Levine P H, Sladdin D G, Krinsky N I
Thromb Haemost. 1981 Jun 30;45(3):290-3.
In the course of studying the effects on platelets of the oxidant species superoxide (O2.-), O2.- was generated by the interaction of xanthine oxidase plus xanthine. Surprisingly, gel-filtered platelets, when exposed to xanthine oxidase in the absence of xanthine substrate, were found to generate superoxide (O2.-), as determined by the reduction of added cytochrome c and by the inhibition of this reduction in the presence of superoxide dismutase. In addition to generating O2.-, the xanthine oxidase-treated platelets display both aggregation and evidence of the release reaction. This xanthine oxidase induced aggregation is not inhibited by the addition of either superoxide dismutase or cytochrome c, suggesting that it is due to either a further metabolite of O2.0, or that O2.- itself exerts no important direct effect on platelet function under these experimental conditions. The ability of C2.- to modulate platelet reactions in vivo or in vitro remains in doubt, and xanthine oxidase is an unsuitable source of O2.- in platelet studies because of its own effects on platelets.
在研究超氧化物(O2.-)这种氧化剂对血小板的影响过程中,超氧化物是通过黄嘌呤氧化酶与黄嘌呤相互作用产生的。令人惊讶的是,经凝胶过滤的血小板在无黄嘌呤底物的情况下暴露于黄嘌呤氧化酶时,发现会产生超氧化物(O2.-),这是通过添加的细胞色素c的还原以及超氧化物歧化酶存在时这种还原的抑制来确定的。除了产生O2.-外,经黄嘌呤氧化酶处理的血小板还表现出聚集以及释放反应的迹象。这种黄嘌呤氧化酶诱导的聚集不受超氧化物歧化酶或细胞色素c添加的抑制,这表明它要么是由于O2.0的进一步代谢产物,要么是在这些实验条件下O2.-本身对血小板功能没有重要的直接影响。O2.-在体内或体外调节血小板反应的能力仍存在疑问,并且由于黄嘌呤氧化酶自身对血小板的影响,它在血小板研究中不是合适的O2.-来源。