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. 1973 Dec 1;62(6):693–706. doi: 10.1085/jgp.62.6.693

Intracellular Calcium Binding and Release in Frog Heart

Saul Winegrad 1
PMCID: PMC2226138  PMID: 4217348

Abstract

The capacities and affinities of intracellular calcium-binding sites have been studied in frog ventricles, in which the concentration of Ca++ in the sarcoplasm can be controlled as a result of treatment with EDTA. The total calcium content of calcium-depleted and nondepleted muscles at rest and muscles generating considerable tension was 0.8, 1.4, and 5.4 µmol/g of muscle, respectively. Net movement of calcium into or out of the cells occurred without change in tension when the sarcoplasmic concentration of Ca++ was either of two values, less than 10-7 M or approximately 5 x 10-7 M. These data can be explained by the presence of two groups of intracellular calcium sinks which compete with the contractile proteins, one with a capacity of about 0.6 µmol/g and an affinity constant greater than 107 M-1 and a second with a capacity of 4.0 µmol/g and an affinity constant of about 2 x 106 M-1. The higher affinity calcium is released by anoxia, oligomycin, or abrupt changes in sarcoplasmic Ca++. Muscles soaked in Sr-Ringer's contain electron densities in the sarcoplasmic reticulum and to a lesser extent in the mitochondria.

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Selected References

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

  1. Costantin L. L., Podolsky R. J. Depolarization of the internal membrane system in the activation of frog skeletal muscle. J Gen Physiol. 1967 May;50(5):1101–1124. doi: 10.1085/jgp.50.5.1101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Edwards C., Lorković H., Weber A. The effect of the replacement of calcium by strontium on excitation-contraction coupling in frog skeletal muscle. J Physiol. 1966 Oct;186(2):295–306. doi: 10.1113/jphysiol.1966.sp008035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Nauss K. M., Davies R. E. Changes in phosphate compounds during the development and maintenance of rigor mortis. J Biol Chem. 1966 Jun 25;241(12):2918–2922. [PubMed] [Google Scholar]
  4. Page S. G., Niedergerke R. Structures of physiological interest in the frog heart ventricle. J Cell Sci. 1972 Jul;11(1):179–203. doi: 10.1242/jcs.11.1.179. [DOI] [PubMed] [Google Scholar]
  5. Somlyo A. V., Somlyo A. P. Strontium accumulation by sarcoplasmic reticulum and mitochondria in vascular smooth muscle. Science. 1971 Nov 26;174(4012):955–958. doi: 10.1126/science.174.4012.955. [DOI] [PubMed] [Google Scholar]
  6. Sommer J. R., Johnson E. A. Cardiac muscle. A comparative ultrastructural study with special reference to frog and chicken hearts. Z Zellforsch Mikrosk Anat. 1969;98(3):437–468. [PubMed] [Google Scholar]
  7. THOMAS L. J., Jr Increase of labeled calcium uptake in heart muscle during potassium lack contracture. J Gen Physiol. 1960 Jul;43:1193–1206. doi: 10.1085/jgp.43.6.1193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Winegrad S. Studies of cardiac muscle with a high permeability to calcium produced by treatment with ethylenediaminetetraacetic acid. J Gen Physiol. 1971 Jul;58(1):71–93. doi: 10.1085/jgp.58.1.71. [DOI] [PMC free article] [PubMed] [Google Scholar]

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