Histone deacetylase as a potential therapeutic target for memory dysfunction during aging and neurodegenerative disorders.

4区 生物学 Q3 Biochemistry, Genetics and Molecular Biology
Methods in enzymology Pub Date : 2026-01-01 Epub Date: 2026-06-08 DOI:10.1016/bs.mie.2026.05.037
Padmanabh Singh, Mahendra Kumar Thakur
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引用次数: 0

Abstract

Brain aging is a natural biological process characterized by gradual structural, molecular, and functional changes in the brain over time. Aging is the major risk factor for neurodegenerative diseases characterized by progressive neuronal loss, cognitive decline, and impaired motor function. In recent years, growing evidence has highlighted the importance of epigenetic regulation in the development and progression of these disorders. Among these epigenetic regulators, histone deacetylases (HDACs) have emerged as critical modulators of gene expression and neuronal function. Dysregulation of HDAC activity has been increasingly implicated in the pathogenesis of several neurodegenerative diseases. Abnormal HDAC expression or activity can alter transcription of genes involved in neuronal survival and synaptic integrity, which leads to neuronal dysfunction and degeneration. Pharmacological inhibition of HDAC activity has been shown to restore histone acetylation levels, enhance the expression of neuroprotective genes, and improve synaptic plasticity in various experimental models.

组蛋白去乙酰化酶作为衰老和神经退行性疾病记忆功能障碍的潜在治疗靶点。
脑老化是一个自然的生物学过程,其特征是随着时间的推移,大脑的结构、分子和功能逐渐发生变化。衰老是神经退行性疾病的主要危险因素,其特征是进行性神经元丧失、认知能力下降和运动功能受损。近年来,越来越多的证据强调了表观遗传调控在这些疾病的发展和进展中的重要性。在这些表观遗传调节剂中,组蛋白去乙酰化酶(hdac)已成为基因表达和神经元功能的关键调节剂。HDAC活性的失调已越来越多地与几种神经退行性疾病的发病机制有关。异常的HDAC表达或活性可以改变参与神经元存活和突触完整性的基因的转录,从而导致神经元功能障碍和变性。在各种实验模型中,药理抑制HDAC活性已被证明可以恢复组蛋白乙酰化水平,增强神经保护基因的表达,并改善突触可塑性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Methods in enzymology
Methods in enzymology 生物-生化研究方法
CiteScore
2.90
自引率
0.00%
发文量
308
审稿时长
3-6 weeks
期刊介绍: The critically acclaimed laboratory standard for almost 50 years, Methods in Enzymology is one of the most highly respected publications in the field of biochemistry. Each volume is eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. Now with over 500 volumes the series contains much material still relevant today and is truly an essential publication for researchers in all fields of life sciences, including microbiology, biochemistry, cancer research and genetics-just to name a few. Five of the 2013 Nobel Laureates have edited or contributed to volumes of MIE.
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