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在一项使用F344大鼠的亚慢性毒性研究中对作为食品添加剂的鞣花酸进行安全性评估。

Safety assessment of ellagic acid, a food additive, in a subchronic toxicity study using F344 rats.

作者信息

Tasaki M, Umemura T, Maeda M, Ishii Y, Okamura T, Inoue T, Kuroiwa Y, Hirose M, Nishikawa A

机构信息

Division of Pathology, National Institute of Health Sciences, Tokyo, Japan.

出版信息

Food Chem Toxicol. 2008 Mar;46(3):1119-24. doi: 10.1016/j.fct.2007.10.043. Epub 2007 Nov 21.

DOI:10.1016/j.fct.2007.10.043
PMID:18155344
Abstract

Ellagic acid is a phenolic acid compound, used as a food additive for its antioxidative properties. Because of its chemical characteristics, use is also to be expected in cosmetics. The present 90-day subchronic toxicity study was performed in F344 rats at dose levels of 0, 1.25, 2.5 and 5% in powdered basal diet, with actual doses of 9.4, 19.1, 39.1 g/kg b.w., respectively, in males, and 10.1, 20.1, 42.3 g/kg b.w. in females. No mortality or treatment-related clinical signs were observed throughout the experimental period. Body weight gain was significantly reduced from weeks 3 (5% group), 6 (2.5% group) and 7 (1.25% group) to the end of the experiment (except week 8 in the lowest group) in the treated females, the final body weights being decreased in the 5% (92.5%), 2.5% (94.2%) and 1.25% (94.8%) treated groups as compared to the control. Changes in MCV and serum AST, ALP, Ca, Cl and P were sporadically observed, but these were not considered to be treatment-related alterations. There were no obvious histopathological changes in any of the groups. The no-observed-effect level (NOEL) was estimated to be 5% (3011 mg/kg b.w./day) for males and the no-observed-adverse-effect level (NOAEL) and NOEL in females were estimated to be 5% (3254 mg/kg b.w./day) and <1.25% (778 mg/kg b.w./day), respectively.

摘要

鞣花酸是一种酚酸化合物,因其抗氧化特性而用作食品添加剂。由于其化学特性,预计也可用于化妆品中。本研究对F344大鼠进行了为期90天的亚慢性毒性试验,在粉状基础饲料中分别添加0%、1.25%、2.5%和5%的鞣花酸,雄性大鼠的实际剂量分别为9.4、19.1、39.1 g/kg体重,雌性大鼠的实际剂量分别为10.1、20.1、42.3 g/kg体重。在整个实验期间未观察到死亡或与处理相关的临床症状。在处理后的雌性大鼠中,从第3周(5%组)、第6周(2.5%组)和第7周(1.25%组)到实验结束(最低剂量组的第8周除外)体重增加显著减少,与对照组相比,5%(92.5%)、2.5%(94.2%)和1.25%(94.8%)处理组的最终体重下降。偶尔观察到平均红细胞体积(MCV)以及血清谷草转氨酶(AST)、碱性磷酸酶(ALP)、钙(Ca)、氯(Cl)和磷(P)的变化,但这些变化不被认为与处理有关。各实验组均未观察到明显的组织病理学变化。雄性大鼠的未观察到效应水平(NOEL)估计为5%(3011 mg/kg体重/天),雌性大鼠的未观察到有害效应水平(NOAEL)和NOEL分别估计为5%(3254 mg/kg体重/天)和<1.25%(778 mg/kg体重/天)。

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