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The predator odor avoidance model of post-traumatic stress disorder in rats

机译:大鼠创伤后应激障碍的捕食者气味避免模型

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Individuals with post-traumatic stress disorder avoid trauma-related stimuli and exhibit blunted hypothalamic–pituitary–adrenal axis response at the time of trauma. Our laboratory uses predator odor (i.e. bobcat urine) stress to divide adult Wistar rats into groups that exhibit high (avoiders) or low (nonavoiders) avoidance of a predator odor-paired context, modeling the fact that not all humans exposed to traumatic events develop psychiatric conditions. Male avoiders exhibit lower body weight gain after stress, as well as extinction-resistant avoidance that persists after a second stress exposure. These animals also show attenuated hypothalamic–pituitary–adrenal axis response to predator odor that predicts subsequent avoidance of the odor-paired context. Avoiders exhibit unique brain activation profiles relative to nonavoiders and controls (as measured by Fos immunoreactivity), and higher corticotropin-releasing factor levels in multiple brain regions. Furthermore, avoider rats exhibit escalated and compulsive-like alcohol self-administration after traumatic stress. Here, we review the predator odor avoidance model of post-traumatic stress disorder and its utility for tracking behavior and measuring biological outcomes predicted by avoidance. The major strengths of this model are (i) etiological validity with exposure to a single intense stressor, (ii) established approach distinguishing individual differences in stress reactivity, and (iii) robust behavioral and biological phenotypes during and after trauma.
机译:具有创伤后应激障碍的个体避免了创伤相关的刺激,并且在创伤时表现出钝化的下丘脑 - 垂体 - 肾上腺轴反应。我们的实验室使用捕食剂气味(即山猫尿)应力将成人Wistar大鼠分成避免捕食性气味背景的高(避免)或低(犹太人),避免了捕食性气味的背景,这使得并非所有暴露于创伤事件发生的事实精神病条件。男性避免在压力之后表现出较低的体重增加,以及在第二次压力暴露后持续的耐火性避免。这些动物还显示出衰减的下丘脑 - 垂体 - 肾上腺轴响应于预测后续避免气味的上下文的捕食性气味。避免表现出相对于非掠夺者和对照的独特脑激活曲线(通过FOS免疫反应性测量),以及多种脑区中的较高的皮质激素释放因子水平。此外,在创伤应力后,Avoider大鼠表现出升级和强制性的酒精自我给药。在这里,我们审查了创伤后应力障碍的捕食气味避免模型及其借出跟踪行为和测量避免预测的生物学结果。该模型的主要优点是(i)具有暴露于单个强烈的压力源的病因有效性,(ii)建立的方法区分胁迫反应性的个体差异,(iii)创伤期间和后生物表型和生物学表型。

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