Iqbal Z M, Varnes M E, Yoshida A, Epstein S S
Cancer Res. 1977 Apr;37(4):1011-5.
The in vitro microsomal metabolism of the strain 13 guinea pig pancreas was investigated by determining the benzo(a)pyrene (BP) hydroxylase activity in the 9000 x g supernatant and microsomal pellet. BP hydroxylase activity in both 9000 x g supernatant and microsomal pellet of the pancreas was less than 1% of the activity in the respective liver fractions, However, pretreatment of animals with methylcholanthrene or BP at 20 mg/kg, for either 1 day or 3 consecutive days, markedly enhanced the BP hydroxylase activity of pancreatic microsomes over that of controls; the induction in the liver microsomes was less than 2-fold over that of controls. The hydroxylation of BP by pancreatic microsomes was linear with time over a 30-min period, with the rate of hydroxylation dependent on both the enzyme and substrate concentrations.
通过测定9000×g上清液和微粒体沉淀中的苯并(a)芘(BP)羟化酶活性,研究了13号品系豚鼠胰腺的体外微粒体代谢。胰腺9000×g上清液和微粒体沉淀中的BP羟化酶活性均低于相应肝脏组分活性的1%。然而,用甲基胆蒽或20mg/kg的BP对动物进行预处理,无论是1天还是连续3天,均可使胰腺微粒体的BP羟化酶活性显著高于对照组;肝脏微粒体中的诱导作用比对照组高不到2倍。胰腺微粒体对BP的羟化作用在30分钟内随时间呈线性关系,羟化速率取决于酶和底物的浓度。