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组蛋白去乙酰化酶及其亚型特异性抑制剂在缺血性卒中中的作用

Histone Deacetylases and Their Isoform-Specific Inhibitors in Ischemic Stroke.

作者信息

Demyanenko Svetlana, Dzreyan Valentina, Sharifulina Svetlana

机构信息

Laboratory of Molecular Neurobiology, Academy of Biology and Biotechnology, Southern Federal University, pr. Stachki 194/1, Rostov-on-Don 344090, Russia.

出版信息

Biomedicines. 2021 Oct 11;9(10):1445. doi: 10.3390/biomedicines9101445.

Abstract

Cerebral ischemia is the second leading cause of death in the world and multimodal stroke therapy is needed. The ischemic stroke generally reduces the gene expression due to suppression of acetylation of histones H3 and H4. Histone deacetylases inhibitors have been shown to be effective in protecting the brain from ischemic damage. Histone deacetylases inhibitors induce neurogenesis and angiogenesis in damaged brain areas promoting functional recovery after cerebral ischemia. However, the role of different histone deacetylases isoforms in the survival and death of brain cells after stroke is still controversial. This review aims to analyze the data on the neuroprotective activity of nonspecific and selective histone deacetylase inhibitors in ischemic stroke.

摘要

脑缺血是全球第二大死因,因此需要多模式中风治疗。缺血性中风通常会因组蛋白H3和H4乙酰化受抑制而导致基因表达降低。已证明组蛋白脱乙酰酶抑制剂在保护大脑免受缺血性损伤方面有效。组蛋白脱乙酰酶抑制剂可诱导受损脑区的神经发生和血管生成,促进脑缺血后的功能恢复。然而,不同的组蛋白脱乙酰酶同工型在中风后脑细胞存活和死亡中的作用仍存在争议。本综述旨在分析非特异性和选择性组蛋白脱乙酰酶抑制剂在缺血性中风中神经保护活性的数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6741/8533589/0c8ddb09fc47/biomedicines-09-01445-g001.jpg

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