Biochemistry and Pharmacology Graduate Program, Federal University of Espirito Santo, Vitoria, ES, Brazil; Department of Biomolecular Sciences, School of Pharmaceutical Sciences, University of São Paulo, Ribeirão Preto, SP, Brazil; Translational Neuropsychiatry Unit (TNU), Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Department of Pharmaceutical Sciences, Health Science Center, Federal University of Espirito Santo, Vitoria, ES, Brazil.
Prog Neuropsychopharmacol Biol Psychiatry. 2020 Jun 8;100:109878. doi: 10.1016/j.pnpbp.2020.109878. Epub 2020 Jan 23.
Ketamine, a non-competitive N-methyl-D-aspartate (NMDA) receptor antagonist, presents a rapid and sustained antidepressant effect in clinical and preclinical studies. Regarding ketamine effects on anxiety, there is a widespread discordance among pre-clinical studies. To address this issue, the present study reviewed the literature (electronic database MEDLINE) to summarize the profile of ketamine effects in animal tests of anxiety/fear. We found that ketamine anxiety/fear-related effects may depend on the anxiety paradigm, schedule of ketamine administration and tested species. Moreover, there was no report of ketamine effects in animal tests of fear related to panic disorder (PD). Based on that finding, we evaluated if treatment with ketamine and another NMDA antagonist, MK-801, would induce acute and sustained (24 hours later) anxiolytic and/or panicolytic-like effects in animals exposed to the elevated T-maze (ETM). The ETM evaluates, in the same animal, conflict-evoked and fear behaviors, which are related, respectively, to generalized anxiety disorder and PD. Male Wistar rats were systemically treated with racemic ketamine (10, 30 and 80 mg/kg) or MK-801 (0.05 and 0.1 mg/kg) and tested in the ETM in the same day or 24 hours after their administration. Ketamine did not affect the behavioral tasks performed in the ETM acutely or 24 h later. MK-801 impaired inhibitory avoidance in the ETM only at 45 min post-injection, suggesting a rapid but not sustained anxiolytic-like effect. Altogether our results suggest that ketamine might have mixed effects in anxiety tests while it does not affect panic-related behaviors.
氯胺酮是一种非竞争性 N-甲基-D-天冬氨酸(NMDA)受体拮抗剂,在临床和临床前研究中表现出快速和持续的抗抑郁作用。关于氯胺酮对焦虑的影响,临床前研究中存在广泛的不一致。为了解决这个问题,本研究综述了文献(电子数据库 MEDLINE),总结了氯胺酮在动物焦虑/恐惧测试中的作用特征。我们发现,氯胺酮与焦虑/恐惧相关的作用可能取决于焦虑范式、氯胺酮给药方案和测试物种。此外,没有报道氯胺酮在与惊恐障碍(PD)相关的动物恐惧测试中的作用。基于这一发现,我们评估了氯胺酮和另一种 NMDA 拮抗剂 MK-801 是否会在暴露于高架 T 迷宫(ETM)的动物中诱导急性和持续(24 小时后)的抗焦虑和/或惊恐样作用。ETM 在同一动物中评估了冲突诱发的和恐惧行为,分别与广泛性焦虑障碍和 PD 有关。雄性 Wistar 大鼠系统给予外消旋氯胺酮(10、30 和 80 mg/kg)或 MK-801(0.05 和 0.1 mg/kg),并在给药当天或 24 小时后在 ETM 中进行测试。氯胺酮急性或 24 小时后均不影响 ETM 中的行为任务。MK-801 仅在注射后 45 分钟时损害 ETM 中的抑制性回避,表明其具有快速但非持续的抗焦虑样作用。总之,我们的结果表明,氯胺酮在焦虑测试中可能具有混合作用,而不影响与惊恐相关的行为。