Publication:
Comparative effects of pirfenidone and nintedanib in experimental intraabdominal adhesion model

dc.contributor.coauthorErdem, Olgun
dc.contributor.coauthorErdem, Selin Karaman
dc.contributor.coauthorYildiz, Abdullah
dc.contributor.coauthorCakit, Hakan
dc.contributor.coauthorCanbey, Ceren
dc.contributor.coauthorOzkan, Omer Faruk
dc.date.accessioned2025-12-31T08:20:07Z
dc.date.available2025-12-31
dc.date.issued2025
dc.description.abstractBackground: Postoperative peritoneal adhesions (PPA) develop in up to 90% of intraabdominal surgeries and are a major cause of small bowel obstruction, leading to readmissions and morbidity. However, no effective pharmacologic strategy currently exists for PPA prevention. Pirfenidone and Nintedanib are oral antifibrotics approved for idiopathic pulmonary fibrosis, with emerging data on their effects in cardiac and hepatic fibrosis. This study aimed to compare their efficacy in preventing PPA via intraperitoneal (IP) administration in an experimental model. Methods: Twenty-eight rats were randomized into four groups of 7: Pirfenidone (P), Nintedanib (N), combination (P + N), and saline control (C). Adhesions were induced via cecal abrasion. On postoperative day 7, macroscopic fibrosis scores (MFS), affected regions, histopathology, and TGF-beta 1 expression were evaluated. Results: Group P had significantly lower MFS than Group N (P < 0.001) and showed a reduction trend vs. control. TGF-beta 1 HScore was significantly lower in Group P vs. Group N (P = 0.002) and P + N (P = 0.014). Group N showed the highest inflammation and elevated TGF-beta 1 vs. control (P = 0.013). Conclusion: Pirfenidone appears effective in reducing PPA formation via IP administration. In contrast, Nintedanib may be unsuitable for IP use in saline, potentially due to poor solubility.
dc.description.fulltextYes
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.identifier.doi10.1016/j.ajg.2025.07.002
dc.identifier.eissn2090-2387
dc.identifier.embargoNo
dc.identifier.endpage329
dc.identifier.issn1687-1979
dc.identifier.issue4
dc.identifier.pubmed40912938
dc.identifier.quartileN/A
dc.identifier.scopus2-s2.0-105015345119
dc.identifier.startpage322
dc.identifier.urihttps://doi.org/10.1016/j.ajg.2025.07.002
dc.identifier.urihttps://hdl.handle.net/20.500.14288/31488
dc.identifier.volume26
dc.identifier.wos001622326900004
dc.keywordsPirfenidone
dc.keywordsNintedanib
dc.keywordsExperimental
dc.keywordsIntraperitoneal adhesions
dc.keywordsPostoperative adhesions
dc.language.isoeng
dc.publisherELSEVIER
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofArab Journal of Gastroenterology
dc.relation.openaccessYes
dc.rightsCC BY-NC-ND (Attribution-NonCommercial-NoDerivs)
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectGastroenterology & Hepatology
dc.titleComparative effects of pirfenidone and nintedanib in experimental intraabdominal adhesion model
dc.typeJournal Article
dspace.entity.typePublication

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