Department of Pharmacotherapeutics, Graduate School of Pharmacy and Pharmaceutical Sciences, Fukuyama University, Hiroshima, Japan.
Department of Pharmacotherapeutics, Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University, Hiroshima, Japan.
PLoS One. 2023 Feb 8;18(2):e0273037. doi: 10.1371/journal.pone.0273037. eCollection 2023.
In the chronic phase after intracerebral hemorrhage (ICH), the aftereffect-associated lowering of motivation burdens many patients; however, the pathogenic mechanism is unclear. Here, we revealed for the first time that indoleamine 2, 3-dioxygenase (IDO) expression and enzyme activity are increased in the collagenase-induced murine ICH model. IDO is a rate-limiting enzyme situated at the beginning of the kynurenine pathway and converts tryptophan, a source of serotonin (5-hydroxytryptamine; 5-HT), to kynurenine. In this study, we showed that IDO is localized in 5-HTergic neurons. After ICH, the synaptosomal 5-HT level decreased, but this effect was neutralized by subcutaneous injections of 1-methyl tryptophan (MT), a specific IDO inhibitor. These results suggest that ICH-induced IDO weakens the activity of 5-HTergic neurons. Accordingly, we next investigated whether the IDO increase contributes to the depression-like behaviors of ICH mice. The immobility times of tail suspension and forced swimming tests were significantly prolonged after ICH but shortened by the administration of 1-MT. In conclusion, the increased IDO after ICH was found to decrease 5-HT levels and subsequently reduce stress tolerance. These findings indicate that IDO is a novel therapeutic target for the ICH aftereffect-associated lowering of motivation.
在脑出血(ICH)后的慢性期,与后遗症相关的动机降低困扰着许多患者;然而,其发病机制尚不清楚。在这里,我们首次揭示了色氨酸 2,3-双加氧酶(IDO)的表达和酶活性在胶原酶诱导的小鼠 ICH 模型中增加。IDO 是位于犬尿氨酸途径起始处的限速酶,可将色氨酸(5-羟色胺(5-HT)的来源)转化为犬尿氨酸。在这项研究中,我们表明 IDO 位于 5-HT 能神经元中。ICH 后,突触体 5-HT 水平下降,但这一作用被特异性 IDO 抑制剂 1-甲基色氨酸(MT)的皮下注射所中和。这些结果表明,ICH 诱导的 IDO 削弱了 5-HT 能神经元的活性。因此,我们接下来研究了 IDO 增加是否导致 ICH 小鼠出现抑郁样行为。在 ICH 后,悬尾和强迫游泳试验的不动时间明显延长,但 1-MT 给药后缩短。总之,ICH 后 IDO 的增加被发现会降低 5-HT 水平,从而降低应激耐受力。这些发现表明 IDO 是治疗 ICH 后效应相关动机降低的一个新的治疗靶点。