SENSITIZATION OF RAT ALVEOLAR MACROPHAGES TO ENHANCED TNF-ALPHA RELEASE BY INVIVO TREATMENT WITH DEXAMETHASONE

被引:17
作者
RENZ, H
HENKE, A
HOFMANN, P
WOLFF, LJ
SCHMIDT, A
RUSCHOFF, J
GEMSA, D
机构
[1] UNIV MARBURG,INST IMMUNOL,W-3550 MARBURG,GERMANY
[2] UNIV MARBURG,INST PATHOL,W-3550 MARBURG,GERMANY
[3] OREGON HLTH SCI UNIV,DEPT PEDIAT,PORTLAND,OR 97201
关键词
D O I
10.1016/0008-8749(92)90242-H
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Treatment of rats with dexamethasone rapidly induced a marked weight loss which occurred within 3 days and persisted for several weeks. The cachectic state was paralleled by increased serum levels of triglycerides, albumin, and protein and a strong reduction of blood mononuclear leukocytes. In lung sections, an increased number of mononuclear giant cells was found but no bacteria, fungi, or Pneumocystis carinii organisms. Quite strikingly, alveolar macrophages from dexamethasone-treated rats, but not from control animals, were highly sensitive to LPS and released large amounts of TNF-α ex vivo. Also under in vivo conditions, high TNF-α serum concentrations were found in dexamethasone-treated but not control rats when examined 1 1 2 hr after an intravenous LPS injection. These data, suggest that the glucocorticoid-induced cachexia of rats may be linked, at least in part, to readily inducible TNF-α release from primed macrophages. © 1992.
引用
收藏
页码:249 / 257
页数:9
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