Kaneko M, Singal P K, Dhalla N S
Division of Cardiovascular Sciences, St. Boniface General Hospital Research Centre, Winnipeg, Manitoba, Canada.
Basic Res Cardiol. 1990 Jan-Feb;85(1):45-54. doi: 10.1007/BF01907013.
Effects of oxygen free radicals on Ca2+/Mg2+ ATPase and ATP-independent Ca2(+)-binding activities were examined in rat heart sarcolemma. Membranes were incubated with different oxygen radical generating media such as xanthine + xanthine oxidase, hydrogen peroxide, and hydrogen peroxide + Fe2+. In the presence of xanthine + xanthine oxidase, Ca2+ ATPase activity was stimulated and this effect was prevented by the addition of superoxide dismutase. Hydrogen peroxide also showed a significant increase in Ca2(+)-ATPase activity in a dose-dependent manner and this effect was blocked by catalase. On the other hand, a combination of hydrogen peroxide + Fe2+ decreased Ca2(+)-ATPase activity; this depression was prevented by the addition of D-mannitol. The observed change in Ca2(+)-ATPase activity due to oxygen free radicals was associated with changes in Vmax, whereas Ka remained unaffected. Both xanthine + xanthine oxidase and hydrogen peroxide increased whereas, hydrogen peroxide + Fe2+ inhibited the ATP-independent Ca2(+)-binding activities. It is suggested that oxygen free radicals may influence Ca2+ movements in the cell by altering the Ca2+/Mg2+ ATPase and Ca2(+)-binding activities of the membrane and these effects may be oxygen-radical species specific.
在大鼠心肌肌膜中研究了氧自由基对Ca2+/Mg2+ATP酶和非ATP依赖的Ca2+结合活性的影响。将肌膜与不同的氧自由基生成介质一起孵育,如黄嘌呤+黄嘌呤氧化酶、过氧化氢以及过氧化氢+Fe2+。在黄嘌呤+黄嘌呤氧化酶存在的情况下,Ca2+ATP酶活性受到刺激,而超氧化物歧化酶的加入可阻止这种效应。过氧化氢也以剂量依赖的方式使Ca2+ATP酶活性显著增加,而过氧化氢酶可阻断这种效应。另一方面,过氧化氢+Fe2+的组合降低了Ca2+ATP酶活性;加入D-甘露醇可防止这种抑制作用。观察到的由于氧自由基导致的Ca2+ATP酶活性变化与Vmax的变化相关,而Ka保持不变。黄嘌呤+黄嘌呤氧化酶和过氧化氢均可增加非ATP依赖的Ca2+结合活性,而过氧化氢+Fe2+则抑制该活性。提示氧自由基可能通过改变膜的Ca2+/Mg2+ATP酶和Ca2+结合活性来影响细胞内的Ca2+转运,并且这些效应可能具有氧自由基种类特异性。