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Xenobiotica
the fate of foreign compounds in biological systems
Volume 10, 1980 - Issue 9
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Original Article

The role of lipophilicity in the extrahepatic disposition of aminostilbene derivatives following administration to rat

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Pages 675-688 | Received 04 Sep 1979, Published online: 30 Sep 2009
 

Abstract

1. Carcinogenic trans-4-dimethylaminostilbene and its unbound metabolites in rat tissues are highly lipophilic with partition coefficients of 10000 to 80 000. The values for bibenzyl derivatives are somewhat lower.

2. Sulphates and glucuronic acid conjugates are present in liver, kidney, blood and bile, but not to any extent in other extrahepatic tissues.

3. The patterns of unbound metabolites in lung, spleen, adrenals, brain and fat after oral administration of 3H-labelled trans-4-dimethylaminostilbene, cis-4-dimethyl-aminostilbene and 4-dimethylaminobibenzyl have been determined. The concn. of tissue metabolites do not parallel plasma concn. of metabolites and do not correlate with lipophilicity.

4. Binding of trans-4-aminostilbene metabolites to tissue proteins is 3-5 times greater than that of cis-4-aminostilbene metabolites and more than 10 times higher than that of aminobibenzyl metabolites. In Zymbal gland, the target tissue for trans-4-dimethylaminostilbene carcinogenicity, the tissue concn. of reactive metabolites is insufficiently high to account for the tissue specific effect.

5. The analysis of fat tissue provided circumstantial evidence that reactive metabolites bind covalently to fatty acids.

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