Insights into the Pathophysiology of Alzheimer's Disease and Potential Therapeutic Targets: A Current Perspective

被引:17
作者
Kumaran, Kesevan Rajah [1 ]
Yunusa, Suleiman [2 ,4 ]
Perimal, Enoch [5 ,6 ]
Wahab, Habibah [3 ]
Mueller, Christian P. [2 ,7 ]
Hassan, Zurina [2 ,7 ]
机构
[1] Natl Inst Biotechnol Malaysia, Malaysian Inst Pharmaceut & Nutraceut, Gelugor, Pulau Pinang, Malaysia
[2] Univ Sains Malaysia, Ctr Drug Res, Minden 11800, Penang, Malaysia
[3] Univ Sains Malaysia, Sch Pharmaceut Sci, George Town, Malaysia
[4] Bauchi State Univ Gadau, Dept Pharmacol, Gadau, Bauchi State, Nigeria
[5] Curtin Univ, Curtin Med Sch, Bentley, WA, Australia
[6] Univ Putra Malaysia, Fac Med & Hlth Sci, Dept Biomed Sci, Serdang, Malaysia
[7] Friedrich Alexander Univ Erlangen Nuremberg, Univ Clin, Dept Psychiat & Psychotherapy, Sect Addict Med, Erlangen, Germany
关键词
Alzheimer's disease; amyloid plaques; cholinergic; neurodegeneration; neuroinflammation; pharmacological agent; tau tangles; AMYLOID-BETA-PEPTIDE; PROTEIN PHOSPHATASE 2A; NERVE GROWTH-FACTOR; NICOTINIC ACETYLCHOLINE-RECEPTORS; PAIRED HELICAL FILAMENT; KINASE; DELTA; OXIDATIVE STRESS; APOLIPOPROTEIN-E; TAU-PHOSPHORYLATION; UP-REGULATION;
D O I
10.3233/JAD-220666
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The aging population increases steadily because of a healthy lifestyle and medical advancements in healthcare. However, Alzheimer's disease (AD) is becoming more common and problematic among older adults. AD-related cases show an increasing trend annually, and the younger age population may also be at risk of developing this disorder. AD constitutes a primary form of dementia, an irreversible and progressive brain disorder that steadily damages cognitive functions and the ability to perform daily tasks. Later in life, AD leads to death as a result of the degeneration of specific brain areas. Currently, the cause of AD is poorly understood, and there is no safe and effective therapeutic agent to cure or slow down its progression. The condition is entirely preventable, and no study has yet demonstrated encouraging findings in terms of treatment. Identifying this disease's pathophysiology can help researchers develop safe and efficient therapeutic strategies to treat this ailment. This review outlines and discusses the pathophysiology that resulted in the development of AD including amyloid-beta plaques, tau neurofibrillary tangles, neuroinflammation, oxidative stress, cholinergic dysfunction, glutamate excitotoxicity, and changes in neurotrophins level may sound better based on the literature search from Scopus, PubMed, ScienceDirect, and Google Scholar. Potential therapeutic strategies are discussed to provide more insights into AD mechanisms by developing some possible pharmacological agents for its treatment.
引用
收藏
页码:507 / 530
页数:24
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