Mayer V W, Goin C J
Genetic Toxicology Branch, Food and Drug Administration, Washington, DC 20204.
Mutat Res. 1994 Dec;341(2):83-91. doi: 10.1016/0165-1218(94)90090-6.
The neurotoxic hexacarbon compounds n-hexane, 2-hexanone and 2,5-hexanedione were tested in combination with acetone and methyl ethyl ketone for the potential to induce chromosome loss in strain D61.M of Saccharomyces cerevisiae. n-Hexane and 2-hexanone, alone or in combination, induced only marginally positive chromosome loss, whereas the metabolite and presumed proximal genetically active agent 2,5-hexanedione was strongly positive when tested alone and in combination. These observations are discussed in relation to the reported potentiation of the neurotoxic effects of these hexacarbons when exposure results from combinations with other solvents, e.g., acetone and methyl ethyl ketone. Treatments that result in neurotoxicity in experimental animals and humans and those that result in chromosome loss in a yeast genetic test system may be correlated by their activity on a common intracellular target.
对神经毒性六碳化合物正己烷、2-己酮和2,5-己二酮,与丙酮和甲乙酮组合,测试其在酿酒酵母D61.M菌株中诱导染色体丢失的可能性。正己烷和2-己酮单独或组合使用时,仅诱导出轻微阳性的染色体丢失,而代谢产物以及推测的近端遗传活性剂2,5-己二酮单独测试和组合测试时均呈强阳性。结合已报道的这些六碳化合物与其他溶剂(如丙酮和甲乙酮)组合接触时神经毒性作用的增强情况,对这些观察结果进行了讨论。在实验动物和人类中导致神经毒性的处理,以及在酵母遗传测试系统中导致染色体丢失的处理,可能因其对共同细胞内靶点的活性而相互关联。