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Genet Mol Res ; 14(4): 13860-7, 2015 Oct 30.
Artículo en Inglés | MEDLINE | ID: mdl-26535701

RESUMEN

The aim of this study was to examine the expression of macrophage migration-inhibitory factor (MIF) in duodenal ulcer epithelial cells and its relation to Helicobacter pylori (Hp) infection, and to discuss the pathogenic roles of MIF expression and Hp infection in duodenal ulcer. MIF protein and mRNA expression was examined in samples from patients with duodenal ulcer with and without Hp infection (N = 40 each, experimental group), and in normal duodenal bulb mucosal tissue (N = 40, control group) using immunohistochemistry and in situ hybridization. Patients without Hp infection received routine treatment, and treatment was provided to the patients positive for Hp to eradicate Hp infection. Hp and MIF expression levels before treatment and after the ulcer had been cured were compared. The positive rates of MIF protein and mRNA in patients with Hp infection before treatment were 67.5 and 65%, respectively, and were 18.9 and 21.6% in the 37 patients from whom Hp was eliminated. These were statistically different both before and after treatment compared with controls (P < 0.05). In the patients without Hp infection, the positive rates of MIF protein and mRNA expression before (45 and 47.5%, respectively) and after (32.5 and 30%) treatment were not significantly different (P > 0.05). The results of this study suggested that MIF is related to the development of duodenal ulcer, and that the presence of Hp is closely related with the expression of MIF in the duodenal mucosa and the development of duodenal ulcer.


Asunto(s)
Úlcera Duodenal/etiología , Úlcera Duodenal/metabolismo , Infecciones por Helicobacter/complicaciones , Infecciones por Helicobacter/microbiología , Helicobacter pylori , Factores Inhibidores de la Migración de Macrófagos/metabolismo , Adulto , Anciano , Biopsia , Úlcera Duodenal/diagnóstico , Femenino , Expresión Génica , Infecciones por Helicobacter/tratamiento farmacológico , Humanos , Inmunohistoquímica , Hibridación in Situ , Mucosa Intestinal/metabolismo , Mucosa Intestinal/patología , Factores Inhibidores de la Migración de Macrófagos/genética , Masculino , Persona de Mediana Edad , ARN Mensajero/genética , ARN Mensajero/metabolismo , Adulto Joven
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