Department of Physiology, Development and Neuroscience, and Cambridge Centre for Brain Repair, University of Cambridge, Cambridge CB2 3DY, UK.
Neuropharmacology. 2010 Nov;59(6):375-9. doi: 10.1016/j.neuropharm.2010.05.008. Epub 2010 Jun 1.
Agomelatine, a novel melatonin analogue and anti-depressant that acts as an agonist on melatonin receptors 1 and 2 and as an antagonist at the 5HT2C receptor, was tested for its effects on cell proliferation in the dentate gyrus of the adult rat hippocampus under intact and flattened corticosterone rhythm conditions. Agomelatine stimulated mitosis rates in the intact male rat. Flattening the daily corticosterone rhythm by inserting a subcutaneous pellet of this steroid prevented the action of agomelatine. However, adding a daily injection of corticosterone at CT1200 to rats with implanted corticosterone pellets failed to restore agomelatine's efficacy on cell proliferation. The 5HT2C receptor antagonist SB242084 stimulated progenitor cell proliferation in the dentate gyrus, while a 5HT2C agonist (RO600175) had no effect on cell proliferation alone, but counteracted that of agomelatine. These results suggest that agomelatine, a new anti-depressant, can stimulate progenitor cell mitosis in the dentate gyrus. Its action requires an intact diurnal corticosterone rhythm. The action of agomelatine on neurogenesis is likely to reside in its antagonism of the 5HT2C receptor, and suggests a mechanism distinct from that of fluoxetine, another anti-depressant, which, as previous work shows, acts through the 5HT1A receptor, but whose action is also blocked by a flattened corticosterone rhythm.
阿戈美拉汀是一种新型褪黑素类似物和抗抑郁药,作为褪黑素受体 1 和 2 的激动剂,以及 5HT2C 受体的拮抗剂,其在完整和扁平皮质酮节律条件下对成年大鼠海马齿状回细胞增殖的影响进行了测试。阿戈美拉汀刺激雄性大鼠完整状态下的有丝分裂率。通过在皮下插入这种类固醇的小丸来使每日皮质酮节律变平,可防止阿戈美拉汀的作用。然而,向植入皮质酮小丸的大鼠每日 CT1200 注射皮质酮未能恢复阿戈美拉汀对细胞增殖的功效。5HT2C 受体拮抗剂 SB242084 刺激齿状回祖细胞增殖,而 5HT2C 激动剂(RO600175)单独对细胞增殖没有影响,但能抵消阿戈美拉汀的作用。这些结果表明,新型抗抑郁药阿戈美拉汀可刺激齿状回祖细胞有丝分裂。其作用需要完整的昼夜皮质酮节律。阿戈美拉汀对神经发生的作用可能与其对 5HT2C 受体的拮抗作用有关,这表明其作用机制与另一种抗抑郁药氟西汀不同,如前所述,氟西汀通过 5HT1A 受体起作用,但也被扁平的皮质酮节律阻断。