首页> 外文期刊>Japanese Journal of Pharmacology >Anxiety-like behavior in elevated plus-maze tests in repeatedly cold-stressed mice.
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Anxiety-like behavior in elevated plus-maze tests in repeatedly cold-stressed mice.

机译:反复冷应激小鼠在高迷宫测试中的焦虑样行为。

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To clarify the relationship between SART (specific alternation of rhythm in temperature) stress (repeated cold stress) and anxiety, the effects of various types of stress on the behavior of mice were studied in elevated plus-maze tests and then the effects of anxiolytics were evaluated. The percentage of time spent in the open arms of the plus-maze apparatus decreased in mice subjected to SART stress without change in the total number of arm entries. No change was noted in mice subjected to other stresses, such as 1-h, 2-day and 5-day cold stress and 1-h, 15-h and 5 x 15-h restraint stress. The reduction in the percentage of time spent in the open arms caused by SART stress was inhibited by single and repeated administrations of diazepam and alprazolam and by a single administration of buspirone, which have no influence on the percentage of time spent in the open arms in nonstressed mice, but not by flumazenil, WAY-100635 and chronic treatment with buspirone. The effects of diazepam and buspirone were antagonized by flumazenil and WAY-100635, respectively. The behavior of SART-stressed mice in the plus-maze would thus appear to arise from anxiety, to which benzodiazepine and serotonin receptors are related, but the diazepam binding inhibitor, an endogenous anxiogenic protein, is not. Thus SART-stressed animals may be useful for investigating the psychopharmacological and neuropharmacological basis of anxiety.
机译:为了阐明SART(温度的特定节奏变化)应激(反复冷应激)与焦虑之间的关系,在高迷宫试验中研究了各种应激对小鼠行为的影响,然后对抗焦虑药进行了研究。评估。在遭受SART应力的小鼠中,在没有迷宫总数的情况下,加迷宫装置张开的手臂所花费的时间百分比减少了。在遭受其他应激(例如1小时,2天和5天冷应激以及1小时,15小时和5 x 15小时约束应激)的小鼠中,没有发现变化。地塞米松和阿普唑仑的单次和重复给药以及丁螺环酮的单次给药抑制了SART应激导致的张开双臂所花费的时间百分比的减少,而丁苯哌酮的单次给药对服用舒张压的时间所占的百分比没有影响。非应激小鼠,但不接受氟马西尼,WAY-100635和丁螺环酮的慢性治疗。氟马西尼和WAY-100635分别拮抗地西epa和丁螺环酮的作用。因此,SART应激小鼠在迷宫中的行为似乎是由焦虑引起的,焦虑与苯二氮卓和5-羟色胺受体有关,而与地西epa结合抑制剂(一种内源性焦虑源蛋白)无关。因此,SART应激动物可用于研究焦虑的心理药理学和神经药理学基础。

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