Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/6926
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dc.contributor.authorYılmaz, Mustafa-
dc.contributor.authorTopsakal, Şenay-
dc.contributor.authorHerek, Özkan-
dc.contributor.authorÖzmen, Özlem-
dc.contributor.authorŞahinduran, Şima-
dc.contributor.authorBüyükoğlu, Tülay-
dc.contributor.authorYonetci, Nadir-
dc.date.accessioned2019-08-16T12:13:02Z
dc.date.available2019-08-16T12:13:02Z
dc.date.issued2009-
dc.identifier.issn1931-5244-
dc.identifier.urihttps://hdl.handle.net/11499/6926-
dc.identifier.urihttps://doi.org/10.1016/j.trsl.2009.07.009-
dc.description.abstractIn this study, we examined the effects of etanercept (ETA) on experimentally induced pancreatitis. Acute pancreatitis was induced with Na taurocholate. ETA was simultaneously administered to treatment groups. Serum amylase and lipase activity, pancreatic histopathology, apoptosis, malondialdehyde (MDA), and myeloperoxidase enzyme activity (MPO) were assessed. Although rats in the groups 1, 2, and 3 were sacrificed 24h later, groups 4, 5, and 6 were sacrificed 5 days later. ETA treatment significantly decreased serum amylase activity (nontreated, 2636.16 ± 191.94; treated, 1898.71 ± 262.53; control, 506.28 ± 17.31 U/L, P < 0.001), lipase activity (nontreated, 3049.67 ± 972.65; treated, 2538.85 ± 660.45; control, 88.57 ± 7.54 U/L, P < 0.001), histopathologic score (nontreated, 5.43 ± 0.43; treated, 2.57 ± 0.20; control, 0.71 ± 0.18, P < 0.001), MDA (nontreated, 105.77 ± 13.29; treated, 92.89 ± 10.39; control, 41.26 ± 2.54 nmol/g, P < 0.001), and MPO (nontreated, 0.64 ± 1.15; treated, 0.59 ± 0.13; control, 0.17 ± 0.02 units/g/wet weight, P < 0.001) activity in 24-h groups. In 5-day groups, ETA treatment decreased amylase activity (nontreated, 738.67 ± 48.60; treated, 497.14 ± 47.25; control, 389.00 ± 9.17 U/L, P < 0.001), lipase activity (nontreated, 101.33 ± 39.32; treated, 34.57 ± 7.29; control, 23.42 ± 2.12 U/L, P < 0.001), histopathologic score (nontreated, 5.43 ± 0.43; treated, 3.71 ± 0.68; control, 0.00 ± 0.00, P < 0.001), MDA (nontreated, 67.91 ± 4.28; treated, 60.91 ± 3.57; control, 14.85 ± 1.16 nmol/g, P < 0.001), and MPO (nontreated, 0.36 ± 0.04; treated, 0.27 ± 0.02; control, 0.14 ± 0.02 units/g/wet weight, P < 0.001) activity. Caspase-positive cells numbers around the necrosis significantly decreased by ETA treatment in both 24-h groups (nontreated, 74.28 ± 3.26; treated, 67.00 ± 1.15; control, 3.85 ± 0.63, P < 0.001) and 5-day groups (nontreated, 79.85 ± 3.01; treated, 47.85 ± 5.76; control, 2.22 ± 0.63, P < 0.001). These results showed that ETA has an ameliorating effect on sodium taurocholate-induced acute necrotic pancreatitis. © 2009 Mosby, Inc. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherMosby Inc.en_US
dc.relation.ispartofTranslational Researchen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectamylaseen_US
dc.subjectcaspaseen_US
dc.subjectetanercepten_US
dc.subjectmalonaldehydeen_US
dc.subjectmyeloperoxidaseen_US
dc.subjecttaurocholic aciden_US
dc.subjecttriacylglycerol lipaseen_US
dc.subjectacute pancreatitisen_US
dc.subjectanimal experimenten_US
dc.subjectanimal modelen_US
dc.subjectanimal tissueen_US
dc.subjectapoptosisen_US
dc.subjectarticleen_US
dc.subjectcell deathen_US
dc.subjectcell infiltrationen_US
dc.subjectcontrolled studyen_US
dc.subjectdrug effecten_US
dc.subjectenzyme activityen_US
dc.subjectfemaleen_US
dc.subjecthistopathologyen_US
dc.subjectleukocyteen_US
dc.subjectnonhumanen_US
dc.subjectpriority journalen_US
dc.subjectraten_US
dc.subjectscoring systemen_US
dc.subjectAmylasesen_US
dc.subjectAnimalsen_US
dc.subjectApoptosisen_US
dc.subjectBiological Markersen_US
dc.subjectCholagogues and Cholereticsen_US
dc.subjectDisease Models, Animalen_US
dc.subjectFemaleen_US
dc.subjectImmunoenzyme Techniquesen_US
dc.subjectImmunoglobulin Gen_US
dc.subjectImmunosuppressive Agentsen_US
dc.subjectLipaseen_US
dc.subjectMalondialdehydeen_US
dc.subjectNecrosisen_US
dc.subjectPancreasen_US
dc.subjectPancreatitis, Acute Necrotizingen_US
dc.subjectPeroxidaseen_US
dc.subjectRatsen_US
dc.subjectRats, Wistaren_US
dc.subjectReceptors, Tumor Necrosis Factoren_US
dc.subjectTaurocholic Aciden_US
dc.titleEffects of etanercept on sodium taurocholate-induced acute pancreatitis in ratsen_US
dc.typeArticleen_US
dc.identifier.volume154en_US
dc.identifier.issue5en_US
dc.identifier.startpage241
dc.identifier.startpage241en_US
dc.identifier.endpage249en_US
dc.identifier.doi10.1016/j.trsl.2009.07.009-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid19840765en_US
dc.identifier.scopus2-s2.0-70349943976en_US
dc.identifier.wosWOS:000271485900004en_US
dc.identifier.scopusqualityQ1-
dc.ownerPamukkale University-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.01. Surgical Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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