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논문 기본 정보

자료유형
학술저널
저자정보
Han, Jung-Hee (Korea Institute of Toxicology, KRICT) Cha, Shin-Woo (Korea Institute of Toxicology, KRICT) Kim, Choong-Yong (Korea Institute of Toxicology, KRICT) Lee, Gab-Soo (Korea Institute of Toxicology, KRICT) Suh, Jeong-Eun (Korea Institute of Toxicology, KRICT) Kim, Joon-Kyum (Medicinal Research Center, Chong Kun Dang Co.) Kim, Jong-Choon (College of Veterinary Medicine, Chonnam National University) Kang, Boo-Hyon (Korea Institute of Toxicology, KRICT)
저널정보
한국응용약물학회 The journal of applied pharmacology : the official journal of the Korean Society of Applied Pharmacology The journal of applied pharmacology : the official journal of the Korean Society of Applied Pharmacology 제12권 제1호
발행연도
2004.1
수록면
49 - 54 (6page)

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초록· 키워드

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The present study was conducted to investigate the potential subacute toxicity of CKD-602 by a 5-day repeated intravenous administration in Sprague-Dawley rats. CKD-602 was administered intravenously to male rats at dose levels of 0, 0.08, 0.2, and 0.5 mg/kg for 5 days. Studies included general observation, body weight changes, ophthalmoscopic examination, hematology, se겨m biochemistry, gross findings at necropsy and organ weight measurement. There were no deaths in any treatment group and treatment related clinical sign was depilation in the 0.5 mg/kg groups. The decrease or suppression of body weight was also observed dose-dependently in all treatment groups. Decreased leukocyte in all treatment groups, decreased platelet in the above 0.2 mg/kg groups and increase in the serum levels of total cholesterol in the 0.5 mg/kg group were considered as a treatment related toxic effects. Decreased weight of thymus in all treatment groups anti decreased weight of spleen in the above 0.2 mg/kg group were observed. The intravenous administration of CKD-602 caused depilation and decreased weight and had toxic effect on the leukocyte, platelet, spleen and thymus. In the condition of this study, the target organs were spleen and thymus and the toxic effect level was determined to be 0.2 mg/kg, but no-observed-adverse-effect level (NOAEL) was considered to be lower than 0.08 mg/kg.

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