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N-乙酰-L-天冬氨酸对斯普拉格-道利大鼠的急性和重复剂量经口毒性

Acute and repeated dose oral toxicity of N-acetyl-l-aspartic acid in Sprague-Dawley rats.

作者信息

Delaney Bryan, Amanda Shen Z, Powley Charles R, Gannon Shawn, Munley Susan A, Maxwell Carl, Barnett John F

机构信息

Pioneer Hi-Bred International Inc., 7250 NW 62nd Avenue, P.O. Box 552, Johnston, IA 50131, United States.

出版信息

Food Chem Toxicol. 2008 Jun;46(6):2023-34. doi: 10.1016/j.fct.2008.01.042. Epub 2008 Feb 2.

DOI:10.1016/j.fct.2008.01.042
PMID:18329151
Abstract

N-acetyl-l-aspartic acid (NAA) is a constituent of the mammalian central nervous system (CNS) that has been identified in a number of commonly consumed foods. The current study reports the outcome of acute and repeated dose oral toxicology studies conducted with NAA in Sprague-Dawley (SD) rats. No mortalities or evidence of adverse effects were observed in SD rats following acute oral administration of 2000mg/kg NAA. In a separate study, NAA was added to the diets of SD rats (n=10/sex group) at concentrations corresponding to daily doses of 10, 100, or 1000mg/kg/day for 14 consecutive days and 100, 500, and 1000mg/kg/day for another 14 days. All rats survived until scheduled sacrifice and no differences in body weights, feed consumption values, or clinical signs were observed in any of the treatment groups. No biologically significant differences were observed in functional observational battery (FOB), motor activity evaluations, ophthalmologic examinations, hematology, coagulation, clinical chemistry, or organ weights of any of the NAA treatment groups. Further, no test substance-related gross or microscopic changes were observed in NAA exposure groups. Based on these results, NAA was not considered acutely toxic following oral exposure to 2000mg/kg and the no-observed-adverse-effect-level (NOAEL) for systemic toxicity from repeated dose dietary exposure to NAA is 1000mg/kg/day.

摘要

N-乙酰-L-天门冬氨酸(NAA)是哺乳动物中枢神经系统(CNS)的一种成分,已在多种常见食用食物中被发现。本研究报告了用NAA对斯普拉格-道利(SD)大鼠进行急性和重复剂量口服毒理学研究的结果。给SD大鼠急性口服2000mg/kg NAA后,未观察到死亡或不良反应迹象。在另一项研究中,将NAA以相当于每日剂量10、100或1000mg/kg/天的浓度添加到SD大鼠(每组雌雄各10只)的饮食中,持续14天,然后以100、500和1000mg/kg/天的浓度再持续14天。所有大鼠均存活至预定处死时间,各治疗组在体重、饲料消耗量或临床体征方面均未观察到差异。在任何NAA治疗组的功能观察组合(FOB)、运动活动评估、眼科检查、血液学、凝血、临床化学或器官重量方面,均未观察到生物学上的显著差异。此外,在NAA暴露组中未观察到与受试物相关的大体或显微镜下变化。基于这些结果,口服暴露于2000mg/kg的NAA不被认为具有急性毒性,重复剂量经饮食暴露于NAA的全身毒性未观察到不良反应水平(NOAEL)为1000mg/kg/天。

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