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矛盾的发现可能会挑战急性有机磷中毒的正统推理。

Paradox findings may challenge orthodox reasoning in acute organophosphate poisoning.

机构信息

Walther-Straub-Institute of Pharmacology and Toxicology, Ludwig-Maximilians-University, Goethestr. 33, 80336 Munich, Germany.

出版信息

Chem Biol Interact. 2010 Sep 6;187(1-3):270-8. doi: 10.1016/j.cbi.2009.10.014. Epub 2009 Oct 31.

Abstract

It is generally accepted that inhibition of acetylcholinesterase (AChE) is the most important acute toxic action of organophosphorus compounds, leading to accumulation of acetylcholine followed by a dysfunction of cholinergic signaling. However, the degree of AChE inhibition is not uniformly correlated with cholinergic dysfunction, probably because the excess of essential AChE varies among tissues. Moreover, the cholinergic system shows remarkable plasticity, allowing modulations to compensate for dysfunctions of the canonical pathway. A prominent example is the living (-/-) AChE knockout mouse. Clinical experience indicates that precipitous inhibition of AChE leads to more severe poisoning than more protracted yet finally complete inhibition. The former situation is seen in parathion, the latter in oxydemeton methyl poisoning. At first glance, this dichotomy is surprising since parathion is a pro-poison and has to be activated to the oxon, while the latter is still the ultimate inhibitor. Also oxime therapy in organophosphorus poisoning apparently gives perplexing results: Oximes are usually able to reactivate diethylphosphorylated AChE, but the efficiency may be occasionally markedly smaller than expected from kinetic data. Dimethylphosphorylated AChE is in general less amenable to oxime therapy, which largely fails in some cases of dimethoate poisoning where aging was much faster than expected from a dimethylphosphorylated enzyme. Similarly, poisoning by profenofos, an O,S-dialkyl phosphate, leads to a rapidly aged enzyme. Most surprisingly, these patients were usually well on admission, yet their erythrocyte AChE was completely inhibited. Analysis of the kinetic constants of the most important reaction pathways, determination of the reactant concentrations in vivo and comparison with computer simulations may reveal unexpected toxic reactions. Pertinent examples will be presented and the potentially underlying phenomena discussed.

摘要

一般认为,乙酰胆碱酯酶(AChE)的抑制是有机磷化合物最重要的急性毒性作用,导致乙酰胆碱的积累,随后胆碱能信号失灵。然而,AChE 的抑制程度与胆碱能功能障碍并不完全相关,这可能是因为组织中必需的 AChE 过量不同。此外,胆碱能系统表现出显著的可塑性,允许调节来补偿经典途径的功能障碍。一个突出的例子是活(-/-)AChE 基因敲除小鼠。临床经验表明,AChE 的急剧抑制比更持久但最终完全抑制导致更严重的中毒。前一种情况见于对硫磷,后一种情况见于氧乐果中毒。乍一看,这种二分法令人惊讶,因为对硫磷是一种前毒物,必须被激活为氧肟,而后者仍然是最终的抑制剂。有机磷中毒的肟治疗也显然给出了令人困惑的结果:肟通常能够使二乙基膦酰化的 AChE 重新活化,但效率偶尔可能明显小于从动力学数据预期的那样。二甲膦酰化的 AChE 通常不易受肟治疗,在某些情况下二甲氧酯中毒肟治疗基本上失败,其中老化速度明显快于从二甲膦酰化酶预期的速度。同样,敌百虫(一种 O,S-二烷基磷酸酯)中毒会导致酶迅速老化。最令人惊讶的是,这些患者通常在入院时情况良好,但他们的红细胞 AChE 已完全被抑制。对最重要反应途径的动力学常数进行分析、测定体内反应物浓度并与计算机模拟进行比较,可能会揭示出意想不到的毒性反应。将呈现相关的例子,并讨论潜在的现象。

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