首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Bile Acid-Induced Increase in Bile Acid-Independent Flow and Plasma Membrane NaK-ATPase Activity in Rat Liver
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Bile Acid-Induced Increase in Bile Acid-Independent Flow and Plasma Membrane NaK-ATPase Activity in Rat Liver

机译:胆汁酸诱导的大鼠肝脏胆汁酸非依赖性血流和血浆膜NaK-ATPase活性增加

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摘要

Previous studies showed that in rats with obstruction of the bile ducts draining the median and left hepatic lobes, and in rats with normal bile ducts in which the bile acid pool size and secretion were augmented by 48-h intraduodenal infusion of taurocholate, bile acid flux through secreting hepatocytes was increased. Under these conditions, taurocholate transport maximum exhibited a time-dependent adaptation to increased secretory load.Unexpectedly, bile acid-independent canalicular flow in these experimental models also was found to be increased when measured at 48 h. Relative to controls, bile acid-independent flow per gram of nonobstructed liver was increased approximately threefold in selectively obstructed rats and 43% in bile acid-loaded rats with normal ducts. In rats infused with bile acids at similar rates for only 16 h, no increase was observed. Studies with [14C]erythritol suggested that the increased bile flow under these conditions was of canalicular origin.NaK-ATPase activity in canaliculi-enriched liver plasma membrane preparations from the nonobstructed lobes of selectively obstructed rats and from 48-h bile acid-loaded rats was increased by 47% and 52%, respectively, relative to controls, but was not increased in membranes from 16-h bile acid-loaded rats. Canalicular membrane 5′-nucleotidase and Mg ATPase also were increased.These studies show that augmented bile acid flux through secreting liver causes an adaptive increase in bile acid-“independent” flow and in the activity of canalicular membrane enzymes. The mechanism by which bile acids modulate this and previously reported aspects of bile secretion remains to be elucidated.
机译:先前的研究表明,在阻塞了引流正中肝叶和左肝叶的胆管的大鼠中,以及在正常胆管的大鼠中,十二指肠内输注牛磺胆酸盐,胆汁酸通量会增加胆汁酸池的大小和分泌通过分泌肝细胞增加。在这些条件下,牛磺胆酸盐的最大转运量表现出对分泌量增加的时间依赖性。出乎意料的是,在这些实验模型中,与胆汁酸无关的小管流量在48 h时也被发现增加。相对于对照,在选择性阻塞的大鼠中,每克非阻塞肝的胆汁酸依赖性流量增加了约三倍,在正常导管的胆汁酸负荷大鼠中,胆汁酸的流量增加了约三倍。在以相似速率注入胆汁酸的大鼠中仅16 h,未观察到增加。用[ 14 C]赤藓糖醇进行的研究表明,在这些条件下胆汁流量的增加是源自小管。来自选择性梗阻大鼠的非梗阻性小叶和来自于小肠梗阻的小叶的富含小管的肝质膜制剂中的NaK-ATPase活性相对于对照,装载48h胆汁酸的大鼠分别增加了47%和52%,但装载16h胆汁酸的大鼠的膜中并未增加。研究还显示,小管膜5'-核苷酸酶和Mg ATPase也增加了。这些研究表明,通过分泌肝脏增加的胆汁酸通量引起了胆汁酸“非独立”流量和小管膜酶活性的适应性增加。胆汁酸调节这种和先前报道的胆汁分泌方面的机制仍有待阐明。

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