血小板活化因子是肿瘤坏死因子/半乳糖胺致死性的中介。

Journal of inflammation Pub Date : 1995-01-01
C Libert, W Van Molle, P Brouckaert, W Fiers
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引用次数: 0

摘要

我们在此报道,WEB2170是一种有效的血小板活化因子(PAF)受体拮抗剂,在半乳糖胺(GalN)致敏的小鼠中,可以防止PAF诱导和小鼠肿瘤坏死因子(TNF)诱导的死亡。此外,我们证明了α 1-酸性糖蛋白(AGP)或白细胞介素-1 (IL-1)预处理可以防止tnf诱导的死亡,但不能防止paf诱导的死亡。我们得出结论,PAF在TNF/ galn诱导的致死性休克中是一种介质,但AGP或IL-1预处理所赋予的保护并没有达到清除PAF的水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Platelet-activating factor is a mediator in tumor necrosis factor/galactosamine-induced lethality.

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.

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