1Translational Neuropsychiatry Unit,Department of Clinical Medicine,Aarhus University,Risskov,Denmark.
2Department of Pharmacology,Biological Section Building,Federal University of Paraná,Curitiba,Paraná,Brazil.
Acta Neuropsychiatr. 2018 Dec;30(6):307-322. doi: 10.1017/neu.2017.39. Epub 2018 Feb 1.
Although monoaminergic-targeted drugs have prompted great advances in the development of treatments for depression, the need for new options persists, since these drugs still have a delayed clinical effect and most patients do not respond properly to them. Recently, the observation of the antidepressant effects of ketamine brought on a new wave of studies regarding the comprehension of the neurobiology of depression and the development of new and more effective antidepressant drugs.
Thus, in this paper, we present a historical review of the development of monoaminergic antidepressant drugs and the role of ketamine as the introductory agent of a new era in the research of the neurobiology of depression.
Firstly, we review how the pharmacological treatment for major depression started, and we point out the main drugs discovered, the researchers involved, and how the studies developed have contributed to the understanding of the neurobiology of depression. Secondly, the major problems regarding the clinical efficacy and acceptance of these drugs are discussed, and the introduction of the glutamatergic system as a target for antidepressant drugs is presented. Finally, we review how ketamine revealed itself as an exciting option towards obtaining pharmacological agents to treat depression, through the understanding of biological markers.DiscussionKetamine contributed to confirm that different targets of the glutamatergic system and neurotrophic pathways are strictly related to the neurobiology of depression. There are several antidepressant drugs based on ketamine's mechanism of action already in the pipeline, and glutamatergic-targeted antidepressants may be on the market in the near future.
尽管单胺能靶向药物在开发抑郁症治疗方法方面取得了重大进展,但仍需要新的选择,因为这些药物仍具有延迟的临床效果,而且大多数患者对其反应不佳。最近,观察到氯胺酮具有抗抑郁作用,这引发了一波新的研究,旨在深入了解抑郁症的神经生物学,并开发新的、更有效的抗抑郁药物。
因此,在本文中,我们对单胺能抗抑郁药物的发展进行了历史回顾,并介绍了氯胺酮作为抑郁症神经生物学研究新时代的先导药物的作用。
首先,我们回顾了抗重性抑郁症的药物治疗是如何开始的,并指出了发现的主要药物、涉及的研究人员,以及研究进展如何有助于对抑郁症神经生物学的理解。其次,讨论了这些药物在临床疗效和可接受性方面的主要问题,并提出了将谷氨酸能系统作为抗抑郁药物的靶点。最后,我们回顾了氯胺酮如何通过对生物标志物的理解,揭示了自身作为治疗抑郁症的药理学药物的令人兴奋的选择。
氯胺酮有助于证实,谷氨酸能系统和神经营养途径的不同靶点与抑郁症的神经生物学密切相关。目前已有几种基于氯胺酮作用机制的抗抑郁药物正在研发中,谷氨酸能靶向抗抑郁药物可能在不久的将来上市。