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Gene Expression of Antioxidant Enzymes in the Resected Intestine in Crohn's Disease
O. Sotona, E. Peterová, J. Örhalmi, T. Dušek, A. Mrkvicová, V. Knoblochová, P. Lochman, O. Malý, J. Páral, J. Bureš
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články
Grantová podpora
PROGRES Q40-15
Univerzita Karlova v Praze
PROGRES Q40-01
Univerzita Karlova v Praze
UHHK, 00179906
Ministerstvo Zdravotnictví Ceské Republiky
Digitální knihovna NLK
Zdroj
Free Medical Journals od 1997
Open Access Digital Library od 1997-01-01
Medline Complete (EBSCOhost) od 2012-06-01
ROAD: Directory of Open Access Scholarly Resources od 1997
Odkazy
PubMed
34779380
DOI
10.14712/18059694.2021.26
Knihovny.cz E-zdroje
- MeSH
- antioxidancia * MeSH
- Crohnova nemoc * genetika metabolismus MeSH
- exprese genu * MeSH
- glutathionperoxidasa genetika MeSH
- lidé MeSH
- messenger RNA genetika MeSH
- reaktivní formy kyslíku MeSH
- střeva MeSH
- superoxid dismutáza 1 * genetika metabolismus MeSH
- superoxiddismutasa genetika MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
INTRODUCTION: The inflammatory process in Crohn's disease (CD) is closely associated with the formation of reactive oxygen species. Antioxidant enzymes can play an important role in the outcome of CD and may influence postoperative recurrence in these patients. The aim of our study was to evaluate gene expression of intracellular antioxidant enzymes in surgically resected intestinal specimens of patients with CD, both in macroscopically normal and in inflamed tissue. METHODS: A total of 28 patients referred for elective bowel resection were enrolled in the study. Full-thickness small intestinal specimens were investigated. Gene expression of antioxidant enzymes - superoxide dismutase (SOD), glutathione peroxidase (GPX), glutathione reductase (GSR) - was evaluated both in macroscopically normal and inflamed samples. RESULTS: There were significantly lower levels of SOD1 mRNA (p = 0.007) and GSR mRNA (p = 0.027) in inflamed tissue compared to macroscopically normal areas. No significant differences were found between affected and non-affected intestinal segments in mRNA for SOD2, SOD3 and GPX. CONCLUSIONS: Our pilot data clearly showed that the gene expression of major antioxidant enzymes is not a uniform mechanism in the pathogenesis of Crohn's disease. Topically decreased gene expression of SOD1 and GSR might facilitate the segmental tissue injury caused by reactive oxygen species.
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- $a Sotona, Otakar $u Department of Field Surgery, Faculty of Military Health Sciences, University of Defence, Hradec Králové, Czech Republic. otakar.sotona@seznam.cz $u Department of Surgery, Charles University, Faculty of Medicine in Hradec Králové and University Hospital Hradec Králové, Czech Republic. otakar.sotona@seznam.cz $7 xx0140744
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- $a INTRODUCTION: The inflammatory process in Crohn's disease (CD) is closely associated with the formation of reactive oxygen species. Antioxidant enzymes can play an important role in the outcome of CD and may influence postoperative recurrence in these patients. The aim of our study was to evaluate gene expression of intracellular antioxidant enzymes in surgically resected intestinal specimens of patients with CD, both in macroscopically normal and in inflamed tissue. METHODS: A total of 28 patients referred for elective bowel resection were enrolled in the study. Full-thickness small intestinal specimens were investigated. Gene expression of antioxidant enzymes - superoxide dismutase (SOD), glutathione peroxidase (GPX), glutathione reductase (GSR) - was evaluated both in macroscopically normal and inflamed samples. RESULTS: There were significantly lower levels of SOD1 mRNA (p = 0.007) and GSR mRNA (p = 0.027) in inflamed tissue compared to macroscopically normal areas. No significant differences were found between affected and non-affected intestinal segments in mRNA for SOD2, SOD3 and GPX. CONCLUSIONS: Our pilot data clearly showed that the gene expression of major antioxidant enzymes is not a uniform mechanism in the pathogenesis of Crohn's disease. Topically decreased gene expression of SOD1 and GSR might facilitate the segmental tissue injury caused by reactive oxygen species.
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