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大鼠吸入异戊二烯的命运:与丁二烯的比较。

The fate of isoprene inhaled by rats: comparison to butadiene.

作者信息

Dahl A R, Birnbaum L S, Bond J A, Gervasi P G, Henderson R F

出版信息

Toxicol Appl Pharmacol. 1987 Jun 30;89(2):237-48. doi: 10.1016/0041-008x(87)90044-5.

Abstract

Isoprene (2-methyl-1,3-butadiene), a volatile monomer occurring in the natural environment and used in the manufacture of elastomers, is a close chemical relative of the animal carcinogen 1,3-butadiene. To obtain toxicokinetic data for inhaled isoprene, male F344 rats were exposed in groups of 30 to 14C-labeled isoprene vapor at four concentrations from 8 to 8200 ppm. The percentage of the inhaled isoprene that was metabolized decreased with increasing exposure concentration. The percentage of the total metabolites (that is, non-isoprene-retained 14C) excreted in urine and feces or expired was determined as a function of vapor concentration. About 75% of the total metabolites was excreted in urine. This was independent of inhaled isoprene concentration. After exposure to 8200 ppm, a larger percentage of the metabolites was excreted in feces than after exposure to lower concentrations. Using vacuum line techniques, blood metabolite concentrations were determined as functions of both vapor concentration and exposure duration. At one exposure concentration (1480 ppm) metabolites were measured in the nose, lungs, liver, kidney, and fat, as well as in blood. A mutagenic metabolite, isoprene diepoxide, was tentatively identified in all tissues examined. Between 0.0018 and 0.031% of the inhaled 14C label was tentatively identified as this metabolite in blood. The relative amount of the metabolites present in blood was highest for low concentrations of inhaled isoprene and for shorter exposure durations. Body fat appeared to be a reservoir for both isoprene metabolites and isoprene itself. The appearance of metabolites in the respiratory tract after short exposure durations together with low blood concentrations of isoprene indicated that substantial metabolism of inhaled isoprene in the respiratory tract may occur.

摘要

异戊二烯(2-甲基-1,3-丁二烯)是一种存在于自然环境中并用于制造弹性体的挥发性单体,它与动物致癌物1,3-丁二烯是化学近亲。为了获得吸入异戊二烯的毒代动力学数据,将30只雄性F344大鼠分为几组,暴露于浓度为8至8200 ppm的四种浓度的14C标记异戊二烯蒸气中。随着暴露浓度的增加,被代谢的吸入异戊二烯的百分比降低。测定了尿液、粪便或呼出物中排泄的总代谢物(即非异戊二烯保留的14C)的百分比与蒸气浓度的函数关系。约75%的总代谢物通过尿液排泄。这与吸入的异戊二烯浓度无关。暴露于8200 ppm后,与较低浓度暴露相比,粪便中排泄的代谢物百分比更高。使用真空管路技术,测定了血液中代谢物浓度与蒸气浓度和暴露持续时间的函数关系。在一个暴露浓度(1480 ppm)下,在鼻子、肺、肝脏、肾脏、脂肪以及血液中测量了代谢物。在所有检查的组织中初步鉴定出一种致突变代谢物异戊二烯二环氧物。在血液中,吸入的14C标记物中有0.0018%至0.031%初步鉴定为这种代谢物。对于低浓度的吸入异戊二烯和较短的暴露持续时间,血液中存在的代谢物相对量最高。身体脂肪似乎是异戊二烯代谢物和异戊二烯本身的储存库。短时间暴露后呼吸道中出现代谢物以及异戊二烯血液浓度较低表明,呼吸道中吸入的异戊二烯可能会发生大量代谢。

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