De Berardis Domenico, Fornaro Michele, Serroni Nicola, Campanella Daniela, Rapini Gabriella, Olivieri Luigi, Srinivasan Venkataramanujam, Iasevoli Felice, Tomasetti Carmine, De Bartolomeis Andrea, Valchera Alessandro, Perna Giampaolo, Mazza Monica, Di Nicola Marco, Martinotti Giovanni, Di Giannantonio Massimo
National Health Service, Department of Mental Health, Psychiatric Service of Diagnosis and Treatment, Hospital "G. Mazzini", ASL 4, 64100 Teramo, Italy.
Department of "Scienze della Formazione", University of Catania, 95121 Catania, Italy.
Int J Mol Sci. 2015 Jan 5;16(1):1111-30. doi: 10.3390/ijms16011111.
Agomelatine, a melatonergic antidepressant with a rapid onset of action, is one of the most recent drugs in the antidepressant category. Agomelatine's antidepressant actions are attributed to its sleep-promoting and chronobiotic actions mediated by MT1 and MT2 receptors present in the suprachiasmatic nucleus, as well as to its effects on the blockade of 5-HT2c receptors. Blockade of 5-HT2c receptors causes release of both noradrenaline and dopamine at the fronto-cortical dopaminergic and noradrenergic pathways. The combined actions of agomelatine on MT1/MT2 and 5-HT2c receptors facilitate the resynchronization of altered circadian rhythms and abnormal sleep patterns. Agomelatine appeared to be effective in treating major depression. Moreover, evidence exists that points out a possible efficacy of such drug in the treatment of bipolar depression, anxiety disorders, alcohol dependence, migraines etc. Thus, the aim of this narrative review was to elucidate current evidences on the role of agomelatine in disorders other than major depression.
阿戈美拉汀是一种起效迅速的褪黑素能抗抑郁药,是抗抑郁药类别中最新的药物之一。阿戈美拉汀的抗抑郁作用归因于其通过视交叉上核中存在的MT1和MT2受体介导的促睡眠和生物钟调节作用,以及其对5-HT2c受体的阻断作用。阻断5-HT2c受体会导致去甲肾上腺素和多巴胺在前额叶皮质多巴胺能和去甲肾上腺素能通路释放。阿戈美拉汀对MT1/MT2和5-HT2c受体的联合作用有助于使改变的昼夜节律和异常睡眠模式重新同步。阿戈美拉汀似乎对治疗重度抑郁症有效。此外,有证据表明该药物在治疗双相抑郁症、焦虑症、酒精依赖、偏头痛等方面可能有效。因此,本叙述性综述的目的是阐明关于阿戈美拉汀在重度抑郁症以外的疾病中的作用的现有证据。