Targeting TrkB neurotrophin receptor to treat depression

被引:0
|
作者
Rantamaki, Tomi [1 ]
Castren, Eero [1 ]
机构
[1] Univ Helsinki, Ctr Neurosci, Helsinki, Finland
关键词
BDNF cleavage; chromatin remodeling; pro-BDNF; p75(NTR) receptor; transactivation; TrkB agonist; truncated TrkB receptor;
D O I
10.1517/14728220802121472
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: An increasing number of findings point out the key role of the BDNF (brain-derived neurotrophic factor) receptor, tyrosine kinase receptor B (TrkB), in the regulation of antidepressant drug actions. Therefore, targeting TrkB receptors might be a rational strategy to develop novel antidepressant drugs. Objective/methods: In this review we will discuss several approaches to targeting the TrkB receptor using existing or novel drugs. We will mainly concentrate on the following issues: i) synthesis, release and cleavage of neurotrophins; ii) augmentation of the actions of neurotrophins; iii) synthesis of TrkB; iv) developing agonists for TrkB; and v) TrkB transactivation. Conclusions: Different molecular approaches can be used to screen antidepressant drugs acting through TrkB receptors but it remains to be seen whether they demonstrate therapeutic antidepressant effects.
引用
收藏
页码:705 / 715
页数:11
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