Spustová V, Dzúrik R
Medical Bionics Research Institute, Bratislava, Czechoslovakia.
Ren Physiol Biochem. 1991;14(1-2):42-7.
Hippurate action on glucose utilization was evaluated in rat kidney cortex slices. Studies have shown the following. (1) Hippurate inhibits markedly basal as well as insulin-stimulated glucose utilization and basal gluconeogenesis. (2) Ca deficiency and specific Ca channel blockers diltiazem and isradipine abolish the hippurate inhibition of glucose utilization. (3) K+ channel blockers, i.e. the increased K+ concentration in incubation medium, procaine and sulfonylurea drugs also abolish the hippurate inhibition of glucose utilization. It is concluded that hippurate and benzoate operate through the ATP-dependent K+ channel.
在大鼠肾皮质切片中评估了马尿酸对葡萄糖利用的作用。研究结果如下:(1) 马尿酸显著抑制基础及胰岛素刺激的葡萄糖利用以及基础糖异生。(2) 钙缺乏以及特异性钙通道阻滞剂地尔硫䓬和伊拉地平可消除马尿酸对葡萄糖利用的抑制作用。(3) 钾通道阻滞剂,即孵育培养基中钾离子浓度升高、普鲁卡因和磺脲类药物也可消除马尿酸对葡萄糖利用的抑制作用。得出的结论是,马尿酸和苯甲酸通过ATP依赖性钾通道发挥作用。