基于病理网络的多靶点阿尔茨海默病治疗创新方法

IF 10.9 1区 医学 Q1 CHEMISTRY, MEDICINAL Medicinal Research Reviews Pub Date : 2024-04-28 DOI:10.1002/med.22045
Paloma Mayo, Jorge Pascual, Enrique Crisman, Cristina Domínguez, Manuela G. López, Rafael León
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摘要

阿尔茨海默病(AD)是最普遍的神经退行性疾病,也是对全球健康的一大威胁。由于全球人口老龄化,预计在未来 30 年内,阿尔茨海默病的发病率将呈指数级增长。目前,已获批准的药物仅能对症治疗,无法有效延缓或阻止疾病的无情发展。对注意力缺失症的深入研究表明,这种疾病是一种高度复杂的多因素疾病。在过去二十年里,新病理途径及其相互联系的揭示对针对老年痴呆症的药物化学研发产生了重大影响。发病过程中涉及的复杂病理事件网络促使了多靶点药物的开发。这些化学实体结合了针对两个或多个药物靶点的药理活性。这些多靶点配体可改变病理网络中的不同节点,从而延缓甚至阻止疾病的发展。在此,我们回顾了过去十年中针对多发性硬化症的多靶点药物开发策略。
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Innovative pathological network-based multitarget approaches for Alzheimer's disease treatment

Alzheimer's disease (AD) is the most prevalent neurodegenerative disease and is a major health threat globally. Its prevalence is forecasted to exponentially increase during the next 30 years due to the global aging population. Currently, approved drugs are merely symptomatic, being ineffective in delaying or blocking the relentless disease advance. Intensive AD research describes this disease as a highly complex multifactorial disease. Disclosure of novel pathological pathways and their interconnections has had a major impact on medicinal chemistry drug development for AD over the last two decades. The complex network of pathological events involved in the onset of the disease has prompted the development of multitarget drugs. These chemical entities combine pharmacological activities toward two or more drug targets of interest. These multitarget-directed ligands are proposed to modify different nodes in the pathological network aiming to delay or even stop disease progression. Here, we review the multitarget drug development strategy for AD during the last decade.

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来源期刊
CiteScore
29.30
自引率
0.00%
发文量
52
审稿时长
2 months
期刊介绍: Medicinal Research Reviews is dedicated to publishing timely and critical reviews, as well as opinion-based articles, covering a broad spectrum of topics related to medicinal research. These contributions are authored by individuals who have made significant advancements in the field. Encompassing a wide range of subjects, suitable topics include, but are not limited to, the underlying pathophysiology of crucial diseases and disease vectors, therapeutic approaches for diverse medical conditions, properties of molecular targets for therapeutic agents, innovative methodologies facilitating therapy discovery, genomics and proteomics, structure-activity correlations of drug series, development of new imaging and diagnostic tools, drug metabolism, drug delivery, and comprehensive examinations of the chemical, pharmacological, pharmacokinetic, pharmacodynamic, and clinical characteristics of significant drugs.
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