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水氯化副产物氯羟基呋喃酮混合物的细菌和哺乳动物细胞遗传毒性。

Bacterial and mammalian-cell genotoxicity of mixtures of chlorohydroxyfuranones, by-products of water chlorination.

作者信息

Mäki-Paakkanen Jorma, Komulainen Hannu, Kronberg Leif

机构信息

Laboratory of Toxicology, National Public Health Institute, Kuopio, Finland.

出版信息

Environ Mol Mutagen. 2004;43(4):217-25. doi: 10.1002/em.20017.

Abstract

The genotoxic responses of mixtures of four chlorohydroxyfuranones (CHFs), 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone (MX), 3,4-dichloro-5-hydroxy-2(5H)-furanone (MCA), 3-chloro- 4-(chloromethyl)-5-hydroxy-2(5H)-furanone (CMCF) and 3-chloro-4-methyl-5-hydroxy-2(5H)-furanone (MCF), were compared with the genotoxicity of the individual compounds. Genotoxicity was evaluated in the Salmonella reversion assay (Ames test), the in vitro Chinese hamster ovary (CHO) cell Hprt mutation assay, and in the CHO chromosome aberration test. When tested individually, the concentrations of the chemicals that were chosen for the mixtures induced no or only a modest increase in the genotoxic effects, and caused little or no cytotoxicity. In the Ames test, the genotoxic responses caused by the mixtures of CHFs did not follow simple additivity. Synergism was observed with strains TA97 and TA98, and antagonism with strain TA100. In the CHO/Hprt mutation assay, the mutagenic response of the mixtures was inconsistent, with near additivity seen with a mixture of CHFs that resulted in 12% cell survival. In contrast, the four CHFs together consistently caused more structural chromosome damage (mainly chromatid-type breaks and exchanges) compared to the sum of net effects of the four CHFs tested alone. Also, a potentiating effect was consistently seen for the cytotoxicity of the CHF mixtures both in the CHO/Hprt mutation assay and the chromosome aberration test. The present results indicate that the genotoxic effects of CHF mixtures can be greater than additive. Such effects may be worth considering in the cancer risk assessment of chlorinated drinking water.

摘要

比较了四种氯代羟基呋喃酮(CHFs)混合物,即3-氯-4-(二氯甲基)-5-羟基-2(5H)-呋喃酮(MX)、3,4-二氯-5-羟基-2(5H)-呋喃酮(MCA)、3-氯-4-(氯甲基)-5-羟基-2(5H)-呋喃酮(CMCF)和3-氯-4-甲基-5-羟基-2(5H)-呋喃酮(MCF)的遗传毒性反应与各单一化合物的遗传毒性。通过沙门氏菌回复突变试验(Ames试验)、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(Hprt)突变试验以及CHO染色体畸变试验评估遗传毒性。单独测试时,为混合物选择的化学物质浓度未诱导遗传毒性效应增加或仅使其适度增加,且几乎未引起细胞毒性或仅引起轻微细胞毒性。在Ames试验中,CHFs混合物引起的遗传毒性反应不遵循简单相加性。在TA97和TA98菌株中观察到协同作用,而在TA100菌株中观察到拮抗作用。在CHO/Hprt突变试验中,混合物的诱变反应不一致,在导致12%细胞存活的CHFs混合物中观察到接近相加性。相比之下,与单独测试的四种CHFs的净效应总和相比,四种CHFs共同作用始终导致更多的结构性染色体损伤(主要是染色单体型断裂和交换)。此外,在CHO/Hprt突变试验和染色体畸变试验中,CHF混合物的细胞毒性始终呈现增强效应。目前的结果表明,CHF混合物的遗传毒性效应可能大于相加效应。在氯化饮用水的癌症风险评估中,此类效应可能值得考虑。

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