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Ischemia-reperfusion induces myocardial infarction through mitochondrial Ca²⁺ overload.

Abstract
Both mitochondria and the sarcoplasmic reticulum (SR) are essential for myocardial homeostasis and control of cardiac function. Uptake of Ca(2+) from the cytosol into SR is mediated by the Ca(2+)-dependent ATPase SERCA2a, which is reversibly inhibited by phospholamban (PLN). We previously showed that removal of PLN inhibition of SERCA2a with an antibody to (anti-) PLN reduces cytosolic Ca(2+) overload, thereby attenuating the spread of contraction bands and fodrin proteolysis, during reperfusion after cardiac ischemia. We have now examined the effects of anti-PLN injection into the heart on the development of myocardial infarction (MI) after ischemia-reperfusion in rats. Whereas anti-PLN injection attenuated cytosolic Ca(2+) overload, it did not affect MI size 6h after the onset of reperfusion and actually increased it at 30 min. The antibody also increased the release of apoptosis-inducing factor (AIF) from mitochondria into the cytosol, indicative of enhanced opening of the mitochondrial permeability transition pore (mPTP). Administration of an mPTP blocker at the time of reperfusion or of a blocker of the mitochondrial Ca(2+) uniporter significantly suppressed the release of AIF and the development of MI. These results indicate that the enhancement of SR Ca(2+) loading by anti-PLN injection facilitated Ca(2+) uniporter-dependent mitochondrial Ca(2+) uptake and thereby induced mPTP opening and MI development during early reperfusion. The enhancement of SR Ca(2+) loading thus aggravates MI in a manner independent of cytosolic Ca(2+) overload. Given that cytosolic Ca(2+) overload induces contraction bands, our findings are inconsistent with a causal relation between contraction bands and MI.
AuthorsKaori Shintani-Ishida, Makoto Inui, Ken-Ichi Yoshida
JournalJournal of molecular and cellular cardiology (J Mol Cell Cardiol) Vol. 53 Issue 2 Pg. 233-9 (Aug 2012) ISSN: 1095-8584 [Electronic] England
PMID22659291 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2012 Elsevier Ltd. All rights reserved.
Chemical References
  • Apoptosis Inducing Factor
  • Calcium-Binding Proteins
  • Lactones
  • Mitochondrial Membrane Transport Proteins
  • Mitochondrial Permeability Transition Pore
  • Ru 360
  • Ruthenium Compounds
  • Spiro Compounds
  • phospholamban
  • sanglifehrin A
  • Cyclosporine
  • Calcium
Topics
  • Animals
  • Apoptosis Inducing Factor (metabolism)
  • Calcium (metabolism)
  • Calcium-Binding Proteins (pharmacology)
  • Cyclosporine (pharmacology)
  • Lactones (pharmacology)
  • Male
  • Mitochondria (drug effects, metabolism)
  • Mitochondrial Membrane Transport Proteins (drug effects)
  • Mitochondrial Permeability Transition Pore
  • Myocardial Infarction (etiology, metabolism)
  • Rats
  • Rats, Sprague-Dawley
  • Reperfusion Injury (metabolism, physiopathology)
  • Ruthenium Compounds (pharmacology)
  • Sarcoplasmic Reticulum (drug effects, metabolism)
  • Spiro Compounds (pharmacology)

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