Current therapeutic targets for the treatment of Alzheimer's disease

被引:62
作者
Grill, Joshua D. [1 ]
Cummings, Jeffrey L. [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Deane F Johnson Ctr Neurotherapeut, Mary S Easton Ctr Alzheimers Dis Res,Dept Neurol, Los Angeles, CA 90095 USA
关键词
amyloid-beta; beta-secretase; gamma-secretase; Alzheimer's disease; dementia; immunotherapy; tau; therapeutic; treatment; AMYLOID-BETA-PEPTIDE; CYCLIN-DEPENDENT KINASE-5; GAMMA-SECRETASE INHIBITOR; PLACEBO-CONTROLLED TRIAL; HISTAMINE H-3 RECEPTOR; LONG-TERM POTENTIATION; TRANSGENIC MOUSE MODEL; GLYCATION END-PRODUCTS; BLOOD-BRAIN-BARRIER; FACTOR GENE-THERAPY;
D O I
10.1586/ERN.10.29
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Alzheimer's disease is a progressive neurodegenerative disease for which no cure exists. There is a substantial need for new therapies that offer improved symptomatic benefit and disease-slowing capabilities. In recent decades there has been substantial progress in understanding the molecular and cellular changes associated with Alzheimer's disease pathology. This has resulted in identification of a large number of new drug targets. These targets include, but are not limited to, therapies that aim to prevent production of or remove the amyloid-beta protein that accumulates in neuritic plaques; to prevent the hyperphosphorylation and aggregation into paired helical filaments of the microtubule-associated protein tau; and to keep neurons alive and functioning normally in the face of these pathologic challenges. We provide a review of these targets for drug development.
引用
收藏
页码:711 / 728
页数:18
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