• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

苯妥英钠和苯巴比妥预防小鼠茶碱诱发癫痫发作的相对疗效

Relative efficacy of phenytoin and phenobarbital for the prevention of theophylline-induced seizures in mice.

作者信息

Blake K V, Massey K L, Hendeles L, Nickerson D, Neims A

机构信息

Department of Pediatrics, College of Medicine, University of Florida, Gainesville 32610.

出版信息

Ann Emerg Med. 1988 Oct;17(10):1024-8. doi: 10.1016/s0196-0644(88)80439-6.

DOI:10.1016/s0196-0644(88)80439-6
PMID:3177989
Abstract

We evaluated the efficacy of pretreatment with phenytoin and phenobarbital to prevent seizures in mice given convulsive doses of theophylline. The control LD50 for theophylline was determined in 48 mice by intraperitoneal injections of increasing doses without anticonvulsant treatment. Anticonvulsant effects were determined in 105 additional mice pretreated with either phenytoin 30 mg/kg (n = 35), phenobarbital 35 mg/kg (n = 30), or phenobarbital 60 mg/kg (n = 40) one hour before theophylline administration. The theophylline LD50 (95% confidence interval) was 239 mg/kg (range, 229 to 248 mg/kg) for controls, 204 mg/kg (range, 194 to 214 mg/kg) for phenytoin, 305 mg/kg (range, 288 to 323 mg/kg) for low-dose phenobarbital, and 319 mg/kg (range, 307 to 331 mg/kg) for high-dose phenobarbital. Each LD50 differed significantly from control (P less than .05). The phenobarbital groups were significantly different from phenytoin (P less than .05) but not from each other. Theophylline serum concentrations were not significantly different among groups after adjustment for different doses. The mean +/- SEM time to seizure in minutes after adjustment for theophylline dose was 23.5 +/- 4.0 minutes for controls, 5.7 +/- 7.5 minutes for phenytoin, 44.1 +/- 7.1 minutes for low-dose phenobarbital, and 63.7 +/- 6.5 minutes for high-dose phenobarbital.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们评估了苯妥英钠和苯巴比妥预处理对给予惊厥剂量氨茶碱的小鼠预防癫痫发作的效果。通过腹腔注射递增剂量且不进行抗惊厥治疗,在48只小鼠中测定了氨茶碱的对照半数致死量(LD50)。在另外105只小鼠中,于给予氨茶碱前1小时分别用30 mg/kg苯妥英钠(n = 35)、35 mg/kg苯巴比妥(n = 30)或60 mg/kg苯巴比妥(n = 40)进行预处理,以确定抗惊厥效果。对照的氨茶碱LD50(95%置信区间)为239 mg/kg(范围229至248 mg/kg),苯妥英钠组为204 mg/kg(范围194至214 mg/kg),低剂量苯巴比妥组为305 mg/kg(范围288至323 mg/kg),高剂量苯巴比妥组为319 mg/kg(范围307至331 mg/kg)。各LD50与对照均有显著差异(P小于0.05)。苯巴比妥组与苯妥英钠组有显著差异(P小于0.05),但两组之间无显著差异。调整不同剂量后,各组间氨茶碱血清浓度无显著差异。调整氨茶碱剂量后,以分钟计的平均惊厥发作时间(均值±标准误),对照组为23.5±4.0分钟,苯妥英钠组为5.7±7.5分钟,低剂量苯巴比妥组为44.1±7.1分钟,高剂量苯巴比妥组为63.7±6.5分钟。(摘要截断于250字)

相似文献

1
Relative efficacy of phenytoin and phenobarbital for the prevention of theophylline-induced seizures in mice.苯妥英钠和苯巴比妥预防小鼠茶碱诱发癫痫发作的相对疗效
Ann Emerg Med. 1988 Oct;17(10):1024-8. doi: 10.1016/s0196-0644(88)80439-6.
2
Phenobarbital improves survival in theophylline-intoxicated rabbits.
J Toxicol Clin Toxicol. 1986;24(3):203-11. doi: 10.3109/15563658608990458.
3
A comparative study of the effects of phenytoin and phenobarbital on electrically induced maximal seizures in frogs and mice.
J Pharmacol Exp Ther. 1982 Apr;221(1):132-8.
4
Effects of three N-(carboxyanilinomethyl) derivatives of p-isopropoxyphenylsuccinimide on the anticonvulsant action of carbamazepine, phenobarbital, phenytoin and valproate in the mouse maximal electroshock-induced seizure model.三种 N-(对异丙氧基苯甲酰基)琥珀酰亚胺的衍生物对卡马西平、苯巴比妥、苯妥英和丙戊酸钠在小鼠最大电休克惊厥模型中抗惊厥作用的影响。
Eur J Pharmacol. 2010 Dec 1;648(1-3):74-9. doi: 10.1016/j.ejphar.2010.08.017. Epub 2010 Sep 6.
5
Adenosine receptors are not involved in theophylline-induced seizures.
J Toxicol Clin Toxicol. 1994;32(3):257-65. doi: 10.3109/15563659409017958.
6
2-phosphonomethyl-pentanedioic acid (glutamate carboxypeptidase II inhibitor) increases threshold for electroconvulsions and enhances the antiseizure action of valproate against maximal electroshock-induced seizures in mice.2-膦酰甲基-戊二酸(谷氨酸羧肽酶II抑制剂)可提高小鼠电惊厥阈值,并增强丙戊酸盐对最大电休克诱导惊厥的抗惊厥作用。
Eur J Pharmacol. 2006 Feb 15;531(1-3):66-73. doi: 10.1016/j.ejphar.2005.11.045. Epub 2006 Jan 3.
7
Evidence for a synergistic interaction between phenytoin and phenobarbital in experimental animals.
J Pharmacol Exp Ther. 1981 Jun;217(3):805-11.
8
Anticonvulsant activity of phenobarbital and phenytoin in combination.
J Pharmacol Exp Ther. 1977 Mar;200(3):570-5.
9
Kinetics of drug action in disease states. XXXVII. Effects of acute fluid overload and water deprivation on the hypnotic activity of phenobarbital and the neurotoxicity of theophylline in rats.疾病状态下药物作用的动力学。三十七。急性液体超负荷和缺水对大鼠苯巴比妥催眠活性及茶碱神经毒性的影响。
J Pharmacol Exp Ther. 1989 Dec;251(3):827-32.
10
Imperatorin enhances the protective activity of conventional antiepileptic drugs against maximal electroshock-induced seizures in mice.欧前胡素增强传统抗癫痫药物对小鼠最大电休克诱导癫痫发作的保护作用。
Eur J Pharmacol. 2007 Nov 28;574(2-3):133-9. doi: 10.1016/j.ejphar.2007.07.008. Epub 2007 Jul 13.

引用本文的文献

1
Theophylline reverses oxycodone's but not fentanyl's respiratory depression in mice while caffeine is ineffective against both opioids.茶碱可逆转小鼠体内羟考酮的呼吸抑制作用,但对芬太尼无效,而咖啡因对这两种阿片类药物均无效。
Pharmacol Biochem Behav. 2023 Aug;229:173601. doi: 10.1016/j.pbb.2023.173601. Epub 2023 Jul 4.
2
Treatment of drug-induced seizures.药物性癫痫发作的治疗。
Br J Clin Pharmacol. 2016 Mar;81(3):412-9. doi: 10.1111/bcp.12720. Epub 2015 Sep 17.
3
Comparative behavioral and neurochemical analysis of phenytoin and valproate treatment on epilepsy induced learning and memory deficit: Search for add on therapy.
苯妥英钠和丙戊酸盐治疗癫痫所致学习和记忆缺陷的比较行为学与神经化学分析:寻找辅助治疗方法。
Metab Brain Dis. 2015 Aug;30(4):951-8. doi: 10.1007/s11011-015-9650-8. Epub 2015 Jan 23.
4
Riboswitches for intracellular study of genes involved in Francisella pathogenesis.用于研究弗朗西斯菌发病机制相关基因的细胞内研究的核糖开关。
mBio. 2012 Nov 20;3(6):e00253-12. doi: 10.1128/mBio.00253-12.
5
Caffeine toxicity in a bodybuilder.一名健美运动员的咖啡因中毒
J Accid Emerg Med. 1998 May;15(3):196-7. doi: 10.1136/emj.15.3.196.