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氯化石蜡:一种高氯化多氯十六烷在小鼠和鹌鹑体内的处置情况。

Chlorinated paraffins: disposition of a highly chlorinated polychlorohexadecane in mice and quail.

作者信息

Biessmann A, Darnerud P O, Brandt I

出版信息

Arch Toxicol. 1983 May;53(1):79-86. doi: 10.1007/BF01460004.

Abstract

Uniformly 14C-labelled 1-chloro-polychlorohexadecane (PCHD) of high chlorine content (69% w/w) was given to Japanese quail and to C57Bl mice perorally (p.o.) and intravenously (i.v.). The degradation of PCHD to 14CO2, measured during 8 h, was found to be minute (about 1% of dose) in both species after either route of administration. In mice 66 and 43% of dose was eliminated in the feces during 96 h following p.o. and i.v. administration, respectively; the urinary excretion was about 3% in both cases. In quail, the combined fecal and urinary excretion during 96 h after p.o. administration was 58% of dose. The autoradiographic distribution following p.o. administration showed some general similarities between mice and quail; high radioactivities were present in bile, liver, kidney, and intestinal contents up to 24 h after administration. In addition, in quail high radioactivity was present in the hypophysis, retina, blood, and egg yolk. In mice strong accumulation and retention was observed in the corpora lutea up to 30 days after administration. A long time retention in fat occurred in both species.

摘要

将高氯含量(69%重量/重量)的均匀14C标记的1-氯-多氯十六烷(PCHD)经口(p.o.)和静脉内(i.v.)给予日本鹌鹑和C57Bl小鼠。在给药后的8小时内测量PCHD降解为14CO2的情况,发现两种给药途径后,两种物种中PCHD降解为14CO2的量都很少(约为剂量的1%)。在小鼠中,经口和静脉内给药后,分别在96小时内粪便中排出剂量的66%和43%;两种情况下尿液排泄量约为3%。在鹌鹑中,经口给药后96小时内粪便和尿液的总排泄量为剂量的58%。经口给药后的放射自显影分布显示小鼠和鹌鹑之间有一些总体相似性;给药后24小时内,胆汁、肝脏、肾脏和肠内容物中存在高放射性。此外,在鹌鹑中,垂体、视网膜、血液和蛋黄中存在高放射性。在小鼠中,给药后30天内黄体中观察到强烈的积累和滞留。两种物种的脂肪中都出现了长时间的滞留。

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