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胆汁盐通过肝细胞的微管依赖性转运:胆酸与牛磺胆酸。

Microtubule-dependent transport of bile salts through hepatocytes: cholic vs. taurocholic acid.

作者信息

Crawford J M, Crawford A R, Strahs D C

机构信息

Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts 02115.

出版信息

Hepatology. 1993 Oct;18(4):903-11. doi: 10.1002/hep.1840180423.

Abstract

Studies with taurine-conjugated bile salts have demonstrated two pathways for hepatocellular delivery of bile salts to bile: a cytosolic, microtubule-independent pathway and a membrane-based, microtubule-dependent pathway. However, a significant portion of circulating bile salts may be unconjugated. To determine whether free bile salts utilize similar pathways, we examined the effect of colchicine on the biliary excretion of intravenously administered cholic acid and taurocholate in intact rats. Basal rats were pretreated with low-dose colchicine or its inactive isomer, lumicolchicine, 1 hr before placement of intravenous and biliary cannulas and 2.75 hr before intravenous injection of [14C]cholic acid and [3H]taurocholate. Superfused rats were prepared as above but with intravenous infusion of taurocholate at 200 nmol/min.100 gm beginning 0.75 hr before [14C]cholic acid/[3H]taurocholate injection. Depleted/reinfused rats were subjected to biliary diversion for 20 hr before colchicine or lumicolchicine pretreatment, infusion of taurocholate and [14C]cholic acid/[3H]taurocholate injection. In each group, biliary excretion of [14C]taurocholate and [3H]taurocholate was inhibited equally by colchicine; for peak excretion rates the respective inhibition values were 33% and 35% in basal rats, 63% and 65% in superfused rats, and 74% and 76% in depleted/reinfused rats. Biliary excretion of [14C]taurocholate occurred consistently later than excretion of [3H]taurocholate, and maximal rates of excretion were reduced. In contrast, plasma uptake rates of [14C]cholic acid and [3H]taurocholate were essentially the same in depleted/reinfused rats. Deconvolution analysis of [14C]taurocholate vs. [3H]taurocholate biliary excretion curves revealed no significant differences among experimental groups. We conclude that conversion of [14C]cholic acid to [14C]taurocholate slightly retards its biliary excretion and diminishes its peak excretion rate compared with exogenous [3H]taurocholate.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对牛磺酸结合型胆汁盐的研究已证明,肝细胞将胆汁盐输送至胆汁存在两条途径:一条是胞质内、不依赖微管的途径,另一条是基于膜、依赖微管的途径。然而,循环中的胆汁盐有很大一部分可能是未结合的。为了确定游离胆汁盐是否利用类似途径,我们研究了秋水仙碱对完整大鼠静脉注射胆酸和牛磺胆酸盐后胆汁排泄的影响。基础大鼠在插入静脉和胆管插管前1小时以及静脉注射[14C]胆酸和[3H]牛磺胆酸盐前2.75小时,用低剂量秋水仙碱或其无活性异构体光秋水仙碱进行预处理。灌流大鼠的制备方法同上,但在注射[14C]胆酸/[3H]牛磺胆酸盐前0.75小时开始以200 nmol/min.100 gm的速度静脉输注牛磺胆酸盐。排空/再灌注大鼠在秋水仙碱或光秋水仙碱预处理、输注牛磺胆酸盐以及注射[14C]胆酸/[3H]牛磺胆酸盐之前,先进行20小时的胆汁引流。在每组中,秋水仙碱对[14C]牛磺胆酸盐和[3H]牛磺胆酸盐的胆汁排泄抑制作用相同;基础大鼠的峰值排泄率抑制值分别为33%和35%,灌流大鼠为63%和65%,排空/再灌注大鼠为74%和76%。[14C]牛磺胆酸盐的胆汁排泄始终比[3H]牛磺胆酸盐的排泄晚,且最大排泄率降低。相比之下,排空/再灌注大鼠中[14C]胆酸和[3H]牛磺胆酸盐的血浆摄取率基本相同。对[14C]牛磺胆酸盐与[3H]牛磺胆酸盐胆汁排泄曲线的去卷积分析显示,各实验组之间无显著差异。我们得出结论,与外源性[3H]牛磺胆酸盐相比,[14C]胆酸转化为[14C]牛磺胆酸盐会略微延迟其胆汁排泄并降低其峰值排泄率。(摘要截短于250字)

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