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头孢氨苄和四环素对大鼠小肠半乳糖吸收的影响。

Effect of cephalexin and tetracycline on galactose absorption in rat small intestine.

作者信息

Barcina Y, Alcalde A I, Ilundain A, Larralde J

出版信息

Drug Nutr Interact. 1986;4(3):299-307.

PMID:3956390
Abstract

The effects of cephalexin and tetracycline HCl on D-galactose absorption in rat small intestine were investigated. Both antibiotics inhibited D-galactose uptake into isolated intestinal mucosa in a dose-dependent fashion. In vivo studies showed that cephalexin and tetracycline HCl reduced D-galactose absorption and that the transport defect was not reversible on cessation of antibiotic perfusion. Both the active and passive components of D-glactose absorption were inhibited by the antibiotics tested. Furthermore, both drugs reduced mucosa O2 consumption and inhibited D-galactose absorption when they were perfused in a contiguous loop. We conclude that the diminished D-galactose transport by rat small intestine after tissue exposure to either cephalexin or tetracycline HCl appears to be in part due to an insufficient energy supply.

摘要

研究了头孢氨苄和盐酸四环素对大鼠小肠中D-半乳糖吸收的影响。两种抗生素均以剂量依赖性方式抑制D-半乳糖摄取到分离的肠黏膜中。体内研究表明,头孢氨苄和盐酸四环素降低了D-半乳糖的吸收,并且在停止抗生素灌注后转运缺陷不可逆。所测试的抗生素抑制了D-半乳糖吸收的主动和被动成分。此外,当两种药物在相邻肠袢中灌注时,它们都会降低黏膜耗氧量并抑制D-半乳糖吸收。我们得出结论,大鼠小肠在组织暴露于头孢氨苄或盐酸四环素后D-半乳糖转运减少似乎部分是由于能量供应不足。

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