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. 1983 Jul;43(1):1–4. doi: 10.1016/S0006-3495(83)84316-1

Determination of ionic calcium in frog skeletal muscle fibers.

J R López, L Alamo, C Caputo, R DiPolo, S Vergara
PMCID: PMC1329261  PMID: 6603872

Abstract

Ionic calcium concentrations were measured in frog skeletal muscle fibers using Ca-selective microelectrodes. In fibers with resting membrane potentials more negative than -85 mV, the mean pCa value was 6.94 (0.12 microM). In fibers depolarized to -73 mV with 10-mM K the mean pCa was 6.43 (0.37 microM). This increase in the intracellular [Ca2+] could be related to the higher oxygen consumption and heat production (Solandt effect) reported to occur under these conditions. Caffeine, 3 mM, also produced an increase in the free ionic calcium to a pCa of 6.52 (0.31 microM) without changes in the membrane potential. Lower caffeine concentrations, 1 and 2 mM, did not change the fiber pCa. Lower Ca concentrations in the external medium effectively reduced the internal ionic calcium to an estimated pCa of 7.43 (0.03 microM).

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Selected References

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  1. Alvarez-Leefmans F. J., Rink T. J., Tsien R. Y. Free calcium ions in neurones of Helix aspersa measured with ion-selective micro-electrodes. J Physiol. 1981 Jun;315:531–548. doi: 10.1113/jphysiol.1981.sp013762. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Caputo C., Gottschalk G., Lüttgau H. C. The control of contraction activation by the membrane potential. Experientia. 1981 Jun;37(6):580–581. doi: 10.1007/BF01990061. [DOI] [PubMed] [Google Scholar]
  3. DiPolo R., Rojas H., Vergara J., Lopez R., Caputo C. Measurements of intracellular ionized calcium in squid giant axons using calcium-selective electrodes. Biochim Biophys Acta. 1983 Mar 9;728(3):311–318. doi: 10.1016/0005-2736(83)90500-x. [DOI] [PubMed] [Google Scholar]
  4. Dipolo R., Requena J., Brinley F. J., Jr, Mullins L. J., Scarpa A., Tiffert T. Ionized calcium concentrations in squid axons. J Gen Physiol. 1976 Apr;67(4):433–467. doi: 10.1085/jgp.67.4.433. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. 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]
  6. Lüttgau H. C., Oetliker H. The action of caffeine on the activation of the contractile mechanism in straited muscle fibres. J Physiol. 1968 Jan;194(1):51–74. doi: 10.1113/jphysiol.1968.sp008394. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Novotný I., Vyskocil F. Possible role of Ca ions in the resting metabolism of frog sartorius muscle during potassium depolarization. J Cell Physiol. 1966 Feb;67(1):159–168. doi: 10.1002/jcp.1040670118. [DOI] [PubMed] [Google Scholar]
  8. Solandt D. Y. The effect of potassium on the excitability and resting metabolism of frog's muscle. J Physiol. 1936 Feb 8;86(2):162–170. doi: 10.1113/jphysiol.1936.sp003351. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Tsien R. Y., Rink T. J. Neutral carrier ion-selective microelectrodes for measurement of intracellular free calcium. Biochim Biophys Acta. 1980 Jul;599(2):623–638. doi: 10.1016/0005-2736(80)90205-9. [DOI] [PubMed] [Google Scholar]

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