Beer-Sheva Mental Health Center, The State of Israel Ministry of Health, Anxiety and Stress Research Unit, Faculty of Health Sciences, Ben-Gurion University of the Negev, Israel.
Eur Neuropsychopharmacol. 2012 Mar;22(3):205-21. doi: 10.1016/j.euroneuro.2011.07.012. Epub 2011 Sep 16.
In mammals, the circadian and stress systems are involved in adaptation to predictable and unpredictable stimuli, respectively. A series of experiments examined the relationship between stress-induced posttraumatic stress (PTSD)-like behavioral response patterns in rats and brain levels of genes related to circadian rhythms. The effects of agomelatine, administered immediately after exposure, on stress-related behavior and on local expression of Per1 and Per2 were assessed. Animals were exposed to predator scent stress. The outcome measures included behavior in an elevated plus-maze (EPM) and acoustic startle response (ASR) 7days after the exposure. Pre-set cut-off behavioral criteria classified exposed animals according to behavioral responses in EPM and ASR paradigms as those with 'extreme behavioral response' (EBR), 'minimal behavioral response (MBR),' or 'partial behavioral response' (PBR). Per1 and Per2 expression in hippocampal subregions, frontal cortex and suprachiasmatic nucleus (SCN) 8days after exposure were evaluated using immunohistochemical and RT-PCR techniques at zeitgeber-times 19 and 13. The effects of agomelatine, on behavioral tests were evaluated on Day 8. Local brain expression of Per1 and Per2 mRNA was subsequently assessed. Data were analyzed in relation to individual behavior patterns. Animals with extreme behavioral response (EBR) displayed a distinct pattern of Per1 and Per2 expression in the SCN, which was the opposite of that observed in the control and MBR animals. In the DG, no variation in Per2 expression was observed in the EBR and PBR animals. Immediate post-exposure treatment with agomelatine significantly reduced percentage of extreme-responders and normalized the expression of Per1 and Per2 as compared to controls. Stress-induced alterations in Per genes in the EBR animals may represent an imbalance between normally precisely orchestrated physiological and behavioral processes and psychopathological processes. These findings indicate that these circadian-related genes play a role in the neurobiological response to predator scent stress and provide supportive evidence that the use of agomelatine immediately after traumatic experience may be protective against the subsequent development of PTSD.
在哺乳动物中,昼夜节律系统和应激系统分别参与适应可预测和不可预测的刺激。一系列实验研究了大鼠应激后创伤后应激(PTSD)样行为反应模式与大脑中与昼夜节律相关基因之间的关系。评估了暴露后立即给予阿戈美拉汀对应激相关行为以及 Per1 和 Per2 局部表达的影响。动物暴露于捕食者气味应激下。评估的结果测量包括暴露后 7 天在高架十字迷宫(EPM)和听觉惊跳反应(ASR)中的行为。预设的行为标准根据 EPM 和 ASR 范式中的行为反应将暴露动物分为“极端行为反应”(EBR)、“最小行为反应”(MBR)或“部分行为反应”(PBR)。暴露后 8 天,使用免疫组织化学和 RT-PCR 技术在 Zeitgeber-times 19 和 13 评估海马亚区、前额皮质和视交叉上核(SCN)中 Per1 和 Per2 的表达。在第 8 天评估阿戈美拉汀对行为测试的影响。随后评估 Per1 和 Per2 mRNA 的局部脑表达。数据分析与个体行为模式有关。具有极端行为反应(EBR)的动物在 SCN 中显示出明显的 Per1 和 Per2 表达模式,与对照和 MBR 动物观察到的模式相反。在 DG 中,EBR 和 PBR 动物的 Per2 表达没有变化。暴露后立即给予阿戈美拉汀治疗可显著降低极端反应者的比例,并使 Per1 和 Per2 的表达正常化,与对照组相比。EBR 动物应激诱导的 Per 基因变化可能代表正常精确协调的生理和行为过程与精神病理过程之间的不平衡。这些发现表明这些与昼夜节律相关的基因在对捕食者气味应激的神经生物学反应中起作用,并提供了支持性证据,表明创伤后立即使用阿戈美拉汀可能对随后 PTSD 的发展具有保护作用。