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豚鼠离体黏膜中2-萘酚的代谢及代谢物转运:肠道药物代谢区室化的进一步证据

2-Naphthol metabolism and metabolite transport in the isolated guinea pig mucosa: further evidence for compartmentation of intestinal drug metabolism.

作者信息

Sund R B, Lauterbach F

机构信息

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

出版信息

Pharmacol Toxicol. 1993 Feb;72(2):84-9. doi: 10.1111/j.1600-0773.1993.tb00295.x.

Abstract

As an extension of a previous study on the metabolism of 14C-1-naphthol (1-N) by the isolated guinea pig mucosa (Sund & Lauterbach 1986), the isomeric compound 2-naphthol (2-N, 50-130 nmol/ml) has now been examined. 14C-Labelled drug was added to the luminal or contraluminal fluid bathing the two sides of jejunal or colonic mucosal sheets in a symmetrical set up. After aerobic incubation for 45 min. at 37 degrees, the fluid compartments and the tissue were analysed for parent drug and metabolites. Like 1-N 2-N was transformed into its sulphate and glucuronide. In the jejunum, 2-N was more extensively sulphated than 1-N, whereas in the colon the metabolite profiles (sulphate:glucuronide ratio) of the two isomers were similar. Generally, the metabolism rate of 2-N, its metabolite profile and metabolite transport pattern (lumen: blood distribution ratio) as well as the tissue accumulation of parent drug and metabolites, depended on the side of drug administration and on the tissue studied. Thus, changing the drug administration had a pronounced impact on the jejunal metabolism and transport, but caused only minor effects in the colon. In summary, this study emphasizes that drug metabolism and metabolite transport differ in the small and large intestine. The data further support the hypothesis that jejunal drug metabolism takes place in two compartments, of which the most active one is accessible from the lumen side and the other from the blood side. The possibility that colonic drug metabolism may also involve compartmentation should be considered although the present study provided very little evidence for this.

摘要

作为先前关于豚鼠离体黏膜对14C-1-萘酚(1-N)代谢研究(Sund和Lauterbach,1986年)的扩展,现已对同分异构体化合物2-萘酚(2-N,50 - 130 nmol/ml)进行了研究。在对称设置中,将14C标记的药物添加到灌流空肠或结肠黏膜片两侧的肠腔或对侧腔液中。在37℃需氧孵育45分钟后,分析液腔和组织中的母体药物和代谢物。与1-N一样,2-N也转化为其硫酸盐和葡萄糖醛酸苷。在空肠中,2-N比1-N更易硫酸化,而在结肠中,两种异构体的代谢物谱(硫酸盐:葡萄糖醛酸苷比率)相似。一般来说,2-N的代谢率、其代谢物谱和代谢物转运模式(肠腔:血液分布比率)以及母体药物和代谢物在组织中的积累,取决于给药侧和所研究的组织。因此,改变给药方式对空肠代谢和转运有显著影响,但对结肠只有轻微影响。总之,本研究强调药物代谢和代谢物转运在小肠和大肠中存在差异。数据进一步支持了这样的假设,即空肠药物代谢发生在两个隔室中,其中最活跃的一个可从肠腔侧进入,另一个可从血液侧进入。尽管本研究对此提供的证据很少,但应考虑结肠药物代谢也可能涉及分隔的可能性。

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