Boyer J L, Schwarz J, Smith N
Gastroenterology. 1976 Feb;70(2):254-6.
The hepatic metabolism of 35S-sulfobromophthalein was studied in the free-swimming Elasmobranchs, Squalus acanthias (spiny dogfish shark) and Raja erinacea (small skate), to evaluate the physiological significance of biliary excretion of organic anions in marine vertebrates. Twenty-four hours after intra-arterial injection, 85.8 +/- 15.7% of the administered dose was recovered in bile and liver in dogfish and 78.4 +/- 9.9% in skates. More than 85% of BSP in bile was in unconjugated form in both species. Furthermore, selective hepatic uptake and biliary excretion of 35S-sulfobromophthalein occurred despite very little specific binding protein (Ligandin). These studies demonstrate that transport systems for biliary excretion of organic anions evolved before migration of marine life from the sea and independent of conjugation and organic anion binding proteins which facilitate biliary excretion of compounds such as 35S-sulfobromophthalein in higher vertebrates.
在自由游动的板鳃亚纲动物棘鲨(Squalus acanthias,棘鲛)和小鳐(Raja erinacea,小鳐鱼)中研究了35S-磺溴酞的肝脏代谢,以评估海洋脊椎动物中有机阴离子胆汁排泄的生理意义。动脉内注射24小时后,在棘鲛的胆汁和肝脏中回收了85.8±15.7%的给药剂量,在小鳐鱼中为78.4±9.9%。在这两个物种中,胆汁中超过85%的磺溴酞呈未结合形式。此外,尽管特异性结合蛋白(配体蛋白)很少,但仍发生了35S-磺溴酞的选择性肝脏摄取和胆汁排泄。这些研究表明,有机阴离子胆汁排泄的转运系统在海洋生物从海洋迁移之前就已经进化,并且独立于促进高等脊椎动物中35S-磺溴酞等化合物胆汁排泄的结合和有机阴离子结合蛋白。