Morphological Andbiochemical Evaluation of Effects Of<i> Myrtus</I><i> Communis</I> L. Extract on Heart and Aorta in High Fat-Diet Obese Rats

dc.authoridErcan, Feriha/0000-0003-2339-5669
dc.authoridSener, Goksel/0000-0001-7444-6193
dc.authoridSen, Ali/0000-0002-2144-5741
dc.authorwosidErcan, Feriha/A-1655-2018
dc.contributor.authorŞener, Göksel
dc.contributor.authorAyci, Nurdan Bulbul
dc.contributor.authorKaya, Rumeysa Keles
dc.contributor.authorSen, Ali
dc.contributor.authorSener, Goksel
dc.contributor.authorErcan, Feriha
dc.contributor.otherEczacılık Meslek Bilimleri Bölümü
dc.date.accessioned2025-01-11T13:02:06Z
dc.date.available2025-01-11T13:02:06Z
dc.date.issued2023
dc.departmentFenerbahçe Universityen_US
dc.department-temp[Yay, Nagehan Ozyilmaz; Ayci, Nurdan Bulbul] Marmara Univ, Inst Hlth Sci, Dept Histol & Embryol, Istanbul, Turkiye; [Yay, Nagehan Ozyilmaz; Ayci, Nurdan Bulbul; Ercan, Feriha] Marmara Univ, Sch Med, Dept Histol & Embryol, Istanbul, Turkiye; [Kaya, Rumeysa Keles] Marmara Univ, Sch Pharm, Dept Pharmacol, Istanbul, Turkiye; [Sen, Ali] Marmara Univ, Sch Pharm, Dept Pharmacognosy, Istanbul, Turkiye; [Sener, Goksel] Fenerbahce Univ, Fac Pharm, Dept Pharmacol, Istanbul, Turkiyeen_US
dc.descriptionErcan, Feriha/0000-0003-2339-5669; Sener, Goksel/0000-0001-7444-6193; Sen, Ali/0000-0002-2144-5741en_US
dc.description.abstractObjective: The purpose of this study was to examine the protective effects of Myrtus communis L. (MC) extract on high fat-diet (HFD) induced heart and aorta damage by evaluating oxidative stress and the endothelial nitric oxide system (eNOS).Materials and Methods: Wistar albino male rats were divided into 3 groups (n=7) as control, HFD, and HFD+MC. Rats in HFD and HFD+MC groups were HFD fed for 16 weeks and in the last 4 weeks saline or MC (100 mg/kg) was administered orally (5 days/week). Triglyceride, cholesterol, and high-density lipoprotein (HDL) were estimated in blood serum. Tissue oxidative stress and inflammatory parameters were evaluated biochemically. Tissue morphologies, eNOS, inducible NOS (iNOS), and NADPH oxidase-2 (NOX-2)-immunopositive and apoptotic cells were evaluated histologically.Results: Altered serum lipid profiles, degenerated heart, and aorta morphology, increased malondialdehyde, 8-hydroxy-2-deoxyguanosine, tumor necrosis factor-alpha, monocyte chemoattractant protein-1 and myeloperoxidase levels, and iNOS, NOX-2 immunopositive and apoptotic cells, decreased NO levels, eNOS-immunopositive cells in both tissues were observed in HFD group. All these parameters improved in the HFD+MC group. Conclusion: This study revealed that HFD-induced obesity increased iNOS activation and oxidative stress in the cardiac and aortic tissues of the rats. MC improved oxidant/antioxidant balance and prevented heart and aorta damage via eNOS involvement.en_US
dc.description.sponsorshipMarmara University Research Fund [SAG-C-DRP-250.919.0292]en_US
dc.description.sponsorshipFinancial Support: This study was supported by Marmara University Research Fund (SAG-C-DRP-250.919.0292) .en_US
dc.description.woscitationindexEmerging Sources Citation Index
dc.identifier.citation1
dc.identifier.doi10.5472/marumj.1302544
dc.identifier.endpage170en_US
dc.identifier.issn1309-9469
dc.identifier.issue2en_US
dc.identifier.scopusqualityQ4
dc.identifier.startpage162en_US
dc.identifier.urihttps://doi.org/10.5472/marumj.1302544
dc.identifier.urihttps://hdl.handle.net/20.500.14627/208
dc.identifier.volume36en_US
dc.identifier.wosWOS:001008168200003
dc.language.isoenen_US
dc.publisherMarmara Univ, Fac Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectHigh -Fat Dieten_US
dc.subjectObesityen_US
dc.subjectMyrtus Communis Len_US
dc.subjectExtracten_US
dc.subjectHearten_US
dc.subjectAortaen_US
dc.titleMorphological Andbiochemical Evaluation of Effects Of<i> Myrtus</I><i> Communis</I> L. Extract on Heart and Aorta in High Fat-Diet Obese Ratsen_US
dc.typeArticleen_US
dspace.entity.typePublication
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relation.isOrgUnitOfPublication5052e089-e75d-4aec-a280-6353973e4819
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