Key result
HOE-642 improved postischemic recovery of left ventricular developed pressure to 45% vs 15% in controls (P<.05) and enhanced the protective effect of ischemic preconditioning in isolated rat hearts.
Population
Isolated rat ventricular myocytes and isolated rat hearts
Comparison
HOE-642, an NHE inhibitor, infused for 5 minutes… vs Control, ischemic preconditioning alone, or…
Design
Preclinical
Authors
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NHE inhibition may enhance experimental preconditioning; leaves open clinical translation in ischemia-reperfusion.
Absolute Event Rate: 45% vs 15%
p-value: p=<.05
In an isolated rat heart model, NHE inhibition with HOE-642 did not reduce the efficacy of ischemic preconditioning and enhanced protection during prolonged ischemia.
Shipolini et al. (1997) studied Ischemia. HOE-642 vs. Control was evaluated on Postischemic recovery of left ventricular developed pressure (LVDP) after 40 minutes of ischemia (p=<.05). HOE-642 improved postischemic recovery of left ventricular developed pressure to 45% vs 15% in controls (P<.05) and enhanced the protective effect of ischemic preconditioning in isolated rat hearts.
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