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心脏起搏诱导犬心脏基因表达变化的时程分析。

Time course analysis of cardiac pacing-induced gene expression changes in the canine heart.

机构信息

Department of Pharmacology and Pharmacotherapy, Faculty of Medicine, University of Szeged, Dóm tér 12, 6720 Szeged, Hungary.

出版信息

Mol Cell Biochem. 2013 Jan;372(1-2):257-66. doi: 10.1007/s11010-012-1467-8. Epub 2012 Sep 27.

DOI:10.1007/s11010-012-1467-8
PMID:23014934
Abstract

Rapid right ventricular pacing in anesthetized dogs results in marked protection against ischemia and reperfusion-induced ventricular arrhythmias, 24 h later. We have previous evidence that this protection associates with altered expression of genes, encoding proteins involved in the delayed cardioprotection. However, the sequence of transcriptional changes occurring between the pacing stimulus and the test ischemia has not yet been elucidated. Thus, we designed studies in which the expression of 29 genes was examined by real-time PCR at various time intervals, i.e., immediately (0 h), 6, 12, and 24 h after short periods (4 times 5 min) of rapid (240 beats min(-1)) right ventricular pacing in the canine. Sham-operated dogs (the pacing electrode was introduced but the dogs were not paced) served as controls. Compared with these dogs, pacing induced an early up-regulation of genes which encode, for example, HSP90, MnSOD, ERK1, PKCε, Bcl2, and sGC; all these somehow relate to the early phase of the protection. These genes remained either up-regulated or, after a transient lower expression (around 6 h), were up-regulated again, suggesting their involvement in the delayed protection. There were also some genes which down-regulated soon after the pacing stimulus (e.g., Bax, Casp3, Casp9, MMP9, GSK3β), and showed also low expression 24 h later. Genes encoding eNOS and iNOS, as well as Cx43 were only up-regulated 12 h after pacing. We conclude that cardiac pacing induces time-dependent changes in gene expression, and the sequence of these changes is important in the development of the delayed protection.

摘要

在麻醉犬中快速右心室起搏可显著预防缺血再灌注引起的室性心律失常,24 小时后也是如此。我们之前有证据表明,这种保护与编码参与延迟性心脏保护的蛋白的基因表达改变有关。然而,起搏刺激与测试缺血之间发生的转录变化的顺序尚未阐明。因此,我们设计了研究,通过实时 PCR 在不同时间间隔(即起搏刺激后立即(0 小时)、6、12 和 24 小时)检查 29 个基因的表达,在犬中进行短暂(4 次 5 分钟)快速(240 次/分钟)右心室起搏。假手术组(起搏电极被引入但未起搏的狗)作为对照组。与这些狗相比,起搏诱导了编码 HSP90、MnSOD、ERK1、PKCε、Bcl2 和 sGC 等基因的早期上调;所有这些都与保护的早期阶段有关。这些基因要么保持上调,要么在短暂的低表达(约 6 小时)后再次上调,表明它们参与了延迟保护。也有一些基因在起搏刺激后很快下调(例如,Bax、Casp3、Casp9、MMP9、GSK3β),24 小时后表达也较低。编码 eNOS 和 iNOS 的基因以及 Cx43 仅在起搏后 12 小时上调。我们得出结论,心脏起搏诱导基因表达的时间依赖性变化,这些变化的顺序对于延迟性保护的发展很重要。

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本文引用的文献

1
The involvement of gap junctions in the delayed phase of the protection induced by cardiac pacing in dogs.缝隙连接在心脏起搏诱导的犬心肌保护延迟相中的作用。
Clin Sci (Lond). 2012 Jul;123(1):39-51. doi: 10.1042/CS20110501.
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Changes in gene expression following cardiac pacing-induced delayed cardioprotection in the canine heart.
Acta Biol Hung. 2010 Dec;61(4):434-48. doi: 10.1556/ABiol.61.2010.4.7.
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Mechanisms underlying acute protection from cardiac ischemia-reperfusion injury.急性心脏缺血再灌注损伤的保护机制。
Physiol Rev. 2008 Apr;88(2):581-609. doi: 10.1152/physrev.00024.2007.
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Mapping preconditioning's signaling pathways: an engineering approach.绘制预处理的信号通路:一种工程学方法。
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Cardiac genomic response following preconditioning stimulus.预处理刺激后的心脏基因组反应。
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Glycogen synthase kinase-3beta mediates convergence of protection signaling to inhibit the mitochondrial permeability transition pore.糖原合酶激酶-3β介导保护信号的汇聚以抑制线粒体通透性转换孔。
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