Effects of lexipafant (BB-882), a platelet activating factor receptor antagonist, on liver damage due to bile duct ligation in rats
dc.contributor.author | Oeztuerk, Hulya | |
dc.contributor.author | Oeztuerk, Hayrettin | |
dc.contributor.author | Dokucu, Ali Ihsan | |
dc.contributor.author | Otcu, Selcuk | |
dc.date.accessioned | 2024-04-24T17:33:42Z | |
dc.date.available | 2024-04-24T17:33:42Z | |
dc.date.issued | 2006 | |
dc.department | Dicle Üniversitesi | en_US |
dc.description.abstract | Background and study aims : Extrahepatic cholestasis is one of the main factors causing liver fibrosis. In this study, we aimed to evaluate the effects of lexipafant (BB-882), a platelet activating factor receptor antagonist, on liver damage in rats with bile duct ligation. Methods: A total of 30 male Sprague-Dawley rats weighing 160-190 g were used in this study. Group I (Sham-control, n = 10) rats were undergone laparotomy alone and bile duct was just dissected from the surrounding tissue. Group 2 rats (BDL/Untreated, n = 10) were subjected to bile duct ligation and no drug was applied. Group 3 rats (BDUBB-882, n = 10) received a daily dose of BB-882 intraperitoneally for 14 days after BDL. At the end of the two-week period, biochemical and histological evaluation was processed. Results : The mean serum bilirubin and liver enzymes level significantly decreased, and Superoxide dismutase, catalase and glutathione peroxidase values were significantly increased in BDL/BB-882 group when compared to BDUUntreated group. The histopathological score was significantly less in the BDUBB-882 group compared to the BDL/Untreated rats. In the BDL/BB-882 group was observed less fibrosis and neutrophil infiltration. Conclusions : These results suggest that BB-882 (lexipafant) may reduce the severity of the inflammatory response to liver injury produced by bile duct ligation in rats. | en_US |
dc.identifier.endpage | 202 | en_US |
dc.identifier.issn | 1784-3227 | |
dc.identifier.issue | 2 | en_US |
dc.identifier.pmid | 16929615 | |
dc.identifier.scopus | 2-s2.0-33747621139 | |
dc.identifier.scopusquality | Q3 | |
dc.identifier.startpage | 197 | en_US |
dc.identifier.uri | https://hdl.handle.net/11468/20806 | |
dc.identifier.volume | 69 | en_US |
dc.identifier.wos | WOS:000240612900003 | |
dc.identifier.wosquality | Q4 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.language.iso | en | en_US |
dc.publisher | Univ Catholique Louvain-Ucl | en_US |
dc.relation.ispartof | Acta Gastro-Enterologica Belgica | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Bile Duct Ligation | en_US |
dc.subject | Bb-882 | en_US |
dc.subject | Lexipafant | en_US |
dc.subject | Rat | en_US |
dc.title | Effects of lexipafant (BB-882), a platelet activating factor receptor antagonist, on liver damage due to bile duct ligation in rats | en_US |
dc.title | Effects of lexipafant (BB-882), a platelet activating factor receptor antagonist, on liver damage due to bile duct ligation in rats | |
dc.type | Article | en_US |