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Quinone reductase 2 and antidepressant effect of melatonin derivatives

机译:醌还原酶2和褪黑激素衍生物的抗抑郁作用

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Melatonin and its immediate precursor, N-acetylserotonin (NAS), exert antidepressant effects in experimental models and clinical studies. We reported that melatonin and NAS decreased immobility time (an indicator of antidepressant activity) in the mouse tail suspension test. Melatonin type 3 receptor (MT3) was identified as the same protein as quinone reductase 2 (QR2) detoxifying and antioxidant enzyme. To further elucidate the role of QR2/MT3 in antidepressant action of NAS and melatonin, we studied the effect of QR2/MT3 agonist and antagonist in a tail suspension test. QR2/MT3 agonist 5-MCA-NAT decreased, while the QR2/MT3 antagonist prazosin increased the duration of immobility in the tail suspension test in a dose-dependent manner. Prazosin, in a dose that did not affect the duration of immobility, attenuated the antidepressant-like effect of NAS, melatonin, and typical tricydic antidepressant, amitriptyline, in the tail suspension test. Our results suggest that the modulation of QR2/MT3 might contribute to mechanism(s) of antidepressant effect. New antidepressants might be searched among the agonists of QR2/MT3.
机译:褪黑素及其直接前体N-乙酰羟色胺(NAS)在实验模型和临床研究中发挥抗抑郁作用。我们报道了褪黑激素和NAS减少了小鼠尾部悬吊试验的固定时间(抗抑郁活性的指标)。褪黑素3型受体(MT3)被鉴定为与醌还原酶2(QR2)解毒和抗氧化酶相同的蛋白质。为了进一步阐明QR2 / MT3在NAS和褪黑激素的抗抑郁作用中的作用,我们在尾部悬吊试验中研究了QR2 / MT3激动剂和拮抗剂的作用。 QR2 / MT3激动剂5-MCA-NAT降低,而QR2 / MT3拮抗剂prazosin以剂量依赖性方式增加尾部悬吊试验中固定的持续时间。吡唑嗪的剂量不影响固定持续时间,在尾部悬吊试验中减弱了NAS,褪黑激素和典型的三联抗抑郁药阿米替林的类抗抑郁药作用。我们的结果表明,QR2 / MT3的调节可能有助于抗抑郁作用的机制。可以在QR2 / MT3的激动剂中寻找新的抗抑郁药。

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