硫代溴代眼啡(BSP)及其谷胱甘肽偶联物(BSP- gsh)肝胆运输的质的差异。

Z Gregus, E Fischer
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引用次数: 0

摘要

苯巴比妥预处理(PB);75 mg/kg,每日1次,连用5天),同时给予牛磺胆酸酯(TC;200 μ mol/kg静脉注射),伊红(EO;40-160 μ mol/kg静脉注射)和碘胺酸(IA;研究了马来酸二乙酯(DEM)预处理大鼠对BSP(30—120 mumol/kg i.v)和BSP—GSH(40—160 mumol/kg i.v)肝脏摄取和胆汁排泄的影响。BSP的胆汁排泄量不受PB和EO的影响,而TC增加,IA减少。相比之下,BSP- GSH的排泄不受TC和IA的影响,PB会刺激BSP- GSH的分泌,EO会抑制BSP- GSH的分泌。在不同的实验条件下,肝脏对BSP和BSP- GSH的摄取变化相似:PB不影响,TC、EO和IA减少了BSP和BSP- GSH在肝脏中的积累。这些结果表明,BSP和BSP- GSH在肝胆运输中存在质的差异,这种差异在肝脏摄取后表现出来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Qualitative differences in the hepatobiliary transport of sulfobromophthalein (BSP) and its glutathione conjugate (BSP-GSH).

The effect of phenobarbital pretreatment (PB; 75 mg/kg i.p. once daily for 5 days) and the simultaneous administration of taurocholate (TC; 200 mumol/kg i.v.), eosin(EO; 40-160 mumol/kg i.v.) and iodoxamic acid (IA; 125--500 mumol/kg i.v.) on the hepatic uptake and biliary excretion of BSP (30--120 mumol/kg i.v.) and BSP--GSH (40--160 mumol/kg i.v.) was investigated on diethyl maleate (DEM)-pretreated rats. The biliary excretion of BSP was not influenced by PB and EO, while it was increased by TC and decreased by IA. In contrast, the excretion of BSP--GSH was not influenced by TC or IA, it was stimulated by PB and inhibited by EO. In the different experimental conditions the hepatic uptake of BSP and BSP--GSH changed similarly: PB did not influence, TC, EO and IA decreased the accumulation of BSP and BSP--GSH in the liver. These results indicate that qualitative differences exist in the hepatobiliary transport of BSP and BSP--GSH, which manifest themselves following their hepatic uptake.

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