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Stress the Autonomic Nervous System and the Immune-kynurenine Pathway in the Etiology of Depression

机译:抑郁症病因中的压力自主神经系统和免疫-犬尿氨酸途径

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摘要

The autonomic nervous system is one of the major neural pathways activated by stress. In situations that are often associated with chronic stress, such as major depressive disorder, the sympathetic nervous system can be continuously activated without the normal counteraction of the parasympathetic nervous system. As a result, the immune system can be activated with increased levels of pro-inflammatory cytokines. These inflammatory conditions have been repeatedly observed in depression. In the search for the mechanism by which the immune system might contribute to depression, the enhanced activity of indoleamine 2,3-dioxygenase by pro-inflammatory cytokines has been suggested to play an important role. Indoleamine 2,3-dioxygenase is the first enzyme in the kynurenine pathway that converts tryptophan to kynurenine. Elevated activity of this enzyme can cause imbalances in downstream kynurenine metabolites. This imbalance can induce neurotoxic changes in the brain and create a vulnerable glial-neuronal network, which may render the brain susceptible to depression. This review focuses on the interaction between stress, the autonomic nervous system and the immune system which can cause imbalances in the kynurenine pathway, which may ultimately lead to major depressive disorder.
机译:自主神经系统是压力激活的主要神经途径之一。在通常与慢性压力相关的情况下,例如重度抑郁症,交感神经系统可以连续激活而副交感神经系统没有正常的抵抗作用。结果,可以用增加的促炎细胞因子水平来激活免疫系统。在抑郁症中已经反复观察到这些炎性疾病。在寻找免疫系统可能导致抑郁的机制中,促炎细胞因子增强吲哚胺2,3-二加氧酶的活性被认为起重要作用。吲哚胺2,3-二加氧酶是犬尿氨酸途径中的第一个将色氨酸转化为犬尿氨酸的酶。该酶的活性升高会导致下游犬尿氨酸代谢产物失衡。这种失衡会诱发大脑中的神经毒性变化,并形成脆弱的神经胶质神经网络,从而使大脑容易患上抑郁症。这篇综述着重于压力,自主神经系统和免疫系统之间的相互作用,这些相互作用可能导致犬尿氨酸途径的失衡,最终可能导致严重的抑郁症。

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