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Oxygen surrounding the heart during ischemic conservation determines the myocardial injury during reperfusion

机译:缺血保存期间心脏周围的氧气决定了再灌注期间的心肌损伤

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摘要

There is discrepancy regarding the duration of reperfusion required using 2,3,5-triphenyl-2H-tetrazolium chloride (TTC) staining to assess myocardial infarction in an isolated, perfused heart model. Several investigators prefer long-term reperfusion (120 minutes) to determine myocardial injury, while others have used a shorter duration (30-40 minutes). We investigated whether oxygen surrounding the myocardium during ischemia plays a critical role in the installation of myocardial infarction during reperfusion. Mice hearts were perfused with a Langendorff apparatus using Krebs Henseleit (KH) buffer oxygenated with 95% O2 plus 5% CO2 at 37°C. Hearts were either immersed in KH or suspended in air during 18 minutes of global ischemia in a normothermic, water-jacketed chamber. Hearts then were reperfused for 40, 60, or 90 minutes. We found that hearts immersed in KH had decreased recovery of function and increased myocardial infarct size, reaching a steady-state level after 40 minutes of reperfusion. In contrast, hearts suspended in air approached steady-state after 90 minutes of reperfusion. Thus, mitochondrial reactive oxygen species (ROS) production was much lower in air-maintained hearts than in KH-immersed hearts. To investigate whether an increase in oxygen surrounding the myocardium during ischemia might cause further damage, we bubbled the KH solution with nitrogen (KH+N2) rather than oxygen (KH+O2). With this alteration, recovery of cardiac function was improved and myocardial infarct size and mitochondrial ROS production were reduced compared with hearts immersed in KH+O2. In conclusion, short-term (40 minutes) reperfusion is sufficient to reach steady-state myocardial infarct size when hearts are immersed in physiologic solution during ischemia; however, a longer duration of reperfusion (90 minutes) is required if hearts are suspended in air. Thus, oxygen surrounding the heart during ischemia determines the extent of myocardium injury during reperfusion.
机译:关于使用2,3,5-三苯基-2H-氯化四唑(TTC)染色来评估孤立的灌注心脏模型中的心肌梗塞所需的再灌注持续时间存在差异。一些研究者倾向于长期再灌注(120分钟)来确定心肌损伤,而其他研究者则使用较短的持续时间(30-40分钟)。我们调查了缺血期间心肌周围的氧气是否在再灌注过程中心肌梗死的形成中起关键作用。在37℃下,使用用95%O2加5%CO2氧化的Krebs Henseleit(KH)缓冲液,用Langendorff仪器灌注小鼠心脏。在正常缺血,水套腔中,在全球缺血18分钟内,将心脏浸入KH或悬浮于空气中。然后将心脏再灌注40、60或90分钟。我们发现,浸泡在KH中的心脏的功能恢复下降,心肌梗死面积增加,在再灌注40分钟后达到稳态。相反,在90分钟的再灌注后,悬浮在空气中的心脏接近稳态。因此,空气维持型心脏的线粒体活性氧(ROS)产生要比浸入KH的心脏低得多。为了研究缺血期间心肌周围氧的增加是否会引起进一步的损害,我们向KH溶液中通入了氮气(KH + N2)而不是氧气(KH + O2)。与浸入KH + O2的心脏相比,这种改变可以改善心脏功能的恢复,并减少心肌梗塞的大小和线粒体ROS的产生。总之,当心脏在缺血期间浸入生理溶液中时,短期(40分钟)再灌注足以达到稳态心肌梗塞的大小。但是,如果心脏悬浮在空气中,则需要更长的再灌注时间(90分钟)。因此,缺血期间心脏周围的氧气决定了再灌注过程中心肌损伤的程度。

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