McFee A F
Medical and Health Sciences Division, Oak Ridge Associated Universities, Tennessee 37831-0117.
Environ Mol Mutagen. 1989;13(4):325-31. doi: 10.1002/em.2850130408.
In vitro assays of the genotoxicity of quinoline compounds have yielded varying indications of their potency, and only limited determinations have been reported following in vivo administrations. We have quantified chromosome aberrations (CA) and sister chromatid exchanges (SCE) in the marrow cells of mice that had been injected with quinoline, 8-hydroxyquinoline, or 4-nitroquinoline-1-oxide up to levels approaching lethal. Treatments with quinoline produced no consistent increase in the number of aberrations at either 17 or 36 hr after treatment and no significant increase in SCE numbers at either 23 or 42 hr. Similarly, 8-hydroxyquinoline had no measurable effect on either CA or SCE but did tend to prolong the cell cycle. 4-Nitroquinoline-1-oxide was a very potent inducer of both CA and SCE as well as an inhibitor of cell division.
喹啉化合物遗传毒性的体外试验对其效力给出了不同的结果,而体内给药后的测定报告有限。我们已对注射了喹啉、8-羟基喹啉或4-硝基喹啉-1-氧化物直至接近致死剂量的小鼠骨髓细胞中的染色体畸变(CA)和姐妹染色单体交换(SCE)进行了定量分析。喹啉处理在处理后17小时或36小时均未使畸变数量持续增加,在23小时或42小时SCE数量也未显著增加。同样,8-羟基喹啉对CA或SCE均无可测影响,但确实倾向于延长细胞周期。4-硝基喹啉-1-氧化物是CA和SCE的强效诱导剂,也是细胞分裂的抑制剂。