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논문 기본 정보

자료유형
학술저널
저자정보
Ji-Yeong Jo (Laboratories of Pharmacology) Tae-Hyung Kim (부산대학교) Hye-Young Jeong (Laboratories of Pharmacology) Sung-Mee Lim (동명대학교) Hyung-Sik Kim (부산대학교) Dong-Soon Im (Laboratories of Pharmacology)
저널정보
한국독성학회 Toxicological Research Toxicological Research Vol.27 No.3
발행연도
2011.9
수록면
185 - 190 (6page)

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초록· 키워드

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Di-(2-ethylhexyl)-phthalate (DEHP), the most widely utilized industrial plastizer and a ubiquitous environmental contaminant, can act on peroxisome proliferators-activated nuclear hormone receptor family (PPAR) isoforms. To understand the contribution of sphingolipid metabolism to DEHP-induced hepatotoxicity, effect of DEHP exposure on activities of sphingolipid metabolic enzymes in rat liver was investigated. DEHP (250, 500 or 750 ㎎/㎏) was administered to the rats through oral gavage daily for 28 days. The activities of acidic and alkaline ceramidases were slightly increased in 250 ㎎/㎏ DEHP-administered rat livers and significantly elevated in 500 ㎎/㎏ DEHP-administered ones, although the level of 750 ㎎/㎏ DEHP-administered ones was not increased. Neutral ceramidase, acidic and neutral sphingomyelinases, sphingomyeline synthase and ceramide syhthase were not changed at all by DEHP exposure. Therefore, acidic and alkaline ceramidases might play important roles in DEHP-induced hepatotoxicity.

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INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
ACKNOWLEDGEMENT
REFERENCES

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