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首页> 外文期刊>Regulatory peptides. >Evidence for calcitonin gene-related peptide-mediated ischemic preconditioning in the rat heart.
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Evidence for calcitonin gene-related peptide-mediated ischemic preconditioning in the rat heart.

机译:降钙素基因相关肽介导的大鼠心脏缺血预处理的证据。

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摘要

Previous studies have suggested that calcitonin gene-related peptide (CGRP) may play an important role in the mediation of ischemic preconditioning. In the present study, we examined the release of CGRP during ischemic preconditioning and the effect of preconditioning frequency on this effect in the isolated rat heart. Thirty minutes of global ischemia and 40 min of reperfusion caused a significant cardiac dysfunction and an increase in the release of creatine kinase (CK) during reperfusion. Preconditioning with one, two or three cycles of 5-min ischemia and 5-min reperfusion caused a marked improvement of cardiac function and a decrease in the release of CK, and there was no difference in the degree of improvement among groups. The protective effects of ischemic preconditioning were abolished by the CGRP receptor antagonist CGRP(8-37). A single preconditioning cycle induced a significant increase in the release of CGRP in the coronary effluent. In the hearts treated with two or three preconditioning cycles, the level of CGRP was highest in the first cycle, and was gradually decreased with increasing number of cycles of preconditioning. These results suggest that the protective effects of ischemic preconditioning are mediated by endogenous CGRP in the isolated rat heart.
机译:先前的研究表明降钙素基因相关肽(CGRP)可能在缺血预处理的介导中起重要作用。在本研究中,我们检查了缺血预处理中CGRP的释放以及预处理频率对离体大鼠心脏的影响。 30分钟的整体缺血和40分钟的再灌注会导致严重的心脏功能障碍,并在再灌注期间增加肌酸激酶(CK)的释放。一,两个或三个周期的5分钟局部缺血和5分钟再灌注的预处理可显着改善心功能并降低CK的释放,并且各组之间的改善程度没有差异。 CGRP受体拮抗剂CGRP(8-37)取消了缺血预处理的保护作用。一个单独的预处理循环会导致冠状流出物中CGRP的释放显着增加。在经过两个或三个预处理周期的心脏中,CGRP的水平在第一个周期最高,并随着预处理周期的增加而逐渐降低。这些结果表明,缺血预处理的保护作用是由离体大鼠心脏中的内源性CGRP介导的。

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