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乌头碱治疗对大鼠有机磷中毒癫痫持续状态模型的有益影响。

Beneficial Outcome of Urethane Treatment Following Status Epilepticus in a Rat Organophosphorus Toxicity Model.

机构信息

Department of Pharmacology, Emory University, Atlanta, GA 30322.

出版信息

eNeuro. 2018 Apr 17;5(2). doi: 10.1523/ENEURO.0070-18.2018. eCollection 2018 Mar-Apr.

DOI:10.1523/ENEURO.0070-18.2018
PMID:29766039
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5952304/
Abstract

The efficacy of benzodiazepines to terminate electrographic status epilepticus (SE) declines the longer a patient is in SE. Therefore, alternative methods for ensuring complete block of SE and refractory SE are necessary. We compared the ability of diazepam and a subanesthetic dose of urethane to terminate prolonged SE and mitigate subsequent pathologies. Adult Sprague Dawley rats were injected with diisopropylfluorophosphate (DFP) to induce SE. Rats were administered diazepam (10 mg/kg, ip) or urethane (0.8 g/kg, s.c.) 1 h after DFP-induced SE and compared to rats that experienced uninterrupted SE. Large-amplitude and high-frequency spikes induced by DFP administration were quenched for at least 46 h in rats administered urethane 1 h after SE onset as demonstrated by cortical electroencephalography (EEG). By contrast, diazepam interrupted SE but seizures with high power in the 20- to 70-Hz band returned 6-10 h later. Urethane was more effective than diazepam at reducing hippocampal neurodegeneration, brain inflammation, gliosis and weight loss as measured on day 4 after SE. Furthermore, rats administered urethane displayed a 73% reduction in the incidence of spontaneous recurrent seizures after four to eight weeks and a 90% reduction in frequency of seizures in epileptic rats. By contrast, behavioral changes in the light/dark box, open field and a novel object recognition task were not improved by urethane. These findings indicate that in typical rodent SE models, it is the return of SE overnight, and not the initially intense 1-2 h of SE experience, that is largely responsible for neurodegeneration, accompanying inflammation, and the subsequent development of epilepsy.

摘要

苯二氮䓬类药物终止癫痫持续状态(SE)的疗效随着患者处于 SE 状态的时间延长而下降。因此,需要寻找其他方法来确保完全阻断 SE 和难治性 SE。我们比较了地西泮和亚麻醉剂量的尿烷在终止延长 SE 和减轻随后的病理方面的能力。成年 Sprague Dawley 大鼠用二异丙基氟膦(DFP)注射诱导 SE。大鼠在 DFP 诱导 SE 后 1 小时给予地西泮(10 mg/kg,ip)或尿烷(0.8 g/kg,sc),并与未接受不间断 SE 的大鼠进行比较。皮质脑电图(EEG)显示,DFP 给药后诱导的大振幅和高频尖峰在 SE 发作后 1 小时给予尿烷的大鼠中至少被抑制了 46 小时。相比之下,地西泮中断了 SE,但在 20-70 Hz 频段具有高功率的癫痫发作在 6-10 小时后再次出现。尿烷在减少海马神经退行性变、脑炎症、神经胶质增生和 SE 后第 4 天的体重减轻方面比地西泮更有效。此外,给予尿烷的大鼠在 4 至 8 周后自发性复发性癫痫发作的发生率降低了 73%,癫痫大鼠的癫痫发作频率降低了 90%。相比之下,在光暗箱、开阔场和新物体识别任务中的行为变化并没有因尿烷而改善。这些发现表明,在典型的啮齿动物 SE 模型中,导致神经退行性变、伴随炎症以及随后发生癫痫的主要原因是 SE 在夜间的复发,而不是最初强烈的 1-2 小时 SE 经历。

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2
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Ann Neurol. 2016 Dec;80(6):896-908. doi: 10.1002/ana.24804.
3
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Epilepsia. 2025 Apr;66(4):1329-1342. doi: 10.1111/epi.18212. Epub 2025 Feb 11.
4
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5
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4
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5
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6
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7
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8
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