Kordowiak A M, Stachura J, Tomecki J, Kapusta P
Department of Animal Biochemistry, Jagiellonian University, Cracow, Poland.
J Physiol Pharmacol. 1993 Dec;44(4):383-90.
Addition in vitro of ethanol solution of PGE1 to isolated Golgi-rich membrane fraction caused great alterations in galactosyltransferase activity, marker enzyme of these membranes. Ethanol as a solvent of PGE1 has an influence on the activity of the enzyme as well as the membrane permeability, different drugs penetration and availability of substrates. Then, additional control with ethanol in identical concentration as in the investigated sample was performed. In a dose 1 microgram PGE1 per 1 mg of protein (and lower concentration of ethanol c. 0.09%) the stimulation of this enzyme activity (excluding 2 and 6 hours s after Golgi membrane isolation) was above 30% in comparison with the control.
在富含高尔基体的分离膜组分中体外添加前列腺素E1(PGE1)的乙醇溶液,会导致这些膜的标记酶——半乳糖基转移酶的活性发生巨大变化。乙醇作为PGE1的溶剂,对该酶的活性以及膜通透性、不同药物的渗透和底物的可用性都有影响。然后,用与被研究样品浓度相同的乙醇进行额外对照实验。在每毫克蛋白质中加入1微克PGE1(乙醇浓度约为0.09%且较低)时,与对照组相比,该酶活性的刺激作用(高尔基体膜分离后2小时和6小时除外)超过30%。