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异丙醇致突变性的体外和体内试验。

In vitro and in vivo assays of isopropanol for mutagenicity.

作者信息

Kapp R W, Marino D J, Gardiner T H, Masten L W, McKee R H, Tyler T R, Ivett J L, Young R R

机构信息

Toxicology Division, BioTox, Inc., Richmond, Virginia 23236.

出版信息

Environ Mol Mutagen. 1993;22(2):93-100. doi: 10.1002/em.2850220207.

Abstract

To assess the mutagenic potential of isopropanol, an in vitro Chinese hamster ovary (CHO) cell/HGPRT gene mutation assay and a bone marrow micronucleus study in mice were conducted. In the CHO/HGPRT assay, concentration levels ranged from 0.5 to 5.0 mg/ml. No elevated mutant frequencies attributable to treatment were observed in the test under either activated or non-activated conditions. In the micronucleus assay, mice were injected intraperitoneally (IP) with either 350, 1,173, or 2,500 mg/kg of isopropanol at constant volumes of 10 ml/kg. No increased incidence of micronuclei was observed in bone marrow polychromatic erythrocytes (PCEs) harvested at 24, 48, or 72 hr post-dosing. In both assays, negative and positive control mutant frequencies were within historical control ranges. These results, in conjunction with previously published data, clearly demonstrate that isopropanol is not a mutagen.

摘要

为评估异丙醇的致突变潜力,开展了一项体外中国仓鼠卵巢(CHO)细胞/次黄嘌呤鸟嘌呤磷酸核糖转移酶(HGPRT)基因突变试验以及一项小鼠骨髓微核研究。在CHO/HGPRT试验中,浓度水平为0.5至5.0毫克/毫升。在活化或非活化条件下的试验中,均未观察到因处理导致的突变频率升高。在微核试验中,以10毫升/千克的恒定体积给小鼠腹腔注射350、1173或2500毫克/千克的异丙醇。给药后24、48或72小时采集的骨髓嗜多染红细胞(PCE)中,未观察到微核发生率增加。在这两项试验中,阴性和阳性对照的突变频率均在历史对照范围内。这些结果与先前发表的数据一起,清楚地表明异丙醇不是诱变剂。

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