TOXIC EQUIVALENCY FACTORS OF POLYBROMINATED DIBENZO-P-DIOXIN, DIBENZOFURAN, BIPHENYL, AND POLYHALOGENATED DIPHENYL ETHER CONGENERS BASED ONRAINBOW-TROUT EARLY-LIFE STAGE MORTALITY

Citation
Mw. Hornung et al., TOXIC EQUIVALENCY FACTORS OF POLYBROMINATED DIBENZO-P-DIOXIN, DIBENZOFURAN, BIPHENYL, AND POLYHALOGENATED DIPHENYL ETHER CONGENERS BASED ONRAINBOW-TROUT EARLY-LIFE STAGE MORTALITY, Toxicology and applied pharmacology, 140(2), 1996, pp. 227-234
Citations number
44
Categorie Soggetti
Pharmacology & Pharmacy",Toxicology
ISSN journal
0041008X
Volume
140
Issue
2
Year of publication
1996
Pages
227 - 234
Database
ISI
SICI code
0041-008X(1996)140:2<227:TEFOPD>2.0.ZU;2-K
Abstract
Polybrominated and polychlorinated biphenyls (PBBs/PCBs), dibenzo-p-di oxins (PBDDs/PCDDs), dibenzofurans (PBDFs/PCDFs), and diphenyl ethers (PBDEs/PCDEs) are persistent, lipophilic environmental contaminants th at may pose a risk to fish early life stage survival. To determine thi s potential risk, a rainbow trout early life stage mortality bioassay was used in which the potency of individual polybrominated chemicals w as compared to the potency of the most potent polychlorinated chemical in these classes, 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Followi ng injection of newly fertilized rainbow trout eggs, fish-specific tox ic equivalency factors (TEFs) were calculated as the molar ratio of TC DD LD50 to brominated compound LD50. Signs of toxicity were identical to those produced by polychlorinated TCDD-like chemicals and included yolk sac edema, pericardial edema, multifocal hemorrhages, reduced gro wth, and craniofacial malformations. Polybrominated dibenzo-p-dioxins, dibenzofurans, and biphenyls exhibited decreased potency with increas ed bromine substitution. Only 2,3,7,8-TBDD was more potent than 2,3,7, 8-TCDD, whereas other polybrominated dibenzo-p-dioxins were equipotent or less potent than identically substituted polychlorinated dibenzo-p -dioxins in this assay. Although two PBDF congeners were equipotent to identically substituted PCDFs, 2,3,7,8-TBDF was 9-fold more potent th an 2,3,7,8-TCDF. Both 3,3',4,4'-TBB and 3,3',4,4',5,5'-HxBB were 10-fo ld more potent than identically substituted polychlorinated biphenyls. The halogenated diphenyl ethers and di-ortho polybrominated biphenyls were inactive in this assay. Thus, in this in vivo assay the polybrom inated and polychlorinated TCDD-like chemicals were not always equally potent. To assess the risk posed by mixtures of these chemicals to fe ral fish populations, fish-specific TEFs for both polybrominated and p olychlorinated chemicals should be used. (C) 1996 Academic Press, Inc.