posted on 2004-02-15, 00:00authored byHeather M. Stapleton, Robert J. Letcher, Joel E. Baker
Polybrominated diphenyl ether (PBDE) congener patterns
in biota are often enriched in tetra-, penta-, and hexabrominated diphenyl ethers, which is believed to result
from the use of the commercial “pentaBDE” formulation.
However, our evidence suggests that debromination of PBDEs
occurs within fish tissues leading to appreciable ac
cumulation of less brominated congeners. This suggests
that PBDE body burdens can reflect both direct uptake from
exposure and debromination of more highly brominated
congeners. We conducted two independent dietary exposure
studies using the common carp (Cyprinus carpio) to
trace the fate of 2,2‘,4,4‘,5-pentabromodiphenyl ether (BDE
99) and 2,2‘,3,4,4‘,5‘,6-heptabromodiphenyl ether (BDE
183) in fish tissues. Carp were fed food spiked with individual
BDE congeners for 62 d, and depuration was monitored
during the following 37 d. Significant debromination was
observed, converting BDE 99 to 2,2‘,4,4‘-tetrabromodiphenyl
ether (BDE 47) and BDE 183 to 2,2‘,4,4‘,5,6-hexabromodiphenyl
ether (BDE 154) and another as yet unidentified hexa-BDE congener. The BDE 99 concentration rapidly declined
from 400 ± 40 ng/g ww in the food to 53 ± 12 ng/g ww
in the gut content material sampled 2.5 ± 1 h following
feeding. At least 9.5 ± 0.8% of the BDE 99 mass in the
gut was debrominated to BDE 47 and assimilated in carp
tissues. In the BDE 183 exposure, approximately 17% of the
BDE 183 mass was debrominated and accumulated in
carp tissues in the form of two hexa-BDE congeners. In
both exposure studies, the concentration of the exposure
compound decreased significantly in the gut within 2.5
± 1 h following ingestion. This rapid decrease in the
concentration of the BDE congeners could not be explained
entirely by debromination to quantified products or fecal
egestion. Reactions occurring within the gut transform BDE
congeners to other products that may accumulate or be
excreted. Further studies are needed to identify and determine
the effects of these BDE metabolites.