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Antidepressant-like activity of agomelatine in the mouse unpredictable chronic mild stressed model

机译:在小鼠不可预测的慢性轻度胁迫模型中抗抑郁的致癌物活性

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Agomelatine, acts as an agonist of melatonergic MT1 and MT2 receptors and as an antagonist of 5-HT2C receptors (Millan et al., 2003). The present study was undertaken to investigate whether chronicagomelatine treatment would block unpredictable chronic mild stress-induced depression-like behavior in micecompared to fluoxetine and endogenous melatonergic agonist melatonin. Results:(1) Agomelatine, significantlyreversed the ucms-induced degradation in the coat state; the magnitude was comparable to melatonin andfluoxetine (2) All drugs tested blocked the stress-induced deficit in total number of grooming in splash test ,decreased the attack frequency in resident intruder test, reduced the immobility time in tail suspension test andforced swimming test (3) All drugs decreased enhanced levels of plasma acth, il-6 and Tnf-α levels in stressedmice. Results of this study support the assumption that agomelatine, with a novel mode of action and afavourable clinical safety and tolerability profile is effective as much as fluoxetine for the treatment ofdepression.
机译:Agomelatine,用作褪黑素能MT1和MT2受体的激动剂,作为5-HT2C受体的拮抗剂(Millan等,2003)。本研究进行了研究ChericagoMelatine治疗是否会阻断MiceComparetine和内源溶解剂激动剂褪黑素中不可预测的慢性轻微应激诱导的抑郁状行为。结果:(1)Agomelatine,显着提高了涂层状态的UCMS引起的降解;尺寸与褪黑素和氟辛醚相当(2)所有测试的药物阻断了溅射试验中梳理总数的应力诱导的缺陷,降低了常驻入侵者试验中的攻击频率,降低了尾悬架试验和施加的游泳试验中的不动时间(3 )所有药物的所有药物都会降低应激性血浆ACTH,IL-6和TNF-α水平的增强水平。该研究的结果支持胍葡萄酒的假设,具有新的作用模式和可追踪的临床安全和耐受性型材,与氟西汀有效,用于治疗Drecumple。

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