Inhibition of acrolein-induced apoptosis by the antioxidant selenium

dc.authoridsagir, dilek/0000-0002-6862-988X
dc.contributor.authorGokce, Ayse Basardi
dc.contributor.authorEren, Banu
dc.contributor.authorSagir, Dilek
dc.contributor.authorYilmaz, Burcu Demirel
dc.date.accessioned2025-03-23T19:30:44Z
dc.date.available2025-03-23T19:30:44Z
dc.date.issued2020
dc.departmentSinop Üniversitesi
dc.description.abstractIn this study, the effects of a potent antioxidant, selenium, on apoptosis induced by acrolein, a cytotoxic and genotoxic environmental pollutant, were investigated by immunohistochemical and electron microscopic methods. One hundred adult male Wistar albino rats were used in the study. The rats were divided into four main groups: control, acrolein, selenium, and acrolein + selenium. The animals in the experimental groups were given 1 mg/kg/day selenium and 4 mg/kg/day acrolein daily for 7 days by gavage. After drug administration, each group was divided into subgroups according to the time they were to be euthanized: 12th hour, 1st, 2nd, 3rd, and 5th day. The rats in each group at the determined time were euthanized and their livers were removed. Routine histological procedures were performed for light and electron microscopy examinations. After applying the Terminal Deoxynucleotidyl Transferase dUTP nick end labeling assay on the liver sections, apoptotic index values were calculated. Comparing the liver sections of the rats in the acrolein group and the control group, acrolein was found to cause a significant increase in the apoptotic index. The apoptotic index values of the acrolein + selenium group decreased compared to the acrolein group. In the electron microscopic examinations, apoptotic findings were observed in the liver tissues of the rats given acrolein, such as chromatin condensation in the nucleus of hepatocytes, dilatations in the perinuclear space, and cytoplasmic vacuolization. These apoptotic findings were not observed in the acrolein + selenium group after the 12th hour. These findings show that selenium may potentially be useful as a protective agent for people exposed to acrolein.
dc.identifier.doi10.1177/0748233720909043
dc.identifier.endpage92
dc.identifier.issn0748-2337
dc.identifier.issn1477-0393
dc.identifier.issue2
dc.identifier.pmid32279646
dc.identifier.scopus2-s2.0-85083155938
dc.identifier.scopusqualityQ2
dc.identifier.startpage84
dc.identifier.urihttps://doi.org/10.1177/0748233720909043
dc.identifier.urihttps://hdl.handle.net/11486/5153
dc.identifier.volume36
dc.identifier.wosWOS:000526672000004
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherSage Publications Inc
dc.relation.ispartofToxicology and Industrial Health
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250323
dc.subjectAcrolein
dc.subjectselenium
dc.subjectliver
dc.subjectapoptosis
dc.subjecthistopathology
dc.subjectrat
dc.titleInhibition of acrolein-induced apoptosis by the antioxidant selenium
dc.typeArticle

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