Wolff R K, Bond J A, Sun J D, Henderson R F, Harkema J R, Griffith W C, Mauderly J L, McClellan R O
Inhalation Toxicology Research Institute, Lovelace Biomedical and Environmental Research Institute, Albuquerque, New Mexico 87185.
Toxicol Appl Pharmacol. 1989 Feb;97(2):289-99. doi: 10.1016/0041-008x(89)90334-7.
Exposure of rodents to benzo[a]pyrene (BaP) associated with particles has previously been shown to result in increased retention of BaP and metabolites in lungs. To determine if DNA damage might be enhanced, DNA adducts were measured in lungs of F344 rats following inhalation of pure BaP aerosols or BaP absorbed on carbon black particles. Groups of rats were exposed nose only to filtered air, [14C]BaP (2 mg/m3), or [14C]BaP (2 mg/m3) adsorbed on carbon black (97 mg/m3) (BaP/CB) for 4 hr/day, 1 day/week, for 12 weeks. Groups of rats were terminated at 4, 8, 12, 16, 20, and 24 weeks after the beginning of the 12-week exposure period. Retention of total 14C in lungs was used as an indicator of total reactive metabolites. DNA isolated from lungs was analyzed for adducts using a 32P-postlabeling assay. Inhalation of BaP/CB resulted in 100-fold higher levels of 14C in lungs at the end of the 12-week exposure than did inhalation of pure BaP. The halftime for the decline in 14C levels was 34 +/- 3 weeks (mean +/- SE) for rats exposed to BaP/CB and 6 +/- 2 weeks for rats exposed to pure BaP. At the end of 12 weeks of exposure, DNA adducts in lungs of rats exposed to pure BaP ranged from 2-15 adducts per 10(9) bases (mean = 7, n = 4) and in rats exposed to pure BaP absorbed on carbon black ranged from 10-12 adducts per 10(9) bases (mean = 11, n = 4); DNA adducts in lungs of sham-exposed rats ranged from 0-2 adducts per 10(9) bases (mean = 1, n = 4). The halftimes for the decline in DNA adducts in lungs were 3 +/- 1 weeks (mean +/- SE) for the rats exposed to BaP/CB and 5 +/- 2 weeks for the rats exposed to BaP. One of the DNA adducts found following exposure to both BaP and BaP/CB was tentatively identified as the BaP diol epoxide deoxyguanosine (BPDE) adduct. Levels of both total and BPDE DNA adducts were significantly increased (p less than 0.05) in lungs of rats exposed to both BaP and BaP/CB compared to levels in lungs of sham-exposed rats. There were no significant differences in levels of DNA adducts in lungs of rats exposed to BaP or BaP/CB, although the pattern of adducts was different between the two exposure modes.(ABSTRACT TRUNCATED AT 400 WORDS)
先前的研究表明,将啮齿动物暴露于与颗粒物相关的苯并[a]芘(BaP)中,会导致肺部对BaP及其代谢产物的滞留增加。为了确定DNA损伤是否会增强,研究人员在F344大鼠吸入纯BaP气雾剂或吸附在炭黑颗粒上的BaP后,对其肺部的DNA加合物进行了测量。将大鼠分组,使其仅经鼻暴露于过滤空气、[14C]BaP(2毫克/立方米)或吸附在炭黑(97毫克/立方米)上的[14C]BaP(2毫克/立方米)(BaP/CB),每天暴露4小时,每周暴露1天,共暴露12周。在12周暴露期开始后的4、8、12、16、20和24周,将大鼠分组处死。肺部总14C的滞留量用作总活性代谢产物的指标。使用32P后标记分析法分析从肺部分离的DNA中的加合物。在12周暴露期结束时,吸入BaP/CB的大鼠肺部14C水平比吸入纯BaP的大鼠高100倍。暴露于BaP/CB的大鼠中,14C水平下降的半衰期为34±3周(平均值±标准误),而暴露于纯BaP的大鼠为6±2周。在暴露12周结束时,暴露于纯BaP的大鼠肺部DNA加合物的含量为每10(9)个碱基2 - 15个加合物(平均值 = 7,n = 4),暴露于吸附在炭黑上的纯BaP的大鼠为每10(9)个碱基10 - 12个加合物(平均值 = 11,n = 4);假暴露大鼠肺部DNA加合物的含量为每10(9)个碱基0 - 2个加合物(平均值 = 1,n = 4)。暴露于BaP/CB的大鼠肺部DNA加合物下降的半衰期为3±1周(平均值±标准误),暴露于BaP的大鼠为5±2周。在暴露于BaP和BaP/CB后发现的一种DNA加合物初步鉴定为苯并[a]芘二氢二醇环氧化物脱氧鸟苷(BPDE)加合物。与假暴露大鼠肺部的水平相比,暴露于BaP和BaP/CB的大鼠肺部总DNA加合物和BPDE DNA加合物的水平均显著升高(p < 0.05)。暴露于BaP或BaP/CB的大鼠肺部DNA加合物水平没有显著差异,尽管两种暴露方式下加合物的模式不同。(摘要截断于400字)