Species differences in the metabolism and hepatotoxicity of coumarin
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 rin...
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Veröffentlicht in: | Comparative Biochemistry and Physiology. Part C, Comparative Pharmacology Comparative Pharmacology, 1993, Vol.104 (1), p.1-8 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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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ISSN: | 0306-4492 0742-8413 |
DOI: | 10.1016/0742-8413(93)90102-Q |