首页> 外文期刊>Archives of Toxicology >Nerve agent poisoning in primates: antilethal, anti-epileptic and neuroprotective effects of GK-11.
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Nerve agent poisoning in primates: antilethal, anti-epileptic and neuroprotective effects of GK-11.

机译:灵长类动物的神经药中毒:GK-11的抗致死,抗癫痫和神经保护作用。

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Organophosphorus nerve agents are still in use today in warfare and as terrorism compounds. Classical emergency treatment of organophosphate poisoning includes the combined administration of a cholinesterase reactivator (an oxime), a muscarinic cholinergic receptor antagonist (atropine) and a benzodiazepine anticonvulsant (diazepam). However, recent experiments with primates have demonstrated that such treatment, even when administered immediately after organophosphate exposure, does not rapidly restore normal electroencephalographic (EEG) activity and fails to totally prevent neuronal brain damage. The objective of this study was to evaluate, in a realistic setting, the therapeutic benefit of administration of GK-11 (gacyclidine), an antiglutamatergic compound, as a complement to the available emergency therapy against organophosphate poisoning. GK-11 was injected at a dose of 0.1 mg/kg (i.v) after a 45-min latency period to heavily intoxicated (8 LD50) primates. Just after intoxication, man-equivalent doses of one autoinjector containing atropine/pralidoxime/diazepam were administered. The effects of GK-11 were examined on survival, EEG activity, signs of toxicity, recovery after challenge and central nervous system histology. The present data demonstrate that treatment with GK-11 prevents the mortality observed after early administration of classical emergency medication alone. EEG recordings and clinical observations also revealed that GK-11 prevented soman-induced seizures and motor convulsions. EEG analysis within the classical frequency bands (beta, theta, alpha, delta) demonstrated that central activity was totally restored to normal after GK-11 treatment, but remained profoundly altered in animals receiving atropine/pralidoxime/diazepam alone. GK-11 also markedly accelerated clinical recovery of soman-challenged primates. Lastly, this drug totally prevented the neuropathology observed 3 weeks after soman exposure in animals treated with classical emergency treatment alone. GK-11 represents a promising adjuvant therapy to the currently available emergency polymedication to ensure optimal management of organophosphate poisoning in man. This drug is presently being evaluated in a human clinical trial for a different neuroprotective indication.
机译:今天,有机磷神经毒剂仍在战争中和作为恐怖主义化合物使用。有机磷酸盐中毒的经典紧急治疗方法包括联合施用胆碱酯酶活化剂(肟),毒蕈碱胆碱能受体拮抗剂(阿托品)和苯二氮卓类抗惊厥药(地西p)。但是,最近关于灵长类动物的实验表明,即使在有机磷酸酯暴露后立即施用,这种治疗也不能迅速恢复正常的脑电图(EEG)活性,并且不能完全防止神经元脑损伤。这项研究的目的是在现实的环境中评估抗谷氨酸能化合物GK-11(加环利定)的治疗效果,作为对有机磷中毒的应急治疗的补充。在45分钟潜伏期后,以0.1 mg / kg(i.v)的剂量向严重中毒(8 LD50)的灵长类动物注射GK-11。在中毒后,立即给予相当于人剂量的一种含有阿托品/吡咯肟/地西p的自动注射器。检查了GK-11对存活率,EEG活性,毒性迹象,激发后恢复和中枢神经系统组织学的影响。目前的数据表明,用GK-11进行的治疗可防止仅在早期施用经典急诊药物后观察到的死亡率。脑电图记录和临床观察结果还表明,GK-11可以防止梭曼诱发的癫痫发作和运动性抽搐。在经典频带(β,θ,α,δ)内的脑电图分析表明,在GK-11治疗后,中枢活性完全恢复正常,但在单独接受阿托品/普利多肟/地西ze的动物中,其中枢活动仍发生了深远的变化。 GK-11还显着加速了人类挑战性灵长类动物的临床康复。最后,在单独接受经典紧急治疗的动物中,在梭曼接触三周后,该药物完全预防了神经病理。 GK-11代表了对目前可用的紧急多药治疗的有希望的辅助疗法,以确保对人体有机磷酸盐中毒的最佳管理。目前,该药物正在人类临床试验中评估其不同的神经保护适应症。

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