Iqbal Z M, Yoshida A, Epstein S S
Drug Metab Dispos. 1979 Jan-Feb;7(1):44-8.
Following intravenous administration of [3H]benzo[a]pyrene ([3H]BP) to rats, uptake of radioactivity by the pancreas, per g of tissue, was approximately 16% of that of the liver. At 5 min following administration, unmetabolized BP in the pancreas, liver, and blood constituted 79, 50, and 49% of total BP uptake, respectively. The total uptake and unmetabolized BP in these tissues declined in a biphasic manner over the 2-hr observation period, during which only 0.03% of the total administered dose was excreted in pancreatic juice, as compared to 39% in bile; all radioactivity in pancreatic juice and bile was due to polar BP metabolites, including 3-hydroxy-BP. Pretreatment of rats with methylcholanthrene induced a significant increase in biliary, but not pancreatic, excretion of radioactivity. Administration of secretagogues caused a 2-fold increase in pancreatic, but not biliary, radioactivity.
给大鼠静脉注射[3H]苯并[a]芘([3H]BP)后,每克胰腺组织对放射性的摄取量约为肝脏的16%。给药后5分钟,胰腺、肝脏和血液中未代谢的BP分别占总BP摄取量的79%、50%和49%。在2小时的观察期内,这些组织中的总摄取量和未代谢的BP呈双相下降,在此期间,胰腺分泌液中仅排出了0.03%的给药总剂量,而胆汁中为39%;胰腺分泌液和胆汁中的所有放射性均归因于极性BP代谢物,包括3-羟基-BP。用甲基胆蒽预处理大鼠可显著增加胆汁中放射性的排泄,但对胰腺无此作用。给予促分泌剂可使胰腺中的放射性增加2倍,但对胆汁无此作用。