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转录因子在充血性心力衰竭致心律失常基质形成中的作用。

The role of transcription factors in the formation of an arrhythmogenic substrate in congestive human heart failure.

机构信息

Institute of Pharmacology and Toxicology, University of Munster, Domagkstr. 12, 48149 Munster, Germany.

出版信息

Curr Med Chem. 2014;21(11):1281-98. doi: 10.2174/09298673113209990172.

Abstract

Human congestive heart failure is accompanied by structural and electrical alterations leading to the development of an arrhythmogenic substrate. This substrate is associated with the "sudden cardiac death" due to ventricular tachycardia or ventricular fibrillation. Multiple studies link distinct transcription factors to the transcriptional regulation of genes related to the formation of an arrhythmogenic substrate. In addition to cardiac hypertrophy the up- or downregulation of ion channels, calcium-handling proteins, and proteins forming gap junctions play a pivotal role in the progression of heart failure. This review summarizes the transcriptional regulation of selected genes implicated in the formation of an arrhythmogenic substrate. In this context we provide an overview of relevant transcription factors, activating stimuli and pathways, the evidence of binding to respective elements in the promoter of target genes and the associated mRNA regulation in animal models. Finally, possible therapeutic consequences are discussed.

摘要

人类充血性心力衰竭伴随着结构和电的改变,导致心律失常基质的发展。这种基质与由于室性心动过速或心室颤动导致的“心源性猝死”有关。多项研究将不同的转录因子与与心律失常基质形成相关的基因的转录调控联系起来。除了心肌肥厚外,离子通道、钙处理蛋白和形成间隙连接的蛋白的上调或下调在心力衰竭的进展中起着关键作用。这篇综述总结了参与心律失常基质形成的选定基因的转录调控。在这方面,我们提供了相关转录因子、激活刺激和途径的概述,以及在靶基因启动子中相应元件上结合的证据,以及在动物模型中的相关 mRNA 调节。最后,讨论了可能的治疗后果。

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