| Objective To investigate the effects of dexmedetomidine preconditioning on myocar-dial ischemia-reperfusion injury in isolated rat hearts.Methods Thirty-two male wistar rats weighing230~260g were heparinized with heparin sodium500IU/kg inter-peritoneally and anesthetized with10%chloral hydrate400mg/kg. After thoracotomy the hearts were immediately removed and perfused retrogradely at75cmH20with Krebs-Hensleit(K-H) solution aerated with95%O2and5%CO2in a Langendorff apparatus.After10min stabilization,the thirty-two isolated hearts were randomly divided to4groups(n=8earch):â‘ I/R group in which the hearts were perfused for30min after10min stabilization;â‘¡D1group in which the hearts were perfused with K-H solution containing dexmedetomidine (0.23ng/ml) for20min followed by10min washout before ischemia;(3)D2group in which the hearts were perfused with K-H solution containing dexmedetomidine (2.3ng/ml) for20min followed by10min washout before ischemia;â‘£D3group in which the hearts were perfused with K-H solution containing dexmedetomidine (2.3ng/ml) and yohmbine(1μM) for20min followed by10min washout before ischemia. Hearts were subjected to30min ischemia followed by120min reperfusion with K-H solution.Hemodynamic parameters:Heart rate(HR)ã€Left ventricular developed pressure(LVDP)ã€+differential pressure timemaxium(+dp/dtmax) and-differential pressure timemaxium(-dp/dtmax) were recorded at the end of balance〠before ischemia and at60minã€120min during reperfusion.The activity of creatine kinase(CK) and lactate dehydrogenase(LDH) in coronary effluent were measured at the end of balance and5minã€30minã€60minã€120min during reperfusion. At the end of reperfusion,the activity of SOD and the content of MDA in the myocardium were measured.Results (1) Influence on hemodynamic:There were no differences of HRã€LVDPã€+dp/dtmaxã€-dp/dtmax among groups before ischemic(P>0.05).After ischemia,there were no statistical significance of HR among four groups(P>0.05) and LVDPã€+dp/dtmax and-dp/dtmax tends to decrease in each group; Compared with I/R group,the LVDPã€+dp/dtmaxã€-dp/dtmax were higher in the group of D1and D2(P<0.05), there were no statistical significance in group D3(P>0.05); Compared with D1group, the LVDPã€+dp/dtmaxã€-dp/dtmax were higher in the group of D2and were lower in group D3(P<0.05); Compared with D2group, the LVDPã€+dp/dtmaxã€-dp/dtmax were lower in group of D3(P<0.05).(2)Influene on the myocardical enzyme leak:There were no statistical significance of CK and LDH among four groups at the end of balance(P>0.05);Compared with I/R group, the CK and LDH release decreased in the group of D1and D2(P<0.05), there were no statistical significance in group D3(P>0.05);Compared with D1group, the CK and LDH release decreased in the group of D2(P<0.05)(P<0.05),the CK and LDH were higher in group D3(P<0.05); Compared with D2group,the CK and LDH were higher in group D3(P<0.05).(3)Influence on the content of MDA and the activity of SOD:Compared with I/R group,the content of MDA decreased and the SOD activity was higher in the group of D1and D2(P<0.05), there were no statistical significance in group D3(P>0.05); Compared with D1group, the content of MDA decreased and the SOD activity was higher in the group of D2(P<0.05), the content of MDA increased and the SOD activity was lower in the group of D3(P<0.05); Compared with D2group, the content of MDA increased and the SOD activity was lower in the group of D3(P<0.05).Conclusion Dexmedetomidine preconditioning can protect myocardial ischemia-reperfusion injury relating to concentration and the mechanism of the protection maybe concerned with α2adrenergic receptor. |