Tsai Shih-Jen
Department of Psychiatry, Taipei Veterans General Hospital, No. 201, Shih-Pai Road, Sec. 2, 11217, Taipei, Taiwan, ROC.
Med Hypotheses. 2004;62(2):215-8. doi: 10.1016/S0306-9877(03)00299-8.
Major depressive disorder (MDD) is a common mental disease with unknown etiology. Recent studies have suggested that decreased brain-derived neurotrophic factor (BDNF) may be implicated in the pathogenesis of MDD. Instead of a decrease in central BDNF, however, studies utilizing genetic depression animal models have found elevated levels of the factor. In the brain, BDNF exerts its influence chiefly by signaling through tyrosine receptor kinase B (Trk-B). In this report, it is suggested that Trk-B pathway down-regulation may be the major pathogenesis for MDD, while stress, which may reduce central BDNF, acts as a precipitation factor to further dampen central BDNF activity and contribute to the development of depression. Further, several possible mechanisms of Trk-B pathway down-regulation, and the implications for this down-regulation in MDD are discussed.
重度抑郁症(MDD)是一种病因不明的常见精神疾病。最近的研究表明,脑源性神经营养因子(BDNF)水平降低可能与MDD的发病机制有关。然而,利用遗传性抑郁症动物模型的研究发现,该因子的水平升高,而非中枢BDNF水平降低。在大脑中,BDNF主要通过酪氨酸受体激酶B(Trk-B)信号传导发挥作用。本报告表明,Trk-B信号通路下调可能是MDD的主要发病机制,而压力可能会降低中枢BDNF,作为一个促发因素进一步抑制中枢BDNF活性并导致抑郁症的发展。此外,还讨论了Trk-B信号通路下调的几种可能机制,以及这种下调在MDD中的意义。