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蝇蕈醇和咪达唑仑对大鼠睡眠脑电图的影响不会相互增强。

Muscimol and midazolam do not potentiate each other's effects on sleep EEG in the rat.

作者信息

Lancel M, Faulhaber J, Schiffelholz T, Mathias S, Deisz R A

机构信息

Max-Planck Institute of Psychiatry, Clinical Institute, Munich, Germany.

出版信息

J Neurophysiol. 1997 Mar;77(3):1624-9. doi: 10.1152/jn.1997.77.3.1624.

DOI:10.1152/jn.1997.77.3.1624
PMID:9084625
Abstract

The interaction of a gamma-aminobutyric acid-A (GABAA) receptor agonist and a benzodiazepine-type modulator of GABAA receptors on sleep was investigated. Low doses of muscimol (0.3 mg/kg) and the benzodiazepine midazolam (1.5 mg/kg) were administered alone and in combination, in random order, to eight rats. All injections were given intraperitoneally at light onset. Electroencephalogram (EEG) and electromyogram were recorded during the first 6 h post injection. Compared with vehicle, muscimol hardly affected the time spent in non-rapid eye movement sleep (non-REMS) and REMS, but significantly enhanced EEG activity in the frequency range between 2 and 6 Hz during non-REMS. Midazolam significantly increased the time spent in non-REMS, reduced EEG activity at frequencies < 12 Hz, and elevated EEG activity in most higher frequencies during this state. The combined administration of muscimol and midazolam affected non-REMS-specific EEG activity in an unexpected fashion: the effects were intermediate between those of muscimol and midazolam. These results indicate that muscimol and midazolam have dissimilar effects on EEG within non-REMS and demonstrate that midazolam does not augment but attenuates the muscimol-induced changes in sleep EEG. Our data are at variance with established mechanisms, according to which agonistic modulators would have similar effects and should potentiate the effects of GABAA agonists. The present data suggest that application of agonists and agonistic modulators of GABAA receptors causes differential net effects on sleep parameters.

摘要

研究了γ-氨基丁酸-A(GABAA)受体激动剂与GABAA受体的苯二氮䓬类调节剂对睡眠的相互作用。将低剂量的蝇蕈醇(0.3毫克/千克)和苯二氮䓬类药物咪达唑仑(1.5毫克/千克)单独及联合使用,以随机顺序给予8只大鼠。所有注射均在光照开始时腹腔内给药。在注射后的前6小时记录脑电图(EEG)和肌电图。与赋形剂相比,蝇蕈醇几乎不影响非快速眼动睡眠(非REMS)和快速眼动睡眠(REMS)的时间,但显著增强了非REMS期间2至6赫兹频率范围内的EEG活动。咪达唑仑显著增加了非REMS的时间,降低了<12赫兹频率下的EEG活动,并在此状态下提高了大多数较高频率下的EEG活动。蝇蕈醇和咪达唑仑联合给药对非REMS特异性EEG活动产生了意想不到的影响:其效果介于蝇蕈醇和咪达唑仑之间。这些结果表明,蝇蕈醇和咪达唑仑对非REMS内的EEG有不同影响,并表明咪达唑仑不会增强而是减弱蝇蕈醇诱导的睡眠EEG变化。我们的数据与既定机制不同,根据既定机制,激动性调节剂应具有相似的作用并应增强GABAA激动剂的作用。目前的数据表明,GABAA受体激动剂和激动性调节剂的应用对睡眠参数产生不同的净效应。

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