胆碱酯酶抑制剂的神经保护作用:阿尔茨海默病治疗方法的现状与未来展望》。

Natália Chermont Dos Santos Moreira, Jéssica Ellen Barbosa de Freitas Lima, Marcelo Fiori Marchiori, Ivone Carvalho, Elza Tiemi Sakamoto-Hojo
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引用次数: 0

摘要

阿尔茨海默病(AD)是一种缓慢进展的神经退行性疾病,概念上是一个连续的过程,从轻度认知障碍(MCI)到轻度、中度和重度阿尔茨海默病痴呆的临床阶段。AD 被认为是一种复杂的多因素疾病。目前,使用胆碱酯酶抑制剂(ChEI),如他克林、多奈哌齐、利伐斯敏和加兰他敏,是治疗 AD 患者的主要方法。有趣的是,有证据表明胆碱酯酶抑制剂还能促进神经保护作用,给注意力缺失症患者带来一些益处。人们对 ChEI 在注意力缺失症中的作用机制进行了研究。ChEI 可以调节 PI3K/AKT 通路,而 PI3K/AKT 通路是一个重要的信号级联,能够通过激活细胞存活通路来促进神经保护作用,从而对神经元的功能产生重大影响。然而,神经保护领域仍然面临着巨大的挑战,但在揭示 PI3K/AKT 通路细节的背景下,开发作用于多个蛋白靶点的更高效药物的新局面已经出现。因此,本综述将讨论 ChEI 促进神经保护作用的机制以及开发治疗 AD 候选新药的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuroprotective Effects of Cholinesterase Inhibitors: Current Scenario in Therapies for Alzheimer's Disease and Future Perspectives.

Alzheimer's disease (AD) is a slowly progressive neurodegenerative disease conceptualized as a continuous process, ranging from mild cognitive impairment (MCI), to the mild, moderate, and severe clinical stages of AD dementia. AD is considered a complex multifactorial disease. Currently, the use of cholinesterase inhibitors (ChEI), such as tacrine, donepezil, rivastigmine, and galantamine, has been the main treatment for AD patients. Interestingly, there is evidence that ChEI also promotes neuroprotective effects, bringing some benefits to AD patients. The mechanisms by which the ChEI act have been investigated in AD. ChEI can modulate the PI3K/AKT pathway, which is an important signaling cascade that is capable of causing a significant functional impact on neurons by activating cell survival pathways to promote neuroprotective effects. However, there is still a huge challenge in the field of neuroprotection, but in the context of unravelling the details of the PI3K/AKT pathway, a new scenario has emerged for the development of more efficient drugs that act on multiple protein targets. Thus, the mechanisms by which ChEI can promote neuroprotective effects and prospects for the development of new drug candidates for the treatment of AD are discussed in this review.

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