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Future Directions forSerotonin and Antidepressants

机译:的未来方向血清素和抗抑郁药

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摘要

Despite the widespread use of antidepressant medications that block serotonin (5-hydroxytryptamine; 5-HT) and/or norepinephrine (NE) transporters, such as SSRIs (selective serotonin reuptake inhibitors) or SNRIs (serotonin and norepinephrine reuptake inhibitors), the underlying neurobiological basis of action of these agents is poorly understood. Increases in serotonergic function are hypothesized to have beneficial effects on depressive symptoms. However, which of the 14 different neuronal receptors sensitive to 5-HT accounts for the therapeutic effects of SSRIs and SNRIs remains undetermined. The development of drugs that activate or block specific 5-HT receptors may help to circumvent the two main limitations of current antidepressants: low efficacy and delayed onset of therapeutic action. What follows is a short summary of the author’s views on this matter.
机译:尽管广泛使用抗抑郁药物来阻断5-羟色胺(5-羟色胺; 5-HT)和/或去甲肾上腺素(NE)转运蛋白,例如SSRIs(选择性5-羟色胺再摄取抑制剂)或SNRIs(5-羟色胺和去甲肾上腺素再摄取抑制剂),但它们是潜在的神经生物学药物这些药物作用的基础知之甚少。假设血清素能功能的增强对抑郁症状具有有益作用。但是,对5-HT敏感的14种不同的神经元受体中,哪一种是SSRI和SNRI的治疗作用尚不清楚。激活或阻断特定5-HT受体的药物的开发可能有助于规避当前抗抑郁药的两个主要局限:疗效低和治疗作用延迟。以下是作者对此事的观点的简短摘要。

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