首页> 外文期刊>Behavioural Brain Research: An International Journal >The change in muscarinic receptor subtypes in different brain regions of rats treated with fluoxetine or propranolol in a model of post-traumatic stress disorder
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The change in muscarinic receptor subtypes in different brain regions of rats treated with fluoxetine or propranolol in a model of post-traumatic stress disorder

机译:创伤后应激障碍模型中氟西汀或普萘洛尔治疗的大鼠不同脑区毒蕈碱受体亚型的变化

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This study shows the possible contribution of muscarinic receptors in the pathophysiology of post-traumatic stress disorder. Sprague-Dawley rats of both sexes were exposed to dirty cat litter (trauma) for 10min and the protocol was repeated 1 week later with a trauma reminder (clean litter). The rats also received intraperitoneal fluoxetine (2.5, 5 or 10mg/kg/day), propranolol (10mg/kg/day) or saline for 7 days between two exposure sessions. Functional behavioral experiments were performed using elevated plus maze, following exposure to trauma reminder. Western blot analyses for M 1, M 2, M 3, M 4 and M 5 receptor proteins were employed in the homogenates of the hippocampus, the frontal cortex and the amygdaloid complex. The anxiety indices increased from 0.63±0.02 to 0.89±0.04 in rats exposed to the trauma reminder. The freezing times were also recorded as 47±6 and 133±12s, in control and test animals respectively. Fluoxetine or propranolol treatments restored the increases in the anxiety indices and the freezing times. Female rats had higher anxiety indices compared to males. Western blot data showed increases in M 2 and M 5 expression in the frontal cortex. Expression of M 1 receptors increased and M 4 subtype decreased in the hippocampus. In the amygdaloid complex of rats, we also detected a down-regulation of M 4 receptors. Fluoxetine and propranolol only corrected the changes occurred in the frontal cortex. These results may imply that muscarinic receptors are involved in this experimental model of post-traumatic stress disorder.
机译:这项研究表明毒蕈碱受体可能在创伤后应激障碍的病理生理中的作用。将两个性别的Sprague-Dawley大鼠暴露于肮脏的猫砂(创伤)中10分钟,并在1周后用创伤提醒(干净的猫砂)重复该方案。在两次接触之间,大鼠还接受了7天的腹膜内氟西汀(2.5、5或10mg / kg /天),普萘洛尔(10mg / kg /天)或生理盐水。暴露于创伤后,使用高架迷宫进行功能性行为实验。在海马,额叶皮层和杏仁状体复合体的匀浆中采用M1,M 2,M 3,M 4和M 5受体蛋白的蛋白质印迹分析。暴露于创伤提示的大鼠的焦虑指数从0.63±0.02增加到0.89±0.04。对照组和测试动物的冻结时间也分别记录为47±6和133±12s。氟西汀或普萘洛尔治疗恢复了焦虑指数和冰冻时间的增加。与雄性相比,雌性大鼠的焦虑指数更高。蛋白质印迹数据显示额叶皮层中M 2和M 5表达增加。海马中M 1受体的表达增加而M 4亚型的表达减少。在大鼠的杏仁状复合体中,我们还检测到M 4受体的下调。氟西汀和普萘洛尔只能纠正额叶皮质中发生的变化。这些结果可能暗示毒蕈碱受体参与了创伤后应激障碍的这一实验模型。

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