Instituto de Ciências Biomédicas, Universidade Federal de Alfenas (Unifal-MG), Alfenas, Brazil.
Instituto de Ciências Biomédicas, Universidade Federal de Alfenas (Unifal-MG), Alfenas, Brazil.
Behav Brain Res. 2020 Apr 20;384:112557. doi: 10.1016/j.bbr.2020.112557. Epub 2020 Feb 20.
The relationship between individuals with post-traumatic stress disorder (PTSD) and the development of metabolic syndrome (MS) is well understood, but the relationship between individuals with preexisting MS and the development of PTSD is not yet known. Therefore, we evaluated the course of PTSD development in preexisting MS rats and we quantified the glial fibrillary acidic protein (GFAP) and ionized the calcium binding adaptor molecule 1 (Iba-1) in the cortex and hippocampus of the experimental animals. Male Wistar rats were divided into two groups: control or 10 % fructose for 5 weeks. After 5 weeks of MS induction, a group of animals was used to characterize MS. In another group, after 5 weeks of MS induction, animals were exposed to or not exposed to inescapable footshocks, followed by social isolation. After 14 days of a retention interval, the animals were re-exposed to the inescapable footshocks box, and the freezing time was evaluated. Over the following days, the animals were tested using the open field, social interaction and forced swimming tests, respectively. In another group of animals, after induction of MS and PTSD as previously described, elevated plus maze and object recognition tests were performed. Our results demonstrate that fructose solution for 5 weeks was able to induce MS, and animals with MS had more pronounced PTSD-like symptoms and a greater increase in GFAP and Iba-1 in the hippocampus and prefrontal cortex. In conclusion, MS accentuated PTSD-like symptoms that may be related to increased glial activation. This study helps reveal factors that may predispose individuals to the development of PTSD, such as metabolic disorders.
创伤后应激障碍(PTSD)个体与代谢综合征(MS)的发展之间的关系已经得到很好的理解,但患有预先存在的 MS 的个体与 PTSD 的发展之间的关系尚不清楚。因此,我们评估了预先存在的 MS 大鼠中 PTSD 发展的过程,并对实验动物的皮质和海马中的胶质纤维酸性蛋白(GFAP)和钙结合衔接蛋白 1(Iba-1)进行了定量。雄性 Wistar 大鼠分为两组:对照组或 5 周 10%果糖。MS 诱导 5 周后,一组动物用于表征 MS。在另一组中,在 MS 诱导 5 周后,动物暴露于或不暴露于无法逃避的足部电击,然后进行社会隔离。在 14 天的保留间隔后,动物重新暴露于无法逃避的足部电击箱中,并评估冻结时间。在接下来的几天里,分别使用旷场试验、社交互动试验和强迫游泳试验对动物进行测试。在另一组动物中,在如上所述诱导 MS 和 PTSD 后,进行高架十字迷宫和物体识别试验。我们的结果表明,5 周的果糖溶液能够诱导 MS,并且患有 MS 的动物表现出更明显的 PTSD 样症状,以及海马体和前额叶皮质中 GFAP 和 Iba-1 的增加更为明显。总之,MS 加重了 PTSD 样症状,这可能与神经胶质激活增加有关。这项研究有助于揭示可能使个体易患 PTSD 的因素,例如代谢紊乱。