Lin W W, Chang P L, Lee C Y, Joubert F J
Proc Natl Sci Counc Repub China B. 1987 Apr;11(2):155-63.
The pharmacological properties of three phospholipases A2 (CM-I, CM-II and CM-III) purified from Naja mossambica mossambica venom were studied. The order of their catalytic and indirect hemolytic potencies was CM-I = CM-II greater than CM-III. Among them, only CM-III had a direct hemolytic action on the guinea-pig RBC, which was greatly inhibited by heparin. In the chick biventer cervicis nerve- muscle preparation, both CM-II and CM-III caused neuromuscular blockade with a gradual contracture and a decreased sensitivity to ACh and KCl, whereas no complete neuromuscular block was observed with CM-I up to 30 micrograms/ml. In the mouse phrenic nerve-diaphragm preparation, these three PLA2s abolished twitches evoked by indirect stimulation earlier than those by direct stimulation. Contracture was also produced by CM-II and CM-III. However only the latter was inhibited by pretreatment with heparin. These PLA2s caused myonecrosis in the hind-leg muscle of the mouse when injected intramuscularly. From these results, it is concluded that all of these PLA2s are both neurotoxic and myotoxic.
对从莫桑比克射毒眼镜蛇毒液中纯化得到的三种磷脂酶A2(CM-I、CM-II和CM-III)的药理特性进行了研究。它们的催化和间接溶血能力顺序为CM-I = CM-II大于CM-III。其中,只有CM-III对豚鼠红细胞有直接溶血作用,且该作用受到肝素的强烈抑制。在鸡双颈肌神经-肌肉标本中,CM-II和CM-III均引起神经肌肉阻滞,并伴有逐渐的挛缩以及对乙酰胆碱和氯化钾的敏感性降低,而在浓度高达30微克/毫升时,CM-I未观察到完全的神经肌肉阻滞。在小鼠膈神经-膈肌标本中,这三种磷脂酶A2消除间接刺激诱发的抽搐比直接刺激诱发的抽搐更早。CM-II和CM-III也会引起挛缩。然而,只有后者可被肝素预处理抑制。当肌肉注射时,这些磷脂酶A2会导致小鼠后腿肌肉坏死。从这些结果可以得出结论,所有这些磷脂酶A2均具有神经毒性和肌肉毒性。