脑缺血预处理中基因表达的调控。

Conditioning medicine Pub Date : 2017-12-01 Epub Date: 2017-12-15
Tuo Yang, Qianqian Li, Feng Zhang
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引用次数: 0

摘要

中风是第三大死亡原因和长期残疾的主要原因,有效的治疗方法很少,在寻找新的治疗方法方面进展有限。亚致死性缺血损伤诱导对随后严重缺血的保护,称为缺血预处理(IPC),这一现象代表了一种针对缺血性脑损伤的内源性保护方法,并可能指导未来治疗策略的突破。人们普遍认为,ipc介导的长期神经保护需要新的蛋白质合成;然而,它们的相关调控机制却知之甚少。在本文中,我们总结了基于基因组学的基因表达和蛋白质合成改变的研究,特别是IPC调节的潜在途径的分类。我们还回顾了表观遗传学在ipc介导的神经保护中的作用,表观遗传学是一种不改变DNA序列的遗传调控机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulation of gene expression in ischemic preconditioning in the brain.

Stroke is the third leading cause of death and the leading cause of long-term disability, with very few effective treatments and limited progress in the effort to search for novel therapeutic approaches. The phenomenon that a sublethal ischemic insult induces protection against a subsequent severe ischemia, termed ischemic preconditioning (IPC), represents an endogenous protective approach against ischemic brain injury, and may direct a breakthrough to future therapeutic strategies. It is broadly accepted that new protein synthesis is required for IPC-mediated long-term neuroprotection; however, their relative regulatory mechanisms are poorly understood. In the present review, we summarize genomic-based studies on alterations in gene expression and protein synthesis, particularly categorizing potential pathways regulated by IPC. We also review the role of epigenetics, an inheritable genetic regulatory mechanism without changes in DNA sequence, in IPC-mediated neuroprotection.

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