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논문 기본 정보

자료유형
학술저널
저자정보
Je-Won Ko (Chonnam National University) In-Chul Lee (Chonnam National University) Sung-Hyuk Park (Chonnam National University) Changjong Moon (Chonnam National University) Seong-Soo Kang (Chonnam National University) Sung-Ho Kim (Chonnam National University) Jong-Choon Kim (Chonnam National University)
저널정보
한국실험동물학회 Laboratory Animal Research Laboratory Animal Research Vol.30 No.4
발행연도
2014.12
수록면
174 - 180 (7page)

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초록· 키워드

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We investigated the protective effects of pine bark extract (pycnogenol<SUP>®</SUP>, PYC) against cisplatin-induced hepatotoxicity and oxidative stress in rats. Twenty-four male rats were divided into the following four groups: (1) vehicle control, (2) cisplatin (7.5 mg/kg), (3) cisplatin & PYC 10 (10 mg/kg/day), and (4) cisplatin & PYC 20 (20 mg/kg/day). A single intraperitoneal injection of cisplatin induced hepatotoxicity, as evidenced by an increase in serum aminotransferase and histopathological alterations, including degeneration/necrosis of hepatocytes, vacuolation, and sinusoidal dilation. In addition, an increase in the malondialdehyde (MDA) concentration and a decrease in the reduced glutathione (GSH) content and catalase (CAT), superoxide dismutase (SOD), and glutathione S-transferase (GST) activities were observed in the cisplatin-treated rat hepatic tissues. In contrast, PYC treatment effectively prevented cisplatin-induced hepatotoxicity, including the elevation of aminotransferase and histopathological lesions, in a dosedependent manner. Moreover, PYC treatment also induced antioxidant activity by decreasing MDA level and increasing GSH content and SOD and GST activities in liver tissues. These results indicate that PYC has a protective effect against acute hepatotoxicity induced by cisplatin in rats, and that the protective effects of PYC may be due to inhibiting lipid peroxidation and increasing antioxidant activity.

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Materials and Methods
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