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January 1, 1993Journal of Cardiovascular Pharmacology58 citations

Comparative Effects of Na+/H+ Exchange Inhibitors Against Cardiac Injury Produced by Ischemia/Reperfusion, Hypoxia/Reoxygenation, and the Calcium Paradox

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MKMorris KarmazynMRMadhur RayJHJames V. Haist

Key Points

  • To compare the cardioprotective efficacy of the Na+/H+ exchange inhibitors amiloride and 5-(N,N-hexamethylene) amiloride (HMA) against myocardial injury caused by ischemia/reperfusion, hypoxia/reoxygenation, and the calcium paradox.
  • Tested isolated hearts subjected to 15 minutes of ischemia followed by reperfusion, 12 minutes of hypoxia followed by reoxygenation, or calcium depletion and repletion (the calcium paradox).

Structured PICO

P
Population
Preclinical model of cardiac injury produced by ischemia/reperfusion, hypoxia/reoxygenation, and the calcium paradox
I
Intervention
Amiloride (174 microM), 5-(N,N-hexamethylene) amiloride (HMA, 1 microM), or bepridil (10 microM)
C
Comparator
Control (untreated hearts)
O
Outcome
Recovery in contractility and resting tensionsurrogate

Na+/H+ exchange inhibitors amiloride and HMA significantly improve recovery of cardiac contractility following ischemia/reperfusion and hypoxia/reoxygenation in a preclinical model.

Abstract

To examine the role of Na+/H+ exchange in cardiac injury, we compared the effect of amiloride (174 microM) with the markedly more specific and potent inhibitor 5-(N,N-hexamethylene) amiloride (HMA, 1 microM) against cardiac injury produced by reperfusion, reoxygenation, and the calcium paradox. Reperfusion after 15-min ischemia resulted in a 55 +/- 4% recovery in contractility, whereas in the presence of amiloride or HMA, recovery was increased to 82 +/- 5.8 and 72 +/- 7.8%, respectively (p 0.05), but no increases were observed with amiloride or HMA. Bepridil (10 microM), a purported Na+/Ca2+ exchange inhibitor, exerted a salutary effect against reperfusion dysfunction identical to that of amiloride and HMA, whereas in reoxygenated hearts the effects were identical to those observed with HMA. The protective effects of the drugs were not related to improved energy metabolic status. None of the pharmacologic interventions exerted beneficial effects against the calcium paradox.(ABSTRACT TRUNCATED AT 250 WORDS)

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Cite This Study

Karmazyn et al. (1993) studied this question.

synapsesocial.com/papers/6a74d8769c92392688b1e442https://doi.org/10.1097/00005344-199301000-00025
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