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자료유형
학술저널
저자정보
Jeon, Tae-Won (College of Pharmacy, Yeungnam University) Kim, Chun-Hwa (College of Pharmacy, Yeungnam University) Lee, Sang-Kyu (College of Pharmacy, Yeungnam University) Shin, Sil (College of Pharmacy, Yeungnam University) Choi, Jae-Ho (College of Pharmacy, Yeungnam University) Kang, Won-Ku (College of Pharmacy, Catholic University of Daegu) Kim, Sang-Hyun (College of Medicine, Kyungpook National University) Kang, Mi-Jeong (College of Pharmacy, Yeungnam University) Lee, Eung-Seok (College of Pharmacy, Yeungnam University) Jeong, Tae-Cheon (College of Pharmacy, Yeungnam University)
저널정보
한국응용약물학회 Biomolecules & Therapeutics(구 응용약물학회지) Biomolecules & therapeutics 제17권 제3호
발행연도
2009.1
수록면
318 - 324 (7page)

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1-Furan-2-yl-3-pyridin-2-yl-propenone (FPP-3) has recently been synthesized and characterized to have an anti-inflammatory activity through the inhibition of the production of nitric oxide. In the present study, adverse effects of FPP-3 on hepatic functions were determined in female BALB/c mice. When mice were administered with FPP-3 at 125, 250 or 500 mg/kg for 7 consecutive days orally, FPP-3 significantly increased absolute and relative weights of liver with a dose-dependent manner. In addition, FPP-3 administration dramatically increased the hepatotoxicity parameters in serum at 500 mg/kg, in association of hepatic necrosis. FPP-3 significantly induced several phase I enzyme activities. To elucidate the possible mechanism(s) involved in FPP-3 induced hepatotoxicity, we investigated the hepatic activities of free radical generating and scavenging enzymes and the level of hepatic lipid peroxidation. FPP-3 treatment significantly elevated the hepatic lipid peroxidation, measured as the thiobarbituric acid-reactive substance, and the activity of superoxide dismutase. Taken together, the present data indicated that reactive oxygen species might be involved in FPP-3-induced hepatotoxicity.

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