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肠道药物硫酸结合作用的区室化。豚鼠空肠和结肠分离黏膜将肠腔和肠腔外的[35S]硫酸盐掺入1-萘酚的过程。

Compartmentation of intestinal drug sulphoconjugation. Incorporation of luminal and contraluminal [35S]sulphate into 1-naphthol by the isolated mucosa of guinea pig jejunum and colon.

作者信息

Lauterbach F, Czekay R P, Sund R B

机构信息

Department of Pharmacology and Toxicology, Ruhr-University of Bochum, Germany.

出版信息

Biochem Pharmacol. 1993 Oct 19;46(8):1339-47. doi: 10.1016/0006-2952(93)90097-g.

Abstract

Compartmentation of 1-naphthol metabolism was inferred from the metabolite pattern and distribution in the isolated mucosa of guinea pig intestine mounted in a flux chamber (Sund and Lauterbach, Arch Pharmacol Toxicol 58: 74-83, 1986). To verify the existence of these compartments the dependence of [35S]sulphate incorporation into 1-naphthol sulphate on the side of administration of 1-naphthol and [35S]sulphate was determined. Isolated mucosae were pre-equilibrated with [35S]-sulphate (5 x 10(6) cpm/mumol, 1 mM) for 30 min and subsequently incubated for 15 min with 50 microM 1-naphthol. The three 1-naphthol sulphate fractions (luminal side, blood side and tissue) were assayed by HPLC and liquid scintillation counting; their specific activity was calculated as percentage of the specific activity of the inorganic sulphate administered. 1-Naphthol glucuronide was also measured. In jejunal experiments: after luminal administration of 1-naphthol, 1-naphthol sulphate appeared almost exclusively in the luminal solution; its specific activity approached 70% and 3%, when [35S]sulphate was added to the luminal and blood side, respectively. After introducing 1-naphthol and [35S]sulphate on the blood side, a high and similar specific activity of 50-60% was observed in all three 1-naphthol sulphate fractions (luminal and blood side, tissue) though adding [35S]sulphate to the lumen side decreased the specific activity to 10-20%. In experiments on colonic mucosa: a specific activity both of luminal and blood side 1-naphthol sulphate of more than 50% was observed with blood side [35S]sulphate irrespective of the side of 1-naphthol administration. When [35S]sulphate was placed on the luminal side the specific activity of blood side 1-naphthol sulphate dropped to only 3%, and that of luminal 1-naphthol sulphate ranged between 6% and 20%. Supplementary experiments in which mucosae were exposed to 1-naphthol and [35S]sulphate for 45 min without preincubation showed a tendency to decrease the lumen: blood distribution ratio of 1-naphthol sulphate. However, the general pattern of 1-naphthol sulphate specific activity remained unchanged. The experiments provide further evidence that the jejunal conjugation of phenolic drugs is being performed in two major compartments, which are accessible from the lumen ("luminal compartment") and blood ("systemic compartment") side. The luminal compartment seems practically inaccessible to blood side sulphate as is the systemic compartment for luminal 1-naphthol. In the colonic mucosa, a major "systemic compartment" receiving its sulphate from the blood side is the site for most of the events, but a minor "luminal compartment" seems to be involved as well.

摘要

根据豚鼠肠黏膜在流通池中分离后的代谢产物模式及分布情况,推断出1 - 萘酚代谢的区室化现象(Sund和Lauterbach,《药理学与毒理学文献》58: 74 - 83, 1986)。为验证这些区室的存在,测定了1 - 萘酚硫酸酯中[35S]硫酸盐掺入量对1 - 萘酚和[35S]硫酸盐给药侧的依赖性。将分离的黏膜用[35S] - 硫酸盐(5×10(6) cpm/μmol,1 mM)预平衡30分钟,随后与50 μM 1 - 萘酚孵育15分钟。通过高效液相色谱法和液体闪烁计数法测定三个1 - 萘酚硫酸酯组分(肠腔侧、血液侧和组织);其比活性以所给药无机硫酸盐比活性的百分比计算。同时也测定了1 - 萘酚葡糖醛酸酯。在空肠实验中:肠腔给药1 - 萘酚后,1 - 萘酚硫酸酯几乎仅出现在肠腔溶液中;当分别向肠腔侧和血液侧加入[35S]硫酸盐时,其比活性分别接近70%和3%。血液侧加入1 - 萘酚和[35S]硫酸盐后,在所有三个1 - 萘酚硫酸酯组分(肠腔侧和血液侧、组织)中均观察到高且相似的比活性,为50 - 60%,尽管向肠腔侧加入[35S]硫酸盐会使比活性降至10 - 20%。在结肠黏膜实验中:无论1 - 萘酚给药侧如何,血液侧加入[35S]硫酸盐时,肠腔侧和血液侧1 - 萘酚硫酸酯的比活性均超过50%。当[35S]硫酸盐置于肠腔侧时,血液侧1 - 萘酚硫酸酯的比活性仅降至3%,而肠腔侧1 - 萘酚硫酸酯的比活性在6%至20%之间。补充实验中,黏膜在未预孵育的情况下暴露于1 - 萘酚和[35S]硫酸盐45分钟,显示出1 - 萘酚硫酸酯肠腔:血液分布比有降低的趋势。然而,1 - 萘酚硫酸酯比活性的总体模式保持不变。这些实验进一步证明,空肠中酚类药物的结合在两个主要区室中进行,这两个区室可分别从肠腔(“肠腔区室”)和血液(“全身区室”)侧进入。肠腔区室似乎实际上无法接触到血液侧的硫酸盐,全身区室对于肠腔侧的1 - 萘酚也是如此。在结肠黏膜中,一个主要从血液侧接收硫酸盐的“全身区室”是大多数反应发生的部位,但一个较小的“肠腔区室”似乎也参与其中。

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