Department of Experimental Pathology, Cancer Institute, 1-37-1, Kami-Ikebukuro, Toshima-ku, Tokyo 170, Japan.
Carcinogenesis. 1980 Feb;1(2):115-20. doi: 10.1093/carcin/1.2.115.
The binding of benzo(a)pyrene (BP) to DNA in the presence of liver microsomal preparations from 3-methylcholanthrene-treated rats was increased 28.5% (P < 0.001) by addition of UDP-glucuronic acid to the incubation mixture at a 100 microM concentration of BP. However this increase was not observed at lower concentrations of BP. Analysis of DNA-hydrolysates by column chromatography on Sephadex LH-20 indicated that this increase was due to greater binding of benzo(a)pyrene-7,8-dihydrodiol-9,10-epoxide. The amount of bound adducts derived from 9-hydroxybenzo(a)pyrene (9-OH BP) was not significantly affected by UDP-glucuronic acid. Addition of UDP-glucuronic acid to incubation mixtures containing microsomes from untreated rat liver caused only a slight increase in total binding. These findings suggest that UDP-glucuronyl transferase may be involved in the activation of BP.
在 3-甲基胆蒽处理的大鼠肝微粒体制剂存在的情况下,结合物苯并(a)芘(BP)与 DNA 的结合通过在孵育混合物中添加 100 μM 浓度的 UDP-葡萄糖醛酸而增加了 28.5%(P < 0.001)。 然而,在 BP 的较低浓度下未观察到这种增加。 通过在 Sephadex LH-20 上的柱色谱分析 DNA 水解物表明,这种增加是由于苯并(a)芘-7,8-二氢二醇-9,10-环氧化物的结合增加所致。 来自 9-羟基苯并(a)芘(9-OH BP)的结合加合物的量不受 UDP-葡萄糖醛酸的显著影响。 UDP-葡萄糖醛酸添加到包含未处理的大鼠肝微粒体的孵育混合物中仅导致总结合的轻微增加。 这些发现表明 UDP-葡萄糖醛酸基转移酶可能参与 BP 的激活。