Kato M, Maegawa H, Okano T, Inui K, Hori R
Department of Pharmacy, Kyoto University Hospital, Faculty of Medicine, Kyoto University, Japan.
J Pharmacol Exp Ther. 1989 Nov;251(2):745-9.
We examined the effect of diethylpyrocarbonate (DEPC), a histidine specific reagent, on H+ coupled transport of cephradine via dipeptide carriers in the intestinal brush-border membranes, in comparison with the effects of other chemical modifiers. Pretreatment of membrane vesicles with DEPC resulted in the inhibition of cephradine transport in the presence or absence of an inward H+ gradient. This inhibition was reversed by subsequent treatment with hydroxylamine, but not with dithiothreitol. The inactivation by DEPC pretreatment was abolished by the presence of cephradine or glycylsarcosine. In the DEPC-pretreated membranes, the V(max) value of cephradine uptake was decreased without any change in the Km value. In contrast, cephradine uptake was not changed by the pretreatment with N-acetylimidazole, a tyrosine specific reagent, or p-chloromercuribenzene sulfonate, a sulfhydryl reagent. These results suggest that histidine residues in the carriers are essential for H+ coupled transport of amiocephalosporins.
我们研究了组氨酸特异性试剂焦碳酸二乙酯(DEPC)对头孢拉定通过肠刷状缘膜中二肽载体进行H⁺偶联转运的影响,并与其他化学修饰剂的作用进行了比较。用DEPC预处理膜囊泡会导致在有或没有内向H⁺梯度的情况下抑制头孢拉定的转运。随后用羟胺处理可逆转这种抑制作用,但用二硫苏糖醇处理则不能。头孢拉定或甘氨酰肌氨酸的存在消除了DEPC预处理导致的失活。在DEPC预处理的膜中,头孢拉定摄取的V(max)值降低,而Km值没有任何变化。相比之下,用酪氨酸特异性试剂N-乙酰咪唑或巯基试剂对氯汞苯磺酸盐预处理不会改变头孢拉定的摄取。这些结果表明,载体中的组氨酸残基对于氨基头孢菌素的H⁺偶联转运至关重要。