College of Life and Environmental Sciences, University of Exeter, Exeter, UK.
Department of Surgical Sciences, University of Uppsala, Uppsala, Sweden.
Br J Clin Pharmacol. 2022 Oct;88(10):4412-4426. doi: 10.1111/bcp.15374. Epub 2022 May 20.
There is a growing interest in the psychiatric properties of the dissociative anaesthetic ketamine, as single doses have been shown to have fast-acting mood-enhancing and anxiolytic effects, which persist for up to a week after the main psychoactive symptoms have diminished. Therefore, ketamine poses potential beneficial effects in patients with refractory anxiety disorders, where other conventional anxiolytics have been ineffective. Ketamine is a noncompetitive antagonist of the N-methyl-d-aspartate (NMDA) glutamate receptor, which underlies its induction of pain relief and anaesthesia. However, the role of NMDA receptors in anxiety reduction is still relatively unknown. To fill this paucity in the literature, this systematic review assesses the evidence that ketamine significantly reduces refractory anxiety and discusses to what extent this may be mediated by NMDA receptor antagonism and other receptors. We highlight the temporary nature of the anxiolytic effects and discuss the high discrepancy among the study designs regarding many fundamental factors such as administration routes, complementary treatments and other treatments.
人们对分离麻醉剂氯胺酮的精神科特性越来越感兴趣,因为单次给药已被证明具有快速改善情绪和抗焦虑作用,并且在主要精神活性症状减轻后持续长达一周。因此,氯胺酮在其他常规抗焦虑药无效的难治性焦虑症患者中具有潜在的有益作用。氯胺酮是 N-甲基-D-天冬氨酸(NMDA)谷氨酸受体的非竞争性拮抗剂,这是其诱导止痛和麻醉的基础。然而,NMDA 受体在减轻焦虑中的作用仍然相对未知。为了填补这一文献空白,本系统评价评估了氯胺酮显著减轻难治性焦虑的证据,并讨论了 NMDA 受体拮抗作用和其他受体在多大程度上可能介导这种作用。我们强调了抗焦虑作用的暂时性,并讨论了研究设计在许多基本因素(如给药途径、补充治疗和其他治疗)方面的高度差异。