The intestine performs many functions, including the processes of digestion, absorption, and secretion. Yet, in addition, the intestine also serves as a barrier which prevents bacteria and endotoxin contained within the gut from reaching systemic organs as well as the portal and systemic circulations. Based, on clinical studies, the mucosal barrier to endotoxin and bacteria appears to be lost under certain circumstances resulting in systemic sepsis. In fact, life-threatening infections with gut-associated bacteria, in which no infective focus can be found even at autopsy, is a major clinical problem in burn and trauma victims, ICU patients and patients developing multiple organ failure. We and others have previously established that bacteria can translocate across the mucosal barrier and spread systemically under a variety of experimental conditions. Thus, that bacterial (endotoxin) translocation occurs appears clear, however, much remains to be learned about the basic biology of this process as well as its ultimate clinical relevance. Consequently, the central goals of this proposal are to 1) mechanistically investigate the systemic consequences of bacterial and endotoxin translocation on other organ systems and 2) to continue our investigations into the mechanisms by which intestinal barrier function is lost after thermal injury, hemorrhagic shock and endotoxin challenge. Specifically, AIM 1 will test the hypothesis that, under certain circumstances, intestinal injury can result in the gut becoming a cytokine generating organ;
while AIM 2 will test the hypothesis that loss of intestinal barrier function and its sequelae result in distant organ injury which is mediated, at least in part, by endothelial cell activation/injury.
In AIM 3, we will utilize both in vivo and in vitro models to investigate the pathobiology associated with loss of intestinal barrier function with special emphasis on the biology of oxidant mediated tissue injury. The investigations outlined in this proposal will help both clarify the role of intestinal barrier failure in the pathogenesis of distant organ injury as well as provide basic information on the biology and pathophysiology of bacterial translocation. Thus, these studies by providing basic information on the biology of the translocation process as well as the role of gut barrier failure in the evolution of distant organ injury will help in developing physiologically-based therapeutic strategies.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM036376-10
Application #
2178329
Study Section
Surgery, Anesthesiology and Trauma Study Section (SAT)
Project Start
1986-12-01
Project End
1997-03-31
Budget Start
1995-04-01
Budget End
1996-03-31
Support Year
10
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Medicine & Dentistry of NJ
Department
Surgery
Type
Schools of Medicine
DUNS #
605799469
City
Newark
State
NJ
Country
United States
Zip Code
07107
Ding, J; Magnotti, L J; Huang, Q et al. (2001) Hypoxia combined with Escherichia coli produces irreversible gut mucosal injury characterized by increased intestinal cytokine production and DNA degradation. Shock 16:189-95
Suzuki, Y; Deitch, E A; Mishima, S et al. (2000) Inducible nitric oxide synthase gene knockout mice have increased resistance to gut injury and bacterial translocation after an intestinal ischemia-reperfusion injury. Crit Care Med 28:3692-6
Suzuki, Y; Deitch, E A; Mishima, S et al. (2000) Endotoxin-induced mesenteric microvascular changes involve iNOS-derived nitric oxide: results from a study using iNOS knock out mice. Shock 13:397-403
Magnotti, L J; Xu, D Z; Lu, Q et al. (1999) Gut-derived mesenteric lymph: a link between burn and lung injury. Arch Surg 134:1333-40;discussion 1340-1
Xu, D Z; Lu, Q; Kubicka, R et al. (1999) The effect of hypoxia/reoxygenation on the cellular function of intestinal epithelial cells. J Trauma 46:280-5
Mishima, S; Xu, D; Deitch, E A (1999) Increase in endotoxin-induced mucosal permeability is related to increased nitric oxide synthase activity using the Ussing chamber. Crit Care Med 27:880-6
Grotz, M R; Deitch, E A; Ding, J et al. (1999) Intestinal cytokine response after gut ischemia: role of gut barrier failure. Ann Surg 229:478-86
Magnotti, L J; Upperman, J S; Xu, D Z et al. (1998) Gut-derived mesenteric lymph but not portal blood increases endothelial cell permeability and promotes lung injury after hemorrhagic shock. Ann Surg 228:518-27
Swank, G M; Lu, Q; Xu, D Z et al. (1998) Effect of acute-phase and heat-shock stress on apoptosis in intestinal epithelial cells (Caco-2). Crit Care Med 26:1213-7
Mishima, S; Xu, D; Lu, Q et al. (1998) The relationships among nitric oxide production, bacterial translocation, and intestinal injury after endotoxin challenge in vivo. J Trauma 44:175-82

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