Neurotrophic and Antidepressant Actions of Brain-Derived Neurotrophic Factor Require Vascular Endothelial Growth Factor

被引:88
作者
Deyama, Satoshi [1 ,2 ]
Bang, Eunyoung [1 ]
Kato, Taro [1 ,3 ]
Li, Xiao-Yuan [1 ]
Duman, Ronald S. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Psychiat, 34 Pk St, New Haven, CT 06519 USA
[2] Kanazawa Univ, Inst Med Pharmaceut & Hlth Sci, Lab Mol Pharmacol, Kanazawa, Ishikawa, Japan
[3] Sumitomo Dainippon Pharma Co Ltd, Drug Dev Res Labs, Suita, Osaka, Japan
关键词
BDNF; Depression; Medial prefrontal cortex; Mood disorder; Rapid antidepressants; VEGF-A; FACTOR VAL66MET POLYMORPHISM; SYNAPTIC-TRANSMISSION; BEHAVIORAL ACTIONS; MAMMALIAN TARGET; TRUNCATED TRKB; FACTOR VEGF; BDNF; RECEPTOR; KETAMINE; STRESS;
D O I
10.1016/j.biopsych.2018.12.014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
BACKGROUND: Activity-dependent release of brain-derived neurotrophic factor (BDNF) in the medial prefrontal cortex (mPFC) is essential for the rapid and sustained antidepressant actions of ketamine, and a recent study shows a similar requirement for vascular endothelial growth factor (VEGF). Since BDNF is reported to stimulate VEGF expression and/or release in neuroblastoma cells, the present study tested the hypothesis that the actions of BDNF are mediated by VEGF. METHODS: The role of VEGF in the antidepressant behavioral actions of BDNF was tested by intra-mPFC coinfusion of a VEGF neutralizing antibody and by neuron-specific deletion of VEGF. The influence of BDNF on the release of VEGF and the role of VEGF in the neurotrophic actions of BDNF were determined in rat primary cortical neurons. The role of BDNF in the behavioral and neurotrophic actions of VEGF was also determined. RESULTS: The results show that the rapid and sustained antidepressant-like actions of intra-mPFC BDNF are blocked by coinfusion of a VEGF neutralizing antibody, and that neuron-specific mPFC deletion of VEGF blocks the antidepressant-like actions of BDNF. Studies in primary cortical neurons demonstrate that BDNF stimulates the release of VEGF and that BDNF induction of dendrite complexity is blocked by a selective VEGF-fetal liver kinase 1 receptor antagonist. Surprisingly, the results also show reciprocal interactions, indicating that the behavioral and neurotrophic actions of VEGF are dependent on BDNF. CONCLUSIONS: These findings indicate that the antidepressant-like and neurotrophic actions of BDNF require VEGF signaling, but they also demonstrate reciprocal interdependence for BDNF in the actions of VEGF.
引用
收藏
页码:143 / 152
页数:10
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