色氨酸-犬尿氨酸代谢途径在抑郁症中的作用及机制。

IF 3.4 3区 医学 Q2 NEUROSCIENCES
Xiaoli Gong, Rui Chang, Ju Zou, Sijie Tan, Zeyi Huang
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引用次数: 10

摘要

重度抑郁症(MDD)是一种常见的精神疾病,以持续的情绪低落和快感缺乏为特征,通常伴有认知障碍。由于其发病率不断上升、复发率和致残率高,重度抑郁症对患者的身心健康构成了重大威胁,也给社会带来了巨大的经济成本。然而,MDD的病因和发病机制尚不清楚。慢性炎症可能会导致吲哚胺-2,3-双加氧酶(IDO)在整个身体和大脑中变得过度活跃,导致大脑中喹啉酸(QUIN)过量,kynuric酸(KYNA)减少。QUIN的神经毒性损害神经胶质细胞和神经元,加速神经元凋亡,阻碍神经可塑性,并因炎症引起抑郁。因此,异常的TRP-KYN代谢途径及其代谢物与MDD密切相关,提示TRP-KYN代谢途径的改变可能与MDD有关。此外,以TRP-KYN为靶点的中药治疗MDD效果良好。本文综述了近年来抑郁症中TRP-KYN代谢途径及其代谢物的研究进展,为探索抑郁症的病因病机提供理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role and mechanism of tryptophan - kynurenine metabolic pathway in depression.

Major depressive disorder (MDD) is a common mental illness characterized by persistent low mood and anhedonia, normally accompanied with cognitive impairment. Due to its rising incidence and high rate of recurrence and disability, MDD poses a substantial threat to patients' physical and mental health, as well as a significant economic cost to society. However, the etiology and pathogenesis of MDD are still unclear. Chronic inflammation may cause indoleamine-2,3-dioxygenase (IDO) to become overactive throughout the body and brain, resulting in excess quinolinic acid (QUIN) and less kynuric acid (KYNA) in the brain. QUIN's neurotoxicity damages glial cells and neurons, accelerates neuronal apoptosis, hinders neuroplasticity, and causes depression due to inflammation. Therefore, abnormal TRP-KYN metabolic pathway and its metabolites have been closely related to MDD, suggesting changes in the TRP-KYN metabolic pathway might contribute to MDD. In addition, targeting TRP-KYN with traditional Chinese medicine showed promising treatment effects for MDD. This review summarizes the recent studies on the TRP-KYN metabolic pathway and its metabolites in depression, which would provide a theoretical basis for exploring the etiology and pathogenesis of depression.

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来源期刊
Reviews in the Neurosciences
Reviews in the Neurosciences 医学-神经科学
CiteScore
9.40
自引率
2.40%
发文量
54
审稿时长
6-12 weeks
期刊介绍: Reviews in the Neurosciences provides a forum for reviews, critical evaluations and theoretical treatment of selective topics in the neurosciences. The journal is meant to provide an authoritative reference work for those interested in the structure and functions of the nervous system at all levels of analysis, including the genetic, molecular, cellular, behavioral, cognitive and clinical neurosciences. Contributions should contain a critical appraisal of specific areas and not simply a compilation of published articles.
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