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Updated: Aug 22, 2026

Purification of H3 and H4 Histone Proteins and the Quantification of Acetylated Histone Marks in Cells and Brain Tissue
Published on: November 30, 2018
Histone deacetylase as a potential therapeutic target for memory dysfunction during aging and neurodegenerative
Padmanabh Singh1, Mahendra Kumar Thakur1
1Biochemistry and Molecular Biology Laboratory, Department of Zoology, Institute of Science, Centre of Advanced Study, Banaras Hindu University, Varanasi, India.
None:
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.
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