无血性
促炎细胞因子
神经科学
犬尿氨酸
多巴胺能
背景(考古学)
犬尿氨酸途径
多巴胺
重性抑郁障碍
四氢生物蝶呤
心理学
炎症
医学
内科学
生物
扁桃形结构
生物化学
色氨酸
一氧化氮合酶
一氧化氮
氨基酸
古生物学
作者
Roger S. McIntyre,Joshua D. Rosenblat,Walter Swardfager,Roger S. McIntyre
标识
DOI:10.2174/1381612823666170111144340
摘要
Anhedonia, characterized by a loss of interest and/or pleasure in previously enjoyable activities, is an important diagnostic criterion of Major Depressive Disorder (MDD). Converging evidence implicates a causal relationship between proinflammatory cytokines and behavioural disturbances that characterize anhedonia in the context of MDD. Additionally, anhedonia has been implicated in disturbances of key central dopaminergic modulatory pathways. Emerging research into the roles of tetrahydrobiopterin, a cytokine-targeted co-enzyme in the synthesis of dopamine, and kynurenine, a product of inflammation-sensitive breakdown of tryptophan via indoleamine 2, 3-dioxygenase, have shed new light into the role of inflammation in mediating anhedonic behaviours. The following narrative review is not meant to be comprehensive, but highlights the roles of both tetrahydrobiopterin and kynurenine pathways in anhedonia, and discusses a potential mechanism of action via oxidative stress and excitotoxicity. Treatment implications are discussed, with an emphasis on anti-inflammatories as complements to current treatments of anhedonia and MDD. Keywords: Anhedonia, Major Depressive Disorder (MDD), inflammation, tetrahydrobiopterin, kynurenine pathway, cytokines, oxidative stress, treatment implications.
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