Dose-Dependent Effects of Ethanol and E. Coli on Gut Permeability and Cytokine Production

被引:24
作者
Amin, Parth B. [1 ]
Diebel, Lawrence N. [1 ]
Liberati, David M. [1 ]
机构
[1] Wayne State Univ, Dept Surg, Univ Hlth Ctr 6C, Detroit, MI 48201 USA
关键词
alcohol; shock; Caco2; inflammation; TNF; IL6; gut permeability; sepsis; BACTERIAL TRANSLOCATION; ALCOHOL INTERVENTIONS; TRAUMA CENTERS; HOST-DEFENSE; BURN INJURY; INTOXICATION; CELLS; SUPPRESSION; CONSUMPTION; SEPSIS;
D O I
10.1016/j.jss.2008.10.028
中图分类号
R61 [外科手术学];
学科分类号
摘要
Introduction. The gut may prime inflammatory responses following shock/trauma insults. Ethanol (EtOH) use is common in trauma patients and may impair intestinal barrier function. We compared varying concentrations of EtOH on proinflammatory cytokine production of Caco2 cell monolayers and the resultant changes in barrier function. We hypothesized that even low concentrations of EtOH would cause significant cytokine release and barrier dysfunction in vitro. Materials and Methods. Confluent Caco2 cell monolayers were grown in a two-chamber culture system and exposed to varying concentrations of EtOH (0.1%, 0.5%, 1.0%, 1.5%, and 2.0%) with/without Escherichia coli C-25 (EC). Supernatants were collected and TNF and IL6 quantified by ELISA (pg/mL). Monolayer integrity was assessed by apoptosis and permeability measurements. Results. Caco2 production of TNF-alpha increased in a dose-dependent manner when incubated with increasing concentrations of EtoH. A synergistic effect was seen when E. coli was added to the apical chamber. A similar result was seen with the production of IL-6. A dose-dependent effect was also noted with EtOH with or without E. coli on apoptosis and permeability measurements. Conclusion. In addition to alterations in gut permeability, increasing concentrations of ethanol have a synergistic effect with E. con on Caco2 production of proinflammatory cytokines TNF and IL-6. The creation of a proinflammatory cytokine milieu with an altered barrier integrity may be a mechanism by which ethanol may increase septic complications in the injured patient. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:187 / 192
页数:6
相关论文
共 21 条
[1]   MAP kinase signaling in diverse effects of ethanol [J].
Aroor, AR ;
Shukla, SD .
LIFE SCIENCES, 2004, 74 (19) :2339-2364
[2]   Modular effects of estradiol on ethanol-induced apoptosis in human intestinal epithelial cells [J].
Asai, K ;
Buurman, WA ;
Reutelingsperger, CPM ;
Schutte, B ;
Kaminishi, M .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2005, 40 (03) :326-335
[3]  
BJARNASON I, 1984, LANCET, V1, P179
[4]   INTESTINAL PERMEABILITY - AN OVERVIEW [J].
BJARNASON, I ;
MACPHERSON, A ;
HOLLANDER, D .
GASTROENTEROLOGY, 1995, 108 (05) :1566-1581
[5]   Effect of alcohol consumption on the gut [J].
Bode, C ;
Bode, JC .
BEST PRACTICE & RESEARCH CLINICAL GASTROENTEROLOGY, 2003, 17 (04) :575-592
[6]   Alcohol intoxication and post-burn complications [J].
Choudhry, MA ;
Chaudry, IH .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2006, 11 :998-1005
[7]   Gut-associated lymphoid T cell suppression enhances bacterial translocation in alcohol and burn injury [J].
Choudhry, MA ;
Fazal, N ;
Goto, M ;
Gamelli, RL ;
Sayeed, MM .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2002, 282 (06) :G937-G947
[8]   ATTACHMENT OF ENTERO-TOXIGENIC ESCHERICHIA-COLI TO HUMAN INTESTINAL-CELLS [J].
DENEKE, CF ;
MCGOWAN, K ;
THORNE, GM ;
GORBACH, SL .
INFECTION AND IMMUNITY, 1983, 39 (03) :1102-1106
[9]   Practical guidelines for performing alcohol interventions in trauma centers [J].
Dunn, CW ;
Donovan, DM ;
Gentilello, LM .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 1997, 42 (02) :299-304
[10]   Acute ethanol exposure prior to thermal injury results in decreased T-cell responses mediated in part by increased production of IL-6 [J].
Faunce, DE ;
Gregory, MS ;
Kovacs, EJ .
SHOCK, 1998, 10 (02) :135-140