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首页> 外文期刊>Toxicology and Applied Pharmacology >Intravenous and inhalation toxicokinetics of sarin stereoisomers in atropinized guinea pigs.
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Intravenous and inhalation toxicokinetics of sarin stereoisomers in atropinized guinea pigs.

机译:沙林立体异构体在豚鼠体内的静脉和吸入毒性动力学。

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摘要

We report the first toxicokinetic studies of (+/-)-sarin. The toxicokinetics of the stereoisomers of this nerve agent were studied in anesthetized, atropinized, and restrained guinea pigs after intravenous bolus administration of a dose corresponding to 0.8 LD50 and after nose-only exposure to vapor concentrations yielding 0.4 and 0.8 LCt50 in an 8-min exposure time. During exposure the respiratory minute volume and frequency were monitored. Blood samples were taken for gas chromatographic analysis of the nerve agent stereoisomers and for measurement of the activity of blood acetylcholinesterase (AChE). In all experiments, the concentration of (+)-sarin was below the detection limit (<5 pg/ml). The concentration-time profile of the toxic isomer, i.e., (-)-sarin, after an intravenous bolus was adequately described with a two-exponential equation. (-)-Sarin is distributed ca. 10-fold faster than C(-)P(-)-soman, whereas its elimination proceeds almost 10-fold slower. During nose-only exposure to 0.4 and 0.8 LCt50 of (+/-)-sarin in 8 min, (-)-sarin appeared to be rapidly absorbed. The blood AChE activity decreased during the exposure period to ca. 15 and 70% of control activity, respectively. There were no effects on the respiratory parameters. A significant nonlinearity of the toxicokinetics with dose was observed for the respiratory experiments. Copyright 2000 Academic Press.
机译:我们报告了(+/-)-沙林的第一个毒代动力学研究。在静脉推注给予0.8 LD50的剂量后,在仅鼻子暴露于蒸气浓度下在8分钟内产生了0.4和0.8 LCt50的麻醉剂量后,在麻醉,萎缩和约束的豚鼠中研究了这种神经制剂立体异构体的毒物动力学接触时间。在暴露期间,监测呼吸分钟的量和频率。采集血样用于神经毒药立体异构体的气相色谱分析,并测量血液乙酰胆碱酯酶(AChE)的活性。在所有实验中,(+)-sarin的浓度均低于检测极限(<5 pg / ml)。用二指数方程式充分描述了静脉推注后有毒异构体即(-)-sarin的浓度-时间曲线。 (-)-Sarin分布于比C(-)P(-)-梭曼快10倍,而消除它的速度却慢了10倍。在8分钟内仅鼻子暴露于0.4和0.8 LCt50的(+/-)-沙林的过程中,(-)-沙林似乎被迅速吸收。血液中的AChE活性在暴露于约200mg / ml的时间内下降。分别为对照活性的15%和70%。对呼吸参数没有影响。对于呼吸实验,观察到毒代动力学与剂量之间存在明显的非线性关系。版权所有2000学术出版社。

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