Castanho Amélie, Bothorel Béatrice, Seguin Laure, Mocaër Elisabeth, Pévet Paul
Département de Neurobiologie des Rythmes, Institut des Neurosciences Cellulaires et Intégratives, UPR 3212 CNRS, Université de Strasbourg , Strasbourg , France and.
Chronobiol Int. 2014 Apr;31(3):371-81. doi: 10.3109/07420528.2013.860457. Epub 2013 Dec 11.
Depression and biological rhythms disturbances are strongly associated. Agomelatine is an antidepressant with melatoninergic MT1-MT2 agonist and serotoninergic 5-HT2c antagonist properties. Both melatonin and 5-HT are known to modulate circadian rhythmicity controlled by the endogenous clock located in the suprachiasmatic nuclei (SCN). The aim of the present study was to compare the effect of an acute injection of agomelatine (Ago), melatonin (MLT) or an antagonist 5-HT2c (S32006), on the rhythms of two robust clock outputs: the pineal MLT secretion and the body temperature rhythm (Tc). Daily endogenous MLT profiles were measured using transpineal microdialysis over 4 consecutive days in rats maintained on a 12 h light/12 h dark cycle. Simultaneously, Tc was recorded. The drugs were injected subcutaneously at three doses (1, 2.5 or 5 mg/kg) at the onset of darkness. Both Ago and MLT, at the dose of 2.5 mg/kg, increased the amplitude of the peak of MLT secretion and this effect was observed 2 d after injection. Moreover, both drugs induced a dose-dependent advance of the rhythm onset which resulted in lengthening of the MLT peak. S32006 had no effect on the rhythm of MLT. Ago, MLT and S32006 increased the amplitude of the rhythm of Tc. These data suggest a central action of Ago, directly on the SCN, via melatoninergic receptors responsible for both the increased amplitude of MLT rhythm and the phase advance. The increase in the amplitude of the body temperature could involve both MLT agonist and/or 5-HT2c antagonist properties of Ago.
抑郁症与生物节律紊乱密切相关。阿戈美拉汀是一种具有褪黑素能MT1 - MT2激动剂和5 - 羟色胺能5 - HT2c拮抗剂特性的抗抑郁药。已知褪黑素和5 - HT都能调节由位于视交叉上核(SCN)的内源性生物钟控制的昼夜节律。本研究的目的是比较急性注射阿戈美拉汀(Ago)、褪黑素(MLT)或5 - HT2c拮抗剂(S32006)对两个强大的生物钟输出节律的影响:松果体褪黑素分泌和体温节律(Tc)。在维持12小时光照/12小时黑暗周期的大鼠中,连续4天使用经松果体微透析法测量每日内源性褪黑素谱。同时记录体温。在黑暗开始时,以三种剂量(1、2.5或5mg/kg)皮下注射药物。Ago和MLT在2.5mg/kg剂量时,均增加了褪黑素分泌峰值的幅度,且在注射后2天观察到该效应。此外,两种药物均诱导节律起始的剂量依赖性提前,导致褪黑素峰值延长。S32006对褪黑素节律无影响。Ago、MLT和S32006均增加了体温节律的幅度。这些数据表明,Ago通过负责增加褪黑素节律幅度和相位提前的褪黑素能受体直接作用于SCN。体温幅度的增加可能涉及Ago的褪黑素激动剂和/或5 - HT2c拮抗剂特性。