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Quinone reductase 2 and antidepressant effect of melatonin derivatives

机译:褪黑素衍生物的醌还原酶2和抗抑郁作用

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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 tricyclic 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:褪黑激素及其直接前体,N-乙酰苯甲肽素(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在小鼠尾悬浮试验中减少了不可用时间(抗抑郁活性的指示剂)。褪黑激素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和褪黑素的抗抑郁作用中的作用,我们研究了QR2 / MT3激动剂和拮抗剂在尾悬浮试验中的作用。 QR2 / MT3激动剂5-MCA-NAT减少,而QR2 / MT3拮抗剂Prazosin以剂量依赖性方式增加了尾悬浮试验中的不动的持续时间。普拉多辛,在一种不影响不动的持续时间的剂量中,减弱了NaS,褪黑素和典型的三环抗抑郁药,氨基型型尾悬浮试验的抗抑郁药物。我们的研究结果表明,QR2 / MT3的调节可能有助于抗抑郁效应的机制。可以在QR2 / MT3的激动剂中搜索新的抗抑郁药。

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