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Toxicokinetics of PCDD, PCDF, and Coplanar PCB Congeners in Baikal Seals, Pusa sibirica : Age-Related Accumulation, Maternal Transfer, and Hepatic Sequestration

โœ Scribed by Iwata, Hisato; Watanabe, Mafumi; Okajima, Yuka; Tanabe, Shinsuke; Amano, Masao; Miyazaki, Nobuyuki; Petrov, Evgeny A.


Book ID
127388406
Publisher
American Chemical Society
Year
2004
Tongue
English
Weight
169 KB
Volume
38
Category
Article
ISSN
0013-936X

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โœฆ Synopsis


To assess the toxicokinetic behavior and potential toxicity of polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), and coplanar polychlorinated biphenyls (PCBs) in Baikal seals, congener-specific levels and tissue distribution were evaluated in the liver and blubber, and the effects of biological factors including sex and growth were assessed. Total 2,3,7,8-TCDD toxic equivalents (TEQs) were in the range of 210-920 pgTEQ/g fat wt (180-800 pgTEQ/g wet wt) in the blubber and 290-7800 pgTEQ/g fat wt (10-570 pgTEQ/wet wt) in the liver. Nonortho coplanar PCB126 was the most TEQ-contributed congener accounting for 37-59% of the total TEQs in the liver. From the unique congener profiles, weak metabolic properties of Baikal seals for 2,3,7,8-TCDF and 1,2,3,7,8-P 5 -CDF are suggested. Concentrations of most congeners linearly increased with age in male seals, whereas in adult females the levels revealed an age-related decline. The increasing and declining rates were congener-specific. Maternal transfer rates of 5 representative congeners from adult female to pup through lactation, which was estimated from male-female differences in the body burden, was 1.1 ngTEQ/kg/day for the first pup and decreased with every lactational epoch. The liver-blubber distribution of 1,2,3,4,7,8-H 6 CDD, 1,2,3,6,7,8-H 6 CDD, PCB81, PCB126, and PCB169 was dependent on the hepatic total TEQ, indicating hepatic sequestration by induced cytochrome P450 (CYP). These results indicate that congener profile in Baikal seals is governed by complex factors including sex, tissue concentration, binding to CYP, and rates of absorption and metabolism/excretion.


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