Gulaia N M, Gubenko E P, Veller E S
Ukr Biokhim Zh (1978). 1981 Jan-Feb;53(1):94-100.
The glucose-6-phosphatase dehydrogenase (EC 1.1.1.49) reaction of mouse organs was studied as affected by PPi and its diphosphonate analogs. It is shown that in vitro and hydroxy-1-ethane-1,1-diphosphonic acid) inhibit the mentioned enzyme of the mouse spleen and liver. The effect of hydroxyl-1-ethane-1,1-diphosphonic acid was used as an example to show that inhibition of glucose-6-phosphate dehydrogeanse by diphosphonates belongs to the mixed type characterized by changes in the Km and Vmax values. For the spleen enzyme Km equals 0.064 mM, Vmax - 4.7 Mg of NADPH per 1 mg of protein-1. h-1. Administration of methylene diphosphonic acid causes an inhibition in vivo of the glucose-6-phosphatase dehydrogenate activity of the liver but not of the spleen and thymus. Basing on the isoenzymic composition of the enzyme for the mentioned organs, it is possible to suppose that the difference in the methylene diphosphonic acid effect in the liver and lymphoid organs may depend on the differences in its isoenzymic spectrum. The fact that in vivo methylene diphosphonic acid in a dose having an immuno-depressive action has no influence on the activity of glucose-6-phosphatase dehydrogenase in the lymphoid organs, may evidence for the absence of the indirect immunodepressive effect of diphosphonate by affecting this enzyme.
研究了焦磷酸(PPi)及其二膦酸盐类似物对小鼠器官葡萄糖-6-磷酸酶脱氢酶(EC 1.1.1.49)反应的影响。结果表明,体外时,焦磷酸和1-羟基乙烷-1,1-二膦酸抑制小鼠脾脏和肝脏中的上述酶。以1-羟基乙烷-1,1-二膦酸的作用为例表明,二膦酸盐对葡萄糖-6-磷酸脱氢酶的抑制作用属于混合型,其特征是Km和Vmax值发生变化。对于脾脏酶,Km等于0.064 mM,Vmax为每1 mg蛋白质每小时4.7 μg NADPH。给予亚甲基二膦酸会在体内抑制肝脏而非脾脏和胸腺的葡萄糖-6-磷酸酶脱氢酶活性。基于上述器官中该酶的同工酶组成,可以推测亚甲基二膦酸在肝脏和淋巴器官中作用的差异可能取决于其同工酶谱的差异。免疫抑制剂量的亚甲基二膦酸在体内对淋巴器官中葡萄糖-6-磷酸酶脱氢酶活性没有影响,这一事实可能证明二膦酸盐不会通过影响该酶产生间接免疫抑制作用。