Synergistic mechanisms involved in the antidepressant effects of agomelatine

被引:41
作者
Tardito, Daniela [1 ,2 ]
Molteni, Raffaella [1 ,2 ]
Popoli, Maurizio [1 ,2 ]
Racagni, Giorgio [1 ,2 ,3 ]
机构
[1] Univ Milan, Dipartimento Sci Farmacol & Biomol, Ctr Neurofarmacol, I-20133 Milan, Italy
[2] Univ Milan, Dipartimento Sci Farmacol & Biomol, Ctr Eccellenza Malattie Neurodegenerat, I-20133 Milan, Italy
[3] IRCCS San Giovanni Dio Fatebenefratelli, Brescia, Italy
关键词
Agomelatine; Melatonergic receptors; 5-HT2C receptors; Synergism; RAT PREFRONTAL/FRONTAL CORTEX; 5-HT2C RECEPTOR; MELATONIN RECEPTORS; GLUTAMATE RELEASE; STRESS; DEPRESSION; BLOCKADE; ANTAGONIST; EXPRESSION; S-20098;
D O I
10.1016/j.euroneuro.2012.06.016
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Agomelatine is a novel and clinically effective antidepressant drug with melatonergic (MT1/MT2) agonist and 5-HT2C receptor antagonist properties. Both receptorial components are widely expressed in the central nervous system and it seems that this compound could act synergistically on both the melatonergic and the 5-HT2C receptors. In this review we will briefly summarize the oreclinical evidence suggesting that the molecular-cellular effects of agomelatine and in turn its antidepressant activity are the result of a synergistic action between its agonism at MT1/M12 and antagonism at 5-HT2C receptors. The antidepressant properties of agomelatine related to its effect on neurogenesis, cell survival, brain-derived neurotrophic factor (BDNF), activity-regulated cytoskeleton associated protein (Arc) and stress-induced glutamate release, appear to be due to this synergistic action. Compared with traditional antidepressants which also affect these parameters, agomelatine is the only one able to resynchronize these effectors at distinct levels, circuital and intracellular. This suggests that agomelatine effects in restoring circadian rhythms and relieving depressive symptoms result from a synergistic interaction between melatonergic and serotonergic receptors. (C) 2012 Elsevier B.V. and ECNP. All rights reserved.
引用
收藏
页码:S482 / S486
页数:5
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