Ml. Grondahl et al., SECRETORY PATHWAYS IN SALMONELLA TYPHIMURIUM-INDUCED FLUID ACCUMULATION IN THE PORCINE SMALL-INTESTINE, Journal of Medical Microbiology, 47(2), 1998, pp. 151-157
The involvement of 5-hydroxytryptamine (5-HT) and 5-HT3 receptors and
prostaglandin E-2 (PGE(2)) in Salmonella Typhimurium-induced fluid acc
umulation in the porcine small intestine was investigated. Salmonella
Typhimurium (10(8) and 10(10) cfu) and cholera toxin (CT; 20 mu g) wer
e instilled for 8 and 11 h in ligated loops in the porcine jejunum and
ileum. Fluid accumulation and concentrations of Na+, K+, Cl-, 5-HT an
d PGE(2) in the fluid accumulated in the loops were measured. The flui
d accumulation was also measured when Salmonella Typhimurium (10(10) c
fu) and CT (20 mu g) were instilled for 8 h in ligated loops in jejunu
m and ileum in pigs given subcutaneous injections of saline or the 5-H
T3 receptor antagonist ondansetron (200 mu g/kg). Salmonella Typhimuri
um (10(10) cfu) and CT both induced fluid accumulation in jejunum and
ileum after 8 and 11 h. Both treatments also induced an increase in lu
minal release of 5-HT and PGE(2). The accumulated fluid was iso-osmoti
c and hyperosmotic in CT- and Salmonella Typhimurium-treated loops, re
spectively. Ondansetron reduced the Typhimurium-induced fluid accumula
tion in both jejunum and ileum by c. 40%, while it failed to reduce th
e response to CT. These results demonstrate that 5-HT and PGE(2) are r
eleased and 5-HT3 receptors activated in the secretory pathway of Typh
imurium in the porcine small intestine.