Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1987 Aug;84(16):6005–6009. doi: 10.1073/pnas.84.16.6005

Intracellular free calcium concentration measured with 19F NMR spectroscopy in intact ferret hearts.

E Marban, M Kitakaze, H Kusuoka, J K Porterfield, D T Yue, V P Chacko
PMCID: PMC298992  PMID: 3112778

Abstract

Changes in the intracellular free Ca2+ concentration, [Ca2+]i, mediate excitation-contraction coupling in the heart and contribute to cellular injury during ischemia and reperfusion. To study these processes directly, we measured [Ca2+]i in perfused ferret (Mustela putorius furo) hearts using 19F NMR spectroscopy to detect the 5,5'-difluoro derivative of the Ca2+ chelator 1,2-bis(o-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid (BAPTA). To load cells, hearts were perfused with the acetoxymethyl ester derivative of 5,5'-F2-BAPTA. We measured 19F NMR spectra and left ventricular pressure simultaneously, at rest and during pacing at various external Ca concentrations [( Ca]o). Although contractile force was attenuated by the Ca2+ buffering properties of 5,5'-F2-BAPTA, the decrease in pressure could be overcome by raising [Ca]o. Our mean value of 104 nM for [Ca2+]i at rest in the perfused heart agrees well with previous measurements in isolated ventricular muscle. During pacing at 0.6-4 Hz, time-averaged [Ca2+]i increased; the effect of pacing was augmented by increasing [Ca]o. [Ca2+]i more than tripled during 10-20 min of global ischemia, and returned toward control levels upon reperfusion. This approach promises to be particularly useful in investigating the physiology of intact hearts and the pathophysiology of alterations in the coronary circulation.

Full text

PDF
6005

Selected References

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

  1. Allen D. G., Kurihara S. Calcium transients in mammalian ventricular muscle. Eur Heart J. 1980;Suppl A:5–15. doi: 10.1093/eurheartj/1.suppl_1.5. [DOI] [PubMed] [Google Scholar]
  2. Allen D. G., Orchard C. H. Intracellular calcium concentration during hypoxia and metabolic inhibition in mammalian ventricular muscle. J Physiol. 1983 Jun;339:107–122. doi: 10.1113/jphysiol.1983.sp014706. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Arslan P., Di Virgilio F., Beltrame M., Tsien R. Y., Pozzan T. Cytosolic Ca2+ homeostasis in Ehrlich and Yoshida carcinomas. A new, membrane-permeant chelator of heavy metals reveals that these ascites tumor cell lines have normal cytosolic free Ca2+. J Biol Chem. 1985 Mar 10;260(5):2719–2727. [PubMed] [Google Scholar]
  4. Blinks J. R., Wier W. G., Hess P., Prendergast F. G. Measurement of Ca2+ concentrations in living cells. Prog Biophys Mol Biol. 1982;40(1-2):1–114. doi: 10.1016/0079-6107(82)90011-6. [DOI] [PubMed] [Google Scholar]
  5. Clusin W. T., Bristow M. R., Karagueuzian H. S., Katzung B. G., Schroeder J. S. Do calcium-dependent ionic currents mediate ischemic ventricular fibrillation? Am J Cardiol. 1982 Feb 18;49(3):606–612. doi: 10.1016/s0002-9149(82)80019-2. [DOI] [PubMed] [Google Scholar]
  6. Cobbold P. H., Bourne P. K. Aequorin measurements of free calcium in single heart cells. 1984 Nov 29-Dec 5Nature. 312(5993):444–446. doi: 10.1038/312444a0. [DOI] [PubMed] [Google Scholar]
  7. Fabiato A., Fabiato F. Effects of pH on the myofilaments and the sarcoplasmic reticulum of skinned cells from cardiace and skeletal muscles. J Physiol. 1978 Mar;276:233–255. doi: 10.1113/jphysiol.1978.sp012231. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Grinwald P. M. Calcium uptake during post-ischemic reperfusion in the isolated rat heart: influence of extracellular sodium. J Mol Cell Cardiol. 1982 Jun;14(6):359–365. doi: 10.1016/0022-2828(82)90251-6. [DOI] [PubMed] [Google Scholar]
  9. Grynkiewicz G., Poenie M., Tsien R. Y. A new generation of Ca2+ indicators with greatly improved fluorescence properties. J Biol Chem. 1985 Mar 25;260(6):3440–3450. [PubMed] [Google Scholar]
  10. Hochachka P. W. Defense strategies against hypoxia and hypothermia. Science. 1986 Jan 17;231(4735):234–241. doi: 10.1126/science.2417316. [DOI] [PubMed] [Google Scholar]
  11. Kort A. A., Lakatta E. G., Marban E., Stern M. D., Wier W. G. Fluctuations in intracellular calcium concentration and their effect on tonic tension in canine cardiac Purkinje fibres. J Physiol. 1985 Oct;367:291–308. doi: 10.1113/jphysiol.1985.sp015825. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Kusuoka H., Porterfield J. K., Weisman H. F., Weisfeldt M. L., Marban E. Pathophysiology and pathogenesis of stunned myocardium. Depressed Ca2+ activation of contraction as a consequence of reperfusion-induced cellular calcium overload in ferret hearts. J Clin Invest. 1987 Mar;79(3):950–961. doi: 10.1172/JCI112906. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Kusuoka H., Weisfeldt M. L., Zweier J. L., Jacobus W. E., Marban E. Mechanism of early contractile failure during hypoxia in intact ferret heart: evidence for modulation of maximal Ca2+-activated force by inorganic phosphate. Circ Res. 1986 Sep;59(3):270–282. doi: 10.1161/01.res.59.3.270. [DOI] [PubMed] [Google Scholar]
  14. Lattanzio F. A., Jr, Pressman B. C. Alterations in intracellular calcium activity and contractility of isolated perfused rabbit hearts by ionophores and adrenergic agents. Biochem Biophys Res Commun. 1986 Sep 14;139(2):816–821. doi: 10.1016/s0006-291x(86)80063-8. [DOI] [PubMed] [Google Scholar]
  15. Lee C. O., Uhm D. Y., Dresdner K. Sodium-calcium exchange in rabbit heart muscle cells: direct measurement of sarcoplasmic Ca2+ activity. Science. 1980 Aug 8;209(4457):699–701. doi: 10.1126/science.7394527. [DOI] [PubMed] [Google Scholar]
  16. Marban E., Kusuoka H., Yue D. T., Weisfeldt M. L., Wier W. G. Maximal Ca2+-activated force elicited by tetanization of ferret papillary muscle and whole heart: mechanism and characteristics of steady contractile activation in intact myocardium. Circ Res. 1986 Sep;59(3):262–269. doi: 10.1161/01.res.59.3.262. [DOI] [PubMed] [Google Scholar]
  17. Marban E., Rink T. J., Tsien R. W., Tsien R. Y. Free calcium in heart muscle at rest and during contraction measured with Ca2+ -sensitive microelectrodes. Nature. 1980 Aug 28;286(5776):845–850. doi: 10.1038/286845a0. [DOI] [PubMed] [Google Scholar]
  18. Marban E., Robinson S. W., Wier W. G. Mechanisms of arrhythmogenic delayed and early afterdepolarizations in ferret ventricular muscle. J Clin Invest. 1986 Nov;78(5):1185–1192. doi: 10.1172/JCI112701. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Metcalfe J. C., Hesketh T. R., Smith G. A. Free cytosolic Ca2+ measurements with fluorine labelled indicators using 19FNMR. Cell Calcium. 1985 Apr;6(1-2):183–195. doi: 10.1016/0143-4160(85)90043-0. [DOI] [PubMed] [Google Scholar]
  20. Nayler W. G. Calcium and cell death. Eur Heart J. 1983 May;4 (Suppl 100):33–41. doi: 10.1093/eurheartj/4.suppl_c.33. [DOI] [PubMed] [Google Scholar]
  21. Poenie M., Alderton J., Steinhardt R., Tsien R. Calcium rises abruptly and briefly throughout the cell at the onset of anaphase. Science. 1986 Aug 22;233(4766):886–889. doi: 10.1126/science.3755550. [DOI] [PubMed] [Google Scholar]
  22. Radda G. K., Seeley P. J. Recent studies on cellular metabolism by nuclear magnetic resonance. Annu Rev Physiol. 1979;41:749–769. doi: 10.1146/annurev.ph.41.030179.003533. [DOI] [PubMed] [Google Scholar]
  23. Shen A. C., Jennings R. B. Myocardial calcium and magnesium in acute ischemic injury. Am J Pathol. 1972 Jun;67(3):417–440. [PMC free article] [PubMed] [Google Scholar]
  24. Smith G. A., Hesketh R. T., Metcalfe J. C., Feeney J., Morris P. G. Intracellular calcium measurements by 19F NMR of fluorine-labeled chelators. Proc Natl Acad Sci U S A. 1983 Dec;80(23):7178–7182. doi: 10.1073/pnas.80.23.7178. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Tsien R. Y. A non-disruptive technique for loading calcium buffers and indicators into cells. Nature. 1981 Apr 9;290(5806):527–528. doi: 10.1038/290527a0. [DOI] [PubMed] [Google Scholar]
  26. Tsien R. Y. New calcium indicators and buffers with high selectivity against magnesium and protons: design, synthesis, and properties of prototype structures. Biochemistry. 1980 May 27;19(11):2396–2404. doi: 10.1021/bi00552a018. [DOI] [PubMed] [Google Scholar]
  27. Wier W. G., Cannell M. B., Berlin J. R., Marban E., Lederer W. J. Cellular and subcellular heterogeneity of [Ca2+]i in single heart cells revealed by fura-2. Science. 1987 Jan 16;235(4786):325–328. doi: 10.1126/science.3798114. [DOI] [PubMed] [Google Scholar]
  28. Wier W. G., Yue D. T. Intracellular calcium transients underlying the short-term force-interval relationship in ferret ventricular myocardium. J Physiol. 1986 Jul;376:507–530. doi: 10.1113/jphysiol.1986.sp016167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Yue D. T. Intracellular [Ca2+] related to rate of force development in twitch contraction of heart. Am J Physiol. 1987 Apr;252(4 Pt 2):H760–H770. doi: 10.1152/ajpheart.1987.252.4.H760. [DOI] [PubMed] [Google Scholar]
  30. Yue D. T., Marban E., Wier W. G. Relationship between force and intracellular [Ca2+] in tetanized mammalian heart muscle. J Gen Physiol. 1986 Feb;87(2):223–242. doi: 10.1085/jgp.87.2.223. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Yue D. T., Wier W. G. Estimation of intracellular [Ca2+] by nonlinear indicators. A quantitative analysis. Biophys J. 1985 Sep;48(3):533–537. doi: 10.1016/S0006-3495(85)83810-8. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES