de Lima W T, Kwasniewski F H, Sirois P, Jancar S
Departamento de Farmacologia, Universidade de São Paulo, Brasil.
Prostaglandins Leukot Essent Fatty Acids. 1995 Apr;52(4):245-9. doi: 10.1016/0952-3278(95)90044-6.
The present study evaluated the effect of platelet activating factor (PAF) instilled into rat airways on vascular permeability assessed in isolated lung tissues by Evans blue (EB)-labelled plasma protein extravasation. It was found that intratracheal instillation of PAF induces a dose-dependent increase of EB extravasation in the bronchi (upper and inner) but not in the lung parenchyma. The contribution of eicosanoids to PAF-induced increase of vascular permeability was investigated by treating the animals with selected inhibitors prior to PAF administration. Mepacrine (5 mg/kg), L-663,536 (10 mg/kg), indomethacin (4 mg/kg) and dazoxiben (10 mg/kg) significantly reduced EB extravasation in the bronchi. The PAF antagonists BN-52021 (5 mg/kg), WEB-2086 (1 mg/kg), WEB-2170 (5 mg/kg) and PCA-4248 (3 mg/kg) were all effective in reducing the extravasation. These results suggest that PAF-induced increase of vascular permeability in rat bronchi is mediated by cyclooxygenase and lipoxygenase products of arachidonic acid metabolism.
本研究评估了将血小板活化因子(PAF)注入大鼠气道后,通过伊文思蓝(EB)标记的血浆蛋白外渗来评估其对离体肺组织血管通透性的影响。研究发现,气管内注入PAF会导致支气管(上部和内部)中EB外渗呈剂量依赖性增加,但肺实质中未出现这种情况。在给予PAF之前,通过用选定的抑制剂处理动物,研究了类花生酸对PAF诱导的血管通透性增加的作用。米帕林(5mg/kg)、L-663,536(10mg/kg)、吲哚美辛(4mg/kg)和达唑氧苯(10mg/kg)显著降低了支气管中的EB外渗。PAF拮抗剂BN-52021(5mg/kg)、WEB-2086(1mg/kg)、WEB-2170(5mg/kg)和PCA-4248(3mg/kg)均能有效减少外渗。这些结果表明,PAF诱导的大鼠支气管血管通透性增加是由花生四烯酸代谢的环氧化酶和脂氧化酶产物介导的。