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Anticonvulsant effect of clonazepam in the dog: development of tolerance and physical dependence.

作者信息

Scherkl R, Scheuler W, Frey H H

出版信息

Arch Int Pharmacodyn Ther. 1985 Dec;278(2):249-60.

PMID:4096613
Abstract

Dogs were treated with clonazepam, 0.5 mg/kg orally, b.i.d., for 3-6 weeks. The development of tolerance to the anticonvulsant effect was followed by weekly determinations of the convulsive threshold by infusion of pentetrazole, 10 min after i.v. injection of 0.1 mg/kg clonazepam. In all 6 dogs tolerance was apparent after 1-2 weeks of treatment; in 1 dog the anticonvulsant effect had been totally lost after 3 weeks of treatment. Tolerance is regarded to be "functional" since the elimination half-life of clonazepam increased considerably with the duration of the treatment. One day after withdrawal of clonazepam the convulsive threshold had fallen below the control value in all dogs, but 1 week later it had recovered to the control level. Other signs of physical dependence after withdrawal were hyperthermia in 2 dogs as well as anorexia with weight loss in 5 out of the 6 dogs. In anesthetized dogs, relaxed by suxamethonium and ventilated, the effect of repeated injections of clonazepam on the EEG spiking activity maintained by an infusion of pentetrazole was studied; there was no indication for the development of acute tolerance.

摘要

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Abecarnil, a beta-carboline derivative, does not exhibit anticonvulsant tolerance or withdrawal effects in mice.阿贝卡尼,一种β-咔啉衍生物,在小鼠中不表现出抗惊厥耐受性或戒断效应。
Naunyn Schmiedebergs Arch Pharmacol. 1996 Nov;354(5):612-7. doi: 10.1007/BF00170836.
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Changes in benzodiazepine/GABA receptor complex function in benzodiazepine-tolerant mice.苯二氮䓬耐受小鼠中苯二氮䓬/GABA受体复合物功能的变化。
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Chronic benzodiazepine administration. VII. Behavioral tolerance and withdrawal and receptor alterations associated with clonazepam administration.
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