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https://hdl.handle.net/11499/6926
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yılmaz, Mustafa | - |
dc.contributor.author | Topsakal, Şenay | - |
dc.contributor.author | Herek, Özkan | - |
dc.contributor.author | Özmen, Özlem | - |
dc.contributor.author | Şahinduran, Şima | - |
dc.contributor.author | Büyükoğlu, Tülay | - |
dc.contributor.author | Yonetci, Nadir | - |
dc.date.accessioned | 2019-08-16T12:13:02Z | - |
dc.date.available | 2019-08-16T12:13:02Z | - |
dc.date.issued | 2009 | - |
dc.identifier.issn | 1931-5244 | - |
dc.identifier.uri | https://hdl.handle.net/11499/6926 | - |
dc.identifier.uri | https://doi.org/10.1016/j.trsl.2009.07.009 | - |
dc.description.abstract | In 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.iso | en | en_US |
dc.publisher | Mosby Inc. | en_US |
dc.relation.ispartof | Translational Research | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | amylase | en_US |
dc.subject | caspase | en_US |
dc.subject | etanercept | en_US |
dc.subject | malonaldehyde | en_US |
dc.subject | myeloperoxidase | en_US |
dc.subject | taurocholic acid | en_US |
dc.subject | triacylglycerol lipase | en_US |
dc.subject | acute pancreatitis | en_US |
dc.subject | animal experiment | en_US |
dc.subject | animal model | en_US |
dc.subject | animal tissue | en_US |
dc.subject | apoptosis | en_US |
dc.subject | article | en_US |
dc.subject | cell death | en_US |
dc.subject | cell infiltration | en_US |
dc.subject | controlled study | en_US |
dc.subject | drug effect | en_US |
dc.subject | enzyme activity | en_US |
dc.subject | female | en_US |
dc.subject | histopathology | en_US |
dc.subject | leukocyte | en_US |
dc.subject | nonhuman | en_US |
dc.subject | priority journal | en_US |
dc.subject | rat | en_US |
dc.subject | scoring system | en_US |
dc.subject | Amylases | en_US |
dc.subject | Animals | en_US |
dc.subject | Apoptosis | en_US |
dc.subject | Biological Markers | en_US |
dc.subject | Cholagogues and Choleretics | en_US |
dc.subject | Disease Models, Animal | en_US |
dc.subject | Female | en_US |
dc.subject | Immunoenzyme Techniques | en_US |
dc.subject | Immunoglobulin G | en_US |
dc.subject | Immunosuppressive Agents | en_US |
dc.subject | Lipase | en_US |
dc.subject | Malondialdehyde | en_US |
dc.subject | Necrosis | en_US |
dc.subject | Pancreas | en_US |
dc.subject | Pancreatitis, Acute Necrotizing | en_US |
dc.subject | Peroxidase | en_US |
dc.subject | Rats | en_US |
dc.subject | Rats, Wistar | en_US |
dc.subject | Receptors, Tumor Necrosis Factor | en_US |
dc.subject | Taurocholic Acid | en_US |
dc.title | Effects of etanercept on sodium taurocholate-induced acute pancreatitis in rats | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 154 | en_US |
dc.identifier.issue | 5 | en_US |
dc.identifier.startpage | 241 | - |
dc.identifier.startpage | 241 | en_US |
dc.identifier.endpage | 249 | en_US |
dc.identifier.doi | 10.1016/j.trsl.2009.07.009 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 19840765 | en_US |
dc.identifier.scopus | 2-s2.0-70349943976 | en_US |
dc.identifier.wos | WOS:000271485900004 | en_US |
dc.identifier.scopusquality | Q1 | - |
dc.owner | Pamukkale University | - |
item.languageiso639-1 | en | - |
item.openairetype | Article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.01. Surgical Medicine | - |
crisitem.author.dept | 14.02. Internal 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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