Motais R, Cousin J L
Am J Physiol. 1976 Nov;231(5 Pt. 1):1485-9. doi: 10.1152/ajplegacy.1976.231.5.1485.
Ethacrynic acid inhibits anion movements in ox red blood cells. The I50 for chloride is 7 X 10(-6) M. The inhibitory effect is instantaneous and completely reversed by washing the cells with a Ringer solution, suggesting that reaction with a membrane SH group is not involved in this process. Direct proof that ethacrynic acid does not act by its reactivity with thiol groups is given by experiments with dihydroethacrynic acid, a derivative that lacks the ability to combine with SH groups: the characteristics of inhibition are strictly identical (instantaneous and reversible; I50 equals 9 X 10(-6) M). All the phenoxyacetic derivatives tested were also more or less inhibitory. The relative activity of all the derivatives was highly correlated with their liposolubility, indicating that hydrophobic interaction is important in determining drug effect and influence of steric factors is minimal. The data suggest that inhibition essentially results from a hydrophobic interaction between ethacrynic acid and apolar regions of the membrane protein allowing chloride transport.
依他尼酸抑制牛红细胞中的阴离子转运。氯离子的半数抑制浓度(I50)为7×10⁻⁶ M。抑制作用是即时的,用林格溶液洗涤细胞可使其完全逆转,这表明该过程不涉及与膜巯基的反应。用二氢依他尼酸(一种缺乏与巯基结合能力的衍生物)进行的实验直接证明了依他尼酸并非通过与硫醇基团的反应起作用:抑制特性完全相同(即时且可逆;I50等于9×10⁻⁶ M)。所有测试的苯氧基乙酸衍生物或多或少也具有抑制作用。所有衍生物的相对活性与其脂溶性高度相关,表明疏水相互作用在决定药物效应方面很重要,而空间因素的影响最小。数据表明,抑制作用主要源于依他尼酸与允许氯离子转运的膜蛋白非极性区域之间的疏水相互作用。