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논문 기본 정보

자료유형
학술저널
저자정보
Jae Seok Choi (부산대학교) Young Jun Lee (부산대학교) Tae Hyung Kim (부산대학교) Hyun Jung Lim (부산대학교) Mee Young Ahn (부산대학교) Seung Jun Kwack (식품의약품안전청) Tae Seok Kang (식품의약품안전청) Kui Lea Park (식품의약품안전청) Jaewon Lee (식품의약품안전청) Nam Deuk Kim (식품의약품안전청) Tae Cheon Jeong (영남대학교) Sang Geum Kim (충남대학교) Hye Gwang Jeong (충남대학교) Byung Mu Lee (성균관대학교) Hyung Sik Kim (부산대학교)
저널정보
한국독성학회 Toxicological Research Toxicological Research Vol.27 No.2
발행연도
2011.6
수록면
61 - 70 (10page)

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초록· 키워드

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Brominated flame retardants (BFRs) are present in many consumer products ranging from fabrics to plastics and electronics. Wide use of flame retardants can pose an environmental hazard, which makes it important to determine the mechanism of their toxicity. In the present study, dose-dependent toxicity of tetrabromobisphenol A (TBBPA), a flame retardant, was examined in male prepubertal rats (postnatal day 18) treated orally with TBBPA at 0, 125, 250 or 500 ㎎/㎏ for 30 days. There were no differences in body weight gain between the control and TBBPA-treated groups. However, absolute and relative liver weights were significantly increased in high dose of TBBPA-treated groups. TBBPA treatment led to significant induction of CYP2B1 and constitutive androstane receptor (CAR) expression in the liver. In addition, serum thyroxin (T4) concentration was significantly reduced in the TBBPA treated group. These results indicate that repeated exposure to TBBPA induces drug-metabolising enzymes in rats through the CAR signaling pathway. In particular, TBBPA efficiently produced reactive oxygen species (ROS) through CYP2B1 induction in rats. We measured 8-hydroxy-2’-deoxyguanosine (8-OHdG), a biomarker of DNA oxidative damage, in the kidney, liver and testes of rats following TBBPA treatment. As expected, TBBPA strongly induced the production of 8-OHdG in the testis and kidney. These observations suggest that TBBPA-induced target organ toxicity may be due to ROS produced by metabolism of TBBPA in Sprague-Dawley rats.

목차

INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
ACKNOWLEDGEMENTS
REFERENCES

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UCI(KEPA) : I410-ECN-0101-2013-513-000636774