Bougis P E, Marchot P, Rochat H
Toxicon. 1987;25(4):427-31. doi: 10.1016/0041-0101(87)90076-6.
The lethality of elapid snake venoms is due to toxic polypeptides which are alpha-neurotoxins, phospholipases A2 and cardiotoxins. In contrast to alpha-neurotoxins, less is known about the mode of action of phospholipases A2 and cardiotoxins at a cellular and molecular level, although it has been demonstrated that the hemolytic effect of cardiotoxin and its action on muscle can be accelerated in vitro by phospholipase A2. Here we show that when mice are injected i.v. with phospholipase A2, a significant decrease in survival time is observed if a sub-LD50 amount of cardiotoxin is injected simultaneously. Furthermore, the survival time is drastically reduced when phospholipase A2 (2.3 LD50) is injected first, followed 15 min later by doses of cardiotoxin as small as 0.18 LD50. These results strongly suggest a synergy between the two polypeptides.
眼镜蛇科蛇毒的致死性归因于有毒多肽,即α-神经毒素、磷脂酶A2和心脏毒素。与α-神经毒素不同,尽管已经证明磷脂酶A2可在体外加速心脏毒素的溶血作用及其对肌肉的作用,但在细胞和分子水平上,人们对磷脂酶A2和心脏毒素的作用方式了解较少。在此我们表明,当给小鼠静脉注射磷脂酶A2时,如果同时注射低于半数致死剂量(LD50)的心脏毒素,可观察到存活时间显著缩短。此外,当先注射磷脂酶A2(2.3 LD50),15分钟后再注射低至0.18 LD50剂量的心脏毒素时,存活时间会大幅缩短。这些结果有力地表明了这两种多肽之间存在协同作用。