Rice J E, Hosted T J, DeFloria M C, LaVoie E J, Fischer D L, Wiley J C
Carcinogenesis. 1986 Oct;7(10):1761-4. doi: 10.1093/carcin/7.10.1761.
Indeno[1,2,3-cd]pyrene is a ubiquitous environmental pollutant which is active as a tumor initiator and complete carcinogen on mouse skin and is carcinogenic in rat lung. The major metabolites of indeno[1,2,3-cd]pyrene as formed in vivo in mouse skin have been identified. 8-Hydroxyindeno[1,2,3-cd]pyrene is the most abundant metabolite identified. 9-Hydroxyindeno[1,2,3-cd]pyrene and trans-1,2-dihydro-1,2-dihydroxyindeno[1,2,3-cd]pyrene are also major in vivo metabolites in mouse skin. Several minor metabolites were also identified. Among these are trans-1,2-dihydro-1,2,8-trihydroxyindeno[1,2,3-cd]pyrene, trans-1,2-dihydro-1,2,9-trihydroxyindeno[1,2,3-cd]pyrene, indeno[1,2,3-cd]pyrene-1,2-dione, and 10-hydroxyindeno[1,2,3-cd]pyrene. The tumor-initiating activity of several of the major in vivo metabolites of indeno[1,2,3-cd]pyrene has been investigated on mouse skin. Trans-1,2-dihydro-1,2-dihydroxyindeno[1,2,3-cd]pyrene and 1,2-dihydro-1,2-epoxyindeno[1,2,3-cd]pyrene both produced an 80% incidence of tumor-bearing mice at a total initiating dose of 1.0 mg. The activity of this K-region dihydrodiol and K-region oxide was, however, less than that of the parent hydrocarbon. These data suggest that 1,2-dihydro-1,2-epoxyindeno[1,2,3-cd]pyrene, which is an ultimate mutagenic metabolite of indeno[1,2,3-cd]pyrene, is not the ultimate tumorigenic metabolite on mouse skin. 8-Hydroxyindeno[1,2,3-cd]pyrene, which is mutagenic when assayed in the presence of a microsomal activation system, exhibited only weak tumor-initiating activity. These results indicate that the principal metabolic activation pathways associated with the mutagenic activity of indeno[1,2,3-cd]pyrene are not related to its tumor-initiating activity on mouse skin.
茚并[1,2,3 - cd]芘是一种普遍存在的环境污染物,它作为一种肿瘤引发剂在小鼠皮肤上具有活性且是完全致癌物,在大鼠肺部也具有致癌性。已鉴定出茚并[1,2,3 - cd]芘在小鼠皮肤内形成的主要体内代谢产物。8 - 羟基茚并[1,2,3 - cd]芘是已鉴定出的最丰富的代谢产物。9 - 羟基茚并[1,2,3 - cd]芘和顺式 - 1,2 - 二氢 - 1,2 - 二羟基茚并[1,2,3 - cd]芘也是小鼠皮肤中的主要体内代谢产物。还鉴定出了几种次要代谢产物。其中包括反式 - 1,2 - 二氢 - 1,2,8 - 三羟基茚并[1,2,3 - cd]芘、反式 - 1,2 - 二氢 - 1,2,9 - 三羟基茚并[1,2,3 - cd]芘、茚并[1,2,3 - cd]芘 - 1,2 - 二酮和10 - 羟基茚并[1,2,3 - cd]芘。已在小鼠皮肤上研究了茚并[1,2,3 - cd]芘的几种主要体内代谢产物的肿瘤引发活性。反式 - 1,2 - 二氢 - 1,2 - 二羟基茚并[1,2,3 - cd]芘和1,2 - 二氢 - 1,2 - 环氧茚并[1,2,3 - cd]芘在总引发剂量为1.0毫克时,荷瘤小鼠的发生率均为80%。然而,这种K区域二醇和K区域氧化物的活性低于母体烃。这些数据表明,1,2 - 二氢 - 1,2 - 环氧茚并[1,2,3 - cd]芘作为茚并[1,2,3 - cd]芘的一种最终诱变代谢产物,并非小鼠皮肤上的最终致癌代谢产物。8 - 羟基茚并[1,2,3 - cd]芘在微粒体激活系统存在下进行检测时具有诱变活性,但仅表现出微弱的肿瘤引发活性。这些结果表明,与茚并[1,2,3 - cd]芘的诱变活性相关的主要代谢激活途径与其在小鼠皮肤上的肿瘤引发活性无关。