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1991 | 42 | 1 |

Tytuł artykułu

Perpetuation of misinterpretations due to lack of methodical insight. A critical re-evaluation of the determination of 45Ca release from intact guinea-pig atria

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
1. The evaluation of still more pretentious and complicated methods is accompanied by a decline of methodical knowledge outside of the own technical field. Interpretations or extrapolations are taken as granted without critical examination of the methodical steps applied. An example is given by re-evaluating the ⁴⁵Ca release from isolated cardiac tissue and the possible interpretations. 2. ⁴⁵Ca release and tissue Ca content were measured in isolated guinea-pig left atria during Ca equilibrium and under conditions known to induce net Ca movements. 3. At equilibrium condition (1.8 mM Na²⁺ ₀)3 exponential phase of ⁴⁵Ca release from the atria were observed. The compartments contained 61%, 29% and 10% of total ⁴⁵Ca; the were 2, 12 and 90 min, respectively. 4. The release of ⁴⁵Ca from the slowly exchanging compartment (t½ 90 min) decreased during incubation in nominal Ca-free solution, although a net loss of tissue Ca occurred. Addition of EGTA (5 x 10⁻⁵ M) to the washout medium abolished this retardation of ⁴⁵Ca release. 5. At external Na⁺ concentrations below 40 mM (substituted by sucrose), the ⁴⁵Ca release from the slowly exchanging compartment decreased. Simultaneously, the tissue Ca content increased massively. The ⁴⁵Ca release was further reduced in Na-poor, nominal Ca-free solution. Under both conditions, the presence of EGTA in the washout medium normalized the rate of ⁴⁵Ca release. 6. The results suggest that the apparent decline of ⁴⁵Ca release from intact atria upon reduction of the external Ca and Na concentration does not reflect a decrease of the cellular efflux rate, but is the consequence of an enhanced re-uptake of ⁴⁵Ca from the extracellular space into the myocardial cells. The probability for the released ⁴⁵Ca either to escape into the organ bath or to become reabsorbed depends on the specific radioactivity of ⁴⁵Ca in the extracellular space during the washout phase. Thus, this experimental procedure is not suited to demonstrate a Na-Ca exchange at the cardiac sarcolemma.

Wydawca

-

Rocznik

Tom

42

Numer

1

Opis fizyczny

p.37-48,fig.,ref.

Twórcy

autor
  • Department of Pharmacology, University of Kiel, Hospitalstrasse 4-6, D-2300 Kiel 1, Germany
autor
  • Department of Pharmacology, University of Kiel, Hospitalstrasse 4-6, D-2300 Kiel 1, Germany
autor
  • Department of Pharmacology, University of Kiel, Hospitalstrasse 4-6, D-2300 Kiel 1, Germany

Bibliografia

  • 1. Reuter H, Seitz N. The dependence of calcium efflux from cardiac muscle on temperature and' external ion composition. J Physiol 1968; 195: 451-70.
  • 2. Glitsch HG, Reuter H, Scholz H. The effect of the internal sodium concentration on calcium fluxes in isolated guinea-pig auricles. J Physiol 1970; 209: 25-43.
  • 3. Jundt H, Porzig H, Reuter H, Stucki JW. The effect of substances releasing intracellular calcium ions on sodium-dependent calcium efflux from guinea-pig auricles. J Physiol 1975; 246: 229-53.
  • 4. Hein L, Schoch R. Tracer re-uptake interferes with measurement of ⁴⁵ calcium efflux from guinea-pig atria. Naunyn-Schmiedeberg's Arch Pharmacol 1990 ; 341: R55.
  • 5. Zepf S. Eine serienmäßige Calcium-Bestimmung in kleinen Gewebeproben mit dem Spektralfluorometer. Zeiss-Mitteilungen 1966; 4: 43-57.
  • 6. Hoditz H. Lüllmann H. Die Calcium-Umsatzgeschwindigkeit ruhender und kontrahierender Vorhofmuskulatur in vitro. Pflügers Arch 1964; 280: 22-9.
  • 7. Solomon AK. Compartmental methods of kinetic analysis. In: Mineral Metabolism, edited by CL Comar &F Bronner. New York, Academic Press 1960; 1A: 119-67.
  • 8. Grossmann A, Furchgott RF. The effects of frequency of stimulation and calcium concentration on ⁴⁵Ca exchange and contractility of the isolated guinea-pig auricle. J Pharmacol Exp Ther 1964: 143: 120-30.
  • 9. Winegrad S, Shanes AM. Calcium flux and contractility in guinea-pig atria. J Gen Physiol 1962 ; 45: 371-94.
  • 10. Busselen P, Van Kerkhove E. The effect of sodium, calcium and metabolic inhibitors on calcium; efflux from goldfish heart ventricles. J Physiol 1978; 282: 263-83.
  • 11. Philipson KD, Langer GA. Sarcolemmal-bound calcium and contractility in the mammalian myocardium. J Mol Cell Cardiol 1979; 11: 857-75.
  • 12. Saari JT, Johnson JA. Decay of calcium content and contractile force in the rabbit heart. Am J Physiol 1971; 221: 1572-1575.
  • 13. Kuwata JH, Langer GA. Rapid, non-perfusion-limited calcium exchange in cultured neonatal myocardial cells. J Mol Cell Cardiol 1989; 21: 1195-1208.
  • 14. Barry WH, Smith TW. Mechanisms of transmembrane calcium movement in culture chick, embryo ventricular cells. J Physiol 1982; 325: 243-60.
  • 15. Barry WH, Smith TW. Movement of Ca²⁺ accross the sarcolemma: effects of abrupt exposure to zero external Na concentration. J Mol Cardiol 1984; 17: 155-164.
  • 16. Kim D, Smith TW. Inhibition of multiple trans-sarcolemmal cation flux pathways by dichlo- robenzamil in cultured chick heart cells. Mol Pharmacol 1986; 30: 164-70.
  • 17. Langer GA, Nudd LM. Calcium compartmentation in cardiac tissue culture: the effects of extracellular sodium depletion. J Mol Cell Cardiol 1984; 16: 1047-57.
  • 18. Portzehl H, Caldwell PC, Rüegg JC. The dependence of contraction and relaxation of muscle fibers from the crab Maia squinado on the internal concentration of free calcium ions. Biochim Biophys Acta 1964; 79: 581-91.

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Bibliografia

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