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首页> 外文期刊>Japanese Journal of Pharmacology >Impairment of Passive Avoidance Performance in SART-Stressed Mice and the Action of Drugs
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Impairment of Passive Avoidance Performance in SART-Stressed Mice and the Action of Drugs

机译:SART应激小鼠的被动回避性能受损和药物作用

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References(25) Cited-By(11) In order to investigate the behavioral characteristics of the SART-stressed (repeated cold-stressed) animal, a model of dysautonomia, step-down passive avoidance performance was examined in SART-stressed mice. SART-stressed mice exhibited a shortened test trial latency and a decreased incidence of maximum latency of 300 sec, but no change in the training latency. These alterations were blocked by single administration of chlorpromazine or carpipramine prior to the training trial. Repeated, but not single treatments with neurotropin and hopantenate improved the impaired performance due to SART stress. On the other hand, alprazolam and diazepam were ineffective by either mode of administration. Thus, SART-stressed mice appear to have impairment in the process of acquisition of a passive avoidance task.
机译:参考文献(25)被引用者(11)为了研究SART应激(反复冷应激)动物的行为特征,对自主神经失调模型,SART应激小鼠的降压被动回避性能进行了研究。 SART应激小鼠表现出缩短的试验试验潜伏期,最大潜伏期减少了300秒,但训练潜伏期没有变化。在训练试验之前,通过单用氯丙嗪或卡哌拉明可阻止这些改变。反复但非单一的神经营养蛋白和蛇麻酸盐治疗可改善由于SART应激而导致的功能受损。另一方面,阿普唑仑和地西epa对两种给药方式均无效。因此,SART应激的小鼠在获得被动回避任务的过程中似乎有损伤。

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