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首页> 外文期刊>Cardiovascular drugs and therapy >One hour reperfusion is enough to assess function and infarct size with TTC staining in Langendorff rat model.
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One hour reperfusion is enough to assess function and infarct size with TTC staining in Langendorff rat model.

机译:一小时的再灌注足以用Langendorff大鼠模型中的TTC染色评估功能和梗死面积。

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BACKGROUND: There is not general agreement concerning the optimal time of reperfusion necessary to assess myocardial function and necrosis on isolated perfused heart model. Nevertheless, the study of cardioprotection (especially, pre- and postconditioning) requires a reliable and standardized assessment of myocardial necrosis. OBJECTIVE: The objective of this study was thus to evaluate whether 1 h of reperfusion was sufficient to assess rat heart viability on Langendorff preparation. Isolated rat hearts (n = 30) underwent 40 min of global normothermic ischemia followed by 60 or 120 min Langendorff reperfusion. In each group, hearts were also randomly assigned into the 2 following sub-groups: postconditioning (PostC, consisting in 2 episodes of 30 s ischemia and 30 s reperfusion at the onset of reperfusion), and control (no intervention). Coronary flow, heart rate, dP/dt and rate-pressure-product were measured. Myocardial necrosis was assessed by TTC staining and LDH, CK release analysis. RESULTS: Our results indicated that heart function tended to slightly decrease between 60 min and 120 min reperfusion. Infarct size was identical at 60 min and 120 min reperfusion, averaging 33-34% of total LV area in controls versus 17% in PostC (p < 0.001 between control and PostC groups). Similarly, the maximum of enzymatic releases (CK and LDH) measured in coronary effluents was at 60 min of reperfusion, followed by a progressive decrease at 90 min and 120 min. As expected, postconditioning limited enzymatic releases whatever the studied time of reperfusion. CONCLUSION: In conclusion, we showed that prolonged reperfusion beyond 60 min was not useful for function assessment and did not change infarct size measurement, on Langendorff rat model of ischemia-reperfusion.
机译:背景:关于在孤立的灌注心脏模型上评估心肌功能和坏死所需的最佳再灌注时间尚无普遍共识。然而,心脏保护的研究(尤其是预处理和后处理)需要对心肌坏死进行可靠且标准化的评估。目的:因此,本研究的目的是评估再灌注1小时是否足以评估Langendorff制剂对大鼠心脏的生存能力。离体大鼠心脏(n = 30)经历了40分钟的全身常温缺血,然后进行了60或120分钟的Langendorff再灌注。在每组中,心脏也被随机分为以下两个亚组:后处理(PostC,由2次30 s缺血和30 s再灌注开始的再灌注发作)和对照(无干预)组成。测量冠脉流量,心率,dP / dt和心率压积。通过TTC染色和LDH,CK释放分析评估心肌坏死。结果:我们的结果表明,在再灌注60分钟至120分钟之间,心脏功能趋于轻微下降。在再灌注60分钟和120分钟时,梗塞面积相同,对照组平均占左心室总面积的33-34%,而PostC组为17%(对照组和PostC组之间的p <0.001)。同样,在冠脉流出物中测得的最大酶释放量(CK和LDH)是在60分钟再灌注时,随后在90分钟和120分钟时逐渐降低。如预期的那样,无论研究的再灌注时间如何,后处理都会限制酶的释放。结论:总的来说,我们证明了在Langendorff大鼠缺血-再灌注模型中,超过60分钟的再灌注不能用于功能评估,也不能改变梗塞面积的测量。

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