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Hvdroquinone: Assessment of genotoxic potential in the alkaline comet assay.对苯二酚:碱性彗星试验中遗传毒性潜力的评估。 (注:原文中“Hvdroquinone”拼写错误,应为“Hydroquinone”)
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The toxicology of hydroquinone--relevance to occupational and environmental exposure.对苯二酚的毒理学——与职业和环境暴露的相关性。
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In vivo Comet assay on isolated kidney cells to distinguish genotoxic carcinogens from epigenetic carcinogens or cytotoxic compounds.对分离的肾细胞进行体内彗星试验,以区分遗传毒性致癌物与表观遗传致癌物或细胞毒性化合物。
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NTP Toxicology and Carcinogenesis Studies of Hydroquinone (CAS No. 123-31-9) in F344/N Rats and B6C3F1 Mice (Gavage Studies).对F344/N大鼠和B6C3F1小鼠进行的对苯二酚(CAS编号123 - 31 - 9)的NTP毒理学和致癌性研究(灌胃研究)
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Covalent protein adducts of hydroquinone in tissues from rats: quantitation of sulfhydryl-bound forms following single gavage or intraperitoneal administration or repetitive gavage administration.大鼠组织中对苯二酚的共价蛋白加合物:单次灌胃、腹腔注射或重复灌胃给药后巯基结合形式的定量分析
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Down-regulation of Polη expression leads to increased DNA damage, apoptosis and enhanced S phase arrest in L-02 cells exposed to hydroquinone.下调 Polη 的表达会导致 L-02 细胞在暴露于对苯二酚时产生更多的 DNA 损伤、凋亡,并增强 S 期阻滞。
Toxicol Lett. 2012 Oct 17;214(2):209-17. doi: 10.1016/j.toxlet.2012.08.025. Epub 2012 Sep 5.
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Toxicology and carcinogenesis study of styrene-acrylonitrile trimer in F344/N rats (perinatal and postnatal feed studies).F344/N大鼠中苯乙烯-丙烯腈三聚体的毒理学和致癌性研究(围产期和产后饲料研究)
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Measurement of cell proliferation in the kidneys of Fischer 344 and Sprague-Dawley rats after gavage administration of hydroquinone.对经口给予对苯二酚后的Fischer 344大鼠和Sprague-Dawley大鼠肾脏中的细胞增殖进行测量。
Fundam Appl Toxicol. 1994 Oct;23(3):397-406. doi: 10.1006/faat.1994.1121.
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NTP Toxicology and Carcinogenesis Studies of t-Butylhydroquinone (CAS No. 1948-33-0) in F344/N Rats and B6C3F(1) Mice (Feed Studies).叔丁基对苯二酚(CAS编号:1948 - 33 - 0)在F344/N大鼠和B6C3F(1)小鼠中的NTP毒理学与致癌性研究(饲料研究)
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本文引用的文献

1
The effects of strawberry tree water leaf extract, arbutin and hydroquinone on haematological parameters and levels of primary DNA damage in white blood cells of rats.草莓树水叶提取物、熊果苷和对苯二酚对大鼠血液学参数和白细胞初级 DNA 损伤水平的影响。
J Ethnopharmacol. 2018 Apr 6;215:83-90. doi: 10.1016/j.jep.2017.12.039. Epub 2017 Dec 28.
2
Disposition of [C]hydroquinone in Harlan Sprague-Dawley rats and B6C3F1/N mice: species and route comparison.[C]对苯二酚在哈兰·斯普拉格-道利大鼠和B6C3F1/N小鼠体内的处置:物种与给药途径比较
Xenobiotica. 2018 Nov;48(11):1128-1141. doi: 10.1080/00498254.2017.1398847. Epub 2017 Nov 22.
3
HPLC-UV Method for the Identification and Screening of Hydroquinone, Ethers of Hydroquinone and Corticosteroids Possibly Used as Skin-Whitening Agents in Illicit Cosmetic Products.用于鉴定和筛查对苯二酚、对苯二酚醚类以及可能在非法化妆品中用作美白剂的皮质类固醇的高效液相色谱 - 紫外检测法
J Chromatogr Sci. 2016 Mar;54(3):343-52. doi: 10.1093/chromsci/bmv147. Epub 2015 Oct 13.
4
Critical issues with the in vivo comet assay: A report of the comet assay working group in the 6th International Workshop on Genotoxicity Testing (IWGT).体内彗星试验的关键问题:第六届国际遗传毒性测试研讨会(IWGT)彗星试验工作组报告
Mutat Res Genet Toxicol Environ Mutagen. 2015 May 1;783:6-12. doi: 10.1016/j.mrgentox.2014.09.006. Epub 2014 Sep 22.
5
Evaluation of in vivo mutagenicity of hydroquinone in Muta™ mice.对苯二酚在Muta™小鼠体内的致突变性评估。
Mutat Res Genet Toxicol Environ Mutagen. 2014 Dec;775-776:94-8. doi: 10.1016/j.mrgentox.2014.10.009. Epub 2014 Oct 28.
6
International Conference on Harmonisation; guidance on S2(R1) Genotoxicity Testing and Data Interpretation for Pharmaceuticals intended for Human Use; availability. Notice.国际协调会议;人用药品S2(R1)遗传毒性试验和数据解读指南;可获取性。通知。
Fed Regist. 2012 Jun 7;77(110):33748-9.
7
Association of advanced chronic progressive nephropathy (CPN) with renal tubule tumors and precursor hyperplasia in control F344 rats from two-year carcinogenicity studies.在两项为期两年的致癌性研究中,对照F344大鼠的晚期慢性进行性肾病(CPN)与肾小管肿瘤及前期增生的关联。
Toxicol Pathol. 2012 Apr;40(3):473-81. doi: 10.1177/0192623311431948. Epub 2012 Jan 31.
8
Towards a more reliable comet assay: optimising agarose concentration, unwinding time and electrophoresis conditions.迈向更可靠的彗星实验:优化琼脂糖浓度、解旋时间和电泳条件。
Mutat Res. 2011 Sep 18;724(1-2):41-5. doi: 10.1016/j.mrgentox.2011.05.010. Epub 2011 May 30.
9
Final amended safety assessment of hydroquinone as used in cosmetics.关于化妆品中氢醌使用的最终修订安全性评估。
Int J Toxicol. 2010 Nov-Dec;29(6 Suppl):274S-87. doi: 10.1177/1091581810385957.
10
The comet assay as an indicator test for germ cell genotoxicity.彗星试验作为生殖细胞遗传毒性的指示性检测方法。
Mutat Res. 2009 Jan-Feb;681(1):3-12. doi: 10.1016/j.mrrev.2008.03.005. Epub 2008 Mar 30.

对苯二酚:碱性彗星试验中遗传毒性潜力的评估。 (注:原文中“Hvdroquinone”拼写错误,应为“Hydroquinone”)

Hvdroquinone: Assessment of genotoxic potential in the alkaline comet assay.

作者信息

O'Donoghue John L, Beevers Carol, Buard Annie

机构信息

Department of Environmental Medicine, School of Medicine and Dentistry, University of Rochester, Box EHSC, 601 Elmwood Ave., Rochester, NY, 14642, United States.

Exponent International Ltd, The Lenz, Hornbeam Park, Harrogate, HG2 8RE, United Kingdom.

出版信息

Toxicol Rep. 2021 Jan 11;8:206-214. doi: 10.1016/j.toxrep.2021.01.005. eCollection 2021.

DOI:10.1016/j.toxrep.2021.01.005
PMID:33489780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7810912/
Abstract

Hydroquinone (HQ) exposure is common as it is a natural component of plant-based foods and is used in some fingernail polishes, hair dyes, and skin lighteners. Industrially it is used as an antioxidant, polymerization inhibitor, and reducing agent. The current study was undertaken to determine whether HQ may cause DNA damage in an comet assay in F344 rats. DNA strand breaks were assessed in the duodenum as a direct tissue contact site, the testes, and the liver and kidneys, which were tumor sites in bioassays. Rats were exposed to HQ by gavage at 0, 105, 210, or 420 mg/kg/day. At all dose levels, mean % tail intensity and tail moment values for all tissues in animals given HQ were similar to the control. There were no statistically significant increases in tail intensity in any tissue following HQ treatment of male and female rat and data for all animals fell within the available historical control ranges for each tissue. There was no evidence of induction of DNA damage in cells isolated from duodenum, kidney or liver of male and female rats or in the testes of male rats following exposure to HQ at a dose levels up to 420 mg/kg/day, which caused acute renal necrosis.

摘要

对苯二酚(HQ)暴露很常见,因为它是植物性食物的天然成分,并且用于某些指甲油、染发剂和皮肤美白剂中。在工业上,它用作抗氧化剂、聚合抑制剂和还原剂。当前的研究旨在通过彗星试验确定HQ是否会在F344大鼠中导致DNA损伤。在十二指肠(作为直接的组织接触部位)、睾丸以及肝脏和肾脏(在生物测定中为肿瘤发生部位)中评估DNA链断裂情况。大鼠通过灌胃接受0、105、210或420mg/kg/天的HQ暴露。在所有剂量水平下,给予HQ的动物所有组织的平均尾强度百分比和尾矩值与对照组相似。对雄性和雌性大鼠进行HQ处理后,任何组织中的尾强度均无统计学上的显著增加,并且所有动物的数据均落在每个组织可用的历史对照范围内。在暴露于高达420mg/kg/天的HQ后,在雄性和雌性大鼠的十二指肠、肾脏或肝脏分离的细胞中以及雄性大鼠的睾丸中,均没有诱导DNA损伤的证据,该剂量导致了急性肾坏死。