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首页> 外文期刊>Archives of Toxicology >A re-assessment of styrene-induced clastogenicity in mice in a subacute inhalation study.
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A re-assessment of styrene-induced clastogenicity in mice in a subacute inhalation study.

机译:在亚急性吸入研究中,对小鼠中苯乙烯诱导的致胶化性进行了重新评估。

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摘要

To date, a number of in vivo cytogenetic assays have studied the clastogenicity (chromosome aberrations, micronuclei formation) in bone marrow of rodents exposed to styrene by various routes. The majority of all these cytogenetic experiments yielded negative findings (Scott and Preston, Mutat Res 318:175-203, 1994). Recently published data from a micronucleus test in mice exposed via inhalation for up to 21 days showed some positive response, but was not fully conclusive (Vodicka et al., Chem Biol Interact 137:213-227, 2001). Since this exposure regimen has considerable relevance for workplace exposure, the present study was performed to further elucidate these findings. NMRI mice were exposed by whole body inhalation to styrene concentrations of 750 mg/m(3) and 1,500 mg/m(3) for 1, 3, 7, 14 and 21 consecutive days (6 h/day). Animals were killed directly after exposure and bone marrow was sampled for analysis of micronucleus induction. Under the experimental conditions used in the present investigation, there was no evidence of clastogenicity at any concentration or exposure interval.
机译:迄今为止,许多体内细胞遗传学测定方法已经研究了通过各种途径暴露于苯乙烯的啮齿类动物在骨髓中的致分裂性(染色体畸变,微核形成)。所有这些细胞遗传学实验中的大多数产生了阴性结果(Scott和Preston,Mutat Res 318:175-203,1994)。最近发表的通过吸入暴露多达21天的小鼠的微核试验数据显示出一些阳性反应,但尚未完全确定(Vodicka等人,Chem Biol Interact 137:213-227,2001)。由于这种接触方案与工作场所接触有很大关系,因此进行本研究是为了进一步阐明这些发现。将NMRI小鼠通过全身吸入连续1、3、7、14和21天(6小时/天)暴露于750 mg / m(3)和1,500 mg / m(3)的苯乙烯浓度。暴露后直接杀死动物,并取样骨髓以分析微核诱导。在本研究中使用的实验条件下,没有证据表明在任何浓度或暴露间隔下都具有致崩塌性。

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