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Pancreatic secretory trypsin inhibitor in gastrointestinal mucosa and gastric juice


Freeman, TC and Playford, RJ and Quinn, C and Beardshall, K and Poulter, L and Young, J and Calam, J, Pancreatic secretory trypsin inhibitor in gastrointestinal mucosa and gastric juice, Gut: An International Journal of Gastroenterology and Hepatology, 31, (11) pp. 1318-1323. ISSN 0017-5749 (1990) [Refereed Article]

DOI: doi:10.1136/gut.31.11.1318


We studied the distribution of pancreatic secretory trypsin inhibitor (PSTI) in the epithelia of the gastrointestinal tract and determined whether PSTI is secreted into gastric juice. PSTI was measured by a specific radioimmunoassay in biopsy specimens taken from the upper (n = 8) and lower (n = 7) gastrointestinal tract of patients with normal endoscopies. PSTI was present in the stomach, small intestine, and colon. Concentrations (μg/g protein) were highest in the stomach, and significantly higher in the antrum (1240, 670-1700, median and range) than in the gastric body (370, 350-570) (p < 0.01). Concentrations were similar in the duodenum (180, 80-210) and colon (160, 130-360). PSTI determined by immunohistochemistry was present in mucus secreting gastric foveolar cells, duodenal Paneth cells, and colonic non mucus cells. PSTI was present in gastric juice. The median (range) concentration of PSTI in basal gastric juice from 13 patients with duodenal ulcers was 9 (3-21) μg/l and did not change during stimulation with pentagastrin. The rate of secretion, however, did increase significantly (p < 0.05) from 1430 (180-2810) ng/h to 4500 (1250-12770) ng/h during pentagastrin stimulation. PSTI was labile in acid pepsin but stable in the neutral conditions present in the mucus layer. The presence of pancreatic secretory trypsin inhibitor throughout the gut and its secretion into the lumen suggests a hitherto unrecognised mechanism protecting gastrointestinal epithelia against luminal proteases.

Item Details

Item Type:Refereed Article
Research Division:Biomedical and Clinical Sciences
Research Group:Clinical sciences
Research Field:Gastroenterology and hepatology
Objective Division:Health
Objective Group:Clinical health
Objective Field:Clinical health not elsewhere classified
UTAS Author:Playford, RJ (Professor Ray Playford)
ID Code:72798
Year Published:1990
Web of Science® Times Cited:37
Deposited By:Research Division
Deposited On:2011-08-31
Last Modified:2011-09-05

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