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苯巴比妥和咪达唑仑可抑制新生鼠窒息模型的癫痫发作,而布美他尼无效。

Phenobarbital and midazolam suppress neonatal seizures in a noninvasive rat model of birth asphyxia, whereas bumetanide is ineffective.

机构信息

Department of Pharmacology, Toxicology, and Pharmacy, University of Veterinary Medicine, Hannover, Germany.

Center for Systems Neuroscience, Hannover, Germany.

出版信息

Epilepsia. 2021 Apr;62(4):920-934. doi: 10.1111/epi.16778. Epub 2020 Dec 1.

Abstract

OBJECTIVE

Neonatal seizures are the most frequent type of neurological emergency in newborn infants, often being a consequence of prolonged perinatal asphyxia. Phenobarbital is currently the most widely used antiseizure drug for treatment of neonatal seizures, but fails to stop them in ~50% of cases. In a neonatal hypoxia-only model based on 11-day-old (P11) rats, the NKCC1 inhibitor bumetanide was reported to potentiate the antiseizure activity of phenobarbital, whereas it was ineffective in a human trial in neonates. The aim of this study was to evaluate the effect of clinically relevant doses of bumetanide as add-on to phenobarbital on neonatal seizures in a noninvasive model of birth asphyxia in P11 rats, designed for better translation to the human term neonate.

METHODS

Intermittent asphyxia was induced for 30 minutes by exposing the rat pups to three 7 + 3-minute cycles of 9% and 5% O at constant 20% CO . Drug treatments were administered intraperitoneally either before or immediately after asphyxia.

RESULTS

All untreated rat pups had seizures within 10 minutes after termination of asphyxia. Phenobarbital significantly blocked seizures when applied before asphyxia at 30 mg/kg but not 15 mg/kg. Administration of phenobarbital after asphyxia was ineffective, whereas midazolam (0.3 or 1 mg/kg) exerted significant antiseizure effects when administered before or after asphyxia. In general, focal seizures were more resistant to treatment than generalized convulsive seizures. Bumetanide (0.3 mg/kg) alone or in combination with phenobarbital (15 or 30 mg/kg) exerted no significant effect on seizure occurrence.

SIGNIFICANCE

The data demonstrate that bumetanide does not increase the efficacy of phenobarbital in a model of birth asphyxia, which is consistent with the negative data of the recent human trial. The translational data obtained with the novel rat model of birth asphyxia indicate that it is a useful tool to evaluate novel treatments for neonatal seizures.

摘要

目的

新生儿癫痫是新生儿最常见的神经急症类型,通常是围产期窒息时间延长的结果。苯巴比妥目前是治疗新生儿癫痫最广泛使用的抗癫痫药物,但在约 50%的情况下无法阻止癫痫发作。在基于 11 日龄(P11)大鼠的单纯新生儿缺氧模型中,报道 NKCC1 抑制剂布美他尼增强苯巴比妥的抗癫痫作用,而在新生儿的人类试验中则无效。本研究旨在评估布美他尼的临床相关剂量作为苯巴比妥的附加治疗对 P11 大鼠出生窒息非侵入性模型中新生儿癫痫的影响,该模型设计用于更好地转化为人类足月新生儿。

方法

通过将大鼠幼仔暴露于三个 7+3 分钟的 9%和 5%O 循环中,以恒定的 20%CO 进行 30 分钟间歇性窒息。药物治疗在窒息前或窒息后立即通过腹腔内给药。

结果

所有未治疗的大鼠幼仔在窒息结束后 10 分钟内均出现癫痫发作。苯巴比妥在窒息前以 30mg/kg 给药时可显著阻断癫痫发作,但以 15mg/kg 给药时则无效。窒息后给予苯巴比妥无效,而咪达唑仑(0.3 或 1mg/kg)在窒息前或后给药时均具有显著的抗癫痫作用。一般来说,局灶性癫痫发作比全身性惊厥性癫痫发作更难以治疗。布美他尼(0.3mg/kg)单独或与苯巴比妥(15 或 30mg/kg)联合使用对癫痫发作的发生没有显著影响。

意义

这些数据表明,布美他尼在出生窒息模型中不会增加苯巴比妥的疗效,这与最近人类试验的阴性数据一致。使用新型出生窒息大鼠模型获得的转化数据表明,它是评估新生儿癫痫新治疗方法的有用工具。

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