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大鼠体内六氯酚的代谢:肝脏途径。

Hexachlorophene metabolism in rats: the hepatic route.

作者信息

Edelson J, McMullen J P

出版信息

Arch Int Pharmacodyn Ther. 1976 Mar;220(1):140-7.

PMID:952574
Abstract

The terminal elimination rate of radioactivity from the bile of bile-duct cannulated rats, that had received hexachlorophene-14C via the hepatic portal vein, had an apparent first-order half-life of about 10 hr. Tissue distribution studies in these rats indicated that 35-47% of the carbon-14 of the dose was eliminated through the bile within 24 hr. Significant amounts of radioactivity were also found in the liver and carcass at that time; the brain was the only tissue that did not consistently have much higher concentrations of carbon-14 than the blood. The rate limiting step in the disposition of hexachlorophene may be excretion into the bile. A bile-feeding technique demonstrated enterohepatic circulation.

摘要

通过肝门静脉给予六氯酚-14C的胆管插管大鼠胆汁中放射性的终末消除率,其表观一级半衰期约为10小时。对这些大鼠的组织分布研究表明,给药剂量中35-47%的碳-14在24小时内通过胆汁消除。此时在肝脏和胴体中也发现了大量放射性;大脑是唯一碳-14浓度始终不高于血液的组织。六氯酚处置的限速步骤可能是排入胆汁。一种胆汁灌喂技术证明了肠肝循环。

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