Fullerene C60 Decreases Inflammation, Oxidative Stress and Apoptosis Induced by 7,12-Dimethylbenz[a]Anthracene (DMBA) in Muscle Tissue Via Caspase-3 and NRF-2 Protein Signaling Pathway

dc.contributor.authorAslan, Abdullah
dc.contributor.authorBeyaz, Seda
dc.contributor.authorGok, Ozlem
dc.contributor.authorOzercan, Ibrahim Hanifi
dc.contributor.authorAgca, Can Ali
dc.date.accessioned2026-08-12T17:07:47Z
dc.date.issued2024
dc.departmentFırat Üniversitesi
dc.description.abstractFullerene C-60 exhibits potent antioxidant anti-inflammatory activities as well as anticancer activities. In this study using 60 Wistar albino female rats (n = 60, 8 weeks old), they rats were divided into 4 groups, including 15 rats each. The groups were arranged as follows: (i) Control Group: Group fed with standard diet; (ii) C-60 Group: C-60 (1.7 mg/kg bw, oral gavage); (iii) DMBA (7,12-dimethylbenz[a]anthracene) Group: DMBA (45 mg/kg bw, oral gavage); (iv) C-60 and DMBA Group: C-60 (1.7 mg/kg bw, oral gavage) and DMBA (45 mg/kg bw, oral gavage) group. DMBA increased the malondialdehyde levels in muscle tissue, while decreasing GSH and CAT levels; however, treatment with fullerene C-60 reversed these effects. In addition, the oral administration of fullerene C-60 increased caspase-3 and Nrf-2 protein expression and significantly decreased Bcl-2, NF-kappa B, TNF-alpha, COX-2 and p38 alpha (MAPK) protein expression in C60 + DMBA compared to the DMBA group. Moreover, histopathological imaging revealed that the oral administration of fullerene C-60 decreases inflammatory cells, edema formation, and hydropic degeneration in the muscles. Taken together, the results of the present study indicated that fullerene C-60 nanoparticle provides effective protection by preventing muscle tissue damage.
dc.description.sponsorshipFirat University Research Projects Unit (FUBAP) [FF.20.07]; Council of Higher Education (CoHE) 100/2000 Biotechnology priority field doctoral project; Scientific and Technological Research Council of Turkey (TUBITAK) [2211/C]
dc.description.sponsorshipThis study was supported by the Firat University Research Projects Unit (FUBAP) [Project Number: FF.20.07].In addition, this study was supported by the Council of Higher Education (CoHE) 100/2000 Biotechnology priority field doctoral project and The Scientific and Technological Research Council of Turkey (TUBITAK) 2211/C program
dc.identifier.doi10.1007/s11094-024-03207-w
dc.identifier.endpage792
dc.identifier.issn0091-150X
dc.identifier.issn1573-9031
dc.identifier.issue5
dc.identifier.orcid0000-0003-0436-8112
dc.identifier.scopus2-s2.0-85204019380
dc.identifier.scopusqualityQ4
dc.identifier.startpage784
dc.identifier.urihttps://doi.org/10.1007/s11094-024-03207-w
dc.identifier.urihttps://hdl.handle.net/11508/49792
dc.identifier.volume58
dc.identifier.wosWOS:001314156400001
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherSpringer
dc.relation.ispartofPharmaceutical Chemistry Journal
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectapoptosis
dc.subjectCOX-2
dc.subjectDMBA
dc.subjectfullerene C-60
dc.subjectmuscle damage
dc.titleFullerene C60 Decreases Inflammation, Oxidative Stress and Apoptosis Induced by 7,12-Dimethylbenz[a]Anthracene (DMBA) in Muscle Tissue Via Caspase-3 and NRF-2 Protein Signaling Pathway
dc.typeArticle

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