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用别孕烯醇酮和吡仑帕奈作为咪达唑仑的辅助药物治疗大鼠二异丙基氟磷酸酯诱导的癫痫持续状态。

Allopregnanolone and perampanel as adjuncts to midazolam for treating diisopropylfluorophosphate-induced status epilepticus in rats.

机构信息

Department of Neurology, School of Medicine, University of California, Davis, Sacramento, California.

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

出版信息

Ann N Y Acad Sci. 2020 Nov;1480(1):183-206. doi: 10.1111/nyas.14479. Epub 2020 Sep 11.

Abstract

Combinations of midazolam, allopregnanolone, and perampanel were assessed for antiseizure activity in a rat diisopropylfluorophosphate (DFP) status epilepticus model. Animals receiving DFP followed by atropine and pralidoxime exhibited continuous high-amplitude rhythmical electroencephalography (EEG) spike activity and behavioral seizures for more than 5 hours. Treatments were administered intramuscularly 40 min after DFP. Seizures persisted following midazolam (1.8 mg/kg). The combination of midazolam with either allopregnanolone (6 mg/kg) or perampanel (2 mg/kg) terminated EEG and behavioral status epilepticus, but the onset of the perampanel effect was slow. The combination of midazolam, allopregnanolone, and perampanel caused rapid and complete suppression of EEG and behavioral seizures. In the absence of DFP, animals treated with the three-drug combination were sedated but not anesthetized. Animals that received midazolam alone exhibited spontaneous recurrent EEG seizures, whereas those that received the three-drug combination did not, demonstrating antiepileptogenic activity. All combination treatments reduced neurodegeneration as assessed with Fluoro-Jade C staining to a greater extent than midazolam alone, and most reduced astrogliosis as assessed by GFAP immunoreactivity but had mixed effects on markers of microglial activation. We conclude that allopregnanolone, a positive modulator of the GABA receptor, and perampanel, an AMPA receptor antagonist, are potential adjuncts to midazolam in the treatment of benzodiazepine-refractory organophosphate nerve agent-induced status epilepticus.

摘要

咪达唑仑、别孕烯醇酮和吡仑帕奈联合应用于大鼠二异丙基氟磷酸酯(DFP)癫痫持续状态模型中,评估其抗惊厥活性。动物接受 DFP 后,给予阿托品和氯解磷定,表现出持续超过 5 小时的高振幅节律性脑电图(EEG)棘波活动和行为性癫痫发作。治疗在 DFP 后 40 分钟肌肉注射给药。咪达唑仑(1.8mg/kg)治疗后癫痫持续存在。咪达唑仑与别孕烯醇酮(6mg/kg)或吡仑帕奈(2mg/kg)联合应用可终止 EEG 和行为性癫痫持续状态,但吡仑帕奈的作用起效较慢。咪达唑仑、别孕烯醇酮和吡仑帕奈联合应用可迅速完全抑制 EEG 和行为性癫痫发作。在没有 DFP 的情况下,用三药联合治疗的动物表现出镇静但未麻醉。单独给予咪达唑仑的动物表现出自发复发性 EEG 癫痫发作,而给予三药联合治疗的动物则没有,表明具有抗癫痫发生作用。所有联合治疗均较单独给予咪达唑仑更显著地减少氟烷-Jade C 染色评估的神经退行性变,并且大多数治疗还减少了 GFAP 免疫反应性评估的星形胶质细胞增生,但对微胶质细胞激活标志物的影响则不同。我们得出结论,别孕烯醇酮,GABA 受体的正变构调节剂,以及吡仑帕奈,AMPA 受体拮抗剂,可能是咪达唑仑治疗苯二氮䓬类药物难治性有机磷神经毒剂诱导的癫痫持续状态的潜在辅助药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cc3/7756871/ce2e0269794c/NYAS-1480-183-g001.jpg

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