Alzheimer's therapeutics - Neurotrophin small molecule mimetics

被引:28
作者
Massa, SM
Xie, YM
Longo, FM [1 ]
机构
[1] Univ Calif San Francisco, Vet Adm Med Ctr, Dept Neurol, San Francisco, CA USA
[2] Sun Yat Sen Univ Med Sci, Dept Neurol, Guangzhou, Peoples R China
[3] Univ N Carolina, Dept Neurol, Chapel Hill, NC USA
关键词
neurotrophins; mimetics; Alzheimer's disease; neurodegenerative disease;
D O I
10.1007/s12031-002-0019-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A substantial portion of neuronal populations undergoing degeneration in Alzheimer's and other neurodegenerative disorders express neurotrophin receptors. Neurotrophin small molecule mimetics constitute candidate compounds that might be useful in preventing or delaying loss of neuronal function, neural networks or neuronal death in neurodegenerative states. We are testing the hypothesis that pharmacophores based on a combination of the crystal structures of neurotrophins and structure-activity relationships of active neurotrophin peptidomimetics can be used to screen small molecule libraries to identify non-peptide small molecules with neurotrophin agonist or antagonist activity. In preliminary screens using pharmacophores based on two nerve growth factor (NGF) loop domains, a number of small molecules have been identified that display neurotrophic activity using in vitro bioassays. Current studies are focused on determining whether these small molecules function via neurotrophin receptors and whether they activate neurotrophin signaling cascades. Assessment of structure-activity relationships between active and inactive small molecules will allow modification of pharmacophores and provide a basis for the iterative process if identifying compounds with increased potency and efficacy. A collection of such compounds will provide a basis for synthesis of compounds with targeted pharmacological properties.
引用
收藏
页码:107 / 111
页数:5
相关论文
共 15 条
[1]   Alzheimer's disease - Etiologies, pathophysiology, cognitive reserve, and treatment opportunities [J].
Cummings, JL ;
Vinters, HV ;
Cole, GM ;
Khachaturian, ZS .
NEUROLOGY, 1998, 51 (01) :S2-S17
[2]   Enlarged cholinergic forebrain neurons and improved spatial learning in p75 knockout mice [J].
Greferath, U ;
Bennie, A ;
Kourakis, A ;
Bartlett, PF ;
Murphy, M ;
Barrett, GL .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2000, 12 (03) :885-893
[3]  
Hughes RA, 1999, DRUG DEVELOP RES, V46, P268, DOI 10.1002/(SICI)1098-2299(199903/04)46:3/4<268::AID-DDR12>3.0.CO
[4]  
2-G
[5]   Pharmacophore modeling and three-dimensional database searching for drug design using catalyst [J].
Kurogi, Y ;
Güner, OF .
CURRENT MEDICINAL CHEMISTRY, 2001, 8 (09) :1035-1055
[6]   THE INVITRO BIOLOGICAL EFFECT OF NERVE GROWTH-FACTOR IS INHIBITED BY SYNTHETIC PEPTIDES [J].
LONGO, FM ;
VU, TKH ;
MOBLEY, WC .
CELL REGULATION, 1990, 1 (02) :189-195
[7]  
Longo FM, 1997, J NEUROSCI RES, V48, P1, DOI 10.1002/(SICI)1097-4547(19970401)48:1<1::AID-JNR1>3.0.CO
[8]  
2-K
[9]  
Maliartchouk S, 2000, MOL PHARMACOL, V57, P385
[10]   Genuine monovalent ligands of TrkA nerve growth factor receptors reveal a novel pharmacological mechanism of action [J].
Maliartchouk, S ;
Debeir, T ;
Beglova, N ;
Cuello, AC ;
Gehring, K ;
Saragovi, HU .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (14) :9946-9956