Colchicine Protects against Hyperoxic Lung Injury in Neonatal Rats
dc.authorid | OGUZ, SUNA SERIFE/0000-0002-1870-0983 | |
dc.authorid | ERDEVE, OMER/0000-0002-3193-0812 | |
dc.authorid | Uysal, Bulent/0000-0003-1254-9749 | |
dc.authorwosid | OGUZ, SUNA SERIFE/GWZ-7382-2022 | |
dc.authorwosid | TALIM, BERIL/I-9103-2013 | |
dc.authorwosid | ERDEVE, Omer/W-1480-2017 | |
dc.contributor.author | Ozdemir, Ramazan | |
dc.contributor.author | Yurttutan, Sadik | |
dc.contributor.author | Talim, Beril | |
dc.contributor.author | Uysal, Bulent | |
dc.contributor.author | Erdeve, Omer | |
dc.contributor.author | Oguz, Serife Suna | |
dc.contributor.author | Dilmen, Ugur | |
dc.date.accessioned | 2024-08-04T20:36:05Z | |
dc.date.available | 2024-08-04T20:36:05Z | |
dc.date.issued | 2012 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | Background: Bronchopulmonary dysplasia (BPD) is characterized by inflammation, fibrosis and mucosal necrosis, which leads to emphysematous coalescence of alveoli. Objective: We tested whether prophylaxis with colchicine, an anti-inflammatory, antioxidant and antifibrotic drug, would decrease the severity of lung injury in an animal model of BPD. Methods: Twenty-five rat pups were divided into three groups: control (n = 8), hyperoxia (n = 7), and hyperoxia + colchicine (n = 10). The hyperoxia groups were exposed to >95% oxygen from day 1 to 10 of life. On day 10, the animals were sacrificed and the lungs were processed for histology and biochemical analysis. Lung morphology was assessed by the mean linear intercept (MLI), a measure of alveolar size. The degree of lung inflammation and antioxidant capacity were assessed by quantifying lung homogenate tumor necrosis factor-alpha (TNF-alpha), interleukin-1 beta (IL-1 beta), malondialde-hyde (MDA), superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) levels. Results: Colchicine significantly decreased lung damage as determined by the MLI in the c groups (p < 0.01). The median level of lung MDA was significantly higher in the hyperoxia group compared with the control group (p < 0.05) and the colchicine-treated group (p < 0.05). Lung homogenate SOD and GSH-Px activities in the colchicine-treated group were significantly higher than in the hyperoxia group (p < 0.05). Furthermore, colchicine-treated pups had lower lung homogenate TNF-alpha and IL-1 beta levels compared with the hyperoxia group (p < 0.05). Conclusions: Colchicine has favorable effects on alveolarization as well as inflammation and oxidative stress markers in an animal model of BPD. Copyright (C) 2012 S. Karger AG, Basel | en_US |
dc.identifier.doi | 10.1159/000341424 | |
dc.identifier.endpage | 269 | en_US |
dc.identifier.issn | 1661-7800 | |
dc.identifier.issn | 1661-7819 | |
dc.identifier.issue | 4 | en_US |
dc.identifier.pmid | 22922655 | en_US |
dc.identifier.scopus | 2-s2.0-84865281049 | en_US |
dc.identifier.scopusquality | Q1 | en_US |
dc.identifier.startpage | 265 | en_US |
dc.identifier.uri | https://doi.org/10.1159/000341424 | |
dc.identifier.uri | https://hdl.handle.net/11616/95776 | |
dc.identifier.volume | 102 | en_US |
dc.identifier.wos | WOS:000311261100006 | en_US |
dc.identifier.wosquality | Q1 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Karger | en_US |
dc.relation.ispartof | Neonatology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Bronchopulmonary dysplasia | en_US |
dc.subject | Colchicine | en_US |
dc.subject | Tumor necrosis factor-alpha | en_US |
dc.subject | Superoxide dismutase | en_US |
dc.subject | Glutathione peroxidase | en_US |
dc.subject | Hyperoxia | en_US |
dc.title | Colchicine Protects against Hyperoxic Lung Injury in Neonatal Rats | en_US |
dc.type | Article | en_US |