A comprehensive review on therapeutics and diagnostic agents targeting acetyl and butyryl cholinesterases for AD.

International review of neurobiology Pub Date : 2026-01-01 Epub Date: 2026-07-08 DOI:10.1016/bs.irn.2026.05.017
Vishal Chaurasia, Sanjib Das Modak, Gireesh Kumar Singh, Gyan Modi
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Abstract

Alzheimer's disease (AD) is a progressive, irreversible, and multifaceted neurodegenerative disorder characterized by cognitive decline, memory loss, and behavioral impairment, posing a major global health challenge. Its multifactorial pathology includes cholinergic dysfunction, amyloid-β deposition, tau hyperphosphorylation, oxidative stress, and neuroinflammation. Among these, impairment of the cholinergic system, characterized by reduced acetylcholine levels, plays a crucial role in cognitive deficits. The enzymes acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), which hydrolyze acetylcholine, are closely involved in disease progression and serve as important therapeutic and diagnostic targets in AD. This book chapter provides a comprehensive overview of therapeutic and diagnostic agents targeting AChE and BChE in AD, and discusses small-molecule inhibitors, multifunctional ligands, and emerging strategies to modulate cholinesterase activity and restore cholinergic neurotransmission, alleviating disease symptoms. In addition, the chapter highlights advances in diagnostic approaches using fluorescent probes, particularly near-infrared (NIR) probes, for selective detection and imaging of AChE and BChE, including their molecular design, photophysical properties, enzyme selectivity, and mechanisms of action, all of which are critically examined. Targeting AChE and BChE offers a dual advantage in AD by enabling both symptomatic treatment and early-stage diagnosis. This chapter aims to present a clear and comprehensive overview of recent advances in therapeutic and diagnostic approaches, offering meaningful insights for researchers in developing effective strategies for the treatment and monitoring of AD.

针对乙酰胆碱酯酶和丁基胆碱酯酶的AD治疗和诊断药物的综合综述。
阿尔茨海默病(AD)是一种进行性的、不可逆的、多方面的神经退行性疾病,以认知能力下降、记忆丧失和行为障碍为特征,对全球健康构成了重大挑战。其多因素病理包括胆碱能功能障碍、淀粉样蛋白-β沉积、tau过度磷酸化、氧化应激和神经炎症。其中,以乙酰胆碱水平降低为特征的胆碱能系统损伤在认知缺陷中起着至关重要的作用。乙酰胆碱酯酶(AChE)和丁基胆碱酯酶(BChE)水解乙酰胆碱,与疾病进展密切相关,是AD重要的治疗和诊断靶点。本章提供了针对乙酰胆碱酯酶和BChE的AD治疗和诊断药物的全面概述,并讨论了小分子抑制剂,多功能配体和新兴策略,以调节胆碱酯酶活性和恢复胆碱能神经传递,减轻疾病症状。此外,本章强调了使用荧光探针,特别是近红外(NIR)探针,选择性检测和成像AChE和BChE的诊断方法的进展,包括它们的分子设计,光物理性质,酶选择性和作用机制,所有这些都进行了严格的检查。靶向AChE和BChE通过对症治疗和早期诊断为AD提供了双重优势。本章旨在清晰而全面地概述治疗和诊断方法的最新进展,为研究人员制定有效的治疗和监测AD的策略提供有意义的见解。
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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