Rahn C A, Howard G, Riccio E, Doolittle D J
Cellular and Molecular Biology, R.J. Reynolds Tobacco Company, Winston-Salem, NC 27102.
Environ Mol Mutagen. 1991;17(4):244-52. doi: 10.1002/em.2850170405.
Cigarette smokers have been reported to void urine that is more mutagenic, as measured in the Salmonella/microsome assay, than urine voided by nonsmokers. Several previous studies have attempted to correlate indices of tobacco smoke exposure (e.g. nicotine, cotinine, tar intake) with urinary mutagenicity, with conflicting results. These studies generally involved small numbers of smokers and did not carefully control diet, which is known to affect urinary mutagenicity markedly. Our objective was to conduct a controlled study to determine clearly if there were a correlation between urinary nicotine, cotinine, or nicotine + cotinine and urinary mutagenicity and to determine if nicotine or its major metabolite plays a role in the mutagenicity of urine from cigarette smokers. We used a large number of smokers (31), each of whom smoked both a tobacco-burning cigarette and a tobacco-heating cigarette on consecutive weeks, and we prepared and served identical diets to all subjects. Nicotine and cotinine concentrations were determined in small aliquots from urine samples collected over 24 hr, and the remaining urine sample was extracted and concentrated on XAD-2 resin for mutagenicity assays in the Salmonella/microsome test. Nicotine, cotinine, and nicotine + cotinine were statistically correlated with mutagenicity of urine from smokers of the tobacco-burning cigarette, but there was no correlation between nicotine, cotinine, or nicotine + cotinine and mutagenicity of urine from smokers of the tobacco-heating cigarettes. Thus, although urinary nicotine and cotinine concentrations correlate with urinary mutagenicity in smokers of tobacco-burning cigarettes, the present results indicate that nicotine and its metabolite are not responsible for the mutagenicity of smokers' urine.
据报道,吸烟者排出的尿液在沙门氏菌/微粒体试验中测得的致突变性比不吸烟者排出的尿液更高。此前的几项研究试图将烟草烟雾暴露指标(如尼古丁、可替宁、焦油摄入量)与尿液致突变性相关联,但结果相互矛盾。这些研究通常涉及少量吸烟者,且未仔细控制饮食,而饮食已知会显著影响尿液致突变性。我们的目标是进行一项对照研究,以明确确定尿液中的尼古丁、可替宁或尼古丁+可替宁与尿液致突变性之间是否存在关联,并确定尼古丁或其主要代谢物是否在吸烟者尿液的致突变性中起作用。我们使用了大量吸烟者(31人),每人连续几周分别吸食燃烧型香烟和加热型香烟,并且为所有受试者准备并提供相同的饮食。从24小时内收集到的尿液样本的小份样品中测定尼古丁和可替宁浓度,其余尿液样本经提取并浓缩在XAD - 2树脂上,用于沙门氏菌/微粒体试验中的致突变性测定。尼古丁、可替宁以及尼古丁+可替宁与燃烧型香烟吸烟者尿液的致突变性在统计学上相关,但尼古丁、可替宁或尼古丁+可替宁与加热型香烟吸烟者尿液的致突变性之间没有关联。因此,尽管尿液中的尼古丁和可替宁浓度与燃烧型香烟吸烟者的尿液致突变性相关,但目前的结果表明尼古丁及其代谢物并非吸烟者尿液致突变性的原因。