Effects of forced shaking stress at low temperature on pentobarbital-induced sleeping in mice.

K Matsumoto, T Satoh, L H Bing, H Ohta, H Watanabe
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引用次数: 21

Abstract

1. Effects of a new stressful manipulation, forced shaking stress at low temperature (4 degrees C) (FSLT stress), on sleeping induced by pentobarbital were investigated 70 min following its application. 2. Repeated application (7 times) decreased the duration of sleep induced by pentobarbital-Na (45 mg/kg, i.p.) in mice without affecting that induced by ketamine-HCl and chloral hydrate. This effect of FSLT stress disappeared 3 days after termination of application. 3. The latency of nociceptive response in hot-plate test increased in a naloxone-sensitive manner by single and repeated FSLT stress when tested immediately (2 min) after but not 70 min after the last stress application. 4. Diazepam (0.3 mg/kg, i.p.) significantly prolonged the duration of sleep induced by pentobarbital (45 mg/kg, i.p.) in stressed animals without changing that in unstressed animals. The effect of diazepam was blocked by Ro 15-1788 (10 mg/kg, i.p.), a specific benzodiazepine receptor antagonist. 5. Repeated FSLT stress thus appears to decrease pentobarbital sleep by inducing functional changes in the central nervous system and the GABAergic system may partially participate in FSLT stress-induced decrease in pentobarbital sleep.

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低温强制摇应力对戊巴比妥诱导小鼠睡眠的影响。
1. 在戊巴比妥应用70 min后,研究了一种新的应激手法——低温强制摇应力(FSLT应力)对戊巴比妥诱导睡眠的影响。2. 反复应用(7次)可减少戊巴比妥钠(45 mg/kg, i.p)诱导小鼠的睡眠时间,但不影响氯胺酮和水合氯醛诱导的睡眠时间。FSLT应力的这种影响在终止施用3天后消失。3.热板试验中,单次和重复应激对伤害反应的潜伏期在最后一次应激后立即(2 min)而非70 min时呈纳洛酮敏感增加。4. 地西泮(0.3 mg/kg, i.p)显著延长戊巴比妥(45 mg/kg, i.p)诱导的应激动物的睡眠时间,而未改变应激动物的睡眠时间。苯二氮卓受体特异性拮抗剂Ro 15-1788 (10 mg/kg, i.p)可阻断地西泮的作用。5. 因此,反复的FSLT应激似乎通过诱导中枢神经系统的功能改变来减少戊巴比妥睡眠,gaba能系统可能部分参与了FSLT应激诱导的戊巴比妥睡眠减少。
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