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在小肠中存在一种可转运FK089的载体介导转运系统的证据,FK089是一种新型无氨基头孢菌素抗生素。

Evidence for a carrier-mediated transport system in the small intestine available for FK089, a new cephalosporin antibiotic without an amino group.

作者信息

Tsuji A, Hirooka H, Tamai I, Terasaki T

出版信息

J Antibiot (Tokyo). 1986 Nov;39(11):1592-7. doi: 10.7164/antibiotics.39.1592.

Abstract

Transport of a new cephalosporin developed for oral use, FK089, has been studied with the rat everted small intestine in vitro. Uptake was found to be pH-dependent with the maximum rate at an acidic pH below 5 and with a 5-fold lower rate at pH 7.0. The shape of the pH-rate profile was very similar to that of cefixime and different from that of pH-lipophilicity profile of FK089. The saturation kinetics of the uptake of FK089 were demonstrated at pH 5.0. By correcting the nonsaturable rate process, the kinetics of the mutual inhibition of FK089 uptake by cefixime and cefixime uptake by FK089 were all consistent with competitive type inhibition. The results indicate that carrier-mediated transport is responsible for transport of cephem antibiotics without an alpha-amino group in the side chain at the 7-position of the cephem nucleus in the intestinal brush-border membrane.

摘要

已利用大鼠外翻小肠在体外对一种新开发的口服头孢菌素FK089的转运进行了研究。发现摄取呈pH依赖性,在低于5的酸性pH下速率最高,在pH 7.0时速率低5倍。pH-速率曲线的形状与头孢克肟非常相似,与FK089的pH-亲脂性曲线不同。在pH 5.0时证明了FK089摄取的饱和动力学。通过校正非饱和速率过程,头孢克肟对FK089摄取的相互抑制动力学以及FK089对头孢克肟摄取的相互抑制动力学均符合竞争性抑制类型。结果表明,载体介导的转运负责在肠刷状缘膜中头孢烯核7位侧链无α-氨基的头孢烯类抗生素的转运。

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