Early reperfusion levels of Na+ and Ca2+ are strongly associated with postischemic functional recovery but are disassociated from KATP channel-induced cardioprotection

Abstract We previously demonstrated that pinacidil does not affect Na i + accumulation, cellular energy depletion, or acidosis during myocardial ischemia, but dramatically improves the cationic/energetic status during reperfusion. We investigated the role of this latter effect in K ATP channel-induced cardioprotection. Employing 23 Na and 31 P nuclear magnetic resonance spectroscopy with perfused rat hearts, reperfusion Na i + was altered with brief infusions of ouabain and/or RbCl to transiently decrease or increase Na + /K + ATPase activity. The increases and decreases in functional recovery (%LVDP-R) with pinacidil or ouabain, respectively, were largely unaltered by each other’s presence. Early reperfusion Na i + and cellular energy were greatly altered by ouabain and indicated linear relationships with %LVDP-R. Pinacidil shifted these relationships to higher %LVDP-R. Increasing early reperfusion Na i + decreased %LVDP-R but did not diminish pinacidil’s capacity to improve %LVDP-R. Approximately 75% and 45% of the pinacidil-induced improvements in %LVDP-R, could be disassociated from early reperfusion Na i + and cellular energy, respectively. Both pinacidil and RbCl infusion blunted ouabain’s elevation of reperfusion Na i + , but RbCl did not improve %LVDP-R. Atomic absorption tissue Ca 2+ measurements indicated that pinacidil reduced late reperfusion Ca 2+ uptake, but did not reduce early reperfusion Ca 2+ , and its beneficial effects were resistant to ouabain-induced early reperfusion Ca 2+ increases. In conclusion, K ATP channel-induced cardioprotection does not require moderation of Na i + accumulation, cellular energy depletion, or acidosis during ischemia. K ATP channel-induced cardioprotection is largely independent of the accelerated reperfusion Na i + recovery it induces and does not require early reperfusion reductions of tissue Ca 2+ . A larger role for early reperfusion cellular energy cannot be excluded.