Muranushi N, Horie K, Masuda K, Hirano K
Shionogi Research Laboratories, Shionogi & Co., Ltd., Osaka, Japan.
Pharm Res. 1994 Dec;11(12):1761-5. doi: 10.1023/a:1018919517839.
The characteristics of ceftibuten uptake into Caco-2 cells grown in a collagen-coated dish were examined. Ceftibuten showed stereoselective and pH-dependent uptake. The pH-dependency of ceftibuten was more marked than that of cefaclor or cephalexin, but all three antibiotics showed maximal uptake at pH 5.5. Ceftibuten uptake was linear for the initial 1 hr and then reached a plateau. The initial uptake (15 min) was markedly reduced by the addition of 2,4-dinitrophenol or FCCP (a protonophore), or by lowering the incubation temperature. The uptake of ceftibuten into the brush-border membrane vesicles prepared from cultured Caco-2 cells showed an overshoot in the presence of an H(+)-gradient. These findings indicated that the uptake of ceftibuten was energy-dependent, especially H(+)-gradient-dependent. Uptake inhibition by various compounds was compared using Caco-2 cells. Amino acids and a tetrapeptide did not inhibit uptake, whereas di- or tri-peptides were effective inhibitors. These observations suggest that ceftibuten is taken up by a carrier-mediated transport system(s) for dipeptides. Various antibiotics differed in their ability to inhibit uptake, with cyclacillin showing maximum inhibition. Differences in the inhibitory effect may be accounted for by the heterogeneity (multiplicity) of the transport systems.
研究了头孢布烯在胶原包被培养皿中生长的Caco-2细胞中的摄取特性。头孢布烯表现出立体选择性和pH依赖性摄取。头孢布烯的pH依赖性比头孢克洛或头孢氨苄更明显,但这三种抗生素在pH 5.5时均表现出最大摄取量。头孢布烯的摄取在最初1小时呈线性,然后达到平台期。加入2,4-二硝基苯酚或FCCP(一种质子载体),或降低孵育温度,均可显著降低初始摄取量(15分钟)。头孢布烯摄取到从培养的Caco-2细胞制备的刷状缘膜囊泡中,在存在H(+)-梯度时显示出超调现象。这些发现表明头孢布烯的摄取是能量依赖性的,尤其是H(+)-梯度依赖性的。使用Caco-2细胞比较了各种化合物的摄取抑制作用。氨基酸和四肽不抑制摄取,而二肽或三肽是有效的抑制剂。这些观察结果表明,头孢布烯是通过二肽的载体介导转运系统摄取的。各种抗生素在抑制摄取的能力上有所不同,环青霉素表现出最大抑制作用。抑制作用的差异可能是由转运系统的异质性(多样性)造成的。