Is neurotrophin-3 (NT-3): a potential therapeutic target for depression and anxiety?

被引:20
|
作者
de Miranda, A. S. [1 ,2 ]
de Barros, J. L. V. M. [1 ]
Teixeira, Antonio Lucio [3 ]
机构
[1] Univ Fed Minas Gerais, Fac Med, Lab Interdisciplinar Invest Med, Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Morfol, Lab Neurobiol, Belo Horizonte, MG, Brazil
[3] Univ Texas Hlth Sci Ctr Houston, McGovern Med Sch, Dept Psychiat & Behav Sci, Neuropsychiat Program, Houston, TX 77030 USA
关键词
Anxiety; BDNF; depression; dopamine; mood disorders; neurotrophin-3; NT-3; neurotrophic factors; noradrenaline; Trk-C; NERVE GROWTH-FACTOR; ADULT HIPPOCAMPAL NEUROGENESIS; FACTOR BDNF; SYNAPTIC-TRANSMISSION; NOREPINEPHRINE TRANSPORTER; DIFFERENTIAL RESPONSES; DOPAMINERGIC-NEURONS; SIGNAL-TRANSDUCTION; INDUCED MODULATION; NEURITE OUTGROWTH;
D O I
10.1080/14728222.2020.1846720
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Neurotrophin-3 (NT-3) is thought to play a role in the neurobiological processes implicated in mood and anxiety disorders. NT-3 is a potential pharmacological target for mood disorders because of its effects on monoamine neurotransmitters, regulation of synaptic plasticity and neurogenesis, brain-derived neurotrophic factor (BDNF) signaling boosting, and modulation of the hypothalamic-pituitary-adrenal (HPA) axis. The mechanisms underlying NT-3 anxiolytic properties are less clear and require further exploration and definition. Areas covered: The evidence that supports NT-3 as a pharmacological target for anxiety and mood disorders is presented and this is followed by a reflection on the quandaries, stumbling blocks, and future perspectives for this novel target. Expert opinion: There is evidence for miRNAs being key post-transcriptional regulators of neurotrophin-3 receptor gene (NTRK3) in anxiety disorders; however, the anxiolytic properties of NT-3 need further examination and delineation. Moreover, NT-3 expression by non-neuronal cells and its role in brain circuits that participate in anxiety and mood disorders require further scrutiny. Further work is vital before progression into clinical trials can be realized.
引用
收藏
页码:1225 / 1238
页数:14
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