Department of Psychiatry, Duke University Medical Center, Durham, North Carolina, USA.
Curr Neuropharmacol. 2008 Dec;6(4):338-43. doi: 10.2174/157015908787386078.
Depression has been associated with impaired neurotransmission of serotonergic, norepinephrinergic, and dopaminergic pathways, although most pharmacologic treatment strategies for depression enhance only serotonin and norepinephrine neurotransmission. Current drug development efforts are aimed at a new class of antidepressants which inhibit the reuptake of all three neurotransmitters in the hope of creating medications with broader efficacy and/or quicker onset of action. The current review explores limitations of presently available antidepressants and the history and premise behind the movement to devise triple reuptake inhibitors. The evidence for and against the claim that broader spectrum agents are more efficacious is discussed. Examples of triple reuptake inhibitors in development are compared, and preclinical and clinical research with these agents to date is described.
抑郁症与血清素能、去甲肾上腺素能和多巴胺能途径的神经传递受损有关,尽管大多数抗抑郁的药物治疗策略仅增强血清素和去甲肾上腺素能神经传递。目前的药物开发工作旨在开发一类新的抗抑郁药,抑制这三种神经递质的再摄取,希望创造出更有效和/或更快起效的药物。目前的综述探讨了现有抗抑郁药的局限性,以及设计三重再摄取抑制剂背后的历史和前提。讨论了关于更广泛谱的药物更有效的说法的证据。比较了正在开发的三重再摄取抑制剂的例子,并描述了这些药物的临床前和临床研究。