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dc.contributor.authorUlusan, M.
dc.contributor.authorErdogan, M.A.
dc.contributor.authorSimsek, O.
dc.contributor.authorGunes, V.
dc.contributor.authorErbas, O.
dc.date.accessioned2025-01-12T18:55:03Z
dc.date.available2025-01-12T18:55:03Z
dc.date.issued2024
dc.identifier.issn2077-0383
dc.identifier.urihttps://doi.org/10.3390/medicina60101713
dc.identifier.urihttp://hdl.handle.net/11446/5045
dc.description.abstractBackground and Objectives: Non-alcoholic fatty liver disease (NAFLD) is a growing global health concern closely linked to metabolic disorders, including obesity, insulin resistance, and dyslipidemia. Emerging evidence suggests that the gut–liver axis plays a critical role in the pathogenesis of NAFLD, with recent research highlighting the influence of gut microbiota, including fungal species such as Saccharomyces boulardii (S. boulardii). This study aimed to evaluate the effects of S. boulardii on lipid metabolism and oxidative stress in a rat model of fructose-induced NAFLD. Materials and Methods: Thirty Wistar rats were divided into three groups: a control group, a fatty liver group induced by 35% fructose supplementation, and a treatment group receiving S. boulardii (100 mg/kg/day) after fructose induction. Results: Biochemical analyses revealed that the treatment group exhibited significantly lower plasma levels of malondialdehyde (MDA), alanine aminotransferase (ALT), total triglycerides, and cholesterol compared to the untreated fatty liver group (p < 0.05). Furthermore, liver tissue analysis showed a marked reduction in lipid accumulation and fatty infiltration in the treatment group, with no visible lipid vacuoles in hepatocytes. The expression of aquaporin-8 (AQP8) and sirtuin-1 (SIRT1), key markers associated with hepatocyte function and lipid metabolism, was significantly higher in the S. boulardii group compared to the fatty liver group (p < 0.001). Conclusions: These findings indicate that S. boulardii supplementation mitigates the metabolic and oxidative stress-related alterations associated with fructose-induced NAFLD. In conclusion, our study suggests that S. boulardii exerts protective effects on the liver by reducing lipid accumulation and oxidative stress, highlighting its potential as a therapeutic intervention for NAFLD. © 2024 by the authors.en_US
dc.language.isoengen_US
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)en_US
dc.relation.ispartofMedicina (Lithuania)en_US
dc.identifier.doi10.3390/medicina60101713
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectaquaporin-8en_US
dc.subjectfatty liveren_US
dc.subjectfructoseen_US
dc.subjectoxidative stressen_US
dc.subjectsaccharomyces boulardiien_US
dc.subjectsirtuin-1en_US
dc.subjectAnimalsen_US
dc.subjectDisease Models, Animalen_US
dc.subjectFructoseen_US
dc.subjectLipid Metabolismen_US
dc.subjectLiveren_US
dc.subjectMaleen_US
dc.subjectNon-alcoholic Fatty Liver Diseaseen_US
dc.subjectOxidative Stressen_US
dc.subjectProbioticsen_US
dc.subjectRatsen_US
dc.subjectRats, Wistaren_US
dc.subjectSaccharomyces boulardiien_US
dc.subjectfructoseen_US
dc.subjectprobiotic agenten_US
dc.subjectanimalen_US
dc.subjectdisease modelen_US
dc.subjectdrug effecten_US
dc.subjectlipid metabolismen_US
dc.subjectliveren_US
dc.subjectmaleen_US
dc.subjectmetabolismen_US
dc.subjectnonalcoholic fatty liveren_US
dc.subjectoxidative stressen_US
dc.subjectphysiologyen_US
dc.subjectraten_US
dc.subjectSaccharomyces boulardiien_US
dc.subjectWistar raten_US
dc.titleSaccharomyces boulardii Mitigates Fructose-Induced Non-Alcoholic Fatty Liver in Ratsen_US
dc.typearticleen_US
dc.departmentDBÜen_US
dc.identifier.issue10en_US
dc.identifier.volume60en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-tempUlusan M., Department of Internal Medicine, Faculty of Veterinary Medicine, Erciyes University, Kayseri, 38280, Turkey, Department of Internal Medicine, Faculty of Veterinary Medicine, Burdur Mehmet Akif Ersoy University, Burdur, 15030, Turkey; Erdogan M.A., Department of Physiology, Faculty of Medicine, Izmir Katip Celebi University, Izmir, 35620, Turkey; Simsek O., Department of Physiology, Faculty of Veterinary Medicine, Burdur Mehmet Akif Ersoy University, Burdur, 15030, Turkey; Gunes V., Department of Internal Medicine, Faculty of Veterinary Medicine, Erciyes University, Kayseri, 38280, Turkey, Experimental Research and Application Center (DEKAM), Erciyes University, Kayseri, 38280, Turkey; Erbas O., Department of Physiology, Faculty of Medicine, Istanbul Demiroglu Bilim University, Istanbul, 34394, Turkeyen_US
dc.identifier.pmid39459500en_US
dc.identifier.scopus2-s2.0-85207678530en_US
dc.authorscopusid57188931931
dc.authorscopusid57189713929
dc.authorscopusid36549270000
dc.authorscopusid55929313400
dc.authorscopusid55469991100


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