Asadi Kavuma, K Radha, Satarker Sairaj, Gurram Prasada Chowdari
KL College of Pharmacy, Koneru Lakshmaiah Education Foundation, Green Fields, Vaddeswaram, Andhra Pradesh, 522302, India.
Goa University, Taleigao Plateau, Goa, 403206, India.
Mol Neurobiol. 2025 Aug 8. doi: 10.1007/s12035-025-05264-y.
Alzheimer's disease (AD), which is known for causing cognitive decline and significant synaptic dysfunction, continues to pose a significant barrier to good health among the aging population worldwide. While there remain major knowledge gaps in the exact molecular framework of this complex and devastating disease, emerging evidence strongly implicates epigenetic dysregulation as having a major influence on the complexity of the various pathological processes, driving this debilitating disease. This comprehensive review meticulously delves into the critical and multifaceted role of histone deacetylase 2 (HDAC2) as a key player in actively driving the various neurotoxic processes closely connected to AD's characteristic pathological hallmarks and features. We extensively point out the diverse interconnected pathways via which dysregulated HDAC2 activity contributes to the initiation and progression of multiple intricate mechanisms responsible for the observed synaptic dysfunction, the marked accumulation of amyloid-beta (Aβ) plaques and the formation of neurofibrillary tau tangles. Furthermore, we explore the intricate interplay between the aberrant HDAC2 activity and resulting neuroinflammation and oxidative stress within the brain's microenvironment. Additionally, the review summarises the current developments towards HDAC inhibition, carefully identifying the existing limitations in this rapidly evolving field of research, and highlighting promising avenues and potential future directions for developing effective and demonstrably safe therapies. Finally, the approaches that can facilitate the selective modulation of this crucial epigenetic enzyme to combat the devastating effects of AD are suggested and elucidated.
阿尔茨海默病(AD)以导致认知衰退和严重的突触功能障碍而闻名,它仍然是全球老年人口健康的重大障碍。尽管在这种复杂且具有破坏性的疾病的确切分子框架方面仍存在重大知识空白,但新出现的证据强烈表明,表观遗传失调对各种病理过程的复杂性有重大影响,推动了这种使人衰弱的疾病。这篇综述全面深入地探讨了组蛋白去乙酰化酶2(HDAC2)作为关键参与者在积极推动与AD特征性病理特征密切相关的各种神经毒性过程中的关键和多方面作用。我们广泛指出了失调的HDAC2活性通过多种相互关联的途径促成了导致观察到的突触功能障碍、淀粉样β(Aβ)斑块显著积累和神经纤维缠结形成的多种复杂机制的启动和进展。此外,我们探讨了异常的HDAC2活性与大脑微环境中由此产生的神经炎症和氧化应激之间的复杂相互作用。此外,该综述总结了HDAC抑制方面的当前进展,仔细确定了这一快速发展的研究领域中的现有局限性,并强调了开发有效且明显安全的疗法的有前景的途径和潜在未来方向。最后,提出并阐明了能够促进对这种关键表观遗传酶进行选择性调节以对抗AD破坏性影响的方法。