Laboratory of Neuroanatomy and Neuropsychobiology, Department of Pharmacology, Ribeirão Preto Medical School of the University of São Paulo (FMRP-USP), Av. Bandeirantes, 3900, Ribeirão Preto, 14049-900 São Paulo, Brazil; Ophidiarium LNN-FMRP-USP/INeC, Ribeirão Preto Medical School of the University of São Paulo, Av. Bandeirantes, 3900, Ribeirão Preto, 14049-900 São Paulo, Brazil; Behavioural Neurosciences Institute (INeC), Avenida do Café, 2450, Ribeirão Preto, 14050-220 São Paulo, Brazil; Dracena Medical School (UNIFADRA-FUNDEC), Rua Bahia, 332, Dracena, 17900-000 São Paulo, Brazil.
Laboratory of Neuroanatomy and Neuropsychobiology, Department of Pharmacology, Ribeirão Preto Medical School of the University of São Paulo (FMRP-USP), Av. Bandeirantes, 3900, Ribeirão Preto, 14049-900 São Paulo, Brazil; Ophidiarium LNN-FMRP-USP/INeC, Ribeirão Preto Medical School of the University of São Paulo, Av. Bandeirantes, 3900, Ribeirão Preto, 14049-900 São Paulo, Brazil; Behavioural Neurosciences Institute (INeC), Avenida do Café, 2450, Ribeirão Preto, 14050-220 São Paulo, Brazil.
Brain Res. 2020 Oct 1;1744:146907. doi: 10.1016/j.brainres.2020.146907. Epub 2020 May 28.
Confrontation of rodents by natural predators provides a number of advantages as a model for traumatic or stressful experience. Using this approach, one of the aims of this study was to investigate a model for the study of post-traumatic stress disorder (PTSD)-related behaviour in mice. Moreover, because PTSD can facilitate the establishment of chronic pain (CP), and in the same way, patients with CP have an increased tendency to develop PTSD when exposed to a traumatic event, our second aim was to analyse whether this comorbidity can be verified in the new paradigm. C57BL/6 male mice underwent chronic constriction injury of the sciatic nerve (CCI), a model of neuropathic CP, or not (sham groups) and were submitted to different threatening situations. Threatened mice exhibited enhanced defensive behaviours, as well as significantly enhanced risk assessment and escape behaviours during context reexposure. Previous snake exposure reduced open-arm time in the elevated plus-maze test, suggesting an increase in anxiety levels. Sham mice showed fear-induced antinociception immediately after a second exposure to the snake, but 1 week later, they exhibited allodynia, suggesting that multiple exposures to the snake led to increased nociceptive responses. Moreover, after reexposure to the aversive environment, allodynia was maintained. CCI alone produced intense allodynia, which was unaltered by exposure to either the snake stimuli or reexposure to the experimental context. Together, these results specifically parallel the behavioural symptoms of PTSD, suggesting that the snake/exuvia/reexposure procedure may constitute a useful animal model to study PTSD.
自然捕食者对啮齿动物的捕食为创伤或应激体验提供了许多优势,可作为模型。本研究采用这种方法,旨在探讨一种用于研究创伤后应激障碍(PTSD)相关行为的小鼠模型。此外,由于 PTSD 可能促进慢性疼痛(CP)的发生,并且同样,CP 患者在经历创伤事件时更容易发生 PTSD,我们的第二个目的是分析这种合并症是否可以在新的范式中得到验证。C57BL/6 雄性小鼠接受坐骨神经慢性缩窄损伤(CCI),即神经性 CP 模型,或不接受(假手术组),并接受不同的威胁情况。受到威胁的小鼠表现出增强的防御行为,以及在重新暴露于环境时显著增强的风险评估和逃避行为。先前的蛇暴露减少了高架十字迷宫测试中的开臂时间,表明焦虑水平增加。假手术组小鼠在第二次接触蛇后立即表现出恐惧诱导的镇痛,但 1 周后,它们表现出痛觉过敏,表明多次接触蛇会导致疼痛反应增加。此外,重新暴露于厌恶环境后,痛觉过敏持续存在。CCI 本身引起强烈的痛觉过敏,而接触蛇刺激或重新暴露于实验环境均未改变。总之,这些结果特别类似于 PTSD 的行为症状,表明蛇/蜕/重新暴露程序可能是研究 PTSD 的有用动物模型。