Mechanistic insights and emerging therapeutic stratagems for Alzheimer's disease

被引:10
|
作者
Rajendran, Kayalvizhi [1 ,2 ]
Krishnan, Uma Maheswari [1 ,2 ,3 ,4 ]
机构
[1] SASTRA Deemed Univ, Sch Chem & Biotechnol, Thanjavur 613401, India
[2] SASTRA Deemed Univ, Ctr Nanotechnol & Adv Biomat, Thanjavur 613401, India
[3] SASTRA Deemed Univ, Sch Arts Sci Humanities & Educ, Thanjavur 613401, Tamilnadu, India
[4] SASTRA Deemed Univ, Ctr Nanotechnol & Adv Biomat CeNTAB, Sch Arts Sci Humanities & Educ, Sch Chem & Biotechnol, Thanjavur 613401, Tamil Nadu, India
关键词
Alzheimer's disease; Cognitive loss; Polypharmacology; Nanotherapy; Phytotherapy; Immunotherapy; Optogenetics; SIMPLEX-VIRUS TYPE-1; TRANSCRANIAL MAGNETIC STIMULATION; MILD COGNITIVE IMPAIRMENT; MESENCHYMAL STEM-CELLS; AMYLOID-BETA; A-BETA; MEMORY IMPAIRMENT; OXIDATIVE STRESS; MITOCHONDRIAL DYSFUNCTION; NEURONAL DYSFUNCTION;
D O I
10.1016/j.arr.2024.102309
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Alzheimer's disease (AD), a multi-factorial neurodegenerative disorder has affected over 30 million individuals globally and these numbers are expected to increase in the coming decades. Current therapeutic interventions are largely ineffective as they focus on a single target. Development of an effective drug therapy requires a deep understanding of the various factors influencing the onset and progression of the disease. Aging and genetic factors exert a major influence on the development of AD. Other factors like post-viral infections, iron overload, gut dysbiosis, and vascular dysfunction also exacerbate the onset and progression of AD. Further, posttranslational modifications in tau, DRP1, CREB, and p65 proteins increase the disease severity through triggering mitochondrial dysfunction, synaptic loss, and differential interaction of amyloid beta with different receptors leading to impaired intracellular signalling. With advancements in neuroscience tools, new interrelations that aggravate AD are being discovered including pre-existing diseases and exposure to other pathogens. Simultaneously, new therapeutic strategies involving modulation of gene expression through targeted delivery or modulation with light, harnessing the immune response to promote clearance of amyloid deposits, introduction of stem cells and extracellular vesicles to replace the destroyed neurons, exploring new therapeutic molecules from plant, marine and biological sources delivered in the free state or through nanoparticles and use of non-pharmacological interventions like music, transcranial stimulation and yoga. Polypharmacology approaches involving combination of therapeutic agents are also under active investigation for superior therapeutic outcomes. This review elaborates on various disease-causing factors, their underlying mechanisms, the inter-play between different disease-causing players, and emerging therapeutic options including those under clinical trials, for treatment of AD. The challenges involved in AD therapy and the way forward have also been discussed.
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页数:29
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