The influence of inhibitors and other factors on cholinesterases.

J Bajgar
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Abstract

Literature survey dealing with cholinesterases and effects of highly toxic organophosphorus compounds suitable for use as chemical weapons is given in introductory part of this work. There are nerve paralytical agents (NPA)--sarin, soman, VX and a model compound O-ethyl-S-(2-dimethylaminoethyl)-methyl-phosphonothioate (EDMM). On the base of described scheme of intoxication with NPA, inhibition effect on cholinesterases, preferably on AChE as the most important factor involved in the mechanism of acute intoxication with NPA was studied. Intoxication of mice or rats with sarin and soman (2 x LD50) showed that time course of poisoning is faster than that for VX or EDMM. Inhibition of AChE in the blood was in good correlation with symptoms of intoxication and also with inhibition of AChE in the brain. The differences between inhibition effect of soman preferably uniform character of inhibition in the brain parts) and sarin (selective inhibition in the brain parts, with maximum in the frontal cortex and pontomedullar area) were observed. This selectivity was most marked for VX and EDMM intoxication (maximal inhibition in the part of the pontomedullar area containing reticular formation). The dose causing inhibition effect in the brain was assessed to be about 1% of the dose administered. The study of the effect of antidotal therapy (combination of atropine and reactivator) in vivo showed in mice and rats intoxicated with sarin non-uniform increase of AChE activity in the pontomedullar part depending on the dose and type of reactivator. The most marked effect was observed for methoxime. It was demonstrated that there exists good correlation between survival of experimental animals and the rest AChE activity in the pontomedullar part of the brain. AChE activity level critical for survival or death of the organism poisoned with NPA was assessed from these experiments; it was about 1-5% of normal values. By means of original method allowing continual monitoring of AChE activity in the blood, similar AChE reactivation was demonstrated, with highest effect for trimedoxime and methoxime. Using continual determination of the blood AChE activity following sarin, soman, VX and EDMM intoxication demonstrated that only a part of the dose administered caused inhibition effect in the blood; this part was determined to be practically 100% (i. v. administration); for other routes of administration this ratio was as follows: 50-80% (i. m.), 20-40% (i. p.), 6-16% (p. o.) and 1-5% (p. c.), respectively. Using this continual monitoring, the detoxication of sarin and soman was demonstrated. Detoxication of VX and EDMM was not observed.(ABSTRACT TRUNCATED AT 400 WORDS)

抑制剂及其他因素对胆碱酯酶的影响。
关于胆碱酯酶和适合用作化学武器的剧毒有机磷化合物的作用的文献综述在本工作的导论部分给出。有神经麻痹剂(NPA)-沙林,索曼,VX和模型化合物o -乙基-s -(2-二甲氨基乙基)-甲基膦硫酸盐(EDMM)。在所描述的NPA中毒方案的基础上,研究了对胆碱酯酶的抑制作用,尤其是对乙酰胆碱酯酶的抑制作用,这是NPA急性中毒机制中最重要的因素。沙林和索曼(2倍LD50)中毒小鼠或大鼠的中毒时间比VX或EDMM快。血液中乙酰胆碱酯酶的抑制与中毒症状有良好的相关性,也与脑中乙酰胆碱酯酶的抑制有良好的相关性。观察了索曼(具有均匀性的脑区抑制)和沙林(具有选择性的脑区抑制,在额叶皮层和桥脑髓区抑制最大)的抑制效果差异。这种选择性在VX和EDMM中毒中最为明显(在桥脑髓区含有网状结构的部分抑制最大)。在大脑中引起抑制作用的剂量估计约为给药剂量的1%。体内解毒治疗(阿托品联合再激活剂)的效果研究显示,沙林中毒小鼠和大鼠脑桥髓部乙酰胆碱酯酶活性随再激活剂剂量和类型的不同而不均匀升高。甲氧基肟效果最显著。结果表明,实验动物的存活与脑桥脑髓部AChE活性有良好的相关性。从这些实验中评估对NPA中毒生物体的生存或死亡至关重要的乙酰胆碱酯酶活性水平;大约是正常值的1-5%。通过允许持续监测血液中AChE活性的原始方法,证明了类似的AChE再激活,以甲氧苄肟和甲氧苄肟效果最高。通过对沙林、索曼、VX和EDMM中毒后血液AChE活性的持续测定表明,只有部分剂量在血液中产生抑制作用;这部分被确定为几乎100% (i. v.给药);对于其他给药途径,这一比例分别为:50-80% (i.m), 20-40% (i.p), 6-16% (p.o)和1-5% (p.c)。通过这种持续监测,证明了沙林和索曼的解毒作用。未观察到VX和EDMM的解毒作用。(摘要删节为400字)
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