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生育三烯酚富集组分的急性经口毒性和遗传毒性评价OA

Acute oral toxicity and genotoxicity assessment on tocotrienol-rich fraction

中文摘要英文摘要

目的:评价生育三烯酚富集组分(TRF)的急性经口毒性和遗传毒性.方法:依据食品安全国家标准,采用急性经口毒性试验评价其毒性级别,采用细菌回复突变试验、哺乳动物红细胞微核试验及小鼠精母细胞染色体畸变试验评价其遗传毒性.结果:TRF小鼠急性经口半数致死量(LD50)大于19.4 g/kg,属实际无毒级.细菌回复突变的两次独立试验中,加与不加S9其回变菌落数均未超过背景自发突变数的2倍,亦无剂量-反应关系,判定为阴性.哺乳动物红细胞微核试验中,2.5、5.0、10.0 g/kg受试物均未诱发小鼠骨髓嗜多染红细胞微核率的明显升高(P>0.05).小鼠精母细胞染色体畸变试验中,2.5、5.0、10.0 g/kg受试物均未诱发小鼠精母细胞的染色体畸变率及畸变细胞率显著升高(P>0.05).结论:在本实验条件下,TRF属于实际无毒级,未见相关遗传毒性

OBJECTIVE:To evaluate acute oral toxicity and genotoxicity of tocotrienol-rich fraction(TRF).METHODS:According to the national food safety standards,toxicity grade of TRF was evaluated using an acute oral toxicity test.Genotoxicity was assessed using a bacterial reverse mutation test,a mammalian erythrocyte micronucleus test,and a mouse spermatocyte chromosomal aberration test.RESULTS:The acute oral median lethal dose(LD50)of TRF in mice was greater than 19.4 g/kg,classifying it as non-toxic.In the bacterial reverse mutation test,the number of revertant colonies in two independent experiments(with and without S9 metabolic activation)did not exceed twice the background spontaneous mutation rate,and no dose-response relationship was observed,indicating a negative result.In the mammalian erythrocyte micronucleus test,doses of 2.5,5.0 and 10.0 g/kg TRF did not induce a significant increase in the micronucleus rate of mouse bone marrow polychromatic erythrocytes(P>0.05).In the mouse spermatocyte chromosome aberration test,no significant increases in the chromosome aberration rate or the percentage of aberrant cells were observed at any dose levels(P>0.05).CONCLUSION:Under the conditions of this study,TRF can be classified as non-toxic and it shows no evidence of genotoxicity.

胡培丽;张励;刘婷;郑济凡;刘师卜;单纯;李波

中国食品药品检定研究院,北京 102629中国食品药品检定研究院,北京 102629中国食品药品检定研究院,北京 102629中国食品药品检定研究院,北京 102629中国食品药品检定研究院,北京 102629北京市药品检验研究院,北京 102206中国食品药品检定研究院,北京 102629

医药卫生

生育三烯酚富集组分急性毒性遗传毒性小鼠

tocotrienol-rich fractionacute toxicitygenotoxicitymice

《癌变·畸变·突变》 2026 (4)

316-320,5

10.3969/j.issn.1004-616x.2026.04.009

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