A Novel Neurotrophic Drug for Cognitive Enhancement and Alzheimer's Disease

被引:102
作者
Chen, Qi [1 ]
Prior, Marguerite [1 ]
Dargusch, Richard [1 ]
Roberts, Amanda [4 ]
Riek, Roland [2 ,5 ]
Eichmann, Cedric [5 ]
Chiruta, Chandramouli [1 ]
Akaishi, Tatsuhiro [3 ]
Abe, Kazuho [3 ]
Maher, Pamela [1 ]
Schubert, David [1 ]
机构
[1] Salk Inst Biol Studies, Cellular Neurobiol Lab, La Jolla, CA 92037 USA
[2] Salk Inst Biol Studies, Struct Biol Lab, La Jolla, CA 92037 USA
[3] Musashino Univ, Pharmacol Lab, Pharmaceut Sci Res Inst, Nishitokyo, Tokyo, Japan
[4] Scripps Res Inst, La Jolla, CA 92037 USA
[5] ETH, Phys Chem Lab, Zurich, Switzerland
来源
PLOS ONE | 2011年 / 6卷 / 12期
基金
美国国家卫生研究院;
关键词
LONG-TERM POTENTIATION; AMYLOID-BETA-PROTEIN; MOUSE MODEL; HIPPOCAMPAL-LESIONS; LEARNING-DEFICITS; TRANSGENIC MOUSE; MEMORY DEFICITS; STRESS-RESPONSE; CNS DISORDERS; MICE LACKING;
D O I
10.1371/journal.pone.0027865
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Currently, the major drug discovery paradigm for neurodegenerative diseases is based upon high affinity ligands for single disease-specific targets. For Alzheimer's disease (AD), the focus is the amyloid beta peptide (A beta) that mediates familial Alzheimer's disease pathology. However, given that age is the greatest risk factor for AD, we explored an alternative drug discovery scheme that is based upon efficacy in multiple cell culture models of age-associated pathologies rather than exclusively amyloid metabolism. Using this approach, we identified an exceptionally potent, orally active, neurotrophic molecule that facilitates memory in normal rodents, and prevents the loss of synaptic proteins and cognitive decline in a transgenic AD mouse model.
引用
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页数:17
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