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Duodenal epithelial thymidine uptake in patients with duodenal ulcer or endoscopic duodenitis
Authors:Dr Fred S Gorelick  Vincent A Deluca  Daniel G Sheahan  Pierluigi Marignani  Robert S Goldblatt  Jerry Winnan  Elliot M Livstone
Institution:(1) Departments of Medicine and Pathology, Yale University School of Medicine, New Haven, Connecticut;(2) Griffin Hospital, Derby, Connecticut;(3) Department of Internal Medicine, 92 LMP, Yale University School of Medicine, 333 Cedar Street, 06510 New Haven, Connecticut
Abstract:To evaluate the relationship between duodenal ulcer disease and duodenitis, duodenal epithelial cell renewal was measured in mucosal biopsies by the incorporation of 3H]thymidine. When 14 patients with duodenal ulcer were compared to 13 control subjects or 7 with endoscopic duodenitis alone, the crypt size was the same in all groups. Similar to other inflammatory processes of the gastrointestinal tract, patients with endoscopic duodenitis showed increased proliferative indices including a greater number of cells incorporating 3H]thymidine. In contrast, the proliferative indices from the duodenal mucosa of patients with duodenal ulcers did not differ from a control group. In a group of 6 patients with both endoscopic duodenitis and duodenal ulcer, the 3H]thymidine incorporation was intermediate between control subjects or patients with duodenal ulcer alone and those with endoscopic duodenitis alone. When subjects were divided according to the histologic appearance of the duodenal mucosa, those having chronic duodenitis demonstrated enhanced 3H]thymidine incorporation in comparison to a control group or patients with chronic active duodenitis (polymorphonuclear leukocytes present). Although there are many possible explanations of these findings, one may speculate that duodenal ulceration does not stimulate duodenal epithelial proliferation. This project was supported by the Yale Digestive Cancer Research Fund. Dr. Gorelick was supported by a Research Fellowship Award from the National Foundation for Ileitis and Colitis during a portion of this study and is currently a recipient of a Clinical Investigator Award (KO8-AM-00659) from the National Institute of Arthritis, Metabolism and Digestive Diseases.
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