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三氧化二锑的遗传毒理学评估。

An assessment of the genetic toxicology of antimony trioxide.

作者信息

Elliott B M, Mackay J M, Clay P, Ashby J

机构信息

Central Toxicology Laboratory, Macclesfield, Cheshire, UK.

出版信息

Mutat Res. 1998 Jul 8;415(1-2):109-17. doi: 10.1016/s1383-5718(98)00065-5.

Abstract

Antimony trioxide (Sb2O3, CAS 1309-64-4) has been examined in a range of in vitro and in vivo genotoxicity assays. Negative results were obtained with the Salmonella/microsome assay and the L5178Y mutation assay, but a positive response was observed in the in vitro cytogenetic assay using isolated human peripheral lymphocytes. However, in vivo, antimony trioxide was non-clastogenic in the mouse bone marrow micronucleus assay, following oral gavage administration for 1, 7, 14 or 21 days at dose levels of up to 5000 mg/kg (single dose) or 1000 mg/kg (repeat dose). A negative result was also obtained in the in vivo rat liver DNA repair (unscheduled DNA synthesis) assay following a single oral gavage administration of doses up to 5000 mg/kg. These data show no genotoxicity for antimony trioxide in vivo and do not confirm a previous report of clastogenicity in the mouse on repeated dosing. It is concluded that antimony trioxide is not genotoxic in vivo and does not present a genotoxic hazard to humans.

摘要

三氧化二锑(Sb2O3,化学物质登录号1309 - 64 - 4)已在一系列体外和体内遗传毒性试验中进行了检测。沙门氏菌/微粒体试验和L5178Y突变试验结果为阴性,但在使用分离的人外周血淋巴细胞进行的体外细胞遗传学试验中观察到了阳性反应。然而,在体内,经口灌胃给予小鼠长达1、7、14或21天,剂量高达5000 mg/kg(单次剂量)或1000 mg/kg(重复剂量)后,三氧化二锑在小鼠骨髓微核试验中无致断裂作用。单次经口灌胃给予大鼠高达5000 mg/kg的剂量后,在体内大鼠肝脏DNA修复(非程序性DNA合成)试验中也得到了阴性结果。这些数据表明三氧化二锑在体内无遗传毒性,并且不证实之前关于小鼠重复给药有断裂作用的报道。结论是三氧化二锑在体内无遗传毒性,对人类不存在遗传毒性危害。

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