Dzurba A, Breier A, Slezák J, Stankovicová T, Vrbjar N, Ziegelhöffer A
Institute for Heart Research, Slovak Academy of Sciences, Bratislava, CSFR.
Bratisl Lek Listy. 1991 Mar-Apr;92(3-4):155-8.
The effect of calcium entry blocking agents nitrendipine and flunarizine on Mg(2+)-ATPase, (Mg2+ + Na(+)-ATPase, (Na+ + K(+)-ATPase and (Mg2+ + Ca(2+)-ATPase activities was studied. Nitrendipine (1 mumol/l-1) exerted a stimulatory effect on (Mg2+ + Na(+)-ATPase activity. Kinetic analysis of this effect revealed a two-fold rise in Vmax value and lowered Km value for activation of the enzyme by Na+ ions. In concentrations 10(-7) and 10(-5) mol.l-1 flunarizine behaved as a non-specific inhibitor of all sarcolemmal ATPases investigated. Nevertheless, in concentration of 10(-6) mol.l-1 flunarizine inhibited selectively the (Mg2+ + Na(+)-ATPase and (Na+ + K(+)-ATPase activities of myocardial sarcolemma. These observations provided evidence that both flunarizine and nitrendipine, in the concentration 10(-6) mol.l-1, modulate the (Mg2+ + Na(+)-ATPase and (Na+ + K(+)-ATPase activities in cardiac sarcolemma. These side effects of the above drugs particularly that of nitrendipine might have potential physiological relevance.
研究了钙通道阻滞剂尼群地平和氟桂利嗪对Mg(2+)-ATP酶、(Mg2+ + Na(+)-ATP酶、(Na+ + K(+)-ATP酶及(Mg2+ + Ca(2+)-ATP酶活性的影响。尼群地平(1 μmol/l-1)对(Mg2+ + Na(+)-ATP酶活性有刺激作用。对该作用的动力学分析显示,Vmax值升高两倍,且Na+离子激活该酶的Km值降低。在10(-7)和10(-5) mol.l-1浓度下,氟桂利嗪对所有所研究的肌膜ATP酶表现为非特异性抑制剂。然而,在10(-6) mol.l-1浓度下,氟桂利嗪选择性抑制心肌肌膜的(Mg2+ + Na(+)-ATP酶和(Na+ + K(+)-ATP酶活性。这些观察结果证明,氟桂利嗪和尼群地平在10(-6) mol.l-1浓度下均能调节心肌肌膜的(Mg2+ + Na(+)-ATP酶和(Na+ + K(+)-ATP酶活性。上述药物的这些副作用,尤其是尼群地平的副作用,可能具有潜在的生理相关性。