Abstract
Sepsis is a major cause of mortality in patients with common bile duct obstruction. To define possible contributing factors to this phenomenon, this study evaluates the effect of biliary obstruction on the intravascular clearance and organ trapping of viable Escherichia coli using a rat model. Adult male Sprague-Dawley rats were placed in three groups: Group I controls had sham operation, Group II had division and ligation of common bile duct (CDL), and Group III underwent splenectomy. At 21 days following operation 10(9) radiolabeled E. coli were injected intravenously. At varying intervals after infusion, blood samples were obtained for clearance study. At 10 minutes, bacterial distribution in the liver, spleen, kidneys, and lungs was determined (expressed as the mean percentage of injected viable E. coli). Intravascular clearance was similar in all groups. There was a significant decrease in the trapping of bacteria by the liver of CDL rats 14.5% +/- 4.95 (vs. control = 70.0% +/- 13.3) (p less than 0.005). A significant increase of bacterial trapping by the lung was observed in the CDL animals: 63.1% +/- 7.06 (vs. controls 1.4% +/- 0.82) (p less than 0.005). There was no significant change in bacterial localization in splenectomized rats. These data suggest that biliary obstruction decreases hepatic phagocytosis and increases pulmonary localization of viable E. coli. As the Kupffer cells of the liver are usually effective in removal of blood borne bacteria, this phagocytic dysfunction may contribute to the increased susceptibility to infection noted in instances of biliary obstruction.
MeSH Terms
Animals
Blood/microbiology
Body Weight
Cholestasis/microbiology
Common Bile Duct/microbiology
Escherichia coli/isolation & purification
Escherichia coli Infections/microbiology
Kidney/microbiology
Liver/microbiology
Lung/microbiology
Male
Mononuclear Phagocyte System/immunology
Organ Size
Phagocytosis
Rats
Rats, Inbred Strains
Sepsis/microbiology
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Katz S
Grosfeld J L
Gross K
Plager D A
Ross D
Rosenthal R S
Hull M
Weber T R
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