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首页> 外文期刊>The journal of physiological sciences >Emulsified isoflurane postconditioning produces cardioprotection against myocardial ischemiaa??reperfusion injury in rats
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Emulsified isoflurane postconditioning produces cardioprotection against myocardial ischemiaa??reperfusion injury in rats

机译:乳化异氟醚后处理可保护大鼠心肌缺血再灌注损伤

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Emulsified isoflurane (EIso) preconditioning can induce cardioprotection. We investigated whether EIso application after ischemia protects hearts against reperfusion injury and whether it is mediated by the inhibition of apoptosis. Rats were subjected to 30-min coronary occlusion followed by 180-min reperfusion. At the onset of reperfusion, rats were intravenously administered saline (sham, control group), 30??% intralipid (IL group) or 2??ml??kga??1 EIso (EIso group) for 30??min. After reperfusion, infarct sizes, myocardial apoptosis and expression of Bcl-2, Bax and caspase-3 proteins were determined. Hemodynamic parameters were not different among groups. Compared with control and intralipid group, EIso limited infarct size, inhibited apoptosis, increased the expression of Bcl-2, decreased the expression of Bax, cleaved caspase-3, and enhanced Bcl-2/Bax ratio. EIso protects hearts against reperfusion injury when administered at the onset of reperfusion, which may be mediated by the inhibition of apoptosis via modulation of the expression of pro- and anti-apoptotic proteins.
机译:乳化异氟烷(EIso)预处理可以诱导心脏保护作用。我们调查了缺血后EIso的应用是否可以保护心脏免受再灌注损伤,以及是否通过抑制凋亡来介导。对大鼠进行30分钟的冠状动脉闭塞,然后再进行180分钟的再灌注。在再灌注开始时,给大鼠静脉内注射生理盐水(假手术,对照组),30 %%脂质体(IL组)或2毫升/ ml kga -1 EIso(EIso组)30分钟。再灌注后,测定梗塞面积,心肌细胞凋亡以及Bcl-2,Bax和caspase-3蛋白的表达。各组之间的血流动力学参数没有差异。与对照组和血脂内组相比,EIso限制了梗死面积,抑制了细胞凋亡,增加了Bcl-2的表达,降低了Bax的表达,裂解了caspase-3,并提高了Bcl-2 / Bax的比率。 EIso可在再灌注开始时保护心脏免受再灌注损伤,这可以通过调节促凋亡和抗凋亡蛋白的表达来抑制细胞凋亡来介导。

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