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首页> 外文期刊>Chemical research in toxicology >Analysis of highly polar DNA adducts formed in SENCAR mouse epidermis following topical application of dibenz(a,j)anthracene.
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Analysis of highly polar DNA adducts formed in SENCAR mouse epidermis following topical application of dibenz(a,j)anthracene.

机译:苯并(a,j)蒽局部应用后,在SENCAR小鼠表皮中形成的高极性DNA加合物的分析。

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The formation of DNA adducts in mouse epidermis has been examined following topical application of dibenz[a,j]anthracene (DB[a,j]A) and its metabolites, i.e., DB[a,j]A-3,4-diol, DB[a,j]A-3,4-10, 11-bis-diol, DB[a,j]A-3,4-8,9-bis-diol, 10-OH-DB[a,j]A-3,4-diol, or 11-OH-DB[a,j]A-3,4-diol, using a 32P-postlabeling assay. At initiating doses (400-1600 nmol), DB[a,j]A produced at least 23 DNA adduct spots, including four less polar (derived from the bay-region syn- and anti-diol-epoxides) and 19 highly polar DNA adducts. DB[a, j]A-3,4-diol produced 13 DNA adduct spots, four less polar and nine highly polar DNA adducts, and DB[a,j]A-3,4-10,11-bis-diol produced nine highly polar DNA adducts. Eight and seven of the highly polar DNA adducts generated by DB[a,j]A-3,4-diol and DB[a,j]A-3,4-10, 11-bis-diol, respectively, migrated in the chromatography system like the highly polar DNA adducts produced by the parent compound. Sufficient amounts of radioactivity were associated with highly polar adduct spots 11, 13, and 22 to confirm their chromatogaphic identity in DNA samples from DB[a,j]A-, DB[a,j]A-3,4-diol-, and DB[a, j]A-3,4-10,11-bis-diol-treated mice. 10-OH-DB[a,j]A-3,4-diol and 11-OH-DB[a,j]A-3,4-diol did not produce any highly polar DNA adducts that could be detected under our experimental conditions. At an initiating dose of 400 nmol, DB[a,j]A, DB[a,j]A-3,4-diol, and DB[a, j]A-3,4-10,11-bis-diol produced 22.4 +/- 13.0, 15.6 +/- 10.1, and 5. 5 +/- 0.3 (mean +/- SD) adducts/10(9) nucleotides, of which 77, 65, and 100%, respectively, represented highly polar DNA adducts. At the same dose of 400 nmol per mouse, DB[a,j]A and its 3,4-diol were able to initiate papillomas in SENCAR mouse skin (3.08 +/- 1.89 and 3.48 +/- 2.72 papillomas per mouse, respectively, after 16 weeks of promotion with 12-O-tetradecanoyl phorbol 13-acetate), while the 3, 4-10,11-bis-diol of DB[a,j]A was inactive as a tumor initiator. A quantitative correlation (r = 0.935; p = 0.0196) between levels of less polar DNA adducts and tumor-initiating activity of DB[a,j]A, DB[a,j]A-3,4-diol, and anti-DB[a,j]ADE was observed. This study demonstrates that the highly polar DNA adducts formed from DB[a,j]A in mouse epidermis arise primarily from the DB[a,j]A-3,4-10, 11-bis-diol. However, the contribution of this metabolite to the tumor-initiating activity of DB[a,j]A appears to be small.
机译:在局部施用苯并[a,j]蒽(DB [a,j] A)及其代谢物即DB [a,j] A-3,4-二醇后,已经检查了小鼠表皮中DNA加合物的形成。 ,DB [a,j] A-3,4-10,11-双二醇,DB [a,j] A-3,4-8,9-双二醇,10-OH-DB [a,j使用32P后标记测定法检测] A-3,4-二醇或11-OH-DB [a,j] A-3,4-二醇。在起始剂量(400-1600 nmol)下,DB [a,j] A产生至少23个DNA加合物斑点,包括四个极性较小的(来自海湾区域的顺式和反式二醇环氧化合物)和19个高极性的DNA加合物。 DB [a,j] A-3,4-diol产生13个DNA加合物斑点,四个低极性和9个高极性DNA加合物,产生DB [a,j] A-3,4-10,11-双二醇九种高极性DNA加合物。由DB [a,j] A-3,4-二醇和DB [a,j] A-3,4-10,11-双-二醇分别产生的高极性DNA加合物中的八种和七种在其中迁移。色谱系统,如母体化合物产生的高极性DNA加合物。足够的放射性与高极性加合物斑点11、13和22有关,以确认它们在DB [a,j] A-,DB [a,j] A-3,4-二醇-,和DB [a,j] A-3,4-10,11-双-二醇处理的小鼠。 10-OH-DB [a,j] A-3,4-二醇和11-OH-DB [a,j] A-3,4-二醇未产生可在我们的实验中检测到的任何高极性DNA加合物条件。在起始剂量为400 nmol时,DB [a,j] A,DB [a,j] A-3,4-二醇和DB [a,j] A-3,4-10,11-双二醇产生22.4 +/- 13.0、15.6 +/- 10.1和5。5 +/- 0.3(平均+/- SD)加合物/ 10(9)个核苷酸,其中77、65和100%分别代表高度极性DNA加合物。在每只小鼠400 nmol的相同剂量下,DB [a,j] A及其3,4-二醇能够引发SENCAR小鼠皮肤中的乳头状瘤(每只小鼠分别为3.08 +/- 1.89和3.48 +/- 2.72乳头状瘤,在用12-O-十四烷酰佛波醇13-乙酸盐促进16周后),而DB [a,j] A的3,4-10,11-双-二醇作为肿瘤引发剂无效。极性较小的DNA加合物的水平与DB [a,j] A,DB [a,j] A-3,4-二醇和抗-β-环糊精的肿瘤引发活性之间存在定量关系(r = 0.935; p = 0.0196)。观察到DB [a,j] ADE。这项研究表明,在小鼠表皮中由DB [a,j] A形成的高极性DNA加合物主要来自DB [a,j] A-3,4-10,11-双-二醇。然而,这种代谢物对DB [a,j] A的肿瘤启动活性的贡献似乎很小。

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