Fricker G, Wössner R, Drewe J, Fricker R, Boyer J L
Institut für Pharmazeutische Technologie und Biopharmazie, Heidelberg, Germany.
Am J Physiol. 1997 Nov;273(5 Pt 1):G1023-30. doi: 10.1152/ajpgi.1997.273.5.G1023.
The sulfated bile alcohol scymnol sulfate (ScyS), 3 alpha,7 alpha,12 alpha,24 xi, 26,27-hexahydroxy-5 beta-cholestane-26(27)-sulfate, is the major bile salt in bile of an elasmobranch, the little skate. To investigate hepatic transport of bile alcohols in skate liver, [3H]ScyS and a potential precursor, 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestane (chtriol), were used as model compounds. Their transport into isolated hepatocytes was partially saturable, temperature sensitive, and Na+ independent. The uptake of ScyS was inhibited by cholyltaurine, and uptake of cholyltaurine was inhibited by ScyS in a competitive manner. In contrast, uptake of chtriol was not inhibited by cholyltaurine, suggesting separate transport systems. ScyS and chtriol showed a choleretic effect in isolated perfused livers. When ScyS was added to the perfusate of isolated perfused livers, > 25% was found in bile within 7 h. When chtriol was added to the perfusate, 10% of the dose was secreted into the bile mainly in the form of polar metabolites, whereas only nonmetabolized chtriol remained in the livers. The slow bile flow of 40-50 microliters/h and the high recovery in the liver suggest that metabolism may be the rate-limiting step in the hepatic elimination of chtriol. The major metabolites secreted into bile were identified by mass spectrometry and chromatography as scymnol and ScyS. To study the enterohepatic circulation, [3H]ScyS or [3H]chtriol was administered into the duodenum of free-swimming skates, and bile was collected through exteriorized indwelling cannulas over a 4-day period. More than 90% of the radioactivity was recovered from bile, indicating that there was a highly effective absorption in the intestinal epithelium, as well as specific transport mechanisms for hepatic uptake and biliary secretion of these compounds. This is the first direct demonstration of an enterohepatic circulation for a bile alcohol sulfate in fish liver.
硫酸化胆汁醇硫酸鲨胆醇(ScyS),即3α,7α,12α,24ξ,26,27 - 六羟基 - 5β - 胆甾烷 - 26(27) - 硫酸盐,是板鳃亚纲鱼类小斑鳐胆汁中的主要胆盐。为研究鲨肝中胆汁醇的肝脏转运,[3H]ScyS和一种潜在前体3α,7α,12α - 三羟基 - 5β - 胆甾烷(胆三醇)被用作模型化合物。它们进入分离的肝细胞的转运具有部分饱和性、温度敏感性且不依赖钠离子。ScyS的摄取受到胆酰牛磺酸的抑制,而胆酰牛磺酸的摄取则受到ScyS的竞争性抑制。相反,胆三醇的摄取不受胆酰牛磺酸的抑制,表明存在不同的转运系统。ScyS和胆三醇在分离的灌注肝脏中显示出利胆作用。当将ScyS添加到分离的灌注肝脏的灌注液中时,7小时内胆汁中发现超过25%的ScyS。当将胆三醇添加到灌注液中时,10%的剂量主要以极性代谢物的形式分泌到胆汁中,而肝脏中仅保留未代谢的胆三醇。40 - 50微升/小时的缓慢胆汁流量以及肝脏中的高回收率表明,代谢可能是肝脏消除胆三醇的限速步骤。通过质谱和色谱法鉴定出分泌到胆汁中的主要代谢物为鲨胆醇和ScyS。为研究肠肝循环,将[3H]ScyS或[3H]胆三醇注入自由游动的鳐鱼十二指肠,并通过外置留置插管在4天内收集胆汁。超过90%的放射性物质从胆汁中回收,表明在肠上皮中有高效吸收,以及这些化合物肝脏摄取和胆汁分泌的特定转运机制。这是首次直接证明鱼肝中硫酸化胆汁醇的肠肝循环。