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Anxiolytic-like effects of the neurokinin 1 receptor antagonist GR-205171 in the elevated plus maze and contextual fear-potentiated startle model of anxiety in gerbils

机译:神经激肽1受体拮抗剂GR-205171在高架迷宫和情景恐惧增强的沙鼠焦虑模型中的抗焦虑作用

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Gerbils show a neurokinin (NK)1 receptor pharmacological profile, which is similar to that observed in humans, and thus have become a commonly used species to test efficacy of NK1 receptor antagonists. The aim of this study was to determine whether systemic administration of the NK1 receptor antagonist GR-205171 produced anxiolytic-like effects in the elevated plus maze and in a novel contextual conditioned fear test using fear-potentiated startle (FPS). On the elevated plus maze, treatment with GR-205171 at 0, 0.3,1.0, and 5.0mg/kg doses, 30 min before testing produced anxiolytic-like effects in an increasing dose-response manner as measured by the percentage of open arm time and percentage of open arm entries. For contextual fear conditioning, gerbils were given 10 unsignaled footshocks (0.6 mA) at a 2-min variable interstimulus interval in a distinctive training context. Twenty-four hours after training, gerbils received treatment of GR-205171 at 0, 0.3, 1.0, and 5.0 mg/kg doses, 30 min before testing in which startle was elicited in the same context in which they were trained. Contextual FPS was defined as an increase in startle over pretraining baseline values. All drug doselevels (0.3,1.0, and 5.0 mg/kg) significantly attenuated contextual FPS when compared with the vehicle control group. A control group, which received testing in a different context, showed little FPS. These findings support other evidence for anxiolytic activity of NK1 receptor antagonists and provide a novel conditioned fear test that may be an appropriate procedure to test other NK1 antagonists for preclinical anxiolytic activity in gerbils.
机译:沙鼠显示出神经激肽(NK)1受体的药理特性,与人类观察到的相似,因此已成为测试NK1受体拮抗剂功效的常用物种。这项研究的目的是确定系统性施用NK1受体拮抗剂GR-205171是否在高架迷宫中和使用恐惧增强惊吓(FPS)的新型情境条件恐惧测试中产生抗焦虑样作用。在高架迷宫中,在测试前30分钟,以0、0.3、1.0和5.0mg / kg的剂量使用GR-205171进行处理,以按开臂时间百分比衡量的剂量响应方式,产生了类似抗焦虑的作用和张开双臂的百分比。为了进行情境恐惧调节,在有区别的训练环境中,以2分钟的可变刺激间隔为沙鼠提供10条无信号的脚踏电击(0.6 mA)。训练后二十四小时,沙鼠在测试前30分钟以0、0.3、1.0和5.0 mg / kg的剂量接受了GR-205171的治疗,测试时在与他们训练相同的背景下引起惊吓。上下文FPS被定义为惊吓程度超过训练前的基线值。与赋形剂对照组相比,所有药物剂量水平(0.3、1.0和5.0 mg / kg)均显着降低情境FPS。在不同环境中接受测试的对照组显示的FPS很少。这些发现为NK1受体拮抗剂的抗焦虑活性提供了其他证据,并提供了一种新颖的条件恐惧测试,可能是测试其他NK1拮抗剂在沙鼠中临床前抗焦虑活性的合适方法。

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