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5-LOX inhibitor modulates the inflammatory responses provoked by Helicobacter pylori infection.

Authors
Park, S; Han, SU; Lee, KM; Park, KH; Cho, SW; Hahm, KB
Citation
Helicobacter, 12(1):49-58, 2007
Journal Title
Helicobacter
ISSN
1083-43891523-5378
Abstract
BACKGROUND: Arachidonic acid metabolites have been considered as pivotal mediators in Helicobacter pylori-induced inflammatory response, which are mainly metabolized by two distinct enzymes: cyclooxygenase (COX) and lipoxygenase (LOX). While COX has become well known to play a key role in either carcinogenesis or inflammation related to H. pylori infection, little is known regarding the implication of LOX in H. pylori infection. In this study, we evaluated the roles of 5-LOX and its metabolites in H. pylori-induced host responses and further a potential beneficial action of specific LOX inhibitors against H. pylori infection. MATERIALS AND METHODS: Expressions of cytosolic phospholipase A(2) (cPLA(2)), COX-2, and 5-LOX after H. pylori infection were evaluated by immunofluorescence staining and Western blotting. Synthesis of LOX metabolites was measured with reversed-phase high-performance liquid chromatography. For analyzing the influence of 5-LOX inhibitors, nordihydroguaiaretic acid (NDGA) and geraniin, on H. pylori-induced inflammatory responses, RNase protection assay and RT-PCR were performed. RESULTS: H. pylori stimulated the translocation of cPLA(2) from cytoplasm to nucleus and increased the biosynthesis of hydroxyeicosatetraenoic acids (HETEs) as a predominant form of 5S-HETE in gastric epithelium. NDGA exerted a strong suppression activity of H. pylori-induced 5-LOX signaling. The administration of LOX inhibitors was related with down-expression of proinflammatory mediators such as interleukin-8 and tumor necrosis factor-alpha in both H. pylori-infected gastric epithelial cells and macrophage cells. CONCLUSION: LOX modulation with its specific inhibitors could impose significant anti-inflammatory responses after H. pylori infection, based on the fact that H. pylori infection provoked gastric inflammation through metabolizing arachidonic acid by the 5-LOX pathway.
MeSH terms
AnimalsArachidonate 5-Lipoxygenase/metabolism*Arachidonic Acid/metabolism*Cell LineDown-RegulationEpithelial Cells/metabolismEpithelial Cells/microbiologyGlucosides/pharmacologyHelicobacter Infections/metabolism*Helicobacter pylori*HumansHydrolyzable Tannins/pharmacologyInterleukin-8/metabolismLipoxygenase Inhibitors/pharmacologyMacrophages/metabolismMacrophages/microbiologyMitogen-Activated Protein Kinase 3/metabolismNF-kappa B/metabolismNordihydroguaiaretic Acid/pharmacology*Oxidation-Reduction/drug effectsSignal Transduction/drug effectsTumor Necrosis Factor-alpha/metabolism
DOI
10.1111/j.1523-5378.2007.00469.x
PMID
17241301
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Surgery
Journal Papers > School of Medicine / Graduate School of Medicine > Gastroenterology
AJOU Authors
한상욱이기명조성원
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