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对苯二酚在Muta™小鼠体内的致突变性评估。

Evaluation of in vivo mutagenicity of hydroquinone in Muta™ mice.

作者信息

Matsumoto Mariko, Masumori Shoji, Hirata-Koizumi Mutsuko, Ono Atsushi, Honma Masamitsu, Yokoyama Kazuhito, Hirose Akihiko

机构信息

Division of Risk Assessment, National Institute of Health Sciences, Tokyo, Japan; Department of Epidemiology and Environmental Health, Juntendo University Faculty of Medicine, Tokyo, Japan.

Public Interest Incorporated Foundation Biosafety Research Center, Shizuoka, Japan.

出版信息

Mutat Res Genet Toxicol Environ Mutagen. 2014 Dec;775-776:94-8. doi: 10.1016/j.mrgentox.2014.10.009. Epub 2014 Oct 28.

Abstract

Hydroquinone (HQ) is used in skin bleaching agents, hair dyes, and finger nail treatments. Many skin-lightening cosmetics that contain HQ are currently marketed in Japan. Concerns have been expressed regarding health risks to the general population because the carcinogenicity of HQ was previously suggested in animal studies. HQ induced hepatocellular adenomas and forestomach hyperplasias in mice and renal tubular cell adenomas in male rats. In the present study, the lacZ transgenic mutation assay was conducted according to OECD test guideline 488 to determine whether mutagenic mechanisms were involved in HQ-induced carcinogenesis. Male Muta™ mice were repeatedly administered HQ orally at dosages of 0, 25, 50, 100, or 200mg/kg bw/day for 28 days. Body weight gain was decreased in all treatment groups. No significant differences were observed in mutant frequencies in the liver, stomach, lung, or kidney between HQ-treated mice and the concurrent negative controls, whereas the significant induction of mutations was noted in the positive control, N-ethyl-N-nitrosourea. These results suggest that a mutagenic mechanism is not responsible for HQ-induced carcinogenesis.

摘要

对苯二酚(HQ)用于皮肤美白剂、染发剂和指甲护理产品中。目前,许多含HQ的美白化妆品在日本市场销售。由于此前动物研究表明HQ具有致癌性,人们对普通人群的健康风险表示担忧。HQ可诱发小鼠肝细胞腺瘤和前胃增生以及雄性大鼠肾小管细胞腺瘤。在本研究中,根据经合组织(OECD)测试指南488进行了lacZ转基因突变试验,以确定诱变机制是否参与HQ诱导的致癌过程。雄性Muta™ 小鼠连续28天每天按0、25、50、100或200mg/kg体重的剂量口服HQ。所有治疗组的体重增加均减少。在HQ处理的小鼠与同期阴性对照组之间,肝脏、胃、肺或肾脏中的突变频率未观察到显著差异,而在阳性对照N-乙基-N-亚硝基脲中观察到显著的突变诱导。这些结果表明,诱变机制与HQ诱导的致癌作用无关。

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