首页> 美国卫生研究院文献>other >Hot shot induction and reperfusion with a specific blocker of the es-ENT1 nucleoside transporter before and after hypothermic cardioplegia abolishes myocardial stunning in acutely ischemic hearts despite metabolic derangement: Hot shot drug delivery before hypothermic cardioplegia
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Hot shot induction and reperfusion with a specific blocker of the es-ENT1 nucleoside transporter before and after hypothermic cardioplegia abolishes myocardial stunning in acutely ischemic hearts despite metabolic derangement: Hot shot drug delivery before hypothermic cardioplegia

机译:热拍诱导和再灌注前和低温停搏废除尽管心肌代谢紊乱的急性缺血性心脏惊艳后Es-ENT1核苷转运的特异性阻断剂:热拍药物低温停跳前交货

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摘要

ObjectiveSimultaneous inhibition of the cardiac equilibrative-p-nitrobenzylthioinosine (NBMPR)–sensitive (es) type of the equilibrative nucleoside transport 1 (ENT1) nucleoside transporter, with NBMPR, and adenosine deaminase, with erythro-9-[2-hydroxy-3-nonyl]adenine (EHNA), prevents release of myocardial purines and attenuates myocardial stunning and fibrillation in canine models of warm ischemia and reperfusion. It is not known whether prolonged administration of hypothermic cardioplegia influences purine release and EHNA/NBMPR-mediated cardioprotection in acutely ischemic hearts.
机译:目的同时抑制心脏平衡-对硝基苄基硫代肌苷(NBMPR)-敏感的(es)类型的平衡核苷转运1(ENT1)核苷转运蛋白,NBMPR和腺苷脱氨酶,erythro-9- [2-羟基-3-壬基腺嘌呤(EHNA),可防止温暖嘌呤和再灌注犬模型中心肌嘌呤的释放,并减弱心肌的电击和纤颤。尚不明确,长期服用低温体麻痹是否会影响急性缺血心脏的嘌呤释放和EHNA / NBMPR介导的心脏保护作用。

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