Department of Pharmacy and Biotechnology (FaBiT), Pharmaco-Toxicological Analysis Laboratory (PTA Lab), Alma Mater Studiorum - University of Bologna, Bologna, Italy.
Department for Life Quality Studies (QuVi), Alma Mater Studiorum - University of Bologna, Rimini, Italy.
Med Res Rev. 2020 Sep;40(5):1794-1832. doi: 10.1002/med.21671. Epub 2020 Apr 13.
After the development of "classical" tricyclic antidepressants and monoamine oxidase inhibitors, numerous other classes of antidepressant drugs have been introduced onto the market. The selective serotonin reuptake inhibitor class is the best-known one, but many others exist, usually identified by their mechanism of activity. In this second part of the review, focused on new-generation antidepressants not included among selective serotonin reuptake inhibitors, the following classes are considered: noradrenergic and selective serotonergic antidepressants; norepinephrine reuptake inhibitors; serotonin, norepinephrine and dopamine reuptake inhibitors; melatonergic agonists and selective serotonergic antagonists; norepinephrine and dopamine reuptake inhibitors; and so forth. These different mechanisms underlie tolerability and safety profiles that can be very different among the classes, with each one providing significant advantages and disadvantages in comparison with others. The main characteristics of the following antidepressants are described: mianserin, mirtazapine, setiptiline, reboxetine, viloxazine, teniloxazine, atomoxetine, nefazodone, agomelatine, bupropion, esketamine, and tianeptine. The paper is focused on their metabolism and interactions, but also includes brief notes on analytical methods useful for their therapeutic drug monitoring.
在“经典”三环类抗抑郁药和单胺氧化酶抑制剂开发之后,许多其他类别的抗抑郁药已被推向市场。选择性 5-羟色胺再摄取抑制剂类是最知名的一类,但还有许多其他类别的抗抑郁药,通常根据其作用机制来识别。在这篇综述的第二部分,重点介绍了新一代抗抑郁药中不包括选择性 5-羟色胺再摄取抑制剂的药物,考虑了以下几类:去甲肾上腺素和选择性 5-羟色胺能抗抑郁药;去甲肾上腺素再摄取抑制剂;5-羟色胺、去甲肾上腺素和多巴胺再摄取抑制剂;褪黑素激动剂和选择性 5-羟色胺拮抗剂;去甲肾上腺素和多巴胺再摄取抑制剂等。这些不同的机制导致了耐受性和安全性特征在不同类别之间可能有很大差异,每一种都与其他药物相比具有显著的优势和劣势。以下抗抑郁药的主要特征如下:米氮平、米那普仑、噻奈普汀、瑞波西汀、文拉法辛、替奈普汀、阿托西汀、奈法唑酮、阿戈美拉汀、安非他酮、艾司氯胺酮和曲坦辛。本文重点介绍了它们的代谢和相互作用,但也包括了用于治疗药物监测的分析方法的简要说明。