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六氯丁二烯、全氯丁烯酸和全氯丁烯酰氯的诱变性。

Mutagenicity of hexachlorobutadiene, perchlorobutenoic acid and perchlorobutenoic acid chloride.

作者信息

Reichert D, Neudecker T, Schütz S

出版信息

Mutat Res. 1984 Aug-Sep;137(2-3):89-93. doi: 10.1016/0165-1218(84)90096-x.

Abstract

Hexachloro(1,3)butadiene (HCBD) is a well known environmental contaminant. The nephrocarcinogenic potential of HCBD has been shown in long-term studies with rats. Experiments were performed to assist in determining whether this effect is mediated by epigenetic or genotoxic mechanisms and to compare the mutagenic properties of HCBD with those of its monooxidation products, perchloro-3-butenoic acid (PCBA) and perchloro-3-butenoic acid chloride (PCBAC), which are conceivable metabolites of HCBD. All 3 compounds are mutagenic to the Salmonella typhimurium tester strain TA100. The mutagenic effect is dose-dependent and parallels the chemical reactivity of the compounds. HCBD is only mutagenic in the presence of drug-metabolizing enzymes (S9 mix) with an increased protein content. The mutagenic response after incubation with PCBAC and PCBA is 2-3-fold that of HCBD. Additionally, both PCBAC and PCBA exert a mutagenic response in the absence of S9 mix. The experiments support the assumption of a genotoxic potential of HCBD.

摘要

六氯(1,3)丁二烯(HCBD)是一种著名的环境污染物。长期对大鼠的研究已表明HCBD具有肾致癌潜力。开展实验以帮助确定这种效应是由表观遗传机制还是遗传毒性机制介导的,并比较HCBD与其单氧化产物全氯-3-丁烯酸(PCBA)和全氯-3-丁烯酰氯(PCBAC)的诱变性,这两种物质是HCBD可能的代谢产物。所有这3种化合物对鼠伤寒沙门氏菌测试菌株TA100均具有诱变性。诱变效应呈剂量依赖性,且与化合物的化学反应性平行。HCBD仅在存在药物代谢酶(S9混合物)且蛋白质含量增加的情况下具有诱变性。与PCBAC和PCBA孵育后的诱变反应是HCBD的2至3倍。此外,PCBAC和PCBA在不存在S9混合物的情况下均会产生诱变反应。这些实验支持了HCBD具有遗传毒性潜力的假设。

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