首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Effects of taurodihydrofusidate a bile salt analogue on bile formation and biliary lipid secretion in the rhesus monkey.
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Effects of taurodihydrofusidate a bile salt analogue on bile formation and biliary lipid secretion in the rhesus monkey.

机译:胆汁盐类似物taurodihydrofusidate对恒河猴胆汁形成和胆汁脂质分泌的影响。

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摘要

Bile salts play a major role in bile formation and biliary lipid secretion. Sodium taurodihydrofusidate (TDHF), a derivative of the antibiotic fusidic acid, closely resembles bile salts in terms of structure, micellar characteristics, and capacity ot solubilize otherwise insolbule lipids. We have therefore studied the biliary secretion of this bile salt analogue and its influence on bile formation and biliary lipid secretion in primates. Alert, unanesthetized female rhesus monkeys prepared with a total biliary fistula were allowed to reach a steady bile salt secretion rate before each study. In three animals (group I),[14C]TDHF was infused intravenously. Most of the compound was secreted rapidly in bile chemically unchanged. The biliary secretion of this drug produced a twofold increase in bile flow; however, the bile salt output was markedly reduced during the infusion. In spite of this reduction, the phospholipid output remained essentially unchanged whereas the cholesterol output increased almost twofold. In five other animals (group II), the effect of TDHF on the bile salt secretion was further investigated by an intravenous infusion of [14C]taurocholate followed by a combined infusion of [14C]taurocholate and TDHF. When TDHF was added to the infusate, a reduction in the [14C]taurocholate output and a progressive rise in the plasma [14C]taurocholate concentration were observed in each animal. An analysis of the data in both groups indicates that (a) the most likely explanation to account for the decreased bile salt output is that the bile salt analogue, TDHF, interfered with bile salt secretion into the biliary canaliculi; (b) TDHF induces a greater secretion of biliary water than was observed with bile salts, an effect consistent with a stimulation of the bile salt-independent canalicular flow; (c) at similar 3alpha-hydroxysteroid secretion rates TDHF caused a significant increase in cholesterol secretion compared to that induced by bile salt. This finding suggests that TDHF affects cholesterol metabolism or secretion in a way distinct from bile salts. Thus, the solubilization of biliary lipids in mixed micelles, although essential, is only one of the factors which determine their secretion into bile.
机译:胆汁盐在胆汁形成和胆汁脂质分泌中起主要作用。牛磺酸二氢呋喃磺酸钠(TDHF)是一种抗生素夫西地酸的衍生物,就结构,胶束特性和溶解原本不溶的脂质的能力而言,与胆盐极为相似。因此,我们研究了这种胆盐类似物的胆汁分泌及其对灵长类动物胆汁形成和胆汁脂质分泌的影响。在每次研究前,允许将未经麻醉的雌性全鼻瘘雌性猕猴制成胆汁盐稳定分泌。在三只动物(I组)中,静脉内注入[14C] TDHF。大多数化合物在胆汁中快速分泌,化学性质不变。该药物的胆汁分泌使胆汁流量增加了两倍。但是,输注期间胆汁盐的输出明显减少。尽管有这种减少,磷脂的输出量基本上保持不变,而胆固醇的输出量几乎增加了两倍。在另外五只动物(II组)中,通过静脉内输注[14C]牛磺胆酸盐然后联合输注[14C]牛磺胆酸盐和TDHF,进一步研究了TDHF对胆汁盐分泌的影响。当在输注液中添加TDHF时,在每只动物中观察到[14C]牛磺胆酸盐输出的减少和血浆[14C]牛磺胆酸盐的浓度的逐渐升高。对两组数据的分析表明:(a)胆盐输出减少的最可能解释是胆盐类似物TDHF干扰了胆盐向胆管小管的分泌; (b)TDHF诱导的胆汁水分泌量高于胆汁盐所观察到的胆汁水分泌,其作用与刺激非胆汁盐依赖性小管流量相一致; (c)与胆汁盐诱导的胆固醇分泌相比,TDHF在相似的3α-羟基类固醇分泌速率下引起胆固醇分泌显着增加。该发现表明TDHF以不同于胆汁盐的方式影响胆固醇的代谢或分泌。因此,混合胶束中胆脂的增溶虽然必不可少,但这只是决定其分泌成胆汁的因素之一。

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