Tissue distribution, excretion, and metabolism of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in the Golden Syrian hamster

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Abstract

The hamster has been reported to be the least sensitive mammalian species to the acute toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). The fate of a single dose of [3H]- or [14C]TCDD (650 μg/kg, ip or po) was assessed in male hamsters for up to 35 days following treatment. The greatest content (percentage dose/g tissue) of radioactivity was found in the liver, adipose tissue, and adrenals. The radioactivity in liver and adipose tissue was identified as unmetabolized TCDD. The rate of 3H or 14C elimination in urine and feces suggested a first-order process. Similar half-life of elimination (t12) values of 12.0 ± 2.0 and 10.8 ± 2.4 days (mean ± SD) were obtianed with ip administered [3H]- and [14C]TCDD, respectively. With both [3H]- and [14C]TCDD, approximately 35 and 50% of the radioactivity was eliminated in urine and feces, respectively. The t12 for po administered [3H]TCDD was 15.0 ± 2.5 days. High-pressure liquid chromatography of the urine and bile of animals receiving [14C]TCDD revealed one major and several minor radioactive peaks, none of which corresponded to [14C]TCDD. The apparent absence of TCDD metabolites in extracts of liver or adipose tissue indicates that the biotransformed products of TCDD are readily excreted in urine and bile. The enhanced rate of metabolism and excretion of TCDD in hamsters relative to other species may in part contribute to, but not totally explain its unusual resistance to TCDD toxicity.

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1

Present address: Department of Pharmacology and Therapeutics, School of Medicine, State University of New York, Buffalo, N.Y. 14214.

2

Present address: Environmental Health Sciences Center, University of Rochester, Rochester, N.Y. 14642.

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