Rapid adaptation of myocardial calcium homeostasis to short episodes of ischemia in isolated rat hearts

Short episodes of ischemia and reperfusion (ischemic preconditioning) have been shown to attenaute the detrimental rise in intracellular free Ca 2+ ([Ca 2+] i) caused by subsequent sustained ischemia. The purpose of this study was to investigate the detailed time course of [Ca 2+] i during such shor...

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Published inThe American heart journal Vol. 131; no. 6; pp. 1106 - 1112
Main Authors Smith, Geoffrey B., Stefenelli, Thomas, Wu, Shao T., Wikman-Coffelt, Joan, Parmley, William W., Zaugg, Christian E.
Format Journal Article
LanguageEnglish
Published New York, NY Mosby, Inc 01.06.1996
Elsevier
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Summary:Short episodes of ischemia and reperfusion (ischemic preconditioning) have been shown to attenaute the detrimental rise in intracellular free Ca 2+ ([Ca 2+] i) caused by subsequent sustained ischemia. The purpose of this study was to investigate the detailed time course of [Ca 2+] i during such short episodes of ischemia and reperfusion. [Ca 2+] i was measured at a high time resolution by surface fluorometry and indo-1 in isolated perfused rat hearts during three episodes of 5 minutes of ischemia followed by 5 minutes of reperfusion. We found that the rise in systolic [Ca 2+] i was significantly smaller during the second (191% ± 67%) and third (194% ± 75%) episodes of ischemia than during the first episode (289% ± 75%, P < 0.05 vs both subsequent episodes). This attenuated rise in systolic [Ca 2+] i was preserved during perfusion with low extracellular Na + (105.5 mmol/L [Na +] o). During short episodes of ischemia and reperfusion, [Ca 2+] i rises less during the second and third ischemic episode than during the first episode. Thus one transient ischemic stimulus led to a rapid adaptation of [Ca 2+] i homeostasis to subsequent ischemic conditions. Such a rapid adaptation might be an important mechanism of the ischemic preconditioning phenomenon in protecting against ischemic injury.
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ISSN:0002-8703
1097-6744
DOI:10.1016/S0002-8703(96)90084-8