The biliary metabolism of butylated hydroxytoluene (3, 5-di-t-butyl-4-hydroxy-toluene) and its derivatives in the rat

Author:

Holder G M1,Ryan A J1,Watson T R1,Wiebe L I1

Affiliation:

1. Department of Pharmacy, University of Sydney, Sydney, Australia

Abstract

Abstract The biliary metabolism of 3, 5-di-t-butyl-4-hydroxybenzyl alcohol (BHT-CH2OH), 3, 5-di-t-butyl-4-hydroxybenzaldehyde (BHT-CHO) and 3, 5-di-t-butyl-4-hydroxybenzoic acid (BHT-COOH) after parenteral administration has been examined in the rat and compared to that of 3, 5-di-t-butyl-4-hydroxytoluene. Quantitative excretion and chemical examination of bile showed that in the enterohepatic circulation BHT-COOH or its ester glucuronide is the recirculating compound from the four compounds studied. Biliary excretion data are also presented for 1, 2-bis(3, 5-di-t-butyl-4-hydroxyphenyl)ethane.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

Cited by 19 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. 2,6-Di-Tert-Butyl-Hydroxytoluene and Its Metabolites in Foods;Comprehensive Reviews in Food Science and Food Safety;2014-12-12

2. 2,6-Di-tert-butyl-p-cresol (BHT) [MAK Value Documentation, 2007];The MAK-Collection for Occupational Health and Safety;2012-01-31

3. Butylhydroxytoluol (BHT) [MAK Value Documentation in German language, 1986];The MAK-Collection for Occupational Health and Safety;2012-01-31

4. Final Report on the Safety Assessment of BHT;International Journal of Toxicology;2002-10

5. Biological and toxicological consequences of quinone methide formation;Chemico-Biological Interactions;1993-02

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