Secretory pathways in Salmonella Typhimurium-induced fluid accumulation in the porcine small intestine

被引:39
作者
Grondahl, ML
Jensen, GM
Nielsen, CG
Skadhauge, E
Olsen, JE
Hansen, MB
机构
[1] Royal Vet & Agr Univ, Dept Physiol & Anat, DK-1870 Frederiksberg C, Denmark
[2] Royal Vet & Agr Univ, Dept Clin Studies, DK-1870 Frederiksberg C, Denmark
[3] Royal Vet & Agr Univ, Dept Vet Microbiol, DK-1870 Frederiksberg C, Denmark
关键词
D O I
10.1099/00222615-47-2-151
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The involvement of 5-hydroxytryptamine (5-HT) and 5-HT3 receptors and prostaglandin E-2 (PGE(2)) in Salmonella Typhimurium-induced fluid accumulation in the porcine small intestine was investigated. Salmonella Typhimurium (10(8) and 10(10) cfu) and cholera toxin (CT; 20 mu g) were 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 and PGE(2) in the fluid accumulated in the loops were measured. The fluid accumulation was also measured when Salmonella Typhimurium (10(10) cfu) and CT (20 mu g) were instilled for 8 h in ligated loops in jejunum and ileum in pigs given subcutaneous injections of saline or the 5-HT3 receptor antagonist ondansetron (200 mu g/kg). Salmonella Typhimurium (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 luminal release of 5-HT and PGE(2). The accumulated fluid was iso-osmotic and hyperosmotic in CT- and Salmonella Typhimurium-treated loops, respectively. Ondansetron reduced the Typhimurium-induced fluid accumulation in both jejunum and ileum by c. 40%, while it failed to reduce the response to CT. These results demonstrate that 5-HT and PGE(2) are released and 5-HT3 receptors activated in the secretory pathway of Typhimurium in the porcine small intestine.
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页码:151 / 157
页数:7
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