Balansky R M, D'Agostini F, Izzotti A, De Flora S
Department of Health Sciences, University of Genoa, Via A. Pastore 1, I-16132 Genoa, Italy.
Carcinogenesis. 2000 Sep;21(9):1677-82. doi: 10.1093/carcin/21.9.1677.
A combination of tobacco smoking with certain agents has been shown to exert synergistic carcinogenic effects. On the other hand, antagonism betweeen smoke and other pulmonary carcinogens has also been documented by both epidemiological and experimental data. In spite of a very large number of studies carried out for decades in workers exposed to hexavalent chromium, the influence of smoking habits on lung carcinogenesis induced by this metal has not been clarified. For this reason, we performed two studies evaluating clastogenic effects in rodents. In the first one, BDF(1) mice were exposed whole-body to mainstream cigarette smoke for 5 days and, on the last day, they received an i.p. injection of potassium dichromate. In the second study, Sprague-Dawley rats were exposed whole-body to environmental cigarette smoke for 18 consecutive days and for the same period of time they received daily intra-tracheal instillations of sodium dichromate. Individually, the two hexavalent chromium salts and cigarette smoke, either mainstream or environmental, enhanced the frequency of micronuclei in bone marrow polychromatic erythrocytes of both mice and rats. Moreover, individual exposure to either environmental cigarette smoke or sodium dichromate enhanced the frequency of micronuclei and multiple nuclei in pulmonary alveolar macrophages of rats. In both studies, combined exposure to cigarette smoke and hexavalent chromium produced less than additive clastogenic effects. These results are consistent with our previous data, showing that hexavalent chromium and either benzo[a]pyrene or cigarette smoke condensate behave antagonistically in in vitro mutagenicity test systems and that the chromium reducing capacity of human pulmonary alveolar macrophages and peripheral lung parenchyma is enhanced in smokers. Taken together, in the absence of any epidemiological evidence, these findings rule out any occurrence of synergism between cigarette smoke and hexavalent chromium, at least in certain stages of the carcinogenesis process.
吸烟与某些物质的联合作用已被证明具有协同致癌效应。另一方面,流行病学和实验数据也记录了烟雾与其他肺部致癌物之间的拮抗作用。尽管在接触六价铬的工人中进行了数十年的大量研究,但吸烟习惯对这种金属诱发肺癌的影响尚未明确。因此,我们进行了两项评估啮齿动物致突变作用的研究。在第一项研究中,将BDF(1)小鼠全身暴露于主流香烟烟雾中5天,最后一天腹腔注射重铬酸钾。在第二项研究中,将Sprague-Dawley大鼠连续18天全身暴露于环境香烟烟雾中,并在同一时间段内每天经气管内滴注重铬酸钠。单独来看,两种六价铬盐以及主流或环境香烟烟雾均增加了小鼠和大鼠骨髓多染红细胞中的微核频率。此外,单独暴露于环境香烟烟雾或重铬酸钠均可增加大鼠肺泡巨噬细胞中的微核和多核频率。在两项研究中,香烟烟雾与六价铬的联合暴露产生的致突变作用小于相加效应。这些结果与我们之前的数据一致,表明在体外诱变性测试系统中,六价铬与苯并[a]芘或香烟烟雾冷凝物表现出拮抗作用,并且吸烟者的人肺泡巨噬细胞和外周肺实质的铬还原能力增强。综上所述,在缺乏任何流行病学证据的情况下,这些发现排除了香烟烟雾与六价铬之间协同作用的任何发生,至少在致癌过程的某些阶段是如此。