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在一系列标准试验中对[具体物质]的[相关特性]和遗传毒性进行评估。 (注:原文中部分关键信息缺失,翻译只能做到尽量符合结构,完整准确翻译需补充完整信息)

Evaluation of and genotoxicity of in a standard battery of assays.

作者信息

Yun Jun-Won, Kim Yun-Soon, Kwon Euna, Kim Seung-Hyun, You Ji-Ran, Kim Hyeon Hoe, Che Jeong-Hwan, Kang Byeong-Cheol

机构信息

Department of Biotechnology, The Catholic University of Korea, Bucheon, Gyeonggi-do, Korea.

Department of Experimental Animal Research, Biomedical Research Institute, Seoul National University Hospital, Seoul, Korea.

出版信息

Lab Anim Res. 2017 Sep;33(3):231-236. doi: 10.5625/lar.2017.33.3.231. Epub 2017 Sep 27.

Abstract

Among three representative species of Angelica found in Asian countries, including Korea, China, and Japan, (AA) has been used as traditional herbal medicine with antitumor, anti-inflammatory, anti-obesity, and anti-diabetes activities. In this study, the potential genotoxicity and mutagenicity of the AA extract were examined in a battery of and tests (bacterial reverse mutation assay, chromosomal aberrations assay, and micronucleus assay) in accordance with the test guidelines for toxicity testing developed by the Organization for Economic Cooperation and Development. Upon testing in the bacterial mutation assay (Ames test) using five TA98, TA100, TA102, TA1535 and TA1537, no significant increase the number of revertant colonies in the metabolic activation system and non-activation system was noted in the AA extract groups. Also, in the chromosome aberration test, the AA extract did not cause chromosomal aberration with or without metabolic activation by S9 mix. A bone marrow micronucleus test of mice demonstrated that the incidence of micronucleated polychromatic erythrocytes in the AA extract groups (500, 1000 and 2000 mg/kg BW) was equivalent to that of the negative control group. Based on these results from a standard battery of assays, the AA extract was concluded to have no genotoxic at the proper dose.

摘要

在亚洲国家(包括韩国、中国和日本)发现的三种代表性当归属植物中,当归已被用作具有抗肿瘤、抗炎、抗肥胖和抗糖尿病活性的传统草药。在本研究中,根据经济合作与发展组织制定的毒性测试指南,通过一系列测试(细菌回复突变试验、染色体畸变试验和微核试验)对当归提取物的潜在遗传毒性和致突变性进行了检测。在使用五种鼠伤寒沙门氏菌菌株TA98、TA100、TA102、TA1535和TA1537进行的细菌突变试验(艾姆斯试验)中,当归提取物组在代谢活化系统和非活化系统中回复菌落数均未显著增加。此外,在染色体畸变试验中,无论有无S9混合物的代谢活化,当归提取物均未引起染色体畸变。小鼠骨髓微核试验表明,当归提取物组(500、1000和2000mg/kg体重)中微核多染红细胞的发生率与阴性对照组相当。基于这些标准试验的结果,得出当归提取物在适当剂量下无遗传毒性的结论。

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