Nakagawa K, Hidaka T, Kitano M, Asakura M, Kamigaito T, Noguchi T, Hosoe K
Functional Food Ingredients Division, Healthcare Products Business Unit, Kaneka Corporation, 3-2-4, Nakanoshima, Kita-ku, Osaka 530-8288, Japan.
Food Chem Toxicol. 2008 Jul;46(7):2525-32. doi: 10.1016/j.fct.2008.04.008. Epub 2008 Apr 14.
Licorice flavonoid oil (LFO) is a new functional food ingredient. In this study, the genotoxicity of LFO was investigated using a test battery of three different methods. In a reverse mutation assay using four Salmonella typhimurium strains and Escherichia coli, LFO did not increase the number of revertant colonies in any tester strain with or without metabolic activation by rat liver S9 mix. In a chromosomal aberration test using Chinese hamster lung (CHL/IU) cells, LFO did not induce any chromosomal aberrations either in the short period test without rat liver S9 mix or in the continuous treatment (24 h or 48 h) test. However, in the short-period test with rat liver S9 mix, LFO induced structural chromosomal aberrations at concentrations higher than 0.6 mg/mL. A bone marrow micronucleus test using male F344 rats was initially conducted. The animals were dosed by oral gavage at doses up to 5000 mg/kg/day. No significant or dose-dependent increases in the frequency of micronucleated polychromatic erythrocytes (MNPCE) were observed and the high dose suppressed the ratio of polychromatic erythrocytes (PCE) to total erythrocytes. Subsequently, a liver and peripheral blood micronucleus test using male F344 rats was conducted. No micronuclei induction either in hepatocytes or PCE was observed even at the highest dose of 5000 mg/kg/day. From the findings obtained from the genotoxicity assays performed in this study and the published pharmacokinetic studies of LFO, it appears unlikely that dietary consumption of LFO will present any genotoxic hazard to humans.
甘草黄酮油(LFO)是一种新型功能性食品成分。在本研究中,使用三种不同方法的测试组合对LFO的遗传毒性进行了研究。在使用四种鼠伤寒沙门氏菌菌株和大肠杆菌的回复突变试验中,无论有无大鼠肝脏S9混合液的代谢活化作用,LFO在任何测试菌株中均未增加回复菌落的数量。在使用中国仓鼠肺(CHL/IU)细胞的染色体畸变试验中,LFO在无大鼠肝脏S9混合液的短期试验或连续处理(24小时或48小时)试验中均未诱导任何染色体畸变。然而,在有大鼠肝脏S9混合液的短期试验中,LFO在浓度高于0.6mg/mL时诱导了染色体结构畸变。最初进行了一项使用雄性F344大鼠的骨髓微核试验。动物经口灌胃给药,剂量高达5000mg/kg/天。未观察到微核多染红细胞(MNPCE)频率有显著或剂量依赖性增加,且高剂量组抑制了多染红细胞(PCE)与总红细胞的比例。随后,进行了一项使用雄性F344大鼠的肝脏和外周血微核试验。即使在最高剂量5000mg/kg/天的情况下,也未观察到肝细胞或PCE中有微核诱导现象。根据本研究中进行的遗传毒性试验结果以及已发表的LFO药代动力学研究,膳食摄入LFO似乎不太可能对人类造成任何遗传毒性危害。