Toxicology and Immunotherapy Research Unit, Department of Biochemistry, Alex Ekwueme Federal University Ndufu Alike, Abakaliki, Nigeria.
Center for Bio-Computing and Drug Design, Adekunle Ajasin University, Akungba Akoko, Ondo State, Nigeria.
J Biochem Mol Toxicol. 2022 Nov;36(11):e23179. doi: 10.1002/jbt.23179. Epub 2022 Jul 30.
This study investigated the protective effect of quercetin against cyclophosphamide-induced immunosuppressive indoleamine 2,3-dioxygenase (IDO) via the mechanism of oxidative-inflammatory stress and behavioral indices. Cyclophosphamide (CYP) was administered to male Wister rats at a dose of 100 mg/kg with or without quercetin 50 mg/kg every other day for 7 days. Experimental techniques including western blotting, immunohistochemistry analysis, and inflammatory and oxidative stress marker assays were carried out. We also conducted behavioral analyses such as open field, tail suspension, and Y-maze tests for cognitive assessment. The results indicated that quercetin attenuated oxidative-inflammatory stress induced by CYP in the hippocampus and cerebral cortex of male Wister rats by augmenting the activities of antioxidant enzymes and suppressing lipid peroxidation as well as inflammatory mediators such as interleukin-6 and interferon-γ. Concomitantly, quercetin partially prevented the alteration in brain tissue histological architecture and mitigated the activities of IDO/tryptophan 2,3-dioxygenase (TDO) and protein expression of IDO1. This was corroborated by the IDO-quercetin model obtained in silico, revealing a favorable inhibitory interaction between quercetin and the enzyme. Finally, the results of behavioral tests suggested that quercetin significantly prevented the depressive-like posture of the CYP-treated rats. Our study for the first time revealed that quercetin ameliorates the effect of CYP-instigated IDO/TDO activities in the cerebral cortex and hippocampus via restoration of antioxidant enzymes and preventing oxidative-inflammatory stress.
本研究通过氧化应激和炎症反应机制以及行为学指标,研究了槲皮素对环磷酰胺诱导的免疫抑制吲哚胺 2,3-双加氧酶(IDO)的保护作用。雄性 Wistar 大鼠每天给予 100mg/kg 的环磷酰胺(CYP),同时或不给予 50mg/kg 的槲皮素,每隔一天给予一次,共 7 天。采用 Western blot、免疫组织化学分析、炎症和氧化应激标志物检测等实验技术,进行行为分析,如旷场、悬尾和 Y 迷宫测试,以评估认知功能。结果表明,槲皮素通过增加抗氧化酶的活性和抑制脂质过氧化以及白细胞介素-6 和干扰素-γ等炎症介质,减轻 CYP 诱导的雄性 Wistar 大鼠海马和大脑皮质的氧化应激。同时,槲皮素部分防止了脑组织组织学结构的改变,并减轻了 IDO/色氨酸 2,3-双加氧酶(TDO)的活性和 IDO1 的蛋白表达。这一点通过计算机模拟的 IDO-槲皮素模型得到了证实,表明槲皮素与酶之间存在有利的抑制相互作用。最后,行为测试的结果表明,槲皮素显著防止了 CYP 处理大鼠出现抑郁样姿势。本研究首次表明,槲皮素通过恢复抗氧化酶和防止氧化应激,改善了 CYP 诱导的大脑皮质和海马 IDO/TDO 活性。