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托吡酯的治疗剂量对发育中的大鼠大脑无毒。

Therapeutic doses of topiramate are not toxic to the developing rat brain.

作者信息

Glier Carmen, Dzietko Mark, Bittigau Petra, Jarosz Bozena, Korobowicz Elzbieta, Ikonomidou Chrysanthy

机构信息

Department of Pediatric Neurology, Charite, Virchow Clinics, Humboldt University, 13353 Berlin, Germany.

出版信息

Exp Neurol. 2004 Jun;187(2):403-9. doi: 10.1016/j.expneurol.2004.01.025.

Abstract

Antiepileptic drugs (AEDs) used to treat seizures in pregnant women, infants, and young children may cause cognitive impairment. One of the implicated mechanisms is enhancement of apoptotic neuronal death, which occurs physiologically in the developing brain. We investigated whether topiramate, one of the newer antiepileptic drugs, has neurotoxic properties in the developing rat brain. Topiramate slightly but significantly enhanced apoptotic neuronal death in the 7-day-old rat brain at doses of 50 mg/kg and above. These doses are several folds higher than reported ED(50) doses in infant rodent seizure models that respond to topiramate. Electron microscopy confirmed that dying neurons following topiramate treatment displayed the same morphological features as neurons undergoing physiological cell death during development. When compared to the neurotoxicity profile of phenytoin, valproate, and phenobarbital, the separation between the effective anticonvulsant dose and the neurotoxic dose was greater for topiramate and the neurotoxic effect was lower.

摘要

用于治疗孕妇、婴儿和幼儿癫痫发作的抗癫痫药物(AEDs)可能会导致认知障碍。其中一个相关机制是凋亡性神经元死亡增加,这在发育中的大脑中是生理性发生的。我们研究了新型抗癫痫药物之一托吡酯在发育中的大鼠大脑中是否具有神经毒性。在50mg/kg及以上剂量时,托吡酯可轻微但显著地增加7日龄大鼠大脑中的凋亡性神经元死亡。这些剂量比在对托吡酯有反应的幼鼠癫痫模型中报道的半数有效剂量(ED50)高出几倍。电子显微镜证实,托吡酯治疗后死亡的神经元表现出与发育过程中经历生理性细胞死亡的神经元相同的形态特征。与苯妥英、丙戊酸和苯巴比妥的神经毒性特征相比,托吡酯的有效抗惊厥剂量与神经毒性剂量之间的差距更大,且神经毒性作用更低。

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