University Department of Psychiatry, Warneford Hospital, University of Oxford, OX3 7JX, UK.
Oxford Health NHS Foundation Trust, Warneford Hospital, Oxford, UK.
Psychol Med. 2021 May;51(7):1111-1120. doi: 10.1017/S0033291720000604. Epub 2020 Apr 3.
Animal experimental studies suggest that 5-HT4 receptor activation holds promise as a novel target for the treatment of depression and cognitive impairment. 5-HT4 receptors are post-synaptic receptors that are located in striatal and limbic areas known to be involved in cognition and mood. Consistent with this, 5-HT4 receptor agonists produce rapid antidepressant effects in a number of animal models of depression, and pro-cognitive effects in tasks of learning and memory. These effects are accompanied by molecular changes, such as the increased expression of neuroplasticity-related proteins that are typical of clinically useful antidepressant drugs. Intriguingly, these antidepressant-like effects have a fast onset of their action, raising the possibility that 5-HT4 receptor agonists may be a particularly useful augmentation strategy in the early stages of SSRI treatment. Until recently, the translation of these effects to humans has been challenging. Here, we review the evidence from animal studies that the 5-HT4 receptor is a promising target for the treatment of depression and cognitive disorders, and outline a potential pathway for the efficient and cost-effective translation of these effects into humans and, ultimately, to the clinic.
动物实验研究表明,5-HT4 受体激动剂可能成为治疗抑郁症和认知障碍的新靶点。5-HT4 受体是位于纹状体和边缘区域的突触后受体,这些区域与认知和情绪有关。与此一致的是,5-HT4 受体激动剂在许多抑郁症动物模型中产生快速的抗抑郁作用,并在学习和记忆任务中产生认知增强作用。这些作用伴随着分子变化,例如与神经可塑性相关的蛋白质表达增加,这是临床有效抗抑郁药物的典型特征。有趣的是,这些抗抑郁样作用具有快速的作用起始,这增加了 5-HT4 受体激动剂可能是 SSRIs 治疗早期特别有用的增效策略的可能性。直到最近,这些作用在人类中的转化一直具有挑战性。在这里,我们回顾了来自动物研究的证据,表明 5-HT4 受体是治疗抑郁症和认知障碍的有希望的靶点,并概述了将这些作用有效且经济高效地转化为人类并最终转化为临床应用的潜在途径。