학술논문

Endocrine cells distribution in human proximal small intestine: an immunohistochemical and morphometrical study
Research article--Histology and cell biology
Document Type
Report
Source
Italian Journal of Anatomy and Embryology. April 2016, Vol. 121 Issue 1, p112, 10 p.
Subject
Observations
Methods
Health aspects
Immune response -- Observations
Small intestine -- Health aspects
Morphometrics (Biology) -- Methods
Language
English
ISSN
1122-6714
Abstract
Introduction The digestive phase of human exocrine pancreatic secretion occurring after ingestion of a meal is regulated by a network of neurohumoral regulatory systems activated by the duodenal luminal content. [...]
Atrophy of the pancreatic remnant after pancreaticoduodenectomy might be consequent to deregulation of pancreatic endocrine stimuli after duodenal removal. Relative technical surgical solution could be the anastomosis of the 1st jejunal loop to the stomach and the 2nd to the pancreatic stump. Data on the distribution of endocrine cells within the proximal intestine might represent the lacking tile of the problem. Our aims were to investigate the distribution pattern of serotonin, cholecystokinin and secretin cells in the duodenum, the 1st and 2nd jejunal loops of humans. Bowel specimens of ten patients submitted to pancreaticoduodenectomy were collected; immunohistochemical reactions and morphometric analyses were performed. A general ab-oral decrease of enteroendocrine cells was found. The rate of serotonin cells showed a significant 30.67 [+ or -] 8.13% reduction starting from the 1st jejunal loop versus duodenum. The rate of both cholecystokinin and secretin cells in the duodenum was superimposable to that in the 1st jejunal loop, with a significant 62.88 [+ or -] 4.80% loss of cholecystokinin and 39.5 [+ or -] 9.31% of secretin cells in the 2nd loop. After removal of duodenum, preservation of the 1st jejunal loop could impact the function of pancreatic remnant maintaining the physiological enteroendocrine stimulus for pancreatic secretion that can compensate, at least in part for the abolished duodenal hormonal release. Key words Cholecystokinin, enteroendocrine cells, human, secretin, serotonin, small intestine