Neuroscience Center, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.
Department of Pharmacology, Vanderbilt University, Nashville, Tennessee; Vanderbilt Brain Institute, Vanderbilt University, Nashville, Tennessee.
Biol Psychiatry. 2021 Jul 15;90(2):128-136. doi: 10.1016/j.biopsych.2021.05.008. Epub 2021 May 14.
Neurotrophic factors, particularly BDNF (brain-derived neurotrophic factor), have been associated with depression and antidepressant drug action. A variety of preclinical and clinical studies have implicated impaired BDNF signaling through its receptor TrkB (neurotrophic receptor tyrosine kinase 2) in the pathophysiology of mood disorders, but many of the initial findings have not been fully supported by more recent meta-analyses, and more both basic and clinical research is needed. In contrast, increased expression and signaling of BDNF has been repeatedly implicated in the mechanisms of both typical and rapid-acting antidepressant drugs, and recent findings have started to elucidate the mechanisms through which antidepressants regulate BDNF signaling. BDNF is a critical regulator of various types of neuronal plasticities in the brain, and plasticity has increasingly been connected with antidepressant action. Although some equivocal data exist, the hypothesis of a connection between neurotrophic factors and neuronal plasticity with mood disorders and antidepressant action has recently been further strengthened by converging evidence from a variety of more recent data reviewed here.
神经营养因子,特别是脑源性神经营养因子(BDNF),与抑郁症和抗抑郁药物的作用有关。大量的临床前和临床研究表明,通过其受体 TrkB(神经营养受体酪氨酸激酶 2)的 BDNF 信号传导受损与心境障碍的病理生理学有关,但许多最初的发现并没有被最近的荟萃分析完全证实,需要更多的基础和临床研究。相比之下,BDNF 的表达和信号的增加已被反复涉及到典型和快速作用的抗抑郁药物的作用机制中,最近的研究已经开始阐明抗抑郁药调节 BDNF 信号的机制。BDNF 是大脑中各种类型神经元可塑性的关键调节剂,而可塑性越来越与抗抑郁作用有关。尽管存在一些模棱两可的数据,但最近从这里综述的各种更近期的数据中得出的一致证据进一步加强了神经营养因子与神经元可塑性与心境障碍和抗抑郁作用之间联系的假说。