Libert C, Van Molle W, Brouckaert P, Fiers W
Laboratory of Molecular Biology, University of Ghent, Belgium.
J Inflamm. 1995;46(3):139-43.
We here report that administration to mice of WEB2170, a potent platelet-activating factor (PAF) receptor antagonist, prevents both PAF-induced and murine tumor necrosis factor (TNF)-induced lethality in galactosamine (GalN)-sensitized mice. Furthermore, we demonstrate that pretreatment with alpha 1-acid glycoprotein (AGP) or interleukin-1 (IL-1) protects against TNF-induced, but not against PAF-induced lethality. We conclude that PAF is a mediator in TNF/GalN-induced lethal shock, but that the protection conferred by AGP or IL-1 pretreatment is not at the level of scavenging PAF.
我们在此报告,向小鼠给药强效血小板活化因子(PAF)受体拮抗剂WEB2170,可预防PAF诱导的以及鼠肿瘤坏死因子(TNF)诱导的半乳糖胺(GalN)致敏小鼠的致死性。此外,我们证明用α1-酸性糖蛋白(AGP)或白细胞介素-1(IL-1)预处理可预防TNF诱导的致死性,但不能预防PAF诱导的致死性。我们得出结论,PAF是TNF/GalN诱导的致死性休克的介质,但AGP或IL-1预处理所提供的保护并非在清除PAF的水平。