Modulation of the main porcine enteric neuropeptides by a single low-dose of lipopolysaccharide (LPS) Salmonella Enteritidis

• Published in: Gut pathogens Vol. 9; no. 1; p. 73
• Main Authors: Mikołajczyk, Anita, Gonkowski, Sławomir, Złotkowska, Dagmara
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 12-12-2017; BioMed Central; BMC
• Subjects: Animal experimentation; GAL; Low-dose lipopolysaccharide; LPS; Mitogens; Neurons; Neuropeptide Y; Neuropeptides; Pig; Salmonella Enteritidis; Swine; SOM; GAL; NPY; Low-dose lipopolysaccharide; Neuropeptides; VIP; SP; LPS; Salmonella Enteritidis; Pig
• ISSN: 1757-4749; 1757-4749
• DOI: 10.1186/s13099-017-0225-6

The present research was conducted to investigate the influence of a low, single dose of LPS, which does not result in any clinical symptoms of intoxication on the expression of selected neuropeptides within the intestines of the domestic pig.
This experiment was conducted on immature female pigs of the Pitrain × Duroc breed (n = five per group). Seven days after the intravenous injection of 10 mL saline solution for control animals and 5 μg/kg b.w. (in 10 mL saline solution) LPS
Enteritidis for the experimental group, the excised segments of duodenum, jejunum, ileum, ileocecal valve, caecum, descending colon, transverse colon, ascending colon and rectum were prepared to extract the main enteric neuropeptides, including GAL, NPY, SOM, SP, VIP.
The results of this research indicate that single low-dose LPS
Enteritidis produced changes in the content of the selected neuropeptides of the porcine intestine. The most visible changes were observed in the transverse colon, where LPS induced the increase of GAL expression from 19.41 ± 7.121 to 92.92 ± 11.447 ng/g tissue.
The exact functions of the substances studied and mechanisms of responses to LPS action depend on the sections of the intestines. The mechanisms of observed changes are not fully understood, but fluctuations in neuronal active substance levels may be connected with neurodegenerative and/or pro-inflammatory activity of LPS.