Scopus:
Exploring of the ameliorative effects of Nerium (Nerium oleander L.) ethanolic flower extract in streptozotocin induced diabetic rats via biochemical, histological and molecular aspects

dc.contributor.authorBattal A.
dc.contributor.authorDogan A.
dc.contributor.authorUyar A.
dc.contributor.authorDemir A.
dc.contributor.authorKeleş Ö.F.
dc.contributor.authorCelik I.
dc.contributor.authorBaloglu M.C.
dc.contributor.authorAslan A.
dc.date.accessioned2023-04-11T22:11:01Z
dc.date.accessioned2023-04-12T00:30:32Z
dc.date.available2023-04-11T22:11:01Z
dc.date.available2023-04-12T00:30:32Z
dc.date.issued2023-01-01
dc.description.abstractBackground: Nerium oleander L. is ethnopharmacologically used for diabetes. Our aim was to investigate the ameliorative effects of ethanolic Nerium flower extract (NFE) in STZ-induced diabetic rats. Methods: Seven random groups including control group, NFE group (50 mg/kg), diabetic group, glibenclamide group and NFE treated groups (25 mg/kg, 75 mg/kg, and 225 mg/kg) were composed of forty-nine rats. Blood glucose level, glycated hemoglobin (HbA1c), insulin level, liver damage parameters and lipid profile parameters were investigated. Antioxidant defense system enzyme activities and reduced glutathione (GSH) and malondialdehyde (MDA) contents and immunotoxic and neurotoxic parameters were determined in liver tissue. Additionally, the ameliorative effects of NFE were histopathologically examined in liver. mRNA levels of SLC2A2 gene encoding glucose transporter 2 protein were measured by quantitative real time PCR. Results: NFE caused decrease in glucose level and HbA1c and increase in insulin and C-peptide levels. Additionally, NFE improved liver damage biomarkers and lipid profile parameters in serum. Moreover, lipid peroxidation was prevented and antioxidant enzyme activities in liver were regulated by NFE treatment. Furthermore, anti-immunotoxic and anti-neurotoxic effects of NFE were determined in liver tissue of diabetic rats. Histopathogically, significant liver damages were observed in the diabetic rats. Histopathological changes were decreased partially in the 225 mg/kg NFE treated group. SLC2A2 gene expression in liver of diabetic rats significantly reduced compared to healthy rats and NFE treatment (25 mg/kg) caused increase in gene expression. Conclusion: Flower extract of Nerium plant may have an antidiabetic potential due to its high phytochemical content. Graphical Abstract: [Figure not available: see fulltext.].
dc.identifier.doi10.1007/s11033-023-08332-5
dc.identifier.issn3014851
dc.identifier.scopus2-s2.0-85149762790
dc.identifier.urihttps://hdl.handle.net/20.500.12597/4167
dc.relation.ispartofMolecular Biology Reports
dc.rightsfalse
dc.subjectFlower extract | GLUT2 | Nerium oleander | SLC2A2 gene | Streptozotocin
dc.titleExploring of the ameliorative effects of Nerium (Nerium oleander L.) ethanolic flower extract in streptozotocin induced diabetic rats via biochemical, histological and molecular aspects
dc.typeArticle
dspace.entity.typeScopus
person.affiliation.nameYüzüncü Yil Üniversitesi
person.affiliation.nameYüzüncü Yil Üniversitesi
person.affiliation.nameMustafa Kemal Üniversitesi
person.affiliation.nameYüzüncü Yil Üniversitesi
person.affiliation.nameYüzüncü Yil Üniversitesi
person.affiliation.nameYüzüncü Yil Üniversitesi
person.affiliation.nameKastamonu University
person.affiliation.nameYüzüncü Yil Üniversitesi
person.identifier.orcid0000-0001-6098-3908
person.identifier.orcid0000-0002-5438-8560
person.identifier.orcid0000-0003-4345-6756
person.identifier.orcid0000-0002-6867-4410
person.identifier.orcid0000-0002-7869-5311
person.identifier.orcid0000-0003-2199-6348
person.identifier.orcid0000-0003-2976-7224
person.identifier.orcid0000-0002-5122-6646
person.identifier.scopus-author-id25121451300
person.identifier.scopus-author-id54893403000
person.identifier.scopus-author-id57188983805
person.identifier.scopus-author-id57212309307
person.identifier.scopus-author-id57195562796
person.identifier.scopus-author-id8452071500
person.identifier.scopus-author-id36766861600
person.identifier.scopus-author-id58135380400
relation.isPublicationOfScopus5ff50202-a512-4b62-b5ae-9b1676b654a3
relation.isPublicationOfScopus.latestForDiscovery5ff50202-a512-4b62-b5ae-9b1676b654a3

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