Assessment of DNA damage profile and oxidative /antioxidative biomarker level in patients with inflammatory bowel disease.
Adult
Antioxidants
/ metabolism
Biomarkers
/ blood
Case-Control Studies
DNA Damage
/ physiology
Female
Glutathione Peroxidase
/ metabolism
Glutathione Transferase
/ metabolism
Humans
Inflammatory Bowel Diseases
/ blood
Male
Middle Aged
Nitric Oxide
/ blood
Oxidative Stress
/ physiology
Poland
Superoxide Dismutase
/ blood
DNA oxidative damage repair
inflammatory bowel diseases
pro/antioxidant status
Journal
Polski przeglad chirurgiczny
ISSN: 2299-2847
Titre abrégé: Pol Przegl Chir
Pays: Poland
ID NLM: 0376426
Informations de publication
Date de publication:
26 May 2020
26 May 2020
Historique:
entrez:
8
10
2020
pubmed:
9
10
2020
medline:
22
6
2021
Statut:
ppublish
Résumé
<b>Aim:</b> The purpose of this study was to investigate the oxidative DNA damage, pro-antioxidant status in Polish patients with inflammatory bowel disease (IBD). <br><b>Methods:</b> Oxidative DNA damage was measured by comet assay techniques; nitric oxide (NO) and plasmatic lipid peroxidation (MDA) as oxidative stress were valuated by colometric methods; superoxide dismutase (SOD1), catalase (CAT) and glutathione peroxidase (GPx1) as antioxidative defense were determined by spectrophotometric methods. <br><b>Results:</b> The level of oxidative DNA damage in IBD patients was significantly higher in relation to controls (P = 0.01). Alike, in control subject as well as in patients with IBD, lymphocytes are characterized by complete repair of DNA damage. A significant decrease of SOD (P = 0.031), CAT (P = 0.006), GPx1 (P = 0.001) activity was seen in IBD patients vs control. MDA (P = 0.001) and NO (P = 0.001) concentrations were significantly increased in IBD patients as compared to healthy subjects. <br><b>Conclusions:</b> Our results may be due to the induction of DNA repair genes which may occur at the stage of the pathological changes (IBD) that may be caused by excessive oxidative stress. However, the cause of this relationship, and whether it is direct or indirect, remains to be explored.
Identifiants
pubmed: 33028732
doi: 10.5604/01.3001.0014.1548
pii: 01.3001.0014.1548
doi:
Substances chimiques
Antioxidants
0
Biomarkers
0
Nitric Oxide
31C4KY9ESH
Glutathione Peroxidase
EC 1.11.1.9
Superoxide Dismutase
EC 1.15.1.1
Glutathione Transferase
EC 2.5.1.18
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM