Korean J Crit Care Med.  1999 Nov;14(2):137-142.

Physiologic Changes Induced with Lipopolysaccharide in Rats

Affiliations
  • 1Department of Anesthesiology and Critical Care Medicine, Yonsei University, Wonju College of Medicine, Wonju, Korea.

Abstract

BACKGOUND: Bacterial endotoxin or lipopolysaccharide (LPS) is believed to mediate the tissue damage and shock observed in Gram-negative sepsis (GNS) by initiating a cascade of events, including activation of the coagulation, fibrinolytic and complement systems, and release of proinflammatory cytokines. However, the clinical pictures that result from GNS and endotoxin are quite different. The physiologic changes induced with LPS were investigated in this study.
METHODS
Fifty two male Sprague-Dawley rats were injected intraperitoneally with Escherichia coli LPS. Blood samples and bronchoalveolar lavage (BAL) fluid were obtained at baseline and at 2, 4, 8, 16, 24, and 48 hours after injection. Nitrate/nitrite levels were measured from plasma and BAL samples. Lipid peroxide (LPO) levels were measured from plasma. We measured also protein concentration and number of polymorphonuclear leukocytes (PMNL) and macrophages from BAL samples.
RESULTS
Administration of LPS caused significant increase in nitrate/nitrite concentrations of plasma and BAL fluid (p<0.01). ED50 of LPS was 1.76 mg/kg in plasma nitrate/nitrite assay. Plasma LPO levels were increased slightly after administration of LPS, but no statistical significance. Protein concentration was increased significantly (p<0.01) 4 hours after the administration of LPS. LPS induced increase of the number of PMNLs and macrophages of BAL samples significantly (p<0.05).
CONCLUSIONS
LPS increased NO production and alveolar permeability in rats. Also, LPS increased the number of inflammatory cells in the lung.

Keyword

Pharmacology; Lipopolysaccharide; Nitric oxide; Sepsis

MeSH Terms

Animals
Bronchoalveolar Lavage
Complement System Proteins
Cytokines
Escherichia coli
Humans
Lung
Macrophages
Male
Neutrophils
Nitric Oxide
Permeability
Pharmacology
Plasma
Rats*
Rats, Sprague-Dawley
Sepsis
Shock
Complement System Proteins
Cytokines
Nitric Oxide
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