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

Drug-nutrient interactions Pub Date : 1986-01-01
Y Barcina, A I Alcalde, A Ilundain, J Larralde
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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.

头孢氨苄和四环素对大鼠小肠半乳糖吸收的影响。
研究了头孢氨苄和盐酸四环素对大鼠小肠d -半乳糖吸收的影响。两种抗生素均以剂量依赖的方式抑制d -半乳糖进入离体肠粘膜的摄取。体内研究表明,头孢氨苄和四环素HCl减少了d -半乳糖的吸收,并且在停止抗生素灌注后转运缺陷是不可逆的。D-glactose的活性成分和被动成分均被抗生素所抑制。此外,这两种药物在连续循环灌注时均能降低粘膜耗氧量,抑制d -半乳糖吸收。我们得出结论,在组织暴露于头孢氨苄或四环素HCl后,大鼠小肠中d -半乳糖运输的减少似乎部分是由于能量供应不足。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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