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首页> 外文期刊>Basic Research in Cardiology: Official Journal of the German Association of Cardiovascular Research >Inadvertent phosphorylation of survival kinases in isolated perfused hearts: a word of caution.
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Inadvertent phosphorylation of survival kinases in isolated perfused hearts: a word of caution.

机译:孤立的灌注心脏中生存激酶的无意磷酸化:警告。

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The isolated perfused heart is an important model in cardiovascular research. We hypothesized that the perfusion procedure per se will phosphorylate some protein kinases important in pre- and postconditioning. Isolated hearts were Langendorff-perfused for 20 min with or without an intraventricular balloon (rats and mice), or in the working heart mode (mice) and compared to non-perfused controls with respect to protein phosphorylation. Rat hearts were also perfused for 20 and 50 min in the Langendorff mode to investigate the effect of perfusion time on phosphorylation. Western blot analysis showed that perfusion per se induced a massive phosphorylation of ERK 1/2, P38-MAPK, JNK, AMPK, but decreased phosphorylation of AKT in the isolated rat and mouse heart. However, during ongoing perfusion the phosphorylation of these kinases was reduced. Langendorff-perfusion without the intraventricular balloon caused less phosphorylation of ERK 1/2, P38-MAPK and JNK, but had no effect on AMPK. In working hearts phosphorylation of kinases was similar to that of Langendorff-perfused hearts without the balloon. Our findings indicate that excising, handling and perfusion induce a time dependent phosphorylation of stress kinases. The presence of the intraventricular balloon caused the strongest phosphorylation, thus Langendorff-perfused hearts might be partly protected by the perfusion procedure if stress kinases are protective in pre- and postconditioning. This might explain conflicting results obtained with different models of both pre- and postconditioning, and the isolated heart might in some situations be suboptimal for such studies.
机译:离体的灌注心脏是心血管研究的重要模型。我们假设灌注过程本身会磷酸化一些在预处理前后的重要蛋白激酶。在有或没有心室内球囊(大鼠和小鼠)或以工作心脏模式(小鼠)的情况下,对离体心脏进行Langendorff灌注20分钟,并与未灌注的对照组进行蛋白质磷酸化比较。还以Langendorff模式对大鼠心脏进行了20分钟和50分钟的灌注,以研究灌注时间对磷酸化的影响。蛋白质印迹分析表明,灌注本身会诱导ERK 1/2,P38-MAPK,JNK,AMPK大量磷酸化,但会降低离体大鼠和小鼠心脏中AKT的磷酸化。然而,在持续的灌注过程中,这些激酶的磷酸化降低了。没有脑室内球囊的Langendorff灌注导致ERK 1/2,P38-MAPK和JNK的磷酸化程度降低,但对AMPK没有影响。在工作心脏中,激酶的磷酸化与未进行球囊的朗根多夫灌注心脏的磷酸化相似。我们的发现表明,切除,处理和灌注会诱导应激激酶的时间依赖性磷酸化。脑室内球囊的存在引起最强的磷酸化,因此,如果应激激酶在预处理和后处理中具有保护作用,则灌注过程可能会部分保护Langendorff灌注的心脏。这可能解释了用不同的预处理和后处理模型获得的结果相互矛盾,并且在某些情况下离体心脏对于此类研究可能不是最佳的。

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