Small-molecule modulation of neurotrophin receptors: a strategy for the treatment of neurological disease

被引:236
作者
Longo, Frank M. [1 ]
Massa, Stephen M. [2 ]
机构
[1] Stanford Univ, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA
[2] Univ Calif San Francisco, San Francisco Vet Affairs Med Ctr, Dept Neurol, San Francisco, CA 94121 USA
关键词
NERVE GROWTH-FACTOR; TRKB AGONIST 7,8-DIHYDROXYFLAVONE; MILD COGNITIVE IMPAIRMENT; BETA-TURN PEPTIDOMIMETICS; HIGH-AFFINITY; MOUSE MODEL; RAT MODEL; KINASE-B; ERYTHROPOIETIN RECEPTOR; THERAPEUTIC-EFFICACY;
D O I
10.1038/nrd4024
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Neurotrophins and their receptors modulate multiple signalling pathways to regulate neuronal survival and to maintain axonal and dendritic networks and synaptic plasticity. Neurotrophins have potential for the treatment of neurological diseases. However, their therapeutic application has been limited owing to their poor plasma stability, restricted nervous system penetration and, importantly, the pleiotropic actions that derive from their concomitant binding to multiple receptors. One strategy to overcome these limitations is to target individual neurotrophin receptors-such as tropomyosin receptor kinase A (TRKA), TRKB, TRKC, the p75 neurotrophin receptor or sortilin-with small-molecule ligands. Such small molecules might also modulate various aspects of these signalling pathways in ways that are distinct from the programmes triggered by native neurotrophins. By departing from conventional neurotrophin signalling, these ligands might provide novel therapeutic options for a broad range of neurological indications.
引用
收藏
页码:507 / 525
页数:19
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