Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/54860
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dc.contributor.authorUral, C.-
dc.contributor.authorCelik, A.-
dc.contributor.authorOzbal, S.-
dc.contributor.authorGuneli, E.-
dc.contributor.authorArslan, S.-
dc.contributor.authorErgur, B.U.-
dc.contributor.authorCavdar, C.-
dc.contributor.authorAkdoğan, Gül-
dc.contributor.authorCavdar, Zahide-
dc.date.accessioned2023-11-18T09:30:12Z-
dc.date.available2023-11-18T09:30:12Z-
dc.date.issued2023-
dc.identifier.issn0939-4451-
dc.identifier.urihttps://doi.org/10.1007/s00726-023-03342-w-
dc.identifier.urihttps://hdl.handle.net/11499/54860-
dc.description.abstractDiabetic nephropathy (DN), a severe diabetes complication, causes kidney morphological and structural changes due to extracellular matrix accumulation. This accumulation is caused mainly by oxidative stress. Semi-essential amino acid derivative taurine has powerful antioxidant and antifibrotic effects. The aim of this study was to investigate the renoprotective effects of taurine through its possible roles in oxidative stress, extracellular matrix proteins, and the signaling pathways associated with the accumulation of extracellular matrix proteins in DN rats. 29 Wistar albino rats were randomly separated into control, taurine, diabetes, and diabetes + taurine groups. Diabetes animals were injected 45 mg/kg streptozosine. Taurine is given by adding to drinking water as 1% (w/v). Urine, serum, and kidney tissue were collected from rats for biochemical and histological analysis after 12 weeks. According to the studies, taurine significantly reduces the levels of malondialdehyde (MDA), total oxidant status (TOS), and protein expression of NADPH oxidase 4 (NOX4) that increase in diabetic kidney tissue. Also, decreased superoxide dismutase (SOD) activity levels significantly increased with taurine in diabetic rats. Moreover, increased mRNA and protein levels of fibronectin decreased with taurine. The matrix metalloproteinase (MMP)-2 and MMP-9 activities and their mRNA levels increased significantly, and this increase was significantly summed with taurine. There was a decrease in mRNA expression of Extracellular matrix metalloproteinase inducer (EMMPRIN). Taurine significantly increased this decrease. Diabetes increased mRNA expressions of transforming growth factor (TGF)-β and Smad2/3. Taurine significantly reduced this induction. TGF-β protein expression, p38, and Smad2/3 activations were also inhibited, but taurine was suppressed significantly. All these findings indicate that taurine may be an effective practical strategy to prevent renal diabetic injury. © 2023, The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.en_US
dc.description.sponsorshipDokuz Eylül Üniversitesi, DEÜen_US
dc.description.sponsorshipThis research was funded by Dokuz Eylul University Research Project Administration (Project number: 2017.KB.SAG.024) and carried out at Dokuz Eylul University Medical School Learning Resources Center Research Laboratory (R-LAB).en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofAmino Acidsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDiabetic nephropathyen_US
dc.subjectNOX4en_US
dc.subjectOxidative stressen_US
dc.subjectp38 MAPKen_US
dc.subjectSmad2/3en_US
dc.subjectTaurineen_US
dc.titleThe renoprotective effects of taurine against diabetic nephropathy via the p38 MAPK and TGF-β/Smad2/3 signaling pathwaysen_US
dc.typeArticleen_US
dc.departmentPamukkale Universityen_US
dc.identifier.doi10.1007/s00726-023-03342-w-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid56804887400-
dc.authorscopusid55868624600-
dc.authorscopusid24179281500-
dc.authorscopusid22134232700-
dc.authorscopusid8684142100-
dc.authorscopusid8960341600-
dc.authorscopusid6701732727-
dc.identifier.pmid37805666en_US
dc.identifier.scopus2-s2.0-85173734517en_US
dc.identifier.wosWOS:001091525000001en_US
dc.institutionauthor-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.grantfulltextnone-
item.openairetypeArticle-
crisitem.author.dept17.02. Biology-
Appears in Collections:Fen Fakültesi Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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