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药物干预减缓阿尔茨海默病进展:迄今为止的故事。

Pharmacological Interventions to Attenuate Alzheimer's Disease Progression: The Story So Far.

机构信息

Department of Pharmacology & Toxicology, Faculty of Pharmacy, Cairo University, Cairo, Egypt.

出版信息

Curr Alzheimer Res. 2019;16(3):261-277. doi: 10.2174/1567205016666190301111120.

Abstract

Alzheimer's disease (AD) is a progressive neurodegenerative disease and the most common cause of dementia in the elderly. Up to date, the available pharmacological options for AD are limited to cholinesterase inhibitors and memantine that may only provide modest symptomatic management with no significance in slowing down the disease progression. Over the past three decades, the increased interest in and the understanding of AD major pathological hallmarks have provided an insight into the mechanisms mediating its pathogenesis, which in turn introduced a number of hypotheses and novel targets for the treatment of AD. Initially, targeting amyloid-beta and tau protein was considered the most promising therapeutic approach. However, further investigations have identified other major players, such as neuroinflammation, impaired insulin signalling and defective autophagy, that may contribute to the disease progression. While some promising drugs are currently being investigated in human studies, the majority of the previously developed medical agents have come to an end in clinical trials, as they have failed to illustrate any beneficial outcome. This review aims to discuss the different introduced approaches to alleviate AD progression; in addition, provides a comprehensive overview of the drugs in the development phase as well as their mode of action and an update of their status in clinical trials.

摘要

阿尔茨海默病(AD)是一种进行性神经退行性疾病,也是老年人中最常见的痴呆症病因。迄今为止,AD 的可用药物治疗选择仅限于胆碱酯酶抑制剂和美金刚,它们可能仅提供适度的症状管理,而对减缓疾病进展没有意义。在过去的三十年中,人们对 AD 的主要病理学特征越来越感兴趣并加深了理解,这使人们深入了解了介导其发病机制的机制,从而提出了一些治疗 AD 的假说和新靶点。最初,靶向淀粉样蛋白-β和tau 蛋白被认为是最有前途的治疗方法。然而,进一步的研究已经确定了其他主要参与者,如神经炎症、胰岛素信号受损和自噬缺陷,它们可能有助于疾病的进展。虽然一些有前途的药物目前正在人类研究中进行调查,但大多数以前开发的药物在临床试验中都已结束,因为它们未能显示出任何有益的结果。本综述旨在讨论减轻 AD 进展的不同方法;此外,还全面概述了处于开发阶段的药物及其作用方式,并更新了它们在临床试验中的地位。

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