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泛醇的致突变和遗传毒性潜力评估。

Evaluation of the mutagenic and genotoxic potential of ubiquinol.

作者信息

Kitano Mitsuaki, Mizuhashi Fukutaro, Kubo Hiroshi, Kishida Hideyuki, Fujii Kenji, Kitahara Mikio, Hosoe Kazunori

机构信息

Life Science Research Laboratories, Kaneka Corporation, Hyogo, Japan.

出版信息

Int J Toxicol. 2007 Nov-Dec;26(6):533-44. doi: 10.1080/10915810701707460.

Abstract

Ubiquinol (the reduced form of coenzyme Q(10)) is the two-electron reduction product of ubiquinone (the oxidized form of coenzyme Q(10)), and has been shown to be an integral part of living cells, where it functions as an antioxidant in both mitochondria and lipid membranes. To provide information to enable a Generally Regarded as Safe (GRAS) evaluation for the use of ubiquinol in selected foods, a series of Organisation of Economic Cooperation and Development (OECD) and good laboratory practice (GLP) toxicological studies was conducted to evaluate the mutagenic and genotoxic potential of Kaneka QH brand of ubiquinol. Ubiquinol did not induce reverse mutations in Salmonella typhimurium strains TA100, TA1535, TA98, and TA1537 and Escherichia coli WP2uvrA at concentrations up to 5000 mu g/plate, in either the absence and presence of exogenous metabolic activation by rat liver S9. Likewise, ubiquinol did not induce chromosome aberrations in Chinese hamster lung fibroblast (CHL/IU) cells in short-term (6-h) tests with or without rat liver S9 at concentrations up to 5000 mu g/ml or in a continuous (24-h) treatment test at concentrations up to 1201 mu g/ml. Finally, no mortalities, no abnormal clinical signs, and no significant increase in chromosome damage were observed in an in vivo micronucleus test when administered orally at doses up to 2000 mg/kg/day. Thus, ubiquinol was evaluated as negative in the bacterial reverse mutation, chromosomal aberration, and rat bone marrow micronucleus tests under the conditions of these assays.

摘要

泛醇(辅酶Q(10)的还原形式)是泛醌(辅酶Q(10)的氧化形式)的双电子还原产物,并且已被证明是活细胞的一个组成部分,在其中它在线粒体和脂质膜中均作为抗氧化剂发挥作用。为了提供信息以对泛醇在特定食品中的使用进行一般认为安全(GRAS)评估,开展了一系列经济合作与发展组织(OECD)及良好实验室规范(GLP)毒理学研究,以评估Kaneka QH品牌泛醇的致突变和遗传毒性潜力。在高达5000μg/平板的浓度下,无论有无大鼠肝脏S9进行外源性代谢激活,泛醇均未在鼠伤寒沙门氏菌菌株TA100、TA1535、TA98和TA1537以及大肠杆菌WP2uvrA中诱导回复突变。同样,在高达5000μg/ml的浓度下,无论有无大鼠肝脏S9,泛醇在短期(6小时)试验中均未在中国仓鼠肺成纤维细胞(CHL/IU)中诱导染色体畸变,在高达1201μg/ml的浓度下进行连续(24小时)处理试验时也未诱导染色体畸变。最后,在体内微核试验中,当以高达2000mg/kg/天的剂量口服给药时,未观察到死亡、异常临床体征以及染色体损伤的显著增加。因此,在这些试验条件下,泛醇在细菌回复突变、染色体畸变和大鼠骨髓微核试验中被评估为阴性。

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