Epinephrine and endotoxin tolerance differentially modulate serum cytokine levels to high-dose lipopolysaccharide challenge in a murine model

被引:8
作者
Baykal, A
Kaynaroglu, V
Hascelik, G
Sayek, I
Sanac, Y
机构
[1] Univ Hacettepe, Sch Med, Dept Gen Surg, TR-06100 Ankara, Turkey
[2] Univ Hacettepe, Sch Med, Dept Microbiol, TR-06100 Ankara, Turkey
关键词
D O I
10.1016/S0039-6060(99)70008-5
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. The epinephrine tolerance state has been demonstrated to increase survival in endotoxic shock and was claimed to have cross-tolerance with endotoxin tolerance. With use of these data, we aimed to determine the effect of epinephrine and endotoxin tolerance on major cytokine levels in a lipopolysaccharide challenge in mice. Methods. Epinephrine tolerance was induced by beginning with a low dose and gradually increasing to a lethal dose. Endotoxin tolerance was induced by injecting saline solution for 4 days and lipopolysaccharide 1 mg/kg on the fifth day. After these procedures, saline solution or 20 mg/kg lipopolysaccharide was injected into animals. Peak serum levels of tumor necrosis factor-alpha (TNF-alpha), interleukin 1 beta, interleukin 6 (IL-6), interleukin 10 (IL-10), and interleukin 12 (IL-12) were assayed. Results. The lipopolysaccharide injection increased the levels of all the cytokines in the control and epinephrine-tolerant animals. TNF-alpha, IL-6, and IL-10 levels were lower in endotoxin-tolerant animals compared with controls. Epinephrine-tolerant animals had higher levels of TNF-alpha, IL-6, and IL-12 than the controls did. Conclusion. Epinephrine tolerance primes for an exaggerated release of TNF-alpha, IL-6, and IL-12 in response to lipopolysaccharide challenge, suggesting anti-inflammatory and immunosuppressive effects by epinephrine. The anti-inflammatory effect was not mediated through increased IL-10 release. Endotoxin tolerance selectively modulated cytokine release.
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页码:403 / 410
页数:8
相关论文
共 34 条
[1]  
BAYKAL A, IN PRESS AUST NZ J S
[2]  
BAYKAL A, IN PRESS BR J SURG
[3]   INTERLEUKIN-10 IS A CENTRAL REGULATOR OF THE RESPONSE TO LPS IN MURINE MODELS OF ENDOTOXIC-SHOCK AND THE SHWARTZMAN REACTION BUT NOT ENDOTOXIN TOLERANCE [J].
BERG, DJ ;
KUHN, R ;
RAJEWSKY, K ;
MULLER, W ;
MENON, S ;
DAVIDSON, N ;
GRUNIG, G ;
RENNICK, D .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (05) :2339-2347
[4]   POTENTIATION OF ALPHA-ADRENOCEPTOR-MEDIATED RESPONSES FOLLOWING CHRONIC BETA-ADRENOCEPTOR STIMULATION IN THE RAT-HEART [J].
BUTTERFIELD, MC ;
CHESSWILLIAMS, R .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 108 (03) :658-662
[5]  
CHERNOW B, 1989, TXB CRITICAL CARE, P736
[6]  
DIETZMAN RH, 1973, SURG GYNECOL OBSTET, V137, P773
[7]  
DIETZMAN RH, 1969, SURGERY, V65, P623
[8]   HORMONAL-REGULATION OF INFLAMMATORY CELL CYTOKINE TRANSCRIPT AND BIOACTIVITY PRODUCTION IN RESPONSE TO ENDOTOXIN [J].
DOHERTY, GM ;
JENSEN, JC ;
BURESH, CM ;
NORTON, JA .
CYTOKINE, 1992, 4 (01) :55-62
[9]   HEPATIC DRUG-METABOLIZING ENZYME-SYSTEM AND ENDOTOXIN TOLERANCE - STRUCTURAL REQUIREMENT OF LPS IN INDUCTION OF AN EARLY TOLERANCE [J].
EGAWA, K ;
YOSHIDA, M ;
SAKAINO, R ;
KASAI, N .
MICROBIOLOGY AND IMMUNOLOGY, 1984, 28 (11) :1181-1190
[10]  
Elenkov IJ, 1996, P ASSOC AM PHYSICIAN, V108, P374