glucagon-like-peptide-1 has been researched along with Helicobacter-Infections* in 3 studies
3 other study(ies) available for glucagon-like-peptide-1 and Helicobacter-Infections
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Effect of Helicobacter pylori infection on the link between GLP-1 expression and motility of the gastrointestinal tract.
Although Helicobacter pylori (H. pylori) infection is closely associated with the development of peptic ulcer, its involvement in pathophysiology in the lower intestinal tract and gastrointestinal (GI) motility remains unclear. Glucagon-like peptide-1 (GLP-1) is a gut hormone produced in the lower intestinal tract and involved in GI motility. Here, we investigated the effect of H. pylori infection on the link between GLP-1 expression and motility of the GI tract.. C57BL/6 mice were inoculated with a H. pylori strain. Twelve weeks later, the H. pylori-infected mice underwent H. pylori eradication treatment. GI tissues were obtained from the mice at various time intervals, and evaluated for the severity of gastric inflammatory cell infiltration and immunohistochemical expression of GLP-1 and PAX6 in the colonic mucosa. Gastrointestinal transit time (GITT) was measured by administration of carmine-red solution.. GLP-1 was expressed in the endocrine cells of the colonic mucosa, and PAX6 immunoreactivity was co-localized in such cells. The numbers of GLP-1- and PAX6-positive cells in the colon were significantly increased at 12 weeks after H. pylori infection and showed a positive correlation with each other. The GITT was significantly longer in H. pylori-infected mice than in non-infected controls and showed a positive correlation with GLP-1 expression. When H. pylori-infected mice underwent H. pylori eradication, GITT and PAX6/GLP-1 expression did not differ significantly from those in untreated H. pylori-infected mice.. H. pylori infection may impair GI motility by enhancing the colonic GLP-1/PAX6 expression. Topics: Animals; Colon; Female; Gastrointestinal Motility; Glucagon-Like Peptide 1; Helicobacter Infections; Helicobacter pylori; Mice, Inbred C57BL; PAX6 Transcription Factor | 2017 |
Carbohydrate metabolism improvement after Helicobacter pylori eradication.
Topics: Anti-Bacterial Agents; Blood Glucose; Carbohydrate Metabolism; Female; Glucagon-Like Peptide 1; Glucose Tolerance Test; Glycated Hemoglobin; Helicobacter Infections; Helicobacter pylori; Humans; Male; Middle Aged; Prospective Studies | 2016 |
Gastric lipase secretion in children with gastritis.
Gastric lipase is one of the prepancreatic lipases found in some mammalian species and in humans. Our knowledge of the hormonal regulation of gastric lipase secretion in children and adolescents is still very limited. The aim of this study was to compare the activity of human gastric lipase (HGL) in gastric juice in healthy adolescents and in patients with gastritis. The adolescents were allocated to three groups: the first including patients with Helicobacter pylori gastritis (HPG; n = 10), the second including patients with superficial gastritis caused by pathogens other than H. pylori (non-HPG; n = 14) and the control group including healthy adolescents (n = 14). Activity of HGL was measured in gastric juice collected during endoscopy. Plasma concentrations of cholecystokinin (CCK), glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic peptide (GIP) were measured in all adolescents. Activity of HGL in the non-HPG group was significantly lower than in the HPG group (p < 0.005) and the control group (p < 0.005). Mean plasma GIP levels in the control group were lower than in the non-HPG group (p < 0.003) and the HPG group (p < 0.01). We conclude that the regulation of HGL secretion by GLP-1 and CCK is altered in patients with gastritis. Moreover, GIP is a potent controller of HGL activity, both in healthy subjects and in patients with gastritis. Topics: Adolescent; Body Mass Index; Body Weight; Case-Control Studies; Cholecystokinin; Fasting; Gastric Inhibitory Polypeptide; Gastritis; Gastrointestinal Tract; Glucagon-Like Peptide 1; Helicobacter Infections; Humans; Hydrogen-Ion Concentration; Lipase; Young Adult | 2013 |