The impact of ellagic acid on some apoptotic gene expressions: a new perspective for the regulation of pancreatic Nrf-2/NF-?B and Akt/VEGF signaling in CCl4-induced pancreas damage in rats

dc.contributor.authorAslan, Abdullah
dc.contributor.authorBeyaz, Seda
dc.contributor.authorGok, Ozlem
dc.contributor.authorCan, Muhammed Ismail
dc.contributor.authorErman, Fazilet
dc.contributor.authorErman, Orhan
dc.date.accessioned2026-08-12T17:35:49Z
dc.date.issued2021
dc.departmentFırat Üniversitesi
dc.description.abstractObjective: The aim of this study was to evaluate the potential effect of ellagic acid (EA) in the treatment of pancreatic injury. EA has been found to have strong anti-inflammatory, antioxidative, and anticancer properties. The effects of EA on pancreatic star cell (PSC) activation and cell functions have been evaluated and it has been shown that it inhibits the activation of basic cell functions and PSCs and(.) it has antidiabetic activity through its effect on beta-pancreas cells. Materials and methods: In this work, 36 Wistar albino rats (n = 36, 8 weeks old) were used. Rats were divided to 4 groups and 9 rats were each group. Groups: Group 1: control group; Group 2: EA group; Group 3: carbon tetrachloride (CCl4) group; Group 4: EA + CCl4 group. Animals were decapitated after 8 weeks and their pancreas tissue samples were taken and researched. In pancreas tissue, NF-kappa B, TNF-alpha, Nrf-2, VEGF, Bcl-2, caspase-3, and Akt proteins expression ratios were analyzed by western blotting method, CAT activity and GSH levels were determined by spectrophotometer and ROS production was detected by MDA. Results: In our results, the Nrf-2 and caspase-3 protein expressions, catalase activities and GSH levels increased, TNF-alpha, NF-kappa B, Bcl-2, VEGF, and Akt protein expressions and MDA levels reduced in EA + CCl4 group comparable to the CCl4 group. Conclusions: These findings reveal that EA decreases pancreas tissue injury in rats and that EA may also be used as a drug against pancreas tissue injury in the future.
dc.description.sponsorshipFirat University Research Projects Unit (FUBAP)
dc.description.sponsorshipThis work was supported by Firat University Research Projects Unit (FUBAP) [Grant No. FF.16.42].
dc.identifier.doi10.1080/08923973.2020.1869255
dc.identifier.endpage152
dc.identifier.issn0892-3973
dc.identifier.issn1532-2513
dc.identifier.issue2
dc.identifier.orcid0000-0001-8521-6369
dc.identifier.orcid0000-0002-6243-4221
dc.identifier.orcid0000-0003-0436-8112
dc.identifier.orcid0000-0002-0118-2278
dc.identifier.pmid33455449
dc.identifier.scopus2-s2.0-85100034075
dc.identifier.scopusqualityQ2
dc.identifier.startpage145
dc.identifier.urihttps://doi.org/10.1080/08923973.2020.1869255
dc.identifier.urihttps://hdl.handle.net/11508/57691
dc.identifier.volume43
dc.identifier.wosWOS:000608320300001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherTaylor & Francis Ltd
dc.relation.ispartofImmunopharmacology and Immunotoxicology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectProtein kinase B
dc.subjectB-cell lymphoma 2
dc.subjectellagic acid
dc.subjectnuclear factor kappa B
dc.subjectpancreas damage
dc.titleThe impact of ellagic acid on some apoptotic gene expressions: a new perspective for the regulation of pancreatic Nrf-2/NF-?B and Akt/VEGF signaling in CCl4-induced pancreas damage in rats
dc.typeArticle

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