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Genet Mol Res ; 14(4): 13860-7, 2015 Oct 30.
Artigo em Inglês | MEDLINE | ID: mdl-26535701

RESUMO

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.


Assuntos
Úlcera Duodenal/etiologia , Úlcera Duodenal/metabolismo , Infecções por Helicobacter/complicações , Infecções por Helicobacter/microbiologia , Helicobacter pylori , Fatores Inibidores da Migração de Macrófagos/metabolismo , Adulto , Idoso , Biópsia , Úlcera Duodenal/diagnóstico , Feminino , Expressão Gênica , Infecções por Helicobacter/tratamento farmacológico , Humanos , Imuno-Histoquímica , Hibridização In Situ , Mucosa Intestinal/metabolismo , Mucosa Intestinal/patologia , Fatores Inibidores da Migração de Macrófagos/genética , Masculino , Pessoa de Meia-Idade , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Adulto Jovem
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