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在大鼠经二异丙基氟磷酸急性中毒后,急性给予地西泮或咪达唑仑对其大脑长期神经病理学影响的改变极小。

Acute administration of diazepam or midazolam minimally alters long-term neuropathological effects in the rat brain following acute intoxication with diisopropylfluorophosphate.

作者信息

Supasai Suangsuda, González Eduardo A, Rowland Douglas J, Hobson Brad, Bruun Donald A, Guignet Michelle A, Soares Sergio, Singh Vikrant, Wulff Heike, Saito Naomi, Harvey Danielle J, Lein Pamela J

机构信息

Department of Molecular Biosciences, University of California, Davis, School of Veterinary Medicine, Davis, CA, 95616, USA; Department of Molecular Tropical Medicine and Genetics, Faculty of Tropical Medicine, Mahidol University, Bangkok, 10400, Thailand.

Department of Molecular Biosciences, University of California, Davis, School of Veterinary Medicine, Davis, CA, 95616, USA.

出版信息

Eur J Pharmacol. 2020 Nov 5;886:173538. doi: 10.1016/j.ejphar.2020.173538. Epub 2020 Sep 6.

Abstract

Acute intoxication with organophosphorus cholinesterase inhibitors (OPs) can trigger seizures that rapidly progress to life-threatening status epilepticus. Diazepam, long considered the standard of care for treating OP-induced seizures, is being replaced by midazolam. Whether midazolam is more effective than diazepam in mitigating the persistent effects of acute OP intoxication has not been rigorously evaluated. We compared the efficacy of diazepam vs. midazolam in preventing persistent neuropathology in adult male Sprague-Dawley rats acutely intoxicated with the OP diisopropylfluorophosphate (DFP). Subjects were administered pyridostigmine bromide (0.1 mg/kg, i.p.) 30 min prior to injection with DFP (4 mg/kg, s.c.) or vehicle (saline) followed 1 min later by atropine sulfate (2 mg/kg, i.m.) and pralidoxime (25 mg/kg, i.m.), and 40 min later by diazepam (5 mg/kg, i.p.), midazolam (0.73 mg/kg, i.m.), or vehicle. At 3 and 6 months post-exposure, neurodegeneration, reactive astrogliosis, microglial activation, and oxidative stress were assessed in multiple brain regions using quantitative immunohistochemistry. Brain mineralization was evaluated by in vivo micro-computed tomography (micro-CT). Acute DFP intoxication caused persistent neurodegeneration, neuroinflammation, and brain mineralization. Midazolam transiently mitigated neurodegeneration, and both benzodiazepines partially protected against reactive astrogliosis in a brain region-specific manner. Neither benzodiazepine attenuated microglial activation or brain mineralization. These findings indicate that neither benzodiazepine effectively protects against persistent neuropathological changes, and suggest that midazolam is not significantly better than diazepam. Overall, this study highlights the need for improved neuroprotective strategies for treating humans in the event of a chemical emergency involving OPs.

摘要

有机磷胆碱酯酶抑制剂(OPs)急性中毒可引发癫痫发作,并迅速进展为危及生命的癫痫持续状态。长期以来被视为治疗OP诱发癫痫标准疗法的地西泮,正被咪达唑仑所取代。咪达唑仑在减轻急性OP中毒的持续影响方面是否比地西泮更有效,尚未得到严格评估。我们比较了地西泮和咪达唑仑在预防急性中毒的成年雄性Sprague-Dawley大鼠中由OP二异丙基氟磷酸酯(DFP)引起的持续性神经病理学方面的疗效。在注射DFP(4mg/kg,皮下注射)或赋形剂(生理盐水)前30分钟给实验对象腹腔注射溴化吡啶斯的明(0.1mg/kg),1分钟后肌肉注射硫酸阿托品(2mg/kg)和氯解磷定(25mg/kg),40分钟后腹腔注射地西泮(5mg/kg)、肌肉注射咪达唑仑(0.73mg/kg)或赋形剂。在接触后3个月和6个月,使用定量免疫组织化学方法评估多个脑区的神经退行性变、反应性星形胶质细胞增生、小胶质细胞活化和氧化应激。通过体内微型计算机断层扫描(微型CT)评估脑矿化。急性DFP中毒导致持续性神经退行性变、神经炎症和脑矿化。咪达唑仑可短暂减轻神经退行性变,两种苯二氮䓬类药物均以脑区特异性方式部分预防反应性星形胶质细胞增生。两种苯二氮䓬类药物均未减轻小胶质细胞活化或脑矿化。这些发现表明,两种苯二氮䓬类药物均不能有效预防持续性神经病理变化,提示咪达唑仑并不比地西泮显著更好。总体而言,本研究强调了在涉及OPs的化学紧急情况下,需要改进治疗人类的神经保护策略。

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