Okano T, Inui K, Takano M, Hori R
Biochem Pharmacol. 1986 Jun 1;35(11):1781-6. doi: 10.1016/0006-2952(86)90292-3.
The transport of cephalosporin antibiotics in brush-border membrane vesicles isolated from rat small intestine has been studied by a rapid filtration technique, demonstrating a carrier-mediated transport system for aminocephalosporins such as cephradine. In agreement with the transport mechanisms of dipeptides, the uptake of cephradine by brush-border membrane vesicles was Na+-independent and was stimulated in the presence of an inward H+ gradient ([H+]o greater than [H+]i). Cephradine uptake in the presence of an inward H+ gradient was a saturable process with an apparent Km of 9.4 mM, and was markedly inhibited by dipeptides but not inhibited by amino acids. The present data suggest that aminocephalosporins can be transported by a common carrier-mediated system with dipeptides in the intestinal brush-border membranes and this process may be driven by an H+ gradient.
采用快速过滤技术研究了从大鼠小肠分离的刷状缘膜囊泡中头孢菌素抗生素的转运,结果表明存在一种载体介导的氨基头孢菌素(如头孢拉定)转运系统。与二肽的转运机制一致,刷状缘膜囊泡对头孢拉定的摄取不依赖于Na +,且在存在内向H +梯度([H +]o大于[H +]i)时会受到刺激。在存在内向H +梯度的情况下,头孢拉定的摄取是一个可饱和的过程,表观Km为9.4 mM,并且明显受到二肽的抑制,但不受氨基酸的抑制。目前的数据表明,氨基头孢菌素可以通过与二肽共同的载体介导系统在肠道刷状缘膜中转运,并且这个过程可能由H +梯度驱动。