Gallagher J E, Everson R B, Lewtas J, George M, Lucier G W
Health Effects Research Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina.
Teratog Carcinog Mutagen. 1994;14(4):183-92. doi: 10.1002/tcm.1770140405.
Previous studies demonstrated that cigarette smoking is associated with high elevations in levels of both cytochrome P450 1A1 (CYP1A1) and DNA adducts in human placenta. To date, the identity of the smoking related DNA adducts is not known. The DNA adducts identified in placenta of smokers could result from chemicals present in cigarette smoke, substances formed by CYP 1A1 metabolic activation of endogenous compounds, noncigarette related exposures or a combination of these processes. Exposure to contaminated rice oil containing large doses of polychlorinated biphenyls (PCBs) and polychlorinated dibenzofurans (PCDFs) also resulted in massive elevation of CYP 1A1 in human placenta but formation of DNA adducts directly from this exposure has not previously been reported. The purpose for comparing the two populations was to test the hypothesis that if CYP 1A1 induction results in the metabolic activation of endogenous compounds, then DNA adducts should also be present in PCB/PCDF exposed tissues exhibiting high CYP 1A1 activity and some of the adducts detected in the placental DNA from smokers may be identified as those derived from the metabolic activation of endogenous compounds. To test this hypothesis, we measured DNA adducts using 32P-postlabeling to analyze placental DNA from women exposed to PCB/PCDF and from cigarette smokers where levels of CYP 1A1 were similarly elevated. There was no evidence of DNA adducts among specimens obtained from PCB/PCDF exposed individuals. These data suggest that CYP 1A1 induction alone (in the absence of cigarette smoking) does not induce the formation of DNA adducts detectable by this approach, and that smoking related adducts are not a consequence of CYP 1A1 induction mediated activation of endogenous compounds or xenobiotics other than cigarette smoke.
先前的研究表明,吸烟与人类胎盘中细胞色素P450 1A1(CYP1A1)水平和DNA加合物的高度升高有关。迄今为止,与吸烟相关的DNA加合物的身份尚不清楚。在吸烟者胎盘中鉴定出的DNA加合物可能源于香烟烟雾中存在的化学物质、CYP 1A1对内源性化合物的代谢激活形成的物质、与香烟无关的暴露或这些过程的组合。接触含有大量多氯联苯(PCBs)和多氯二苯并呋喃(PCDFs)的受污染米油也会导致人类胎盘中CYP 1A1大量升高,但此前尚未报道过直接由这种暴露形成DNA加合物的情况。比较这两个人群的目的是检验以下假设:如果CYP 1A1诱导导致内源性化合物的代谢激活,那么在表现出高CYP 1A1活性的PCB/PCDF暴露组织中也应该存在DNA加合物,并且在吸烟者胎盘DNA中检测到的一些加合物可能被鉴定为源自内源性化合物代谢激活的加合物。为了检验这一假设,我们使用32P后标记法测量DNA加合物,以分析来自PCB/PCDF暴露女性和CYP 1A1水平同样升高的吸烟者的胎盘DNA。在从PCB/PCDF暴露个体获得的标本中没有DNA加合物的证据。这些数据表明,仅CYP 1A1诱导(在不吸烟的情况下)不会诱导通过这种方法可检测到的DNA加合物的形成,并且吸烟相关的加合物不是CYP 1A1诱导介导的内源性化合物或除香烟烟雾外的外源性物质激活的结果。