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dc.contributor.authorIsildar, Basak
dc.contributor.authorBeydogan, Alisa Bahar
dc.contributor.authorKoyuturk, Ece
dc.contributor.authorYazici, Zeynep Mine Coskun
dc.contributor.authorKoyuturk, Meral
dc.contributor.authorBolkent, Sema
dc.date.accessioned2025-01-12T18:54:57Z
dc.date.available2025-01-12T18:54:57Z
dc.date.issued2024
dc.identifier.issn0948-6143
dc.identifier.issn1432-119X
dc.identifier.urihttps://doi.org/10.1007/s00418-024-02311-y
dc.identifier.urihttp://hdl.handle.net/11446/5018
dc.description.abstractThe consumption of fructose is increasing day by day. Understanding the impact of increasing fructose consumption on the small intestine is crucial since the small intestine processes fructose into glucose. triangle 9-Tetrahydrocannabinol (THC), a key cannabinoid, interacts with CB1 and CB2 receptors in the gastrointestinal tract, potentially mitigating inflammation. Therefore, this study aimed to investigate the effects of the high-fructose diet (HFD) on the jejunum of rats and the role of THC consumption in reversing these effects. Experiments were conducted on Sprague-Dawley rats, with the experimental groups as follows: control (C), HFD, THC, and HFD + THC. The HFD group received a 10% fructose solution in drinking water for 12 weeks. THC groups were administered 1.5 mg/kg/day of THC intraperitoneally for the last four weeks. Following sacrification, the jejunum was evaluated for mucus secretion capacity. IL-6, JNK, CB2 and PCNA expressions were assessed through immunohistochemical analysis and the ultrastructural alterations via transmission electron microscopy. The results showed that fructose consumption did not cause weight gain but triggered inflammation in the jejunum, disrupted the cell proliferation balance, and increased mucus secretion in rats. Conversely, THC treatment displayed suppressed inflammation and improved cell proliferation balance caused by HFD. Ultrastructural examinations showed that the zonula occludens structures deteriorated in the HFD group, along with desmosome shrinkage. Mitochondria were found to be increased due to THC application following HFD. In conclusion, the findings of this research reveal the therapeutic potential of THC in reversing HFD-related alterations and provide valuable insights for clinical application.en_US
dc.description.sponsorshipIstanbul University Cerrahpascedil;aen_US
dc.description.sponsorshipNo Statement Availableen_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.relation.ispartofHistochemistry and Cell Biologyen_US
dc.identifier.doi10.1007/s00418-024-02311-y
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectHigh fructose dieten_US
dc.subjecttriangle-9-Tetrahydrocannabinolen_US
dc.subjectJejunumen_US
dc.subjectEnterocytesen_US
dc.subjectElectron microscopyen_US
dc.subjectCannabis-Sativa Extracten_US
dc.subjectOxidative Stressen_US
dc.subjectSecretionen_US
dc.subjectIl-6en_US
dc.titleEffects of ?-9 tetrahydrocannabinol on the small intestine altered by high fructose diet: A Histopathological studyen_US
dc.typearticleen_US
dc.departmentDBÜen_US
dc.identifier.issue5en_US
dc.identifier.volume162en_US
dc.identifier.startpage363en_US
dc.identifier.endpage372en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Isildar, Basak; Koyuturk, Meral] Istanbul Univ Cerrahpasa, Cerrahpasa Fac Med, Dept Histol & Embryol, Istanbul, Turkiye; [Beydogan, Alisa Bahar; Bolkent, Sema] Istanbul Univ Cerrahpasa, Cerrahpasa Fac Med, Dept Med Biol, Istanbul, Turkiye; [Koyuturk, Ece] Otto von Guericke Univ, Fac Med, Magdeburg, Germany; [Yazici, Zeynep Mine Coskun] Demiroglu Bilim Univ, Fac Arts & Sci, Dept Mol Biol & Genet, Istanbul, Turkiyeen_US
dc.authoridIsildar, Basak/0000-0001-7557-7611
dc.identifier.pmid39110194en_US
dc.identifier.scopus2-s2.0-85200695192en_US
dc.identifier.wosWOS:001285459900001en_US
dc.authorwosidBolkent, Sema/C-9539-2019
dc.authorwosidIsildar, Basak/AAI-2385-2019
dc.authorscopusid57201488048
dc.authorscopusid57118285900
dc.authorscopusid59251169000
dc.authorscopusid36187773300
dc.authorscopusid6603491530
dc.authorscopusid6701612705


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