阿尔茨海默病治疗方法的最新进展:当前和未来的展望。

IF 3.597 Q2 Pharmacology, Toxicology and Pharmaceutics MedChemComm Pub Date : 2024-12-06 DOI:10.1039/D4MD00630E
Amit Sharma, Santosh Rudrawar, Sandip B. Bharate and Hemant R. Jadhav
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引用次数: 0

摘要

阿尔茨海默病(AD)是一种复杂的、无法治愈的神经系统疾病,其特征是认知能力下降、胆碱能神经元减少和神经元丧失。其确切的病理仍不确定,但多种治疗假设已经出现。目前的治疗方法,无论是单一的还是联合的,都只能缓解症状,并且由于其多方面的病理,很难控制AD。发育药物针对的是所设想的假说中涉及的关键疾病因素,包括淀粉样蛋白聚集、过度磷酸化的tau蛋白和胆碱能、肾上腺素能等受体。目前的研究重点是多靶点定向配体(mtdl),它同时抑制多种因素,有助于减缓疾病的进展。本综述试图整理与阿尔茨海默病病原学假说相关的最新信息。它系统地组织了各种阿尔茨海默病治疗方案的进展,特别强调临床候选药物。此外,它有望帮助药物化学家根据现有信息设计新的AD治疗方法,这可能对AD患者有帮助。
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Recent advancements in the therapeutic approaches for Alzheimer's disease treatment: current and future perspective†

Alzheimer's disease (AD) is a complex, incurable neurological condition characterized by cognitive decline, cholinergic neuron reduction, and neuronal loss. Its exact pathology remains uncertain, but multiple treatment hypotheses have emerged. The current treatments, single or combined, alleviate only symptoms and struggle to manage AD due to its multifaceted pathology. The developmental drugs target pivotal disease factors involved in the envisaged hypotheses and include targets such as amyloid aggregation, hyperphosphorylated tau proteins, and receptors like cholinergic, adrenergic, etc. Present-day research focuses on multi-target directed ligands (MTDLs), which inhibit multiple factors simultaneously, helping slow the disease's progression. This review attempts to collate the recent information related to proposed hypotheses for AD etiology. It systematically organizes the advances in various therapeutic options for AD, with a particular emphasis on clinical candidates. Also, it is expected to help medicinal chemists design novel AD treatments based on available information, which could be helpful to AD patients.

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来源期刊
MedChemComm
MedChemComm BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
4.70
自引率
0.00%
发文量
0
审稿时长
2.2 months
期刊介绍: Research and review articles in medicinal chemistry and related drug discovery science; the official journal of the European Federation for Medicinal Chemistry. In 2020, MedChemComm will change its name to RSC Medicinal Chemistry. Issue 12, 2019 will be the last issue as MedChemComm.
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Back cover Back cover Correction: Chiral hydroxymethyl-1H,3H-pyrrolo[1,2-c]thiazoles: the search for selective p53-activating agents for colorectal cancer therapy Back cover Exploration of the cytotoxic and microtubule disruption potential of novel imidazo[1,5-a]pyridine-based chalcones†
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