RELEASE OF SOLUBLE RECEPTORS FOR TUMOR-NECROSIS-FACTOR (TNF) IN RELATION TO CIRCULATING TNF DURING EXPERIMENTAL ENDOTOXINEMIA

被引:232
|
作者
SPINAS, GA
KELLER, U
BROCKHAUS, M
机构
[1] F HOFFMANN LA ROCHE & CO LTD,PHARMACEUT RES NEW TECHNOL,BLDG 69-214,CH-4002 BASEL,SWITZERLAND
[2] UNIV HOSP BASEL,DEPT INTERNAL MED & RES,CH-4031 BASEL,SWITZERLAND
来源
JOURNAL OF CLINICAL INVESTIGATION | 1992年 / 90卷 / 02期
关键词
LIPOPOLYSACCHARIDE; TUMOR NECROSIS FACTOR BINDING PROTEIN; HUMAN; IBUPROFEN; CYCLOOXYGENASE INHIBITOR;
D O I
10.1172/JCI115891
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Serial plasma samples from human volunteers obtained after intravenous administration of Escherichia coli endotoxin were analyzed for the presence of circulating soluble tumor necrosis factor receptors (sTNFR). A four- to fivefold increase of type A (p75) and type B (p55) sTNFR was observed 3 h after endotoxin challenge. Pretreatment of the volunteers with ibuprofen before the injection of endotoxin resulted in a slight increase (3.87+/-0.2 vs. 3.27+/-0.3 ng/ml) and temporal shift of sTNFR-A release concurrent to a marked augmentation of TNF levels (603+/-118 vs. 338+/-56 pg/ml) as compared to the group without ibuprofen pretreatment. There was a significant correlation between peak sTNFR-A levels and peak TNF levels in the individual probands (r = 0.52, P = 0.04). On the contrary, release kinetics and plasma concentrations of sTNFR-B were identical in both groups (7.38+/-0.69 vs. 7.44+/-0.33 ng/ml) and no correlation with individual TNF levels was observed. The amount of sTNFR liberated upon endotoxin challenge was not sufficient to block TNF-mediated cytotoxic effects. Our data indicate that the release in vivo of type A and type B sTNFR upon a short exposure to endotoxin is regulated differently.
引用
收藏
页码:533 / 536
页数:4
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