Comprehensive review of mechanisms of pathogenesis involved in Alzheimer's disease and potential therapeutic strategies

被引:251
|
作者
Sharma, Piyoosh [1 ]
Srivastava, Pavan [1 ]
Seth, Ankit [1 ]
Tripathi, Prabhash Nath [1 ]
Banerjee, Anupam G. [1 ]
Shrivastava, Sushant K. [1 ]
机构
[1] Banaras Hindu Univ, Indian Inst Technol, Dept Pharmaceut Engn & Technol, Pharmaceut Chem Res Lab, Varanasi, Uttar Pradesh, India
关键词
AMYLOID PRECURSOR PROTEIN; ACID AMIDE HYDROLASE; STRUCTURE-BASED DESIGN; MONOAMINE-OXIDASE-B; GLYCOGEN-SYNTHASE KINASE-3; TRANSGENIC MOUSE MODEL; ELEMENT-BINDING PROTEIN; MULTITARGET-DIRECTED LIGANDS; OXIDATIVE STRESS HYPOTHESIS; GAMMA-SECRETASE INHIBITOR;
D O I
10.1016/j.pneurobio.2018.12.006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
AD is a progressive neurodegenerative disorder and a leading cause of dementia in an aging population worldwide. The enormous challenge which AD possesses to global healthcare makes it as urgent as ever for the researchers to develop innovative treatment strategies to fight this disease. An in-depth analysis of the extensive available data associated with the AD is needed for a more comprehensive understanding of underlying molecular mechanisms and pathophysiological pathways associated with the onset and progression of the AD. The currently understood pathological and biochemical manifestations include cholinergic, AD, tau, excitotoxicity, oxidative stress, ApoE, CREB signaling pathways, insulin resistance, etc. However, these hypotheses have been criticized with several conflicting reports for their involvement in the disease progression. Several issues need to be addressed such as benefits to cost ratio with cholinesterase therapy, the dilemma of AChE selectivity over BChE, BBB permeability of peptidic BACE-1 inhibitors, hurdles related to the implementation of vaccination and immunization therapy, and clinical failure of candidates related to newly available targets. The present review provides an insight to the different molecular mechanisms Involved in the development and progression of the AD and potential therapeutic strategies, enlightening perceptions into structural information of conventional and novel targets along with the successful applications of computational approaches for the design of target-specific inhibitors.
引用
收藏
页码:53 / 89
页数:37
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