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Current Topics in Medicinal Chemistry

Editor-in-Chief

ISSN (Print): 1568-0266
ISSN (Online): 1873-4294

Review Article

The Unveiling of Therapeutic Targets for Alzheimer’s Disease: An Integrative Review

Author(s): Pratiksha Madar*, Pooja Nagalapur, Somdatta Chaudhari, Devesh Sharma, Akshada Koparde, Rahul Buchade, Sandip Kshirsagar, Pravin Uttekar, Shailaja Jadhav and Praveen Chaudhari

Volume 24, Issue 10, 2024

Published on: 28 February, 2024

Page: [850 - 868] Pages: 19

DOI: 10.2174/0115680266282492240220101049

Price: $65

Abstract

Alzheimer's disease (AD) is characterized by a complex pathological landscape, necessitating a comprehensive treatment approach. This concise review paper delves into the idea of addressing multiple mechanisms in AD, summarizing the latest research findings on pathogenesis, risk factors, diagnostics, and therapeutic strategies. The etiology of AD is multifaceted, involving genetic, environmental, and lifestyle factors. The primary feature is the accumulation of amyloid-- beta and tau proteins, leading to neuroinflammation, synaptic dysfunction, oxidative stress, and neuronal loss. Conventional single-target therapies have shown limited effectiveness, prompting a shift toward simultaneously addressing multiple disease-related processes. Recent advancements in AD research underscore the potential of multifaceted therapies. This review explores strategies targeting both tau aggregation and amyloid-beta, along with interventions to alleviate neuroinflammation, enhance synaptic function, and reduce oxidative stress. In conclusion, the review emphasizes the growing importance of addressing various pathways in AD treatment. A holistic approach that targets different aspects of the disease holds promise for developing effective treatments and improving the quality of life for Alzheimer's patients and their caregivers.

Keywords: Amyloid plaque, Tau protein, Acetyl cholinesterase (AChE), Butyl cholinesterase (BuChE), N-methyl Di-Aspartate enzyme (NMDA), JNK Signalling, Glycogen synthase kinase-3β (GSK-3β), Cyclin-dependent kinase (CDK-5), Monoamine oxidase (MAO).

Graphical Abstract
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