Cagen S Z, Dent J G, McCormack K M, Rickert D E, Gibson J E
J Pharmacol Exp Ther. 1979 Apr;209(1):1-6.
Polybrominated biphenyls (PBBs) stimulate hepatic drug metabolism in adult and developing rats. The purpose of this investigation was to determine the influence of PBBs on the development of the liver as an organ for chemical excretion. Exposure of developing rats to polybrominated biphenyls (PBBs) by feeding 50 ppm of PBBs to pregnant or lactating mothers and rat weanlings did not produce overt toxicity when compared to controls over a 49-day postnatal period. However, prenatal and postnatal dietary exposure to PBBs resulted in elevated liver weight. In 15-day-old rats, increased liver weight after PBBs was correlated with enhanced ouabain transport from plasma into bile. Liver weight was also elevated in 21-, 35- and 49-day-old rats treated with PBBs, but this effect was not associated with stimulation of ouabain transport in these animals. Stimulation of ouabain transport after PBBs in 15-day-old rats was associated with increased hepatic uptake of ouabain. Stimulation in 15-day-old rats and not older rats may be attributed to the relative importance of uptake for ouabain transport in 15-day-old rats.
多溴联苯(PBBs)可刺激成年大鼠和发育中大鼠的肝脏药物代谢。本研究的目的是确定PBBs对作为化学物质排泄器官的肝脏发育的影响。在产后49天的时间里,与对照组相比,通过给怀孕或哺乳期的母鼠以及断乳幼鼠喂食50 ppm的PBBs,使发育中的大鼠接触多溴联苯(PBBs),并未产生明显的毒性。然而,产前和产后饮食中接触PBBs会导致肝脏重量增加。在15日龄的大鼠中,PBBs处理后肝脏重量增加与哇巴因从血浆转运到胆汁中的能力增强相关。用PBBs处理的21日龄、35日龄和49日龄大鼠的肝脏重量也有所升高,但这种效应与这些动物中哇巴因转运的刺激无关。15日龄大鼠经PBBs处理后哇巴因转运的刺激与肝脏对哇巴因摄取的增加有关。15日龄大鼠而非年龄较大的大鼠出现刺激作用,可能归因于摄取对15日龄大鼠哇巴因转运的相对重要性。