氯仿和甲基氯仿及其代谢物在孕鼠体内的分布。

B R Danielsson, H Ghantous, L Dencker
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引用次数: 0

摘要

在吸入14c标记的氯仿和氯仿甲酯10 min后,以不同的时间间隔(0 ~ 24 h)记录孕鼠体内放射性的分布。使用放射自显影和液体闪烁方法可以区分挥发性(非代谢)、水溶性和牢固组织结合的放射性。与氯仿相比,甲基氯仿在脂肪中保留的时间更长。氯仿的代谢物比甲基氯仿的代谢物丰富得多,它们优先存在于呼吸道(鼻黏膜、气管和支气管)、肝脏和排泄器官中。新生小鼠吸入或腹腔注射氯仿后,在呼吸道和肝脏小叶中心区发现了组织结合活性。在妊娠各阶段吸入氯仿和甲基氯仿后,胎盘和胎儿在短时间间隔内观察到挥发性放射性。虽然在胎儿胎盘单位观察到低水平的甲基氯仿放射性代谢物,但氯仿代谢物随着时间的推移而积累。这一事实在羊水中尤其明显,在4小时时观察到放射性的峰值水平。在妊娠早期,代谢物在胚胎神经组织中积累。在妊娠后期的胎儿呼吸上皮中观察到组织结合的氯仿代谢物,表明这些细胞在妊娠后期具有药物代谢能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Distribution of chloroform and methyl chloroform and their metabolites in pregnant mice.

The distribution of radioactivity in pregnant mice was registered at different time intervals (0-24 h) after a 10-min period of inhalation of 14C-labelled chloroform and methyl chloroform. Autoradiographic and liquid scintillation methods were used to make possible the distinction between volatile (non-metabolized), water-soluble and firmly tissue-bound radioactivity. Methyl chloroform was retained longer in fat as compared to chloroform. Metabolites of chloroform were present in a much greater abundance than those of methyl chloroform and they were found preferentially in the respiratory tract (nasal mucosa, trachea and bronchi), liver and excretory organs. Tissue-bound activity after chloroform inhalation or i.p. injection to newborn mice was found in the respiratory tract and centrilobular areas of the liver. Volatile radioactivity was observed in the placenta and fetuses at short time intervals after inhalation of both chloroform and methyl chloroform at all stages of gestation. While a low level of radioactive metabolites of methyl chloroform was observed in the fetoplacental unit, metabolites of chloroform accumulated with time. This fact was especially marked in the amniotic fluid, where the peak level of radioactivity was observed at 4 h. In early gestation, metabolites accumulated in the embryonic neural tissues. Tissue-bound metabolites of chloroform were observed in the fetal respiratory epithelium in late gestation, indicating a capacity for drug metabolism in these cells in the late fetal period.

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