Exogenous human recombinant interleukin-10 protects the kidney against hypoxia-induced renal injury in immature rats
dc.contributor.author | Ozturk, Hayrettin | |
dc.contributor.author | Onen, Abdurrahman | |
dc.contributor.author | Ozturk, Hulya | |
dc.contributor.author | Buyukbayram, Huseyin | |
dc.date.accessioned | 2024-04-24T17:11:34Z | |
dc.date.available | 2024-04-24T17:11:34Z | |
dc.date.issued | 2006 | |
dc.department | Dicle Üniversitesi | en_US |
dc.description.abstract | Aim: The purpose of this study was to determine the effects of exogenous human recombinant interleukin-10 (rhIL-10) on hypoxia-induced renal injury in immature rats. Method: The study was performed on 1-day-old Sprague-Dawley rat pups. Group 1 (n = 8) served as non-hypoxic controls. Group 2 (untreated, n = 8) rats were subjected to hypoxia-reoxygenation (H/O) and were then returned to their mothers. Group 3 (rhIL-10 treated, n = 8) rats were subjected to H/O, were returned to their mothers, and were treated with rhIL-10 (75 mu g/kg subcutaneously) for the next 3 days. All animals were killed on day 4 and renal specimens were obtained to determine the tissue level of malondialdehyde (MDA) and histological changes. Results: In the untreated group, moderate or severe renal tubular necrosis was observed However, the tubular necrosis score was significantly less in the rhIL-10 treated rats than in the untreated rats (P < 0.05). In the untreated group, MDA levels were significantly increased compared with the control and rhIL-10 groups (P < 0.001 and P < 0.05, respectively). In the rhIL-10 treated group, MDA levels were not significantly different compared with the control group. Conclusion: RhIL-10 has a protective effect against hypoxia-induced renal injury in immature rats by depression of tissue MDA level and renal tubular necrosis score. | en_US |
dc.identifier.doi | 10.1111/j.1442-2042.2006.01304.x | |
dc.identifier.endpage | 400 | en_US |
dc.identifier.issn | 0919-8172 | |
dc.identifier.issue | 4 | en_US |
dc.identifier.pmid | 16734858 | |
dc.identifier.scopus | 2-s2.0-33744823046 | |
dc.identifier.scopusquality | Q1 | |
dc.identifier.startpage | 397 | en_US |
dc.identifier.uri | https://doi.org/10.1111/j.1442-2042.2006.01304.x | |
dc.identifier.uri | https://hdl.handle.net/11468/17602 | |
dc.identifier.volume | 13 | en_US |
dc.identifier.wos | WOS:000237739800014 | |
dc.identifier.wosquality | Q4 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.language.iso | en | en_US |
dc.publisher | Wiley-Blackwell | en_US |
dc.relation.ispartof | International Journal of Urology | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Cytokine | en_US |
dc.subject | Injury | en_US |
dc.subject | Interleukin-10 | en_US |
dc.subject | Renal Ischemia | en_US |
dc.title | Exogenous human recombinant interleukin-10 protects the kidney against hypoxia-induced renal injury in immature rats | en_US |
dc.title | Exogenous human recombinant interleukin-10 protects the kidney against hypoxia-induced renal injury in immature rats | |
dc.type | Article | en_US |