Rantamäki Tomi, Castrén Eero
University of Helsinki, Neuroscience Center, P.O. Box 56, Helsinki, Finland.
Expert Opin Ther Targets. 2008 Jun;12(6):705-15. doi: 10.1517/14728222.12.6.705.
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.
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.
越来越多的研究结果指出脑源性神经营养因子(BDNF)受体——酪氨酸激酶受体B(TrkB)在抗抑郁药物作用调节中的关键作用。因此,靶向TrkB受体可能是开发新型抗抑郁药物的合理策略。
目的/方法:在本综述中,我们将讨论使用现有或新型药物靶向TrkB受体的几种方法。我们将主要关注以下问题:i)神经营养因子的合成、释放和裂解;ii)增强神经营养因子的作用;iii)TrkB的合成;iv)开发TrkB激动剂;以及v)TrkB转活化。
可以使用不同的分子方法来筛选通过TrkB受体起作用的抗抑郁药物,但它们是否具有治疗性抗抑郁作用还有待观察。