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首页> 外文期刊>Japanese Journal of Pharmacology >Modification of the effects of benzodiazepines on the exploratory behaviors of mice on a hole-board by diabetes.
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Modification of the effects of benzodiazepines on the exploratory behaviors of mice on a hole-board by diabetes.

机译:糖尿病改变苯二氮卓类药物对小鼠在洞板上的探索行为的影响。

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摘要

The effect of diabetes on the emotional behavior of mice was examined using an automatic hole-board apparatus. Changes in the emotional state of mice were evaluated in terms of changes in exploratory activity; i.e., total locomotor activity, numbers and duration of rearing and head-dipping, and latency to the first head-dipping. The number and duration of head-dipping in diabetic mice were less than those in non-diabetic mice. Diazepam (0.1-0.56 mg/kg, i.p.) dose-dependently increased the number and duration of head-dipping at doses that did not produce sedation in both diabetic and non-diabetic mice. In contrast, methyl-beta-carboline-3-carboxylate (1 and 2 mg/kg, i.p.) decreased the number and duration of head-dipping in non-diabetic mice, but not in diabetic mice. The number and duration of head-dipping in diabetic mice were increased by treatment with flumazenil (0.1 and 0.3 mg/kg, i.v.). These doses of flumazenil did not affect the number or duration of head-dipping in non-diabetic mice. The present data indicate that diabetic mice exhibited anxiety in the hole-board test and that a benzodiazepine receptor antagonist affected the attenuated number and duration of head-dipping in diabetic mice. The heightened anxiety in diabetic mice may be due to the dysfunction of the benzodiazepine receptor and/or of central inhibitory systems.
机译:使用自动孔板设备检查了糖尿病对小鼠情绪行为的影响。根据探索活动的变化来评估小鼠的情绪状态的变化。即总的运动活动,抚养和浸头的次数和持续时间,以及第一次浸头的等待时间。糖尿病小鼠的头浸次数和持续时间少于非糖尿病小鼠。地西p(0.1-0.56 mg / kg,i.p.)剂量依赖性地增加了在糖尿病和非糖尿病小鼠中均不产生镇静作用的头浸次数和持续时间。相反,β-咔啉-3-羧酸甲酯(1和2 mg / kg,腹膜内)降低了非糖尿病小鼠的头浸药次数和持续时间,但在糖尿病小鼠中却没有。通过用氟马西尼(0.1和0.3mg / kg,i.v。)治疗,增加了糖尿病小鼠中头浸的次数和持续时间。在非糖尿病小鼠中,这些剂量的氟马西尼不会影响头浸的次数或持续时间。目前的数据表明,糖尿病小鼠在孔板试验中表现出焦虑,苯并二氮杂antagonist受体拮抗剂影响了糖尿病小鼠中浸头的数量和持续时间。糖尿病小鼠的焦虑加剧可能是由于苯并二氮杂receptor受体和/或中枢抑制系统的功能障碍。

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