Hydroxytyrosol protects isoproterenol-induced myocardial infarction through activating notch signaling

dc.contributor.authorOnat, Elif
dc.contributor.authorTurk, Ahmet
dc.contributor.authorKocaman, Nevin
dc.contributor.authorHancer, Serhat
dc.contributor.authorSusam, Solmaz
dc.contributor.authorParlar, Ali
dc.contributor.authorOzer, Mehmet Kaya
dc.date.accessioned2026-08-12T17:39:27Z
dc.date.issued2025
dc.departmentFırat Üniversitesi
dc.description.abstractObjective(s): In this investigation, the protective effects of hydroxytyrosol (HT) administered prior to myocardial infarction in rats were examined, with a particular focus on its potential roles within the Notch pathway. Materials and Methods: The animals were categorized into seven groups (n=7): control, myocardial infarction (MI) 6 (th) hr, MI 24(th) hr, MI 7( th) day, MI+HT 6 (th )hr, MI+HT 24(th) hr, MI+HT 7 (th) day. In order to create infarction, the rats received a subcutaneous injection of isoproterenol at a dose of 200 mg/kg. Rats were given 4 ml/kg/day liquid containing HT orally for six weeks before infarction. Histopathological examination was conducted on heart tissue to assess Notch1, Hes1, and DLL4. Biochemical parameters were analyzed in serum using the ELISA method. Results: The study revealed an increase in Notch1 and DLL4 levels, particularly at the 24(th) hr and 7( th )day after the occurrence of myocardial infarction. DLL4 increased at 24 hr and 7 days of infarction after HT administration compared to control. Hes1 levels increased towards the seventh day after infarction and following HT application before infarction. It was noted that the severity of histopathological damage in heart tissue was reduced at the 24(th) hr of infarction in rats treated with HT prior to infarction. A significant decrease in fibrosis was observed on the seventh day of infarction in rats given HT before infarction. The levels of biochemical parameters decreased with the administration of HT before the occurrence of infarction. Conclusion: HT is thought to exert a cardioprotective effect in MI, potentially mediated through the Notch pathway.
dc.description.sponsorshipScientific Research Grants Unit of Adiyaman University, Turkiye [TIPFMAP/2021-0004]
dc.description.sponsorshipThis study was funded by the Scientific Research Grants Unit of Ad & imath;yaman University, Turkiye (grant number TIPFMAP/2021-0004) .
dc.identifier.doi10.22038/ijbms.2024.81495.17637
dc.identifier.endpage223
dc.identifier.issn2008-3866
dc.identifier.issn2008-3874
dc.identifier.issue2
dc.identifier.orcid0000-0003-0903-3522
dc.identifier.pmid39850112
dc.identifier.scopus2-s2.0-85214514764
dc.identifier.scopusqualityQ2
dc.identifier.startpage217
dc.identifier.urihttps://doi.org/10.22038/ijbms.2024.81495.17637
dc.identifier.urihttps://hdl.handle.net/11508/58841
dc.identifier.volume28
dc.identifier.wosWOS:001379175400009
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherMashhad Univ Med Sciences
dc.relation.ispartofIranian Journal of Basic Medical Sciences
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectDLL4
dc.subjectHes1
dc.subjectHydroxytyrosol
dc.subjectMyocardial infarction
dc.subjectNotch1
dc.titleHydroxytyrosol protects isoproterenol-induced myocardial infarction through activating notch signaling
dc.typeArticle

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