ANTRAL ENDOCRINE CELL ALTERATIONS IN IRRITABLE BOWEL SYNDROME: IMPLICATIONS FOR DYSPEPSIA AND GASTROESOPHAGEAL REFLUX
Main Article Content
Keywords
Gastrin, Serotonin, Somatostatin, Irritable Bowel Syndrome (IBS),, Endocrine Cells
Abstract
This study investigates the antral endocrine cell profiles in patients with Irritable Bowel Syndrome (IBS), an area previously unexplored. A total of 152 IBS patients were examined, categorized into 52 with diarrhea-predominant IBS (IBS-D), 42 with mixed IBS (IBS-M), and 58 with constipation-predominant IBS (IBS-C), alongside 86 healthy controls. Gastrin, somatostatin, serotonin transporter (SERT), and GABA immunoreactive cells in stomach antral biopsy specimens were detected using avidin-biotin-complex immunostaining. Computer-aided image analysis was employed to determine the density and intensity of immunopositive cells. The findings revealed that IBS-M patients had significantly fewer serotonin-immunoreactive cells compared to IBS-C patients, who had a notably higher count. No significant differences in serotonin immunoreactivity intensity were observed between IBS-total and controls. Gastrin-immunoreactive cells were significantly denser in IBS patients compared to controls, with IBS-D patients showing a marked difference in immunoreactivity intensity. Somatostatin-immunoreactive cell density was significantly lower in all IBS subtypes compared to controls, while SERT immunoreactivity intensity showed no significant difference between IBS-total and controls. The study concludes that a decrease in somatostatin density and an increase in gastrin density in IBS patients contribute to symptoms such as dyspepsia and gastroesophageal reflux.
References
2. El-Salhy M, Seim I, Chopin L, Gundersen D, Hatlebakk JG and Hausken T: Irritable bowel syndrome: the role of gut neuroendo- crine peptides. Front Biosci (Elite Ed) 4: 2783-2800, 2012.
3. El-Salhy M, Ostgaard H, Gundersen D, Hatlebakk JG and Hausken T: The role of diet in the pathogenesis and management of irritable bowel syndrome (Review). Int J Mol Med 29: 723-731, 2012.
4. El-Salhy M, Gundersen D, Hatlebakk JG and Hausken T: Irritable bowel syndrome: diagnosis, pathogenesis and treatment options. Nova Science Publishers, Inc., New York, 2012.
5. Sternini C, Anselmi L and Rozengurt E: Enteroendocrine cells: a site of 'taste' in gastrointestinal chemosensing. Curr Opin Endocrinol Diabetes Obes 15: 73-78, 2008.
6. Sternini C: Taste receptors in the gastrointestinal tract. IV. Functional implications of bitter taste receptors in gastrointes- tinal chemosensing. Am J Physiol Gastrointest Liver Physiol 292: G457-G461, 2007.
7. Raybould HE: Gut chemosensing: interactions between gut endocrine cells and visceral afferents. Auton Neurosci 153: 41-46, 2010.
8. Raybould HE: Nutrient sensing in the gastrointestinal tract: possible role for nutrient transporters. J Physiol Biochem 64: 349-356, 2008.
9. Bertrand PP and Bertrand RL: Serotonin release and uptake in the gastrointestinal tract. Auton Neurosci 153: 47-57, 2010.
10. Akiba Y and Kaunitz JD: Luminal chemosensing in the duodenal mucosa. Acta Physiol (Oxf) 201: 77-84, 2011.
11. Steinert RE and Beglinger C: Nutrient sensing in the gut: inter- actions between chemosensory cells, visceral afferents and the secretion of satiation peptides. Physiol Behav 105: 62-70, 2011.
12. Nakamura E, Hasumura M, Uneyama H and Torii K: Luminal amino acid-sensing cells in gastric mucosa. Digestion 83 (Suppl 1): 13-18, 2011.
13. Tolhurst G, Reimann F and Gribble FM: Intestinal sensing of nutrients. Handb Exp Pharmacol: 309-335, 2012.
14. Mace OJ, Schindler M and Patel S: The regulation of K- and L-cell activity by GLUT2 and the calcium-sensing receptor CasR in rat small intestine. J Physiol 590: 2917-2936, 2012.
15. El-Salhy M, Lillebo E, Reinemo A and Salmelid L: Ghrelin in patients with irritable bowel syndrome. Int J Mol Med 23: 703-707, 2009.
16. Dizdar V, Spiller R, Singh G, et al: Relative importance of abnormalities of CCK and 5-HT (serotonin) in Giardia-induced post-infectious irritable bowel syndrome and functional dyspepsia. Aliment Pharmacol Ther 31: 883-891, 2010.
17. El-Salhy M, Vaali K, Dizdar V and Hausken T: Abnormal small-intestinal endocrine cells in patients with irritable bowel syndrome. Dig Dis Sci 55: 3508-3513, 2010.
18. El-Salhy M, Gundersen D, Ostgaard H, Lomholt-Beck B, Hatlebakk JG and Hausken T: Low densities of serotonin and peptide YY cells in the colon of patients with irritable bowel syndrome. Dig Dis Sci 57: 873-878, 2012.
19. El-Salhy M, Gundersen D, Hatlebakk JG and Hausken T: Abnormal rectal endocrine cells in patients with irritable bowel syndrome. Regul Pept 188: 60-65, 2014.
20. Coates MD, Mahoney CR, Linden DR, et al: Molecular defects in mucosal serotonin content and decreased serotonin reuptake transporter in ulcerative colitis and irritable bowel syndrome. Gastroenterology 126: 1657-1664, 2004.
21. Wang SH, Dong L, Luo JY, et al: Decreased expression of serotonin in the jejunum and increased numbers of mast cells in the terminal ileum in patients with irritable bowel syndrome. World J Gastroenterol 13: 6041-6047, 2007.
22. Lee KJ, Kim YB, Kim JH, Kwon HC, Kim DK and Cho SW: The alteration of enterochromaffin cell, mast cell, and lamina propria T lymphocyte numbers in irritable bowel syndrome and its rela- tionship with psychological factors. J Gastroenterol Hepatol 23: 1689-1694, 2008.
23. Park JH, Rhee PL, Kim G, et al: Enteroendocrine cell counts correlate with visceral hypersensitivity in patients with diarrhoea- predominant irritable bowel syndrome. Neurogastroenterol Motil 18: 539-546, 2006.