Endotoxin tolerance in rats:: influence on LPS-induced changes in excretory liver function

被引:9
作者
Fernández, ED
Flohé, S
Siemers, F
Nau, M
Schade, FU
机构
[1] Heidelberg Univ, Mannheim Med Sch, Dept Gen Surg, DE-68167 Mannheim, Germany
[2] Univ Essen Gesamthsch, Clin Res Grp Shock & Multi Organ Failure DFG, DE-45122 Essen, Germany
[3] Univ Essen Gesamthsch, Dept Trauma Surg, DE-45122 Essen, Germany
关键词
endotoxin pretreatment; septic shock; liver function; TNF-alpha; bile;
D O I
10.1007/PL00012419
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective and design: We investigated in a rat model of endotoxic shock whether endotoxin tolerance (ETT) prevents lipopolysaccharide (LPS) associated lethality and studied the initial function of liver response to LPS. Animals: Male Sprague-Dawley rats. Treatment: ETT was induced by i.p. injection of LPS (Salmonella friedenau) intraperitoneally over 5 days. Rats (n = 6 each group) received 1 mg LPS/kg b. w. intravenously (Salmonella friedenau). The common bile duct was then canalized and bile was collected every 60 min for 6 h. 1 h after LPS-application liver biopsies were taken for determination of TNF-alpha by RT-PCR. Sham operated animals (n = 6 each group) were treated identically but without application of LPS. Results: All ETT animals survived the duration of the experiment whereas non-tolerant animals (NETT) died before the end of the experiment (5/6). NETT animals showed a continuous decrease in bile flow after 240 min. The amount of bile acids was significantly lower (ANOVA) in NETT animals than in sham operated controls or ETT-animals. Analysis of TNF-alpha mRNA expression in the liver revealed an upregulation 1 h after LPS application, which was significantly lower in LPS-tolerant animals. Conclusions: Our results show that excretory liver failure and death subsequent to intravenous LPS application can be successfully counteracted by induction of ETT.
引用
收藏
页码:500 / 505
页数:6
相关论文
共 26 条
[11]  
Gaeta G B, 1978, Boll Soc Ital Biol Sper, V54, P581
[12]  
HIRATA K, 1980, LAB INVEST, V43, P165
[13]   Bile mediates intestinal pathology in endotoxemia in rats [J].
Jackson, GDF ;
Dai, W ;
Sewell, WA .
INFECTION AND IMMUNITY, 2000, 68 (08) :4714-4719
[14]   Cholestatic liver injury increases circulating TNF-α and IL-6 and mortality after Escherichia coli endotoxemia [J].
Lechner, AJ ;
Velasquez, A ;
Knudsen, KR ;
Johanns, CA ;
Tracy, TF ;
Matuschak, GM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 157 (05) :1550-1558
[15]  
LEVY E, 1967, AM J PATHOL, V51, P269
[16]  
NOLAN JP, 1975, GASTROENTEROLOGY, V69, P1346
[17]  
Schade F U, 1995, Prog Clin Biol Res, V392, P513
[18]  
Schade FU, 1999, ENDOTOXIN IN HEALTH AND DISEASE, P751
[19]   INVOLVEMENT OF TUMOR NECROSIS FACTOR IN ENDOTOXIN-TRIGGERED NEUTROPHIL ADHERENCE TO SINUSOIDAL ENDOTHELIAL-CELLS OF MOUSE-LIVER AND ITS MODULATION IN ACUTE PHASE [J].
SCHLAYER, HJ ;
LAAFF, H ;
PETERS, T ;
WOORTMENKER, M ;
ESTLER, HC ;
KARCK, U ;
SCHAEFER, HE ;
DECKER, K .
JOURNAL OF HEPATOLOGY, 1988, 7 (02) :239-249
[20]   ANTI-CACHECTIN TNF MONOCLONAL-ANTIBODIES PREVENT SEPTIC SHOCK DURING LETHAL BACTEREMIA [J].
TRACEY, KJ ;
FONG, Y ;
HESSE, DG ;
MANOGUE, KR ;
LEE, AT ;
KUO, GC ;
LOWRY, SF ;
CERAMI, A .
NATURE, 1987, 330 (6149) :662-664