Literature DB >> 10860765

Intracellular free calcium and mitochondrial membrane potential in ischemia/reperfusion and preconditioning.

K V Ylitalo1, A Ala-Rämi, E V Liimatta, K J Peuhkurinen, I E Hassinen.   

Abstract

Moderation of calcium perturbations has been implicated in ischemic preconditioning. As mitochondria possess an effective Ca(2+)transporting system driven by the mitochondrial membrane potential, experiments were performed to study time-averaged intracellular free calcium and the mitochondrial membrane potential during preconditioning and ischemia-reperfusion. Isolated rat hearts were subjected to 5 min of preconditioning, a 9-min intervening reperfusion and 21 min of ischemia with subsequent reperfusion. The hearts were preloaded with the Ca(2+)indicator Fura-2 or the mitochondrial membrane potential probe safranine. A method was devised for correction for NADH autofluorescence in time-averaged Ca(2+)probing with Fura-2. The pH dependence of the apparent dissociation constant of the Ca(2+)complex of Fura-2 was determined. Intracellular free Ca(2+)increased during the 5-min ischemia, and this was reversed upon reperfusion. During protracted ischemia a continual Ca(2+)rise was observed when the fluorescence data were corrected for changes in pH. An initial sharp Fura-2 fluorescence spike upon final reperfusion was caused by a pH-dependent change in the dissociation constant of the Ca(2+)complex of Fura-2. In preconditioned hearts the free Ca(2+)was somewhat lower during reperfusion, but a major effect of preconditioning was observed during the prolonged ischemia. The decrease in mitochondrial membrane potential during prolonged ischemia was faster in the preconditioned heart with no difference during the final reperfusion. The effect of preconditioning on cell survival was reflected in a decrease in the post-ischemic washout of creatine kinase. The moderation of the ischemic and post-ischemic intracellular Ca(2+)increase, and the acceleration of the ischemic mitochondrial membrane potential decrease by ischemic preconditioning is in accord with the notion of the involvement of mitochondrial ATP sensitive K(+)channels in preconditioning. In studies on ischemia it is absolutely necessary to correct for the pH-sensitivity of the apparent dissociation constant of the calcium complex of Fura-2 to obtain reliable data for intracellular free calcium. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10860765     DOI: 10.1006/jmcc.2000.1157

Source DB:  PubMed          Journal:  J Mol Cell Cardiol        ISSN: 0022-2828            Impact factor:   5.000


  22 in total

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Review 5.  Mitochondria from anoxia-tolerant animals reveal common strategies to survive without oxygen.

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Review 6.  A technical review of optical mapping of intracellular calcium within myocardial tissue.

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Review 7.  Does the voltage dependent anion channel modulate cardiac ischemia-reperfusion injury?

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8.  Reversible redox-dependent modulation of mitochondrial aconitase and proteolytic activity during in vivo cardiac ischemia/reperfusion.

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Journal:  Proc Natl Acad Sci U S A       Date:  2005-04-19       Impact factor: 11.205

9.  Polyphenol (-)-epigallocatechin gallate during ischemia limits infarct size via mitochondrial K(ATP) channel activation in isolated rat hearts.

Authors:  Dae-Kyu Song; Youngho Jang; June Hong Kim; Kook-Jin Chun; Deokhee Lee; Zhelong Xu
Journal:  J Korean Med Sci       Date:  2010-02-17       Impact factor: 2.153

10.  Time related changes in calcium handling in the isolated ischemic and reperfused rat heart.

Authors:  Zsuzsa Miklós; Tamás Ivanics; Theo H M Roemen; Ger J van der Vusse; László Dézsi; Mária Szekeres; Péter Kemecsei; András Tóth; Márk Kollai; László Ligeti
Journal:  Mol Cell Biochem       Date:  2003-08       Impact factor: 3.396

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