject to various errors, if we accept the value, the twitch recovery is predicted to be either very quick or slow depending upon the variation of [Na]-twitch relation and fiber size. Thus, both quick and slow twitch recoveries can be explained by the diffusion time of Na+ in the T system, and therefore the results are consistent with the idea that the T system is excitable.

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Selected References

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

  1. ADRIAN R. H. The effect of internal and external potassium concentration on the membrane potential of frog muscle. J Physiol. 1956 Sep 27;133(3):631–658. doi: 10.1113/jphysiol.1956.sp005615. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Adrian R. H., Chandler W. K., Hodgkin A. L. The kinetics of mechanical activation in frog muscle. J Physiol. 1969 Sep;204(1):207–230. doi: 10.1113/jphysiol.1969.sp008909. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. 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]
  4. Almers W. Potassium conductance changes in skeletal muscle and the potassium concentration in the transverse tubules. J Physiol. 1972 Aug;225(1):33–56. doi: 10.1113/jphysiol.1972.sp009928. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Barry P. H., Adrian R. H. Slow conductance changes due to potassium depletion in the transverse tubules of frog muscle fibers during hyperpolarizing pulses. J Membr Biol. 1973;14(3):243–292. doi: 10.1007/BF01868081. [DOI] [PubMed] [Google Scholar]
  6. Bastian J., Nakajima S. Action potential in the transverse tubules and its role in the activation of skeletal muscle. J Gen Physiol. 1974 Feb;63(2):257–278. doi: 10.1085/jgp.63.2.257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Bezanilla F., Caputo C., Gonzalez-Serratos H., Venosa R. A. Sodium dependence of the inward spread of activation in isolated twitch muscle fibres of the frog. J Physiol. 1972 Jun;223(2):507–523. doi: 10.1113/jphysiol.1972.sp009860. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Caputo C., Dipolo R. Ionic diffusion delays in the transverse tubules of frog twitch muscle fibres. J Physiol. 1973 Mar;229(2):547–557. doi: 10.1113/jphysiol.1973.sp010153. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Endo M. Entry of fluorescent dyes into the sarcotubular system of the frog muscle. J Physiol. 1966 Jul;185(1):224–238. doi: 10.1113/jphysiol.1966.sp007983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. HAJDU S., LEONARD E. The cellular basis of cardiac glycoside action. Pharmacol Rev. 1959 Jun;11(2 Pt 1):173–209. [PubMed] [Google Scholar]
  11. 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]
  12. HODGKIN A. L., KATZ B. The effect of sodium ions on the electrical activity of giant axon of the squid. J Physiol. 1949 Mar 1;108(1):37–77. doi: 10.1113/jphysiol.1949.sp004310. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Nakajima S., Nakajima Y., Peachey L. D. Speed of repolarization and morphology of glygerol-treated frog muscle fibres. J Physiol. 1973 Oct;234(2):465–480. doi: 10.1113/jphysiol.1973.sp010355. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Valdiosera R., Clausen C., Eisenberg R. S. Impedance of frog skeletal muscle fibers in various solutions. J Gen Physiol. 1974 Apr;63(4):460–491. doi: 10.1085/jgp.63.4.460. [DOI] [PMC free article] [PubMed] [Google Scholar]

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