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长期接触镉对肝脏药物代谢的影响。

Effect of chronic exposure to cadmium on hepatic drug metabolism.

作者信息

Dalvi R R, Robbins T J

出版信息

J Environ Sci Health B. 1979;14(6):603-15. doi: 10.1080/03601237909372154.

Abstract

In an attempt to examine the chronic effect of low levels of cadmium on hepatic drug-metabolizing enzyme system, an experiment was carried out in which growing male rats were given 0, 5, 10, and 20 ppm of cadmium in drinking water for a period of 8 weeks. An ip administration of a hypnotic dose of pentobarbital to the cadmium-treated and the control rats 24 hr following the termination of the experiment exhibited that there was no significant difference in the drug metabolism in control and any of the treated groups. Next, liver microsomes were isolated from animals in all groups to study their ability to metabolize drugs in vitro. The results indicated that the activity of benzphetamine N-demethylase and aniline hydroxylase, and the concentration of microsomal cytochrome P-450 were almost identical in the control and treated groups. On the other hand, a single ip dose of cadmium (2 mg/kg) caused significant decrease in the vivo and in vitro microsomal drug metabolism. These results suggest that although a single ip dose of cadmium (2 mg/kg) causes significant inhibition of drug metabolism, chronic exposure to cadmium up to 20 ppm in drinking water over a period of 8 weeks is unlikely to affect hepatic drug metabolism.

摘要

为了研究低水平镉对肝脏药物代谢酶系统的慢性影响,进行了一项实验,给生长中的雄性大鼠饮用含0、5、10和20 ppm镉的水,持续8周。实验结束24小时后,对镉处理组和对照组大鼠腹腔注射催眠剂量的戊巴比妥,结果显示对照组与任何处理组的药物代谢均无显著差异。接下来,从所有组的动物中分离肝脏微粒体,以研究其体外药物代谢能力。结果表明,对照组和处理组中苄非他明N-脱甲基酶和苯胺羟化酶的活性以及微粒体细胞色素P-450的浓度几乎相同。另一方面,单次腹腔注射镉(2 mg/kg)会导致体内和体外微粒体药物代谢显著下降。这些结果表明,虽然单次腹腔注射镉(2 mg/kg)会显著抑制药物代谢,但在8周内长期饮用含镉量高达20 ppm的水不太可能影响肝脏药物代谢。

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