Laboratory of Experimental Neuropsychobiology, Department of Biochemistry and Molecular Biology, Center of Natural and Exact Sciences, Federal University of Santa Maria. 1000 Roraima Avenue, Santa Maria, RS, 97105-900, Brazil; Graduate Program in Biological Sciences: Toxicological Biochemistry, Federal University of Santa Maria. 1000 Roraima Avenue, Santa Maria, RS, 97105-900, Brazil.
Laboratory of Experimental Neuropsychobiology, Department of Biochemistry and Molecular Biology, Center of Natural and Exact Sciences, Federal University of Santa Maria. 1000 Roraima Avenue, Santa Maria, RS, 97105-900, Brazil; Graduate Program in Biological Sciences: Toxicological Biochemistry, Federal University of Santa Maria. 1000 Roraima Avenue, Santa Maria, RS, 97105-900, Brazil.
Physiol Behav. 2022 Apr 1;247:113708. doi: 10.1016/j.physbeh.2022.113708. Epub 2022 Jan 19.
Ketamine is a dissociative anesthetic in human and veterinary clinic, as well as an abuse drug that acts on several neurotransmitter systems. The use of alternative animal models, such as zebrafish, is emerging to study the effects of drugs on neurobehavioral responses. Here, we evaluated the effects of ketamine on memory consolidation (acute protocol), as well as on anxiety-, aggressive-like behavior, and whole-body cortisol levels in adult zebrafish after a repeated exposure. For the acute protocol, fish were tested in the inhibitory avoidance task (training and testing with a 24-hour interval). Immediately after the training session, fish were exposed to ketamine (0, 2, 20, or 40 mg/L) for 20 min. The exploratory activity was also measured 24 h after acute exposure to exclude the influence of impaired locomotion on memory performance. For the repeated exposure, animals were exposed to the same concentrations of ketamine for 20 min (7 days). After the last exposure (24 h later), anxiety- and aggression-like behaviors were quantified in the novel tank and mirror-induced aggression tests, respectively, as well as whole-body cortisol levels measurements were performed. The highest ketamine concentration tested (40 mg/L) acutely induced a slight memory impairment in the inhibitory avoidance task without changing locomotion and anxiety-like behaviors. Although locomotion, anxiety-, aggressive-like behaviors, and whole-body cortisol levels did not change after repeated exposure, 40 mg/L ketamine increased circling behavior. Overall, our data reinforce that ketamine acutely affects multiple behavioral domains in zebrafish, in which repeated ketamine exposure elicits stereotyped behavior, without changing locomotion, aggression, and anxiety/stress-related parameters.
氯胺酮在人类和兽医临床中是一种分离麻醉剂,也是一种滥用药物,作用于多种神经递质系统。使用替代动物模型,如斑马鱼,来研究药物对神经行为反应的影响正逐渐兴起。在这里,我们评估了氯胺酮对成年斑马鱼记忆巩固(急性方案)的影响,以及在重复暴露后对焦虑样行为、攻击样行为和全身皮质醇水平的影响。对于急性方案,鱼在抑制回避任务中进行测试(训练和测试间隔 24 小时)。在训练后,鱼立即暴露于氯胺酮(0、2、20 或 40 mg/L)20 分钟。在急性暴露 24 小时后还测量了探索性活动,以排除运动障碍对记忆性能的影响。对于重复暴露,动物暴露于相同浓度的氯胺酮 20 分钟(7 天)。最后一次暴露后 24 小时,在新鱼缸和镜像诱导攻击测试中分别量化了焦虑样和攻击样行为,以及全身皮质醇水平的测量。测试的最高氯胺酮浓度(40 mg/L)在抑制回避任务中急性诱导轻微的记忆障碍,而不改变运动和焦虑样行为。尽管重复暴露后运动、焦虑、攻击样行为和全身皮质醇水平没有变化,但 40 mg/L 氯胺酮增加了转圈行为。总的来说,我们的数据强化了氯胺酮在斑马鱼中急性影响多种行为领域的观点,其中重复氯胺酮暴露会引发刻板行为,而不改变运动、攻击和焦虑/应激相关参数。