Center of Excellence in Environmental Toxicology and Center for Cancer Pharmacology, Department of Pharmacology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.
Chem Res Toxicol. 2012 May 21;25(5):993-1003. doi: 10.1021/tx200463s. Epub 2012 May 1.
Benzo[a]pyrene-7,8-dione (B[a]P-7,8-dione) is produced in human lung cells by the oxidation of (±)-B[a]P-7,8-trans-dihydrodiol, which is catalyzed by aldo-keto reductases (AKRs). However, information relevant to the cell-based metabolism of B[a]P-7,8-dione is lacking. We studied the metabolic fate of 2 μM 1,3-[(3)H(2)]-B[a]P-7,8-dione in human lung adenocarcinoma A549 cells, human bronchoalveolar H358 cells, and immortalized human bronchial epithelial HBEC-KT cells. In these three cell lines, 1,3-[(3)H(2)]-B[a]P-7,8-dione was rapidly consumed, and radioactivity was distributed between the organic and aqueous phase of ethyl acetate-extracted media, as well as in the cell lysate pellets. After acidification of the media, several metabolites of 1,3-[(3)H(2)]-B[a]P-7,8-dione were detected in the organic phase of the media by high performance liquid chromatography-ultraviolet-radioactivity monitoring (HPLC-UV-RAM). The structures of B[a]P-7,8-dione metabolites varied in the cell lines and were identified as B[a]P-7,8-dione conjugates with glutathione (GSH) and N-acetyl-l-cysteine (NAC), 8-O-monomethylated-catechol, catechol monosulfate, and monoglucuronide, and monohydroxylated-B[a]P-7,8-dione by liquid chromatography-tandem mass spectrometry (LC-MS/MS). We also obtained evidence for the first time for the formation of an adenine adduct of B[a]P-7,8-dione. Among these metabolites, the identity of the GSH-B[a]P-7,8-dione and the NAC-B[a]P-7,8-dione was further validated by comparison to authentic synthesized standards. The pathways of B[a]P-7,8-dione metabolism in the three human lung cell lines are formation of GSH and NAC conjugates, reduction to the catechol followed by phase II conjugation reactions leading to its detoxification, monohydroxylation, as well as formation of the adenine adduct.
苯并[a]芘-7,8-二酮(B[a]P-7,8-二酮)是由(±)-B[a]P-7,8-反式-二氢二醇在人肺细胞中经醛酮还原酶(AKRs)氧化生成的。然而,目前有关 B[a]P-7,8-二酮的细胞代谢信息还很缺乏。我们研究了 2μM 1,3-[(3)H(2)]-B[a]P-7,8-二酮在人肺腺癌细胞 A549、人支气管肺泡 H358 和永生化人支气管上皮细胞 HBEC-KT 中的代谢命运。在这三种细胞系中,1,3-[(3)H(2)]-B[a]P-7,8-二酮被迅速消耗,放射性物质分布在乙酸乙酯提取介质的有机相和水相以及细胞裂解物沉淀中。在介质酸化后,通过高效液相色谱-紫外-放射性监测(HPLC-UV-RAM)在介质的有机相中检测到几种 1,3-[(3)H(2)]-B[a]P-7,8-二酮代谢物。细胞系中 B[a]P-7,8-二酮代谢物的结构不同,被鉴定为 B[a]P-7,8-二酮与谷胱甘肽(GSH)和 N-乙酰-l-半胱氨酸(NAC)、8-O-单甲基化儿茶酚、儿茶酚单硫酸盐和单葡萄糖醛酸以及单羟基化-B[a]P-7,8-二酮的缀合物通过液相色谱-串联质谱(LC-MS/MS)。我们还首次获得了 B[a]P-7,8-二酮腺嘌呤加合物形成的证据。在这些代谢物中,GSH-B[a]P-7,8-二酮和 NAC-B[a]P-7,8-二酮的身份通过与合成标准品的比较得到进一步验证。在这三种人肺细胞系中,B[a]P-7,8-二酮代谢的途径是形成 GSH 和 NAC 缀合物,还原为儿茶酚,然后进行 II 相缀合反应使其解毒,单羟化以及形成腺嘌呤加合物。