Wang J P, Teng C M
Department of Medical Research, Taichung Veterans General Hospital, Taiwan, R.O.C.
Eur J Pharmacol. 1990 Nov 13;190(3):347-54. doi: 10.1016/0014-2999(90)94199-8.
The edema-producing activity of NNAVPLA2, an acidic phospholipase A2 (PLA2) enzyme from Naja naja atra venom (NNAV), was less potent than that of TMVPLA2 II, a basic PLA2 from Trimeresurus mucrosquamatus venom (TMV). These edema-forming effects were greatly suppressed by pretreatment of rats with diphenhydramine/methysergide or compound 48/80, which reduced the tissue content of histamine and serotonin. Heparin abolished and suppressed the paw edema caused by protamine and TMVPLA2 II, respectively, but had no effect on the NNAVPLA2-induced response. In isolated rat peritoneal mast cells, both PLA2 concentration dependently induced the release of histamine and beta-glucuronidase. Again, TMVPLA2 II was more potent than NNAVPLA2. This degranulation effect of mast cells caused by TMVPLA2 II and protamine was inhibited by heparin, while that caused by NNAVPLA2 was unaffected. The edema-forming and mast cell degranulation effects were greatly decreased in both PBPB-modified NNAVPLA2 and PBPB-modified TMVPLA2 II, in which the catalytic activity of the enzymes was completely lost. PBPB-modified TMVPLA2 II-induced paw edema was also suppressed by heparin. Furthermore, this edematous response was totally reversed in rat pretreated with aspirin in combination with diphenhydramine and methysergide. These results suggest that the edema-forming effect of PLA2 is probably dependent on the presence of catalytic, positive charge and pharmacological sites on its molecule.
中华眼镜蛇毒(NNAV)中的酸性磷脂酶A2(PLA2)即NNAVPLA2的致水肿活性,比竹叶青蛇毒(TMV)中的碱性PLA2即TMVPLA2 II的活性弱。用苯海拉明/甲基麦角新碱或化合物48/80预处理大鼠,可大大抑制这些水肿形成效应,这降低了组胺和5-羟色胺的组织含量。肝素分别消除和抑制了鱼精蛋白和TMVPLA2 II引起的爪部水肿,但对NNAVPLA2诱导的反应没有影响。在分离的大鼠腹膜肥大细胞中,两种PLA2均浓度依赖性地诱导组胺和β-葡萄糖醛酸酶的释放。同样,TMVPLA2 II比NNAVPLA2更有效。肝素抑制了TMVPLA2 II和鱼精蛋白引起的肥大细胞脱颗粒效应,而NNAVPLA2引起的脱颗粒效应则不受影响。在PBPB修饰的NNAVPLA2和PBPB修饰的TMVPLA2 II中,致水肿和肥大细胞脱颗粒效应均大大降低,这两种酶的催化活性完全丧失。肝素也抑制了PBPB修饰的TMVPLA2 II诱导的爪部水肿。此外,在用阿司匹林联合苯海拉明和甲基麦角新碱预处理的大鼠中,这种水肿反应完全逆转。这些结果表明,PLA2的致水肿效应可能取决于其分子上催化、正电荷和药理学位点的存在。