Moura Clarissa A, de Sousa-Silva Anne N, Soares Ana Lívia Mesquita, de Oliveira Torres Carina I, Belchior Hindiael, da Silva Edilson D, Gavioli Elaine C
Department of Biophysics and Pharmacology, Federal University of Rio Grande do Norte, Natal 59078-900, Brazil.
Department of Physical Education, Federal University of Rio Grande do Norte, Av. Senador Salgado Filho, Campus Universitário-Lagoa Nova, Natal 59078-900, Brazil.
Brain Sci. 2024 Dec 22;14(12):1291. doi: 10.3390/brainsci14121291.
BACKGROUND/OBJECTIVES: Recent studies have investigated the effects of ketamine on fear memory in animals. However, it is unclear if ketamine might affect avoidance memory and emotional behaviors concomitantly. In this study, we compared the effects of (,)- and ()-ketamine in modulating avoidance responses, depression- and anxiety-related behaviors in stressed mice.
Mice were previously exposed to inescapable footshock stress, and 24 h later, they were trained in the active avoidance task. (,)-ketamine or ()-isomer was administered 1 h prior to re-exposition to the active avoidance task. Three hours after drug administration, mice were tested in the tail suspension, followed by the open field test.
Neither form of ketamine affected avoidance memory retrieval, while ()-ketamine, and tangentially, (,) reduced avoidance responses during re-exposition to aversive stimulus. In the tail suspension test, (,)- and ()-ketamine equally evoked antidepressant effects. In the open field test, the racemic mixture, but not ()-ketamine, induced anxiolytic actions.
These findings reinforce the therapeutic potential of ketamine for the treatment of stress-related disorders, with (,)-ketamine being more effective in simultaneously inducing antidepressant and anxiolytic responses and reducing avoidance responses in stressed mice.
背景/目的:近期研究已探究了氯胺酮对动物恐惧记忆的影响。然而,尚不清楚氯胺酮是否可能同时影响回避记忆和情绪行为。在本研究中,我们比较了(,)-氯胺酮和()-氯胺酮对应激小鼠回避反应、抑郁和焦虑相关行为的调节作用。
小鼠先前接受不可逃避的足部电击应激,24小时后,对它们进行主动回避任务训练。在再次进行主动回避任务前1小时给予(,)-氯胺酮或()-异构体。给药3小时后,对小鼠进行悬尾试验,随后进行旷场试验。
两种形式的氯胺酮均未影响回避记忆的恢复,而()-氯胺酮以及附带地(,)-氯胺酮在再次暴露于厌恶刺激期间减少了回避反应。在悬尾试验中,(,)-氯胺酮和()-氯胺酮均同样诱发抗抑郁作用。在旷场试验中,消旋混合物而非()-氯胺酮诱导抗焦虑作用。
这些发现强化了氯胺酮治疗应激相关障碍的治疗潜力,(,)-氯胺酮在同时诱导抗抑郁和抗焦虑反应以及减少应激小鼠的回避反应方面更有效。