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首页> 外文期刊>Journal of Molecular and Cellular Cardiology >Cardioprotection by ischemic preconditioning preserves mitochondrial function and functional coupling between adenine nucleotide translocase and creatine kinase.
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Cardioprotection by ischemic preconditioning preserves mitochondrial function and functional coupling between adenine nucleotide translocase and creatine kinase.

机译:通过局部缺血预处理进行的心脏保护可保持线粒体功能以及腺嘌呤核苷酸转运酶和肌酸激酶之间的功能偶联。

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M. N. Laclau, S. Boudina, J. B. Thambo, L. Tariosse, G. Gouverneur, S. Bonoron-Adele, V. A. Saks, K. D. Garlid and P. Dos Santos. Cardioprotection by Ischemic Preconditioning Preserves Mitochondrial Function and Functional Coupling Between Adenine Nucleotide Translocase and Creatine Kinase. Journal of Molecular and Cellular Cardiology (2001) 33, 947-956. This study investigates the effect of ischemic preconditioning on mitochondrial function, including functional coupling between the adenine nucleotide translocase and mitochondrial creatine kinase, which is among the first reactions to be altered in ischemia. Three groups of Langendorff-perfused rat hearts were studied: a control group, a group subjected to 30 min ischemia followed by 15 min reperfusion, and a group subjected to ischemic preconditioning prior to 30 min ischemia and 15 min reperfusion. Ischemic preconditioning significantly delayed the onset and amplitude of contracture during ischemia, decreased enzymatic release, and improved the recovery of heart contractile function after reperfusion. Mitochondrial function was assessed in permeabilized skinned fibers. The protective effect of preconditioning was associated with preservation of mitochondrial function, as evidenced by maintenance of the high K(1/2)for ADP in regulation of mitochondrial respiration and V(max)of respiration, the near absence of respiratory stimulation by exogenous cytochrome c, and preservation of functional coupling between mitochondrial creatine kinase and adenine nucleotide translocase. These data suggest that ischemic preconditioning preserves the structure-function of the intermembrane space, perhaps by opening the mitochondrial ATP-sensitive K(+)channel. The consequence is preservation of energy transfer processes from mitochondria to ATP-utilizing sites in the cytosol. Both of these factors may contribute to cardioprotection and better functional recovery of preconditioned hearts. Copyright 2001 Academic Press.
机译:M. N. Laclau,S。Boudina,J。B. Thambo,L。Tariosse,G。Gouverneur,S。Bonoron-Adele,V。A. Saks,K。D. Garlid和P. Dos Santos。缺血预处理的心脏保护作用保留了线粒体功能以及腺嘌呤核苷酸转位酶和肌酸激酶之间的功能耦合。 Journal of Molecular and Cellular Cardiology(2001)33,947-956。这项研究调查了缺血预处理对线粒体功能的影响,包括腺嘌呤核苷酸转位酶和线粒体肌酸激酶之间的功能偶联,这是缺血性改变的首批反应之一。研究了三组用Langendorff灌注的大鼠心脏:对照组,一组进行30分钟局部缺血再灌注15分钟的大鼠,以及一组在进行30分钟局部缺血再灌注15分钟之前的缺血预处理。缺血预处理可显着延迟缺血过程中挛缩的发作和幅度,减少酶的释放,并改善再灌注后心脏收缩功能的恢复。评估了透化皮肤纤维的线粒体功能。预处理的保护作用与线粒体功能的保持相关,如维持ADP的高K(1/2)调节线粒体呼吸和呼吸V(max),几乎没有外源细胞色素对呼吸的刺激所证明的那样。 c,并保持线粒体肌酸激酶和腺嘌呤核苷酸转位酶之间的功能偶联。这些数据表明缺血预处理可以保留膜间空间的结构功能,也许可以通过打开线粒体ATP敏感的K(+)通道。结果是保留了从线粒体到细胞质中ATP利用位点的能量转移过程。这两个因素都可能有助于心脏保护和预处理心脏更好的功能恢复。版权所有2001学术出版社。

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