[Hepatic lesions in F344 rats treated orally with beta-cyclodextrin for 13 weeks].

K Toyoda, S Hayashi, C Uneyama, T Kawanishi, K Takada, M Takahashi
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引用次数: 0

Abstract

A 13-week oral toxicity study of beta-cyclodextrin was carried out in F344 rats at the dose levels of 10, 5, 2.5, 1.25, 0.6 and 0% in powdered diet. Each group consisted of 10 males and 10 females. All animals survived at the end of the experiment, while a slight decrease in body-weight gain was observed in males of the 10%- and 5%-groups. Dose-dependent increases in serum levels of GOT, GPT and alkaline phosphatase were observed in treated animals of both sexes, and increases in serum levels of urea nitrogen and relative liver weights in treated males. Histopathologically, a dose-dependent increase in the severity of inflammatory cell infiltration was seen in the liver of treated animals, focal hepatocellular necrosis being detected in both sexes of the 10%-group and females of the 5%-group. These findings indicate that beta-cyclodextrin causes hepatocellular injury to rats when it is orally administered.

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[口服β -环糊精13周的F344大鼠肝脏病变]。
本研究对F344大鼠进行了10、5、2.5、1.25、0.6和0%粉饲给药剂量下的-环糊精13周口服毒性研究。每组由10名男性和10名女性组成。在实验结束时,所有的动物都存活了下来,而10%和5%组的雄性体重增加略有下降。治疗前后,雄性动物血清GOT、GPT和碱性磷酸酶水平呈剂量依赖性升高,雄性动物血清尿素氮水平和相对肝脏重量均升高。组织病理学上,治疗动物肝脏炎症细胞浸润的严重程度呈剂量依赖性增加,在10%组的两性和5%组的雌性中均检测到局灶性肝细胞坏死。这些发现表明,口服-环糊精可引起大鼠肝细胞损伤。
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