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四种苯二氮䓬类药物单次及重复给药后在三种小鼠行为模型中的行为效应比较。

Comparison of behavioral effects after single and repeated administrations of four benzodiazepines in three mice behavioral models.

作者信息

Bourin M, Hascoet M, Mansouri B, Colombel M C, Bradwejn J

机构信息

GIS Medicament, Faculty of Medicine, Nantes University, France.

出版信息

J Psychiatry Neurosci. 1992 Jun;17(2):72-7.

Abstract

The behavioral and clinical profiles of various benzodiazepines after acute and chronic treatment are not well defined and may differ. The aim of this study was to evaluate the behavioral profiles of alprazolam, bromazepam, diazepam and lorazepam in mice after single and repeated (every half-life for seven half-lives) administrations using a stimulation-sedation test (actimeter), a myorelaxation test (rotarod), and an anxiolysis test ("four plates"). A dose range from 0.03 to 4 mg/kg was used. A single administration of alprazolam showed stimulating and anxiolytic effects which diminished after repeated administration. Lorezapam's sedative effect diminished but its anxiolytic effect increased upon repeated administration. Except for lorazepam, the myorelaxing effect of all four drugs increased after repeated treatment. These results suggest that the behavioral profile of benzodiazepines may not be identical during acute and chronic treatment. These differences may be present in clinical treatment and warrant investigation in humans.

摘要

各种苯二氮䓬类药物在急性和慢性治疗后的行为和临床特征尚未明确界定,且可能有所不同。本研究的目的是使用刺激-镇静试验(活动计)、肌松试验(转棒试验)和抗焦虑试验(“四板试验”),评估单次和重复给药(每半衰期给药一次,共七个半衰期)后,阿普唑仑、溴西泮、地西泮和劳拉西泮在小鼠中的行为特征。使用的剂量范围为0.03至4mg/kg。单次给予阿普唑仑显示出刺激和抗焦虑作用,重复给药后这些作用减弱。重复给药后,劳拉西泮的镇静作用减弱,但其抗焦虑作用增强。除劳拉西泮外,所有四种药物在重复治疗后的肌松作用均增强。这些结果表明,苯二氮䓬类药物在急性和慢性治疗期间的行为特征可能不相同。这些差异可能存在于临床治疗中,值得在人体中进行研究。

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本文引用的文献

1
A note on a simple apparatus for detecting neurological deficit in rats and mice.
J Am Pharm Assoc Am Pharm Assoc. 1957 Mar;46(3):208-9. doi: 10.1002/jps.3030460322.
2
Tolerance during chronic benzodiazepine treatment associated with decreased receptor binding.
Eur J Pharmacol. 1981 Apr 9;70(4):453-60. doi: 10.1016/0014-2999(81)90356-3.
4
Long-lasting single-dose tolerance to neurologic deficits induced by diazepam.
Psychopharmacology (Berl). 1984;82(3):161-3. doi: 10.1007/BF00427765.
5
Functional tolerance to lorazepam in the rat.
Psychopharmacology (Berl). 1983;81(4):292-4. doi: 10.1007/BF00427565.
8
Rapid development of tolerance to the sedative effects of lorazepam and triazolam in rats.
Psychopharmacology (Berl). 1981;73(3):240-5. doi: 10.1007/BF00422410.
9
[Action of caffeine on the spontaneous motility of the mouse].
Arch Int Pharmacodyn Ther. 1965 Nov;158(1):212-21.

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