EICOSANOIDS REGULATE TUMOR-NECROSIS-FACTOR SYNTHESIS AFTER HEMORRHAGE INVITRO AND INVIVO

被引:22
作者
ERTEL, W
MORRISON, MH
AYALA, A
CHAUDRY, IH
机构
[1] MICHIGAN STATE UNIV,DEPT SURG,CLIN CTR B424,SHOCK & TRAUMA RES LABS,E LANSING,MI 48824
[2] MICHIGAN STATE UNIV,DEPT MICROBIOL & PUBL HLTH,E LANSING,MI 48824
[3] MICHIGAN STATE UNIV,DEPT PHYSIOL,E LANSING,MI 48824
关键词
D O I
10.1097/00005373-199105000-00003
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
The aim of this investigation was to determine whether PGE2 regulates TNF release in vitro and in vivo following hemorrhage. To study this, C3H/HeN mice were bled to a mean blood pressure (BP) of 35 mm Hg, maintained for 60 minutes, and then resuscitated. For in vitro studies, peritoneal (pM-phi) and splenic (sM-phi) macrophages obtained at 2 hours and 24 hours after hemorrhage were stimulated with LPS for 24 or 48 hours with or without ibuprofen (IBU). For in vivo studies, M-phi were harvested 24 hours following hemorrhage with and without IBU treatment and stimulated with LPS for 48 hours. The decreased TNF release by pM-phi but not sM-phi from hemorrhaged mice was restored by IBU in vitro. IBU treatment in vivo significantly enhanced TNF release by pM-phi compared with untreated hemorrhaged animals, while TNF release by sM-phi was only slightly increased. These data indicate a major role of PGE2 in the regulation of TNF release by pM-phi following hemorrhage.
引用
收藏
页码:609 / 616
页数:8
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