Cagen S Z, Gibson J E
Environ Health Perspect. 1978 Apr;23:233-9. doi: 10.1289/ehp.7823233.
The purpose of this investigation was to determine the influence of polybrominated biphenyls (PBBs) on hepatic excretory function in developing and adult rats and mice. Prenatal or postnatal dietary exposure to PBBs (50 ppm in diet of pregnant or lactating mother or in diet of rat weanlings) resulted in elevated liver weight in developing rats. In 15-day-old rats that had been treated with PBBs increased liver weight correlated to enhanced ouabain transport from plasma into bile. Liver weight was also elevated in 21, 35, and 49-day-old rats exposed to PBBs, but this effect was not associated with stimulation of ouabain transport in these animals. However, adult rats fed 100 ppm PBBs for two weeks had significantly lower plasma concentrations of sulfobromophthalein (BSP) and increased biliary excretion of BSP, when compared to controls. PBBs-fed adult rats also excreted a greater percentage conjugated BSP (BSP-GSH) into bile. Two week dietary treatment of 100, 150, and 200 ppm PBBs resulted in enhanced initial disappearance of indocyanine green (ICG) from plasma of adult mice. However, dietary doses of 100 and 200 ppm PBBs to adult mice was not associated with enhanced capacity for ouabain excretion. In contrast, treatment with PBBs through the mother's diet (50 ppm) resulted in an almost twofold increase in cumulative ouabain excretion in 15-day-old mice. The results suggest that PBBs stimulate hepatic drug elimination in rats and mice, but the magnitude of the effect is dependent on age and transported compound.
本研究的目的是确定多溴联苯(PBBs)对发育中的大鼠和小鼠以及成年大鼠和小鼠肝脏排泄功能的影响。产前或产后经饮食接触PBBs(怀孕或哺乳期母鼠或断奶幼鼠的饮食中含50 ppm)会导致发育中的大鼠肝脏重量增加。在经PBBs处理的15日龄大鼠中,肝脏重量增加与哇巴因从血浆转运至胆汁的增强相关。暴露于PBBs的21日龄、35日龄和49日龄大鼠的肝脏重量也有所增加,但这种影响与这些动物中哇巴因转运的刺激无关。然而,与对照组相比,喂食100 ppm PBBs两周的成年大鼠的磺溴酞钠(BSP)血浆浓度显著降低,且BSP的胆汁排泄增加。喂食PBBs的成年大鼠向胆汁中排泄的结合型BSP(BSP-GSH)百分比也更高。对成年小鼠进行为期两周的100、150和200 ppm PBBs饮食处理,会导致吲哚菁绿(ICG)从成年小鼠血浆中的初始消失加快。然而,给成年小鼠喂食100和200 ppm PBBs的饮食剂量与哇巴因排泄能力增强无关。相比之下,通过母鼠饮食(50 ppm)给予PBBs处理,会导致15日龄小鼠中哇巴因累积排泄量增加近两倍。结果表明,PBBs刺激大鼠和小鼠的肝脏药物消除,但影响程度取决于年龄和转运的化合物。