香豆素
代谢物
新陈代谢
羟基化
毒性
化学
药理学
沙鼠
狒狒
生物化学
生物
医学
内分泌学
内科学
酶
有机化学
缺血
作者
Julia H. Fentem,Jeffrey R. Fry
出处
期刊:Comparative Biochemistry and Physiology Part C: Comparative Pharmacology
[Elsevier]
日期:1993-01-01
卷期号:104 (1): 1-8
被引量:56
标识
DOI:10.1016/0742-8413(93)90102-q
摘要
1. Investigations of coumarin metabolism and hepatotoxicity have been reviewed. 2. Species differences in coumarin hepatotoxicity appear to be metabolism-mediated. 3. The rat, in which it is markedly hepatotoxic, primarily metabolises coumarin via 3-hydroxylation and cleavage of the heterocyclic ring. 4. Coumarin is less toxic in the baboon, gerbil and certain strains of mice, which resemble man in their extensive formation of the 7-hydroxy metabolite. 5. Liver toxicity in patients receiving relatively high daily doses of coumarin is very rare. 6. Recent studies indicate that coumarin 3,4-epoxide is the metabolic intermediate responsible for hepatotoxicity in the rat.
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