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In vitro effects of some drugs on human erythrocyte glutathione reductase

机译:某些药物对人红细胞谷胱甘肽还原酶的体外作用

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The effects of ketotifen, meloxicam, phenyramidol–HCl and gadopentetic acid on the enzyme activity of GR were studied using human erythrocyte glutathione reductase (GR) enzymes in vitro. The enzyme was purified 209-fold from human erythrocytes in a yield of 19% with 0.31?U/mg. The purification procedure involved the preparation of haemolysate, ammonium sulphate precipitation, 2′′,5′-ADP Sepharose 4B affinity chromatography and Sephadex G-200 gel filtration chromatography. Purified enzyme was used in the in vitro studies. In the in vitro studies, IC50 values and Ki constants were 0.012?mM and 0.0008?±?0.00021?mM for ketotifen; 0.029?mM and 0.0061?±?0.00127?mM for meloxicam; 0.99?mM and 0.4340?±?0.0890?mM for phenyramidol–HCl; 138?mM and 28.84?±?4.69?mM for gadopentetic acid, respectively, showing the inhibition effects on the purified enzyme. Phenyramidol–HCl showed competitive inhibition, whereas the others showed non-competitive inhibition.
机译:体外使用人红细胞谷胱甘肽还原酶(GR)研究了酮替芬,美洛昔康,苯乙酰胺醇-盐酸和加多戊酸对GR酶活性的影响。该酶从人红细胞中纯化209倍,产率为19%(0.31?U / mg)。纯化步骤包括溶血液的制备,硫酸铵沉淀,2'',5'-ADP Sepharose 4B亲和层析和Sephadex G-200凝胶过滤层析。纯化的酶用于体外研究。在体外研究中,酮替芬的IC 50 值和K i 常数分别为0.012?mM和0.0008?±?0.00021?mM。美洛昔康为0.029?mM和0.0061?±?0.00127?mM;苯乙酰胺-HCl的浓度为0.99?mM和0.4340?±?0.0890?mM; g戊酸分别为138?mM和28.84?±?4.69?mM,显示出对纯化酶的抑制作用。苯乙酰胺-HCl表现出竞争性抑制作用,而其他则表现出非竞争性抑制作用。

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