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丙磺舒及其结构类似物对牛红细胞中有机阴离子和氯离子通透性的抑制作用。

The inhibitor effect of probencid and structural analogues on organic anions and chloride permeabilities in ox erythrocytes.

作者信息

Motais R, Cousin J L

出版信息

Biochim Biophys Acta. 1976 Jan 21;419(2):309-13. doi: 10.1016/0005-2736(76)90356-4.

Abstract

Probenecid inhibits anion movements (organic anions and chloride) in ox erythrocytes. The I50 is 4. 10(-5) M. Structural analogues such as carinamide, p-carboxybenzene sulfonamide and p-carboxy N,N-diethyl benzene sulfonamide, which are drugs of the sulfonamide class, were also found to inhibit anion transport. These results reinforce the previously discussed view based on structural considerations, that sulfonamides act on the red cell membrane as competitors of anion transport. It is possible that probenecid and carinamide act in a similar way in the kidney.

摘要

丙磺舒抑制牛红细胞中的阴离子转运(有机阴离子和氯离子)。半数抑制浓度(I50)为4×10⁻⁵ M。还发现结构类似物如卡尼酰胺、对羧基苯磺酰胺和对羧基N,N -二乙苯磺酰胺等磺胺类药物也能抑制阴离子转运。这些结果强化了先前基于结构考虑所讨论的观点,即磺胺类药物作为阴离子转运的竞争者作用于红细胞膜。丙磺舒和卡尼酰胺在肾脏中可能以类似方式起作用。

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