Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/23172
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dc.contributor.authorTopsakal, Şenay-
dc.contributor.authorOzmen, O-
dc.contributor.authorCankara, FN-
dc.contributor.authorYesilot, S-
dc.contributor.authorBayram, D-
dc.contributor.authorOzdamar, NG-
dc.contributor.authorKayan, S-
dc.date.accessioned2019-08-20T06:50:44Z
dc.date.available2019-08-20T06:50:44Z
dc.date.issued2016-
dc.identifier.issn1424-3903-
dc.identifier.urihttps://hdl.handle.net/11499/23172-
dc.identifier.urihttps://doi.org/10.1016/j.pan.2016.03.001-
dc.description.abstractObjectives: Chronic consumption of high-fructose corn syrup (HFCS) causes several problems such as insulin resistance. The goal of the study was to investigate pancreatic damage induced by chronic HFCS consumption and the protective effects of alpha lipoic acid (ALA) on pancreatic cells.en_US
dc.description.abstractMethods: Wistar Albino, 4-month-old, female rats weighing 250-300 g were randomly distributed into three groups, each containing eight rats. The study included an HFCS group, an HFCS + ALA-administered group and a control group (CON). The prepared 30% solution of HFCS (F30) (24% fructose, 28% dextrose) was added to the drinking water for 10 weeks. ALA treatment was begun 4 weeks after the first HFCS administration (100 mg/kg/oral, last 6 weeks). Rats were anaesthetised and euthanised by cervical dislocation 24 h after the last ALA administration. Blood samples for biochemical tests (amylase, lipase, malondialdehyde (MDA) and catalase (CAT)) and tissue samples for histopathological and immunohistochemical examinations (caspase-3, insulin and glucagon) were collected.en_US
dc.description.abstractResults: Comparing the control and HFCS groups, serum glucose (150.92 +/- 39.77 and 236.50 +/- 18.28, respectively, p < 0.05), amylase (2165.00 +/- 150.76 and 3027.66 +/- 729.19, respectively, p < 0.01), lipase (5.58 +/- 2.22 and 11.51 +/- 2.74, respectively, p < 0.01) and pancreatic tissue MDA (0.0167 +/- 0.004 and 0.0193 +/- 0.006, respectively, p < 0.05) levels were increased, whereas tissue CAT (0.0924 +/- 0.029 and 0.0359 +/- 0.023, respectively, p < 0.05) activity decreased in the HFCS group significantly. Histopathological examination revealed degenerative and necrotic changes in Langerhans islet cells and slight inflammatory cell infiltration in pancreatic tissue in the HFCS group. Immunohistochemically there was a significant decrease in insulin (2.85 +/- 0.37 and 0.87 +/- 0.64, respectively, p < 0.001) and glucagon (2.71 +/- 0.48 and 1.00 +/- 0.75, respectively, p < 0.001) secreting cell scores, whereas a greater increase in caspase-3 (0.14 +/- 0.37 and 1.00 +/- 0.75, respectively, p < 0.05) expression was seen in this group compared with the controls. In the ALA-treated group, all of these pathologic conditions were improved.en_US
dc.description.abstractConclusions: This study indicated HFCS induced pancreatic lesions, but ALA had ameliorative effects. (C) 2016 IAP and EPC. Published by Elsevier B.V. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherKARGERen_US
dc.relation.ispartofPANCREATOLOGYen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHigh-fructose corn syrup; Oxidative stress; Pancreas; Pathology; Alphaen_US
dc.subjectlipoic acid; Immunohistochemistryen_US
dc.titleAlpha lipoic acid attenuates high-fructose-induced pancreatic toxicityen_US
dc.typeArticleen_US
dc.identifier.volume16en_US
dc.identifier.issue3en_US
dc.identifier.startpage347
dc.identifier.startpage347en_US
dc.identifier.endpage352en_US
dc.authorid0000-0003-4575-5653-
dc.identifier.doi10.1016/j.pan.2016.03.001-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid27025195en_US
dc.identifier.scopus2-s2.0-84961792771en_US
dc.identifier.wosWOS:000377555600010en_US
dc.identifier.scopusqualityQ2-
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-
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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