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前额皮质中一氧化氮介导的神经递质传递增加与捕食者暴露的长期焦虑样效应有关。

Increased nitric oxide-mediated neurotransmission in the medial prefrontal cortex is associated with the long lasting anxiogenic-like effect of predator exposure.

机构信息

Departament of Pharmacology, School of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil; Center for Interdisciplinary Research on Applied Neurosciences (NAPNA), University of São Paulo, Brazil; Infectious Diseases and Tropical Medicine Program, Medical School, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.

出版信息

Behav Brain Res. 2013 Nov 1;256:391-7. doi: 10.1016/j.bbr.2013.08.006. Epub 2013 Aug 12.

Abstract

Posttraumatic stress disorder (PTSD) is an anxiety disorder caused by the experience of a severe traumatic event. In rats this disorder has been modeled by exposure to a predator threat. PTSD has been associated to structural and functional changes in the medial prefrontal cortex (mPFC). Direct injections into this brain region of glutamate antagonists or inhibitors of the nitric oxide synthase (NOS) enzyme cause anxiolytic-like effects in rodents. In the present work we investigated if the behavioral changes induced by predator exposure are associated with changes in the mPFC nitrergic system. Since the hippocampus, amygdala and dorsal periaqueductal grey have also been associated to anxiety disorders, including PTSD, we also verified if this procedure would modify the nitrergic system in these regions. Male Wistar rats were exposed to a dummy or live cat for ten minutes and tested in the elevated plus maze test (EPM) seven days later. Immediately after the test their brains were removed for neuronal NOS (nNOS) immunohistochemistry detection and measurements of nitrite/nitrate (NOx) levels. Exposure to the live cat increased freezing responses. One week later the animals that froze when confronted with the cat presented a decreased percentage of entries in the open arms of the EPM and an increased number of nNOS positive neurons in the mPFC and basolateral nucleus of amygdala, but not in the hippocampus, central and medial nuclei of amygdaloid complex or dorsal-lateral periaqueductal grey. Moreover, cat exposed animals showed increased NOx levels in the mPFC but not in the hippocampus one week later. The number of nNOS neurons and NOx levels in the mPFC showed a significant correlation with freezing time during cat exposure. Our results suggest that plastic modifications of the nitrergic system in the mPFC could be related to long lasting behavioral changes induced by severe traumatic events such as predator exposure.

摘要

创伤后应激障碍(PTSD)是一种由严重创伤事件引起的焦虑障碍。在大鼠中,这种疾病是通过暴露于捕食者威胁来建模的。PTSD 与内侧前额叶皮层(mPFC)的结构和功能变化有关。谷氨酸拮抗剂或一氧化氮合酶(NOS)抑制剂直接注射到该脑区会在啮齿动物中引起抗焦虑样作用。在目前的工作中,我们研究了捕食者暴露引起的行为变化是否与 mPFC 硝化系统的变化有关。由于海马体、杏仁核和背侧中脑导水管周围灰质也与焦虑障碍有关,包括 PTSD,我们还检查了该程序是否会改变这些区域的硝化系统。雄性 Wistar 大鼠暴露于假猫或活猫十分钟,然后在高架十字迷宫测试(EPM)中测试七天后。测试后立即取出大脑进行神经元 NOS(nNOS)免疫组织化学检测和硝酸盐/亚硝酸盐(NOx)水平测量。暴露于活猫会增加冻结反应。一周后,当面对猫时冻结的动物在 EPM 的开放臂中的进入百分比降低,并且 mPFC 和杏仁核基底外侧核中的 nNOS 阳性神经元数量增加,但在海马体、杏仁核复合体的中央和内侧核或背外侧中脑导水管周围灰质中没有。此外,暴露于猫的动物在 mPFC 中显示出 NOx 水平升高,但一周后在海马体中没有。mPFC 中的 nNOS 神经元数量和 NOx 水平与猫暴露期间的冻结时间呈显著相关。我们的结果表明,mPFC 硝化系统的可塑性变化可能与严重创伤事件(如捕食者暴露)引起的长期行为变化有关。

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