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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Effects of diazepam and buspirone on the behaviour of wild voles (Microtus socialis) in two models of anxiety.
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Effects of diazepam and buspirone on the behaviour of wild voles (Microtus socialis) in two models of anxiety.

机译:在两种焦虑模型中,地西epa和丁螺环酮对野生田鼠行为的影响。

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摘要

Exploration models of anxiety rely almost universally on the use of laboratory species. Furthermore, the spontaneous patterns of locomotion displayed are often interpreted as being an expression of antipredator defense. However, there is no direct link between the experience of these animals and the proposed motivation for their behaviour. To address this problem, the behaviour of wild trapped voles (Microtus socialis), a small-rodent species that is heavily predated upon, was examined in the elevated plus-maze and the black/white exploration model. It was hypothesised that the patterns of locomotion in these exploration models of anxiety should be similar to those reported for laboratory animals if the reactions of the laboratory animals are related to antipredator defense. Data revealed that voles show a similar preference for the protected areas in these models (closed arms or dark section) and that this preference can be modified by buspirone and diazepam. Interestingly, although the effective doses of each drug was the same within each model, it differed between models, with the minimum effective doses of these compounds being lower in the black/white exploration model (1 mg/kg) than in the elevated plus-maze (4 mg/kg). These data provide valuable information concerning the actions of anxiolytic compounds in wild trapped animals as assessed by formal laboratory models and provide useful verification that findings in these models may be generalised to species other than laboratory rodents.
机译:焦虑的探索模型几乎普遍依赖于实验室物种的使用。此外,所显示的运动的自发模式通常被解释为抗掠食者防御的一种表达。但是,这些动物的经验与它们的行为动机之间没有直接联系。为了解决这个问题,在高架迷宫和黑白勘探模型中检查了野生被困田鼠(Microtus socialis)的行为。假设如果这些实验动物的反应与抗捕食者防御有关,则这些焦虑探索模型中的运动模式应与针对实验动物报道的运动模式相似。数据显示,在这些模型中,田鼠对保护区表现出相似的偏好(闭合臂或深色部分),而丁螺环酮和地西epa可以改变这种偏好。有趣的是,尽管每种药物的有效剂量在每个模型中都是相同的,但在模型之间却有所不同,在黑/白勘探模型中,这些化合物的最小有效剂量(1 mg / kg)低于升高的正负离子剂量。迷宫(4 mg / kg)。这些数据通过正式的实验室模型提供了有关野生被困动物中抗焦虑化合物作用的有价值的信息,并提供了有用的验证方法,证明这些模型中的发现可能会推广到实验室啮齿动物以外的物种。

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