dc.contributor.author | Cadir, Faysal O. | |
dc.contributor.author | Bicakci, Unal | |
dc.contributor.author | Tander, Burak | |
dc.contributor.author | Kilicoglu-Aydin, Birsen | |
dc.contributor.author | Rizalar, Riza | |
dc.contributor.author | Ariturk, Ender | |
dc.contributor.author | Bernay, Ferit | |
dc.date.accessioned | 2020-06-21T15:13:34Z | |
dc.date.available | 2020-06-21T15:13:34Z | |
dc.date.issued | 2008 | |
dc.identifier.issn | 0179-0358 | |
dc.identifier.issn | 1437-9813 | |
dc.identifier.uri | https://doi.org/10.1007/s00383-008-2157-1 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12712/19269 | |
dc.description | Aydin, Birsen/0000-0002-5541-9365 | en_US |
dc.description | WOS: 000256757400010 | en_US |
dc.description | PubMed: 18427813 | en_US |
dc.description.abstract | Evaluation of prophylactic effects of omeprazole and/or vitamin E on the formation of free oxygen radicals (FOR) and bowel histopathology in the newborn rat model of hypoxia/reoxygenation (H/R) that resembles human necrotizing enterocolitis (NEC). Eighty newborn rats were randomly divided into eight groups. H/R was done using airtight chamber. Rats were exposed to 100% CO2 for 15 min followed by a reoxygenation for the next 15 min with 100% O-2. Group 1 (n = 10) was the control group. Group 2 (n = 10) rats received vitamin E. In Group 3 (n = 10) omeprazole was administrated. Group 4 (n = 10) rats received omeprazole and vitamin E. Group 5 (n = 10) rats were subjected to H/R two times for 2 days and one time for 3 days. Group 6 (n = 10) received vitamin E in addition to H/R for 5 days and in Group 7 (n = 10) omeprazole in addition to H/R for 5 days. In Group 8 (n = 10), vitamin E and omeprazole and H/R were applied for 5 days. Rats were killed at the end of the each process and bowel specimens were harvested for histopathological and biochemical investigations. We administrated vitamin E intramuscularly 300 unit/kg per day and omeprazole orally 20 mg/kg per day. Malondialdehyde (MDA), xanthine oxidase (XO), xanthine dehydogenase (XDH) and XO/(XO + XDH) were measured. Vitamin E and/or omeprazole treated rats had significantly less XO% levels than H/R only group (0.36, 0.38 and 0.57, respectively). Similarly, the MDA levels were significantly lower in vitamin E and/or omeprazole received rats than H/R only rats (88.8, 97.9 and 122.6, respectively). All rats treated with omeprazole and/or vitamin E had better biochemical and histopathological levels compared to H/R rats (p < 0.05). Histopathological results show that Group 5 (H/R only) had significantly more intestinal damage when compared with Group 6 (vitamin E + H/R), Group 7 (omeprazole + R/H) and Group 8 (vitamin E + omeprazole + H/R) (p < 0.001). Grade 2 and 3 intestinal damages were only in Group 5 and there were no statistical difference between in Groups 6, 7 and 8 (p > 0.001). Omeprazole and/or vitamin E may protect the biochemical and histopathological intestinal damage of H/R injury in rats. These drugs may be beneficial in the prophylaxis of NEC in humans as well. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Springer | en_US |
dc.relation.isversionof | 10.1007/s00383-008-2157-1 | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | necrotizing enterocolitis | en_US |
dc.subject | intestinal hypoxia-reoxygenation | en_US |
dc.subject | omeprazole | en_US |
dc.subject | vitamin E | en_US |
dc.title | Protective effects of vitamin E and omeprazole on the hypoxia/reoxygenation induced intestinal injury in newborn rats | en_US |
dc.type | article | en_US |
dc.contributor.department | OMÜ | en_US |
dc.identifier.volume | 24 | en_US |
dc.identifier.issue | 7 | en_US |
dc.identifier.startpage | 809 | en_US |
dc.identifier.endpage | 813 | en_US |
dc.relation.journal | Pediatric Surgery International | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |