Efficacy of anti-tumor necrosis factor polyclonal antibody on phosphoenolpyruvate carboxykinase expression in septic and endotoxemic rats

被引:18
作者
Chang, CK
Gatan, M
Schumer, W
机构
[1] Department of Surgery, Finch University of Health Sciences, Mount Sinai Hospital Medical Center, Chicago
[2] Department of Surgery, Finch University of Health Sciences, Mount Sinai Hospital Medical Center, Chicago, IL 60608
来源
SHOCK | 1996年 / 6卷 / 01期
关键词
D O I
10.1097/00024382-199607000-00012
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
We studied the protective effect of anti-tumor necrosis factor-alpha (anti-TNF) polyclonal antibody on phosphoenolpyruvate carboxykinase (PEPCK) expression in lipopolysaccharide-induced endotoxemia and peritonitis sepsis induced by cecal incision. At 3 h after intraperitoneal lipopolysaccharide injection, levels of serum glucose, liver glycogen, and PEPCK expression were decreased and serum TNF was elevated, In contrast, 3 h after cecal incision, levels of serum glucose, serum TNF, and PEPCK expression were elevated, At 6 h after cecal incision (terminal sepsis), serum TNF remained elevated and levels of serum glucose, liver glycogen, and PEPCK expression were decreased. Circulating TNF was not detected in septic and endotoxemic rats pretreated with anti-TNF. Passive immunization with rat anti-TNF antibody restored PEPCK expression in early endotoxemia and sepsis (3 h), but not in terminal sepsis (6 h). Anti-TNF failed to reverse sepsis-induced hypoglycemia and hyperglycemia, suggesting that besides TNF, some other mediators are involved in glucose dyshomeostasis.
引用
收藏
页码:57 / 60
页数:4
相关论文
共 38 条
[1]   EFFICACY AND SAFETY OF MONOCLONAL-ANTIBODY TO HUMAN TUMOR-NECROSIS-FACTOR-ALPHA IN PATIENTS WITH SEPSIS SYNDROME - A RANDOMIZED, CONTROLLED, DOUBLE-BLIND, MULTICENTER CLINICAL-TRIAL [J].
ABRAHAM, E ;
WUNDERINK, R ;
SILVERMAN, H ;
PERL, TM ;
NASRAWAY, S ;
LEVY, H ;
BONE, R ;
WENZEL, RP ;
BALK, R ;
ALLRED, R ;
PENNINGTON, JE ;
WHERRY, JC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 273 (12) :934-941
[2]  
ASTIZ M, 1988, CIRC SHOCK, V26, P311
[3]  
ASTIZ M, 1987, CIRC SHOCK, V21, P300
[4]   DIVERGENT EFFICACY OF ANTIBODY TO TUMOR-NECROSIS-FACTOR-ALPHA IN INTRAVASCULAR AND PERITONITIS MODELS OF SEPSIS [J].
BAGBY, GJ ;
PLESSALA, KJ ;
WILSON, LA ;
THOMPSON, JJ ;
NELSON, S .
JOURNAL OF INFECTIOUS DISEASES, 1991, 163 (01) :83-88
[5]   TUMOR-NECROSIS-FACTOR MEDIATES ENDOTOXIC EFFECTS IN MICE [J].
BAUSS, F ;
DROGE, W ;
MANNEL, DN .
INFECTION AND IMMUNITY, 1987, 55 (07) :1622-1625
[6]   PASSIVE-IMMUNIZATION AGAINST CACHECTIN TUMOR NECROSIS FACTOR PROTECTS MICE FROM LETHAL EFFECT OF ENDOTOXIN [J].
BEUTLER, B ;
MILSARK, IW ;
CERAMI, AC .
SCIENCE, 1985, 229 (4716) :869-871
[7]  
CHANG CK, 1993, CIRC SHOCK, V41, P35
[8]   INTERLEUKIN-1 AFFECTS GLUCOSE-HOMEOSTASIS [J].
DELREY, A ;
BESEDOVSKY, H .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 253 (05) :R794-R798
[9]   SEPSIS-INDUCED ATTENUATION OF GLUCAGON AND 8-BRCAMP MODULATION OF THE PHOSPHOENOLPYRUVATE CARBOXYKINASE GENE [J].
DEUTSCHMAN, CS ;
DEMAIO, A ;
CLEMENS, MG .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1995, 269 (03) :R584-R591
[10]  
DEUTSCHMAN CS, 1993, CIRC SHOCK, V40, P295