Shimada K, Ohishi K, Nambara T
J Pharmacobiodyn. 1985 Jan;8(1):64-8. doi: 10.1248/bpb1978.8.64.
A new method for the assay of Na+, K+-adenosine triphosphatase (Na+, K+-ATPase) inhibition has been devised involving the determination of enzymatically produced adenosine diphosphate (ADP) and unchanged adenosine triphosphate (ATP) by high-performance liquid chromatography (HPLC). The substrate, ATP, was incubated with the enzyme preparation in the presence of an inhibitor. The incubation mixture was filtered through a membrane filter, and ADP and ATP in the filtrate were separated by (HPLC). The inhibitory effect of a cardiac steroid on the enzymic reaction was estimated by measuring the peak area ratio of ADP to ADP plus ATP on the chromatogram. The proposed assay method has proved to be satisfactory with respects to simplicity, sensitivity, and reproducibility.
已设计出一种测定钠钾 - 腺苷三磷酸酶(Na⁺,K⁺ - ATP酶)抑制作用的新方法,该方法涉及通过高效液相色谱法(HPLC)测定酶促产生的二磷酸腺苷(ADP)和未反应的三磷酸腺苷(ATP)。底物ATP在抑制剂存在的情况下与酶制剂一起孵育。孵育混合物通过膜过滤器过滤,滤液中的ADP和ATP通过HPLC分离。通过测量色谱图上ADP与ADP加ATP的峰面积比来评估强心甾对酶反应的抑制作用。所提出的测定方法在简便性、灵敏度和重现性方面已被证明是令人满意的。