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咖啡因对托吡酯、拉莫三嗪和噻加宾抗小鼠全面性强直-阵挛发作作用的影响。

Effect of caffeine on the anticonvulsant effects of oxcarbazepine, lamotrigine and tiagabine in a mouse model of generalized tonic-clonic seizures.

机构信息

Department of Pathophysiology, Medical University of Lublin, Jaczewskiego 8, PL 20-090 Lublin, Poland.

出版信息

Pharmacol Rep. 2009 Sep-Oct;61(5):819-26. doi: 10.1016/s1734-1140(09)70137-9.

Abstract

Caffeine has been reported to be proconvulsant and to reduce the anticonvulsant efficacy of a variety of antiepileptic drugs (carbamazepine, phenobarbital, phenytoin, valproate and topiramate) in animal models of epilepsy and to increase seizure frequency in patients with epilepsy. Using the mouse maximal electroshock model, the present study was undertaken so as to ascertain whether caffeine affects the anticonvulsant efficacy of the new antiepileptic drugs lamotrigine, oxcarbazepine and tiagabine. The results indicate that neither acute nor chronic caffeine administration (up to 46.2 mg/kg) affected the ED(50) values of oxcarbazepine or lamotrigine against maximal electroshock. Similarly, caffeine did not modify the tiagabine electroconvulsive threshold. Furthermore, caffeine had no effect on oxcarbazepine, lamotrigine and tiagabine associated adverse effects such as impairment of motor coordination (measured by the chimney test) or long-term memory (measured by the passive avoidance task). Concurrent plasma concentration measurements revealed no significant effect on lamotrigine and oxcarbazepine concentrations. For tiagabine, however, chronic caffeine (4 mg/kg) administration was associated with an increase in tiagabine concentrations. In conclusion, caffeine did not impair the anticonvulsant effects of lamotrigine, oxcarbazepine, or tiagabine as assessed by electroconvulsions in mice. Also, caffeine was without effect upon the adverse potential of the studied antiepileptic drugs. Thus caffeine may not necessarily adversely affect the efficacy of all antiepileptic drugs and this is an important observation.

摘要

咖啡因已被报道具有致惊厥作用,并降低多种抗癫痫药物(卡马西平、苯巴比妥、苯妥英、丙戊酸钠和托吡酯)在癫痫动物模型中的抗惊厥作用,并增加癫痫患者的癫痫发作频率。本研究采用小鼠最大电休克模型,以确定咖啡因是否影响新型抗癫痫药物拉莫三嗪、奥卡西平和噻加宾的抗惊厥作用。结果表明,急性或慢性咖啡因给药(高达 46.2mg/kg)均不影响奥卡西平和拉莫三嗪对最大电休克的 ED50 值。同样,咖啡因也不改变噻加宾的电惊厥阈值。此外,咖啡因对奥卡西平、拉莫三嗪和噻加宾相关的不良反应(如运动协调能力受损(通过烟囱测试测量)或长期记忆(通过被动回避任务测量))没有影响。同时进行的血浆浓度测量显示,对拉莫三嗪和奥卡西平浓度没有显著影响。然而,对于噻加宾,慢性咖啡因(4mg/kg)给药与噻加宾浓度增加有关。总之,咖啡因并未通过小鼠电惊厥评估降低拉莫三嗪、奥卡西平和噻加宾的抗惊厥作用。此外,咖啡因对研究中的抗癫痫药物的不良潜在影响没有影响。因此,咖啡因不一定会对所有抗癫痫药物的疗效产生不利影响,这是一个重要的观察结果。

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