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针对有机磷杀虫剂和神经毒剂中毒的有效对策。

Effective countermeasure against poisoning by organophosphorus insecticides and nerve agents.

作者信息

Albuquerque Edson X, Pereira Edna F R, Aracava Yasco, Fawcett William P, Oliveira Maristela, Randall William R, Hamilton Tracey A, Kan Robert K, Romano James A, Adler Michael

机构信息

Department of Pharmacology and Experimental Therapeutics, University of Maryland School of Medicine, 655 West Baltimore Street, Baltimore, 21201, USA.

出版信息

Proc Natl Acad Sci U S A. 2006 Aug 29;103(35):13220-5. doi: 10.1073/pnas.0605370103. Epub 2006 Aug 16.

Abstract

The nerve agents soman, sarin, VX, and tabun are deadly organophosphorus (OP) compounds chemically related to OP insecticides. Most of their acute toxicity results from the irreversible inhibition of acetylcholinesterase (AChE), the enzyme that inactivates the neurotransmitter acetylcholine. The limitations of available therapies against OP poisoning are well recognized, and more effective antidotes are needed. Here, we demonstrate that galantamine, a reversible and centrally acting AChE inhibitor approved for treatment of mild to moderate Alzheimer's disease, protects guinea pigs from the acute toxicity of lethal doses of the nerve agents soman and sarin, and of paraoxon, the active metabolite of the insecticide parathion. In combination with atropine, a single dose of galantamine administered before or soon after acute exposure to lethal doses of soman, sarin, or paraoxon effectively and safely counteracted their toxicity. Doses of galantamine needed to protect guinea pigs fully against the lethality of OPs were well tolerated. In preventing the lethality of nerve agents, galantamine was far more effective than pyridostigmine, a peripherally acting AChE inhibitor, and it was less toxic than huperzine, a centrally acting AChE inhibitor. Thus, a galantamine-based therapy emerges as an effective and safe countermeasure against OP poisoning.

摘要

神经性毒剂梭曼、沙林、VX和塔崩是与有机磷杀虫剂有化学关联的致命有机磷化合物。它们的大部分急性毒性源于对乙酰胆碱酯酶(AChE)的不可逆抑制,该酶可使神经递质乙酰胆碱失活。现有针对有机磷中毒的治疗方法存在局限性,这已得到广泛认可,因此需要更有效的解毒剂。在此,我们证明加兰他敏(一种已获批准用于治疗轻至中度阿尔茨海默病的可逆性中枢作用乙酰胆碱酯酶抑制剂)可保护豚鼠免受致死剂量的神经性毒剂梭曼和沙林以及杀虫剂对硫磷的活性代谢产物对氧磷的急性毒性影响。与阿托品联合使用时,在急性暴露于致死剂量的梭曼、沙林或对氧磷之前或之后不久给予单剂量的加兰他敏可有效且安全地对抗它们的毒性。保护豚鼠完全免受有机磷致死作用所需的加兰他敏剂量耐受性良好。在预防神经性毒剂的致死作用方面,加兰他敏比外周作用的乙酰胆碱酯酶抑制剂吡啶斯的明有效得多,且比中枢作用的乙酰胆碱酯酶抑制剂石杉碱毒性更低。因此,基于加兰他敏的疗法成为一种有效且安全的对抗有机磷中毒的对策。

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