Zuliani Juliana P, Fernandes Cristina M, Zamuner Stella R, Gutiérrez José M, Teixeira Catarina F P
Laboratorio de Farmacologia, Instituto Butantan, Sao Paulo, Brazil.
Toxicon. 2005 Mar 1;45(3):335-46. doi: 10.1016/j.toxicon.2004.11.004. Epub 2005 Jan 5.
The inflammatory events induced in the peritoneal cavity of mice by two PLA2s isolated from Bothrops asper snake venom were investigated. MT-III, an Asp-49 catalytically active enzyme and MT-II, a catalytically inactive Lys-49 variant induced increase in vascular permeability. Inhibition of enzymatic activity of MT-III with p-bromophenacyl bromide reduced this effect. MT-III induced a larger neutrophil infiltrate than MT-II. This activity was significantly reduced after inhibition of catalytic activity. Reduction in the number of neutrophils was observed when antibodies against L-selectin, CD18 or LFA-1 were used, suggesting the involvement of these adhesion molecules in the effects of both PLA2s. There was no effect with antibodies against ICAM-1 and PECAM-1. Increase in the levels of LTB4 and TXA2, as well as of IL-1, IL-6 and TNF-alpha, were observed in the peritoneal exudates induced by MT-III. MT-II did not enhance levels of eicosanoids but increased those of cytokines. It is concluded that both PLA2s induce inflammatory events in this model. Since MT-III exerts a stronger proinflammatory effect, the enzymatic phospholipid hydrolysis may be relevant for these phenomena. However, the fact that MT-II induced inflammation suggests that molecular regions distinct from the catalytic site elicit inflammatory events perhaps by interacting with specific cell membrane acceptors.
研究了从矛头蝮蛇毒中分离出的两种磷脂酶A2(PLA2)在小鼠腹腔中诱导的炎症事件。MT-III是一种天冬氨酸-49催化活性酶,MT-II是一种催化无活性的赖氨酸-49变体,它们均可诱导血管通透性增加。用对溴苯甲酰溴抑制MT-III的酶活性可降低这种作用。MT-III诱导的中性粒细胞浸润比MT-II更多。催化活性被抑制后,这种活性显著降低。当使用抗L-选择素、CD18或LFA-1的抗体时,中性粒细胞数量减少,这表明这些黏附分子参与了两种PLA2的作用。抗ICAM-1和PECAM-1的抗体则没有作用。在MT-III诱导的腹腔渗出液中,观察到白三烯B4(LTB4)、血栓素A2(TXA2)以及白细胞介素-1(IL-1)、白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)水平升高。MT-II没有提高类花生酸水平,但增加了细胞因子水平。得出的结论是,在该模型中两种PLA2均可诱导炎症事件。由于MT-III发挥更强的促炎作用,酶促磷脂水解可能与这些现象有关。然而,MT-II诱导炎症这一事实表明,与催化位点不同的分子区域可能通过与特定细胞膜受体相互作用引发炎症事件。