Literature DB >> 9400385

Low efficiency of Ca2+ entry through the Na(+)-Ca2+ exchanger as trigger for Ca2+ release from the sarcoplasmic reticulum. A comparison between L-type Ca2+ current and reverse-mode Na(+)-Ca2+ exchange.

K R Sipido1, M Maes, F Van de Werf.   

Abstract

It has been proposed that Ca2+ entry through the Na(+)-Ca2+ exchanger can contribute significantly to the trigger for Ca2+ release from the sarcoplasmic reticulum (SR). We have compared the characteristics of Ca2+ release triggered by reverse-mode Na(+)-Ca2+ exchange and by L-type Ca2+ current (ICaL) during depolarizing steps in single guinea pig ventricular myocytes (whole-cell voltage clamp, fluo 3 and fura-red as [Ca2+]i indicators, 36 +/- 1 degrees C, K(+)-based pipette solution with 20 mmol/L [Na+]). Conditioning pulses to +60 mV ensured comparable Ca2+ loading of the SR. In the presence of ICaL, [Ca2+]i transients typically have an early and rapid rising phase reflecting Ca2+ release, which has a bell-shaped voltage dependence with a peak at +10 mV. With Ca2+ entry through Na(+)-Ca2+ exchange only (20 mumol/L nisoldipine), Ca2+ release flux from the SR is decreased and directly related to the amplitude of the depolarizing step. Ca2+ release is preceded by a significant delay (81 +/- 21 ms at +20 mV, 24 +/- 4 ms at +70 mV) related to Ca2+ entry through the exchanger. Triggered release interrupts Ca2+ entry, as evidenced by reversal of the exchanger current. At potentials positive to +40 mV, Ca2+ influx through Na(+)-Ca2+ exchange, calculated from the outward exchange current, reaches magnitudes comparable to ICaL, but Ca2+ release due to reverse-mode Na(+)-Ca2+ exchange still has a significant delay. We calculated trigger efficiency as the ratio between the maximal rate of Ca2+ release and the Ca2+ influx preceding this release; efficiency of reverse-mode Na(+)-Ca2+ exchange is approximately four times less than that of ICaL. With both ICaL and reverse-mode Na(+)-Ca2+ exchange present, Ca2+ release is triggered by ICaL, and a contribution of reverse-mode Na(+)-Ca2+ exchange to the trigger could not be detected at potentials below +60 mV. These characteristics of reverse-mode Na(+)-Ca2+ exchange predict that its role as a trigger for Ca2+ release during the action potential is likely to be negligible.

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Year:  1997        PMID: 9400385     DOI: 10.1161/01.res.81.6.1034

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


  60 in total

1.  Local regulation of the threshold for calcium sparks in rat ventricular myocytes: role of sodium-calcium exchange.

Authors:  J I Goldhaber; S T Lamp; D O Walter; A Garfinkel; G H Fukumoto; J N Weiss
Journal:  J Physiol       Date:  1999-10-15       Impact factor: 5.182

2.  Role of the Na(+)-Ca(2+) exchanger as an alternative trigger of CICR in mammalian cardiac myocytes.

Authors:  Chunlei Han; Pasi Tavi; Matti Weckström
Journal:  Biophys J       Date:  2002-03       Impact factor: 4.033

3.  Importance of Ca2+ influx by Na+/Ca2+ exchange under normal and sodium-loaded conditions in mammalian ventricles.

Authors:  Hiroshi Satoh; Masaaki Mukai; Tsuyoshi Urushida; Hideki Katoh; Hajime Terada; Hideharu Hayashi
Journal:  Mol Cell Biochem       Date:  2003-01       Impact factor: 3.396

4.  Alterations in action potential profile enhance excitation-contraction coupling in rat cardiac myocytes.

Authors:  R Sah; R J Ramirez; R Kaprielian; P H Backx
Journal:  J Physiol       Date:  2001-05-15       Impact factor: 5.182

Review 5.  Regulation of cardiac excitation-contraction coupling by action potential repolarization: role of the transient outward potassium current (I(to)).

Authors:  Rajan Sah; Rafael J Ramirez; Gavin Y Oudit; Dominica Gidrewicz; Maria G Trivieri; Carsten Zobel; Peter H Backx
Journal:  J Physiol       Date:  2003-01-01       Impact factor: 5.182

6.  Role of sodium-calcium exchanger in modulating the action potential of ventricular myocytes from normal and failing hearts.

Authors:  Antonis A Armoundas; Ion A Hobai; Gordon F Tomaselli; Raimond L Winslow; Brian O'Rourke
Journal:  Circ Res       Date:  2003-06-12       Impact factor: 17.367

7.  Na+ currents are required for efficient excitation-contraction coupling in rabbit ventricular myocytes: a possible contribution of neuronal Na+ channels.

Authors:  Natalia S Torres; Robert Larbig; Alex Rock; Joshua I Goldhaber; John H B Bridge
Journal:  J Physiol       Date:  2010-11-01       Impact factor: 5.182

8.  Activation of reverse Na+-Ca2+ exchange by the Na+ current augments the cardiac Ca2+ transient: evidence from NCX knockout mice.

Authors:  Robert Larbig; Natalia Torres; John H B Bridge; Joshua I Goldhaber; Kenneth D Philipson
Journal:  J Physiol       Date:  2010-07-19       Impact factor: 5.182

9.  Mechanisms underlying the frequency dependence of contraction and [Ca(2+)](i) transients in mouse ventricular myocytes.

Authors:  Gudrun Antoons; Kanigula Mubagwa; Ines Nevelsteen; Karin R Sipido
Journal:  J Physiol       Date:  2002-09-15       Impact factor: 5.182

10.  Spatial characteristics of sarcoplasmic reticulum Ca2+ release events triggered by L-type Ca2+ current and Na+ current in guinea-pig cardiac myocytes.

Authors:  Peter Lipp; Marcel Egger; Ernst Niggli
Journal:  J Physiol       Date:  2002-07-15       Impact factor: 5.182

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