Effect of Gundelia Tournefortii Extract on Diabetic Gastropathy: Involvement of Inflammation, Apoptosis, Oxidative Stress, and Histopathology

dc.contributor.author Şeker, Uğur
dc.contributor.author Seker, Ugur
dc.contributor.author Demircioglu, Muhammet
dc.contributor.author Demircioglu, Ismail
dc.contributor.other Department of Basic Medical Sciences / Temel Tıp Bilimleri Bölümü
dc.contributor.other 10. Faculty of Medicine / Tıp Fakültesi
dc.contributor.other 01. Mardin Artuklu University / Mardin Artuklu Üniversitesi
dc.date.accessioned 2025-04-16T00:17:04Z
dc.date.available 2025-04-16T00:17:04Z
dc.date.issued 2025
dc.description.abstract In this study, the effect of Gundelia tournefortii (GT) extract against diabetic gastropathy was investigated by pathological methods. The animal groups were designed as the control, diabetes, diabetes + GT50, diabetes + GT100, and diabetes + GT200 groups. No treatment was applied to the control group. The other groups received 45.00 mg kg-1 streptozotocin intraperitoneally on the experimental day. The treatment groups were also given 50.00, 100, and 200 mg kg-1 of GT extract daily by gavage for 21 days. Tissues were stained with Hematoxylin and Eosin for histopathological examination. Immunohistochemical staining was performed to reveal the presence of inflammation (tumor necrosis factor alpha), apoptosis (cysteine aspartate specific proteases-3), and oxidative stress (heat shock protein-27). Histopathological examination revealed no pathological lesion in the control group. In the diabetes group, mucosal tissue damage, and vascular and inflammatory changes were observed. In the treatment groups, GT decreased histopathological findings in parallel with the dose increase. Immunohistochemical examination revealed no immunopositivity in the control group, while severe immunopositivity was observed in the diabetes groups in terms of inflammation, apoptosis, and oxidative stress. In the treatment groups, there was a decrease in the severity of immunopositivity's depending on the dose increase. As a result of this study, which has not been done before, GT was found to have a protective effect against gastropathy, being an important complication of diabetes, and this study is thus an important reference point for future research and promises new hope for the patients. (c) 2025 Urmia University. All rights reserved. en_US
dc.identifier.doi 10.30466/vrf.2024.2027690.4249
dc.identifier.issn 2008-8140
dc.identifier.issn 2322-3618
dc.identifier.scopus 2-s2.0-105000760448
dc.identifier.uri https://doi.org/10.30466/vrf.2024.2027690.4249
dc.identifier.uri https://hdl.handle.net/20.500.12514/8485
dc.language.iso en en_US
dc.publisher Urmia Univ en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Cysteine Aspartate Specific en_US
dc.subject Diabetes en_US
dc.subject Gundelia Tournefortii en_US
dc.subject Heat Shock Protein en_US
dc.subject Tumor Necrosis Factor Alpha en_US
dc.title Effect of Gundelia Tournefortii Extract on Diabetic Gastropathy: Involvement of Inflammation, Apoptosis, Oxidative Stress, and Histopathology en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.scopusid 57202544780
gdc.author.scopusid 55910059600
gdc.author.scopusid 59704685800
gdc.author.scopusid 57194508123
gdc.description.department Artuklu University en_US
gdc.description.departmenttemp [Dortbudak, Muhammet Bahaeddin] Harran Univ, Dept Pathol, Fac Vet Med, Sanliurfa, Turkiye; [Seker, Ugur] Mardin Artuklu Univ, Fac Med, Dept Histol & Embryol, Mardin, Turkiye; [Demircioglu, Muhammet] Dicle Univ, Dept Histol & Embryol, Inst Hlth Sci, Diyarbakir, Turkiye; [Demircioglu, Ismail] Harran Univ, Fac Vet Med, Dept Anat, Sanliurfa, Turkiye en_US
gdc.description.endpage 139 en_US
gdc.description.issue 3 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.startpage 133 en_US
gdc.description.volume 16 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q3
gdc.identifier.wos WOS:001447478400002
gdc.scopus.citedcount 0
gdc.wos.citedcount 0
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