Sentürk Murat, Gülçin Ilhami, Ciftci Mehmet, Küfrevioğlu Omer Irfan
Department of Chemistry, Faculty of Arts and Sciences, Atatürk University, Erzurum, Turkey.
Biol Pharm Bull. 2008 Nov;31(11):2036-9. doi: 10.1248/bpb.31.2036.
Dantrolene, a drug used to treat malignant hyperthermia, inhibits abnormal Ca2+ release from the sarcoplasmic reticulum. Glutathione reductase (Glutathione: NADP+ oxidoreductase, EC 1.8.1.7), a member of the pyridine-nucleotide disulfide oxidoreductase family of flavoenzymes, catalyzes the reduction of glutathione disulfide (GSSG) to reduced form (GSH) in the presence of nicotinamide adenine dinucleotide phosphate (NADPH). In the present study, the in vitro effects of dantrolene on human erythrocyte glutathione reductase were investigated. For this purpose, initially, human erythrocyte glutathione reductase was purified 2555.56 fold in a yield of 29.74% using both 2',5'-ADP Sepharose-4B affinity gel chromatography and Sephadex G-200 gel filtration chromatography. The purity of the enzyme was controlled by sodium dodecyle sulfate (SDS)-polyacrylamide gel electrophoresis (SDS-PAGE) which showed a single band. A constant temperature (+4 degrees C) was maintained during the purification process. Enzyme activity was determined with the Beutler method at 340 nm by means of a spectrophotometer. Dantrolene showed remarkable in vitro inhibitory effects on the enzyme. Ki constant and 50% inhibitory concentration (IC50) value for dantrolene were determined by Lineweaver-Burk graphs and plotting activity % vs. [I], respectively. Ki constant for dantrolene was found to be 0.1116+/-0.04 mM; IC50 value was 0.0523 mM. Dantrolene displayed non-competitive inhibition.
丹曲林是一种用于治疗恶性高热的药物,它能抑制肌浆网中异常的钙离子释放。谷胱甘肽还原酶(谷胱甘肽:NADP+氧化还原酶,EC 1.8.1.7)是黄素酶吡啶核苷酸二硫化物氧化还原酶家族的成员,在烟酰胺腺嘌呤二核苷酸磷酸(NADPH)存在的情况下,催化谷胱甘肽二硫化物(GSSG)还原为还原形式(GSH)。在本研究中,研究了丹曲林对人红细胞谷胱甘肽还原酶的体外作用。为此,首先,使用2',5'-ADP琼脂糖-4B亲和凝胶色谱和Sephadex G-200凝胶过滤色谱法将人红细胞谷胱甘肽还原酶纯化了2555.56倍,产率为29.74%。通过十二烷基硫酸钠(SDS)-聚丙烯酰胺凝胶电泳(SDS-PAGE)控制酶的纯度,结果显示为单一一条带。在纯化过程中保持恒温(+4℃)。通过分光光度计采用Beutler方法在340nm处测定酶活性。丹曲林在体外对该酶表现出显著的抑制作用。通过Lineweaver-Burk图和绘制活性%与[I]的关系分别确定丹曲林的Ki常数和50%抑制浓度(IC50)值。发现丹曲林的Ki常数为0.1116±0.04 mM;IC50值为0.0523 mM。丹曲林表现出非竞争性抑制作用。