Ellagic acid inhibits proinflammatory intermediary manufacture by suppressing NF-?B/Akt, VEGF and activating Nrf-2/Caspase-3 signaling pathways in rat testicular damage: a new way for testicular damage cure and in silico approach

dc.contributor.authorAslan, Abdullah
dc.contributor.authorGok, Ozlem
dc.contributor.authorBeyaz, Seda
dc.contributor.authorUslu, Harun
dc.contributor.authorErman, Fazilet
dc.contributor.authorErman, Orhan
dc.contributor.authorBaspinar, Serpil
dc.date.accessioned2026-08-12T17:20:12Z
dc.date.issued2022
dc.departmentFırat Üniversitesi
dc.description.abstractEllagic acid (EA) has protective effect on testicular damage and this natural compound decreases oxidative damage. The present study aims to examine the preventive effect of ellagic acid (EA) against carbon tetrachloride (CCl4)-induced testicular tissue damage in rats. In testicular tissue, tumor necrosis factor-alpha (TNF-alpha), Nuclear factor erythroid-2 related factor 2 (Nrf-2), B-cell lymphoma-2 (Bcl-2), vascular endothelial growth factor (VEGF), Nuclear factor-kappa B (NF-kappa B), cysteine aspartic proteases (caspase-3) and protein kinase B (Akt) synthesis levels were analyzed by western blot method, reactive oxygen species (ROS) was measured by malondialdehyde (MDA) levels, Glutathione (GSH) level and catalase (CAT) by spectrophotometer. As a result, in comparison with the CCl4 group, caspase-3 and Nrf-2 protein synthesis levels increased in EA + CCl4 group, however, VEGF, Bcl-2, NF-kappa B, TNF-alpha and Akt protein synthesis levels decreased, EA application raised GSH levels and CAT activity, reduced MDA levels. In this study, in silico tools were applied to confirm the activity of EA against the cancer with macromolecules such as the above mentioned transcription factors. EA, turned out to show significant activity similarly to some cocrystal ligands, particularly against cancer. These results points out that EA can be used as a testicular damage cure drug in future.
dc.description.sponsorshipFirat University Scientific Research Projects Unit (FUBAP) [FF.16.42]
dc.description.sponsorshipThis article supported by Firat University Scientific Research Projects Unit (FUBAP) with FF.16.42 project number.
dc.identifier.doi10.1080/15376516.2022.2046668
dc.identifier.endpage476
dc.identifier.issn1537-6516
dc.identifier.issn1537-6524
dc.identifier.issue6
dc.identifier.orcid0000-0001-8521-6369
dc.identifier.orcid0000-0001-5181-4053
dc.identifier.orcid0000-0001-8827-8557
dc.identifier.orcid0000-0003-0436-8112
dc.identifier.orcid0000-0001-9496-2451
dc.identifier.orcid0000-0002-6243-4221
dc.identifier.pmid35236242
dc.identifier.scopus2-s2.0-85126036924
dc.identifier.scopusqualityQ2
dc.identifier.startpage463
dc.identifier.urihttps://doi.org/10.1080/15376516.2022.2046668
dc.identifier.urihttps://hdl.handle.net/11508/53460
dc.identifier.volume32
dc.identifier.wosWOS:000763744000001
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherTaylor & Francis Ltd
dc.relation.ispartofToxicology Mechanisms and Methods
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectEllagic acid
dc.subjectNE-kappa B
dc.subjectNrf-2
dc.subjecttesticular damage
dc.subjectmolecular docking
dc.titleEllagic acid inhibits proinflammatory intermediary manufacture by suppressing NF-?B/Akt, VEGF and activating Nrf-2/Caspase-3 signaling pathways in rat testicular damage: a new way for testicular damage cure and in silico approach
dc.typeArticle

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