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小鼠对苯二氮䓬的交叉耐受性扩展至丙戊酸钠。

Benzodiazepine cross-tolerance in mice extends to sodium valproate.

作者信息

Gent J P, Bentley M, Feely M, Haigh J R

出版信息

Eur J Pharmacol. 1986 Aug 22;128(1-2):9-15. doi: 10.1016/0014-2999(86)90551-0.

DOI:10.1016/0014-2999(86)90551-0
PMID:3093253
Abstract

Slow intravenous infusion of pentylenetetrazol was used to measure the convulsive threshold in mice. The anticonvulsant effects of clobazam, clonazepam, diazepam, lorazepam, sodium phenobarbitone and sodium valproate were assessed in naive animals and compared with the effects of the same compounds in animals which had been pretreated (twice daily for 3 days) with one of the benzodiazepines or sodium valproate. Cross-tolerance was observed between all the benzodiazepines but not between benzodiazepines and sodium phenobarbitone. Animals pretreated with the benzodiazepines were cross-tolerant to valproate, but the converse was not true; nor did sodium valproate induce tolerance to itself.

摘要

采用戊四氮缓慢静脉注射法测定小鼠惊厥阈值。在未用药的动物中评估氯巴占、氯硝西泮、地西泮、劳拉西泮、苯巴比妥钠和丙戊酸钠的抗惊厥作用,并与用其中一种苯二氮䓬类药物或丙戊酸钠预处理(每日两次,共3天)的动物中相同化合物的作用进行比较。所有苯二氮䓬类药物之间均观察到交叉耐受性,但苯二氮䓬类药物与苯巴比妥钠之间未观察到交叉耐受性。用苯二氮䓬类药物预处理的动物对丙戊酸有交叉耐受性,但反之则不然;丙戊酸钠也不会诱导自身耐受性。

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Benzodiazepine cross-tolerance in mice extends to sodium valproate.小鼠对苯二氮䓬的交叉耐受性扩展至丙戊酸钠。
Eur J Pharmacol. 1986 Aug 22;128(1-2):9-15. doi: 10.1016/0014-2999(86)90551-0.
2
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Long-term studies on anticonvulsant tolerance and withdrawal characteristics of benzodiazepine receptor ligands in different seizure models in mice. I. Comparison of diazepam, clonazepam, clobazam and abecarnil.小鼠不同癫痫模型中苯二氮䓬受体配体的抗惊厥耐受性和撤药特性的长期研究。I. 地西泮、氯硝西泮、氯巴占和阿贝卡尼的比较。
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Tolerance to anticonvulsant effects of diazepam, clonazepam, and clobazam in amygdala-kindled rats.杏仁核点燃大鼠对安定、氯硝西泮和氯巴占抗惊厥作用的耐受性。
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Differences in the development of tolerance to two anticonvulsant benzodiazepines in the amygdaloid kindled rat.
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引用本文的文献

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Deconstructing tolerance with clobazam: Post hoc analyses from an open-label extension study.用氯巴占解构耐受性:一项开放标签扩展研究的事后分析
Neurology. 2016 Oct 25;87(17):1806-1812. doi: 10.1212/WNL.0000000000003253. Epub 2016 Sep 28.
2
Basic pharmacology of valproate: a review after 35 years of clinical use for the treatment of epilepsy.丙戊酸盐的基础药理学:用于癫痫治疗35年临床应用后的综述
CNS Drugs. 2002;16(10):669-94. doi: 10.2165/00023210-200216100-00003.
3
Effects of the antiepileptic drug valproate on metabolism and function of inhibitory and excitatory amino acids in the brain.
抗癫痫药物丙戊酸盐对大脑中抑制性和兴奋性氨基酸代谢及功能的影响。
Neurochem Res. 1993 Apr;18(4):485-502. doi: 10.1007/BF00967253.
4
Tolerance, cross-tolerance and dependence measured by operant responding in rats treated with triazolam via osmotic pumps.通过渗透泵给大鼠注射三唑仑后,用操作性反应测量耐受性、交叉耐受性和依赖性。
Psychopharmacology (Berl). 1994 Jun;115(1-2):86-94. doi: 10.1007/BF02244756.
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Proceedings of the British Pharmacological Society. Leeds, 12th-14th July 1989. Abstracts.英国药理学会会议记录。利兹,1989年7月12日至14日。摘要
Br J Pharmacol. 1989 Oct;98 Suppl(Suppl):606P-773P.
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Convulsive thresholds in mice during the recovery phase from anaesthesia induced by propofol, thiopentone, methohexitone and etomidate.小鼠在丙泊酚、硫喷妥钠、甲己炔巴比妥和依托咪酯诱导的麻醉恢复阶段的惊厥阈值。
Br J Pharmacol. 1991 Apr;102(4):879-82. doi: 10.1111/j.1476-5381.1991.tb12270.x.