共 293 条
Current therapeutic targets for the treatment of Alzheimer's disease
被引:62
作者:

Grill, Joshua D.
论文数: 0 引用数: 0
h-index: 0
机构:
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 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

Cummings, Jeffrey L.
论文数: 0 引用数: 0
h-index: 0
机构:
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 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
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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