TY - JOUR
T1 - Toxicity of 3,3’,4,4’- and 2,2’,5,5’- tetrabromobiphenyl
T2 - Correlation of activity with aryl hydrocarbon hydroxylase induction and lack of protection by antioxidants
AU - Robertson, L. W.
AU - Andres, J. L.
AU - Safe, S. H.
AU - Lovering, S. L.
N1 - Funding Information:
The financial assistance of the Texas Agricultural Experiment Station, grant 6376, is gratefully acknowledged. Requests for reprints should be sent to S. Safe, Veterinary Physiology and Pharmacology, Texas A&M University, College Station, Texas 77843.
Copyright:
Copyright 2016 Elsevier B.V., All rights reserved.
PY - 1983/1
Y1 - 1983/1
N2 - 3,3’,4,4’-Tetrabromobiphenyl is a minor component of commercial polybrominated biphenyl (PBB) mixture fireMaster BP-6 and is a potent inducer of aryl hydrocarbon hydroxylase (AHH). A single ip dose of 3,3’,4,4’-tetrabromobiphenyl (750 pmoi/kg) caused significant reduction in the growth rate in the immature male Wistar rat, as well as pale enlarged livers and marked reduction in thymus size. Under light microscopy, hepatocytes were enlarged and vacuolated. The vacuoles, which were most prominent in the midzonal region of the lobule, corresponded to fat droplets in oil-red-O-stained sections. The thymus, especially the cortex, was markedly depleted of lymphocytes. Neither the reduced growth, altered organ weights nor the histo- pathology was reversed for the duration of the study by the coadministration of the antioxidants butylated hydroxy anisole (BHA), butyiated hydroxy toluene (BHT), or vitamin E. Vitamin E did, however counter the negative effect of 3,3’,4,4’-tetra- bromobiphenyl on growth during the first 5 d of the study. 2,2’,5,5’-Tetrabromo- biphenyi, also a minor component of fireMaster BP-6, is a weak phenobarbital-type inducer of cytochrome P-450. When administered at the same dose, 2,2’,5,5’-tetra- bromobiphenyl did not elicit any observed toxic effects. These data confirm the correlation between AHH induction and toxicity for these PBBs and suggest that 3,3’,4,4’-tetrabromobiphenyl may significantly contribute to the toxicity of fireMaster BP-6. Although there is evidence that polychlorinated biphenyls, and perhaps 2,3,7,8-tetrach/orodibenzo-p-dioxin, exert certain toxic effects via a lipid peroxidation mechanism, the toxic changes measured during this study were not reversed by the administration of the antioxidants.
AB - 3,3’,4,4’-Tetrabromobiphenyl is a minor component of commercial polybrominated biphenyl (PBB) mixture fireMaster BP-6 and is a potent inducer of aryl hydrocarbon hydroxylase (AHH). A single ip dose of 3,3’,4,4’-tetrabromobiphenyl (750 pmoi/kg) caused significant reduction in the growth rate in the immature male Wistar rat, as well as pale enlarged livers and marked reduction in thymus size. Under light microscopy, hepatocytes were enlarged and vacuolated. The vacuoles, which were most prominent in the midzonal region of the lobule, corresponded to fat droplets in oil-red-O-stained sections. The thymus, especially the cortex, was markedly depleted of lymphocytes. Neither the reduced growth, altered organ weights nor the histo- pathology was reversed for the duration of the study by the coadministration of the antioxidants butylated hydroxy anisole (BHA), butyiated hydroxy toluene (BHT), or vitamin E. Vitamin E did, however counter the negative effect of 3,3’,4,4’-tetra- bromobiphenyl on growth during the first 5 d of the study. 2,2’,5,5’-Tetrabromo- biphenyi, also a minor component of fireMaster BP-6, is a weak phenobarbital-type inducer of cytochrome P-450. When administered at the same dose, 2,2’,5,5’-tetra- bromobiphenyl did not elicit any observed toxic effects. These data confirm the correlation between AHH induction and toxicity for these PBBs and suggest that 3,3’,4,4’-tetrabromobiphenyl may significantly contribute to the toxicity of fireMaster BP-6. Although there is evidence that polychlorinated biphenyls, and perhaps 2,3,7,8-tetrach/orodibenzo-p-dioxin, exert certain toxic effects via a lipid peroxidation mechanism, the toxic changes measured during this study were not reversed by the administration of the antioxidants.
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U2 - 10.1080/15287398309530322
DO - 10.1080/15287398309530322
M3 - Article
C2 - 6298436
AN - SCOPUS:0020660147
SN - 0098-4108
VL - 11
SP - 81
EP - 91
JO - Journal of Toxicology and Environmental Health
JF - Journal of Toxicology and Environmental Health
IS - 1
ER -