Genotoxic and antigenotoxic potentials of two Usnea species

MakaleAçık ErişimScopus SJRQ2
  • SDG 3 · Sağlık ve Kaliteli Yaşam

Özet

For ages, lichens have long been investigated popularly for biological roles, mainly antitumor, antimicrobial and antioxidant activities. Many positive results were obtained in these previous research. Thus, in this study, we aimed to determine whether extracts of Usnea articulata (UAE) and Usnea filipendula (UFE) possessing a protection against aflatoxin B1(AFB1)-induced genotoxic and oxidative damage. The results of our studies showed that 5 μM concentrations of AFB1increased the frequencies of sister chromatid exchange (SCE) and the level of malondialdehyde (MDA) and decreased the activities of superoxide dismutase (SOD), glutathione (GSH) and glutathione peroxidase (GPx). However, when 5, 10 and 20 µg/mL concentrations of UAE and UFE was added to AFB1, the frequencies of SCE and MDA level were decreased and SOD, GSH and GPx level were increased. The Ames (Salmonella typhimurium TA1535, TA1537) and WP2 (Escherichia coli) test systems carried out evinced that UAE and UFE possess any mutagenicity, but have antimutagenic effects. Consequently, the results of this experiment have clearly shown that UAE and UFE have strong antioxidative and antigenotoxic effects that are associated with its antioxidant nature. A detailed study can be performed to determine the antioxidant properties of each compound that will extend the use of lichen extracts in food and pharmacy industries.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/bayburt/12465Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1177/0748233713485889Yayıncı resmi DOI adresi
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Kaydın indeks veri tabanlarındaki sayfası (aktarımda alınan kayıt numarasıyla). Erişim, indeksin kendi koşullarına bağlıdır.
Atıflar
Scopus
16
WoS
13
OpenAlex
14
Her kaynağın kendi saydığı toplam atıf; aktarım ve zenginleştirme sırasında alındı.
Tam Kayıt
AlanDeğerDil
dc.contributor.authorCeker, Selcuk
dc.contributor.authorOrhan, Furkan
dc.contributor.authorKizil, Hamit Emre
dc.contributor.authorAlpsoy, Lokman
dc.contributor.authorGulluce, Medine
dc.contributor.authorAslan, Ali
dc.contributor.authorAgar, Guleray
dc.date.accessioned2026-10-29T19:09:37.136835522Z
dc.date.available2026-10-29T19:09:37.136835522Z
dc.date.issued2015
dc.description.abstractFor ages, lichens have long been investigated popularly for biological roles, mainly antitumor, antimicrobial and antioxidant activities. Many positive results were obtained in these previous research. Thus, in this study, we aimed to determine whether extracts of Usnea articulata (UAE) and Usnea filipendula (UFE) possessing a protection against aflatoxin B1(AFB1)-induced genotoxic and oxidative damage. The results of our studies showed that 5 μM concentrations of AFB1increased the frequencies of sister chromatid exchange (SCE) and the level of malondialdehyde (MDA) and decreased the activities of superoxide dismutase (SOD), glutathione (GSH) and glutathione peroxidase (GPx). However, when 5, 10 and 20 µg/mL concentrations of UAE and UFE was added to AFB1, the frequencies of SCE and MDA level were decreased and SOD, GSH and GPx level were increased. The Ames (Salmonella typhimurium TA1535, TA1537) and WP2 (Escherichia coli) test systems carried out evinced that UAE and UFE possess any mutagenicity, but have antimutagenic effects. Consequently, the results of this experiment have clearly shown that UAE and UFE have strong antioxidative and antigenotoxic effects that are associated with its antioxidant nature. A detailed study can be performed to determine the antioxidant properties of each compound that will extend the use of lichen extracts in food and pharmacy industries.
dc.identifier.doi10.1177/0748233713485889
dc.identifier.eissn1477-0393
dc.identifier.endpage999
dc.identifier.issn0748-2337
dc.identifier.issue11
dc.identifier.pmid23589403
dc.identifier.scopus2-s2.0-84945128430
dc.identifier.startpage990
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/bayburt/12465
dc.identifier.volume31
dc.identifier.wosWOS:000363351400004
dc.language.isoen
dc.publisherSAGE PUBLICATIONS INC
dc.relation.ispartofToxicology and Industrial Health
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAMES
dc.subjectantigenotoxicity
dc.subjectantioxidant enzymes
dc.subjectSCE
dc.subjectUsnea articulata
dc.subjectUsnea filipendula
dc.subjectWP2
dc.subject.classificationPublic, Environmental & Occupational Health
dc.subject.classificationToxicology
dc.subject.otherAflatoxin B1
dc.subject.otherAntimutagenic Agents
dc.subject.otherAntioxidants
dc.subject.otherDNA Damage
dc.subject.otherEscherichia coli
dc.subject.otherGlutathione
dc.subject.otherGlutathione Peroxidase
dc.subject.otherMalondialdehyde
dc.subject.otherMutagens
dc.subject.otherOxidative Stress
dc.subject.otherSalmonella typhimurium
dc.subject.otherSister Chromatid Exchange
dc.subject.otherSuperoxide Dismutase
dc.subject.otherUsnea
dc.subject.otherantimutagenic agent
dc.subject.otherantioxidant
dc.subject.othermalonaldehyde
dc.subject.othermutagenic agent
dc.subject.otheraminoacridine
dc.subject.othermethanol
dc.subject.othermethylnitronitrosoguanidine
dc.subject.otherplant extract
dc.subject.othersodium azide
dc.subject.otherunclassified drug
dc.subject.otherUsnea articulata extract
dc.subject.otherUsnea filipendula extract
dc.subject.otherchemistry
dc.subject.otherdrug effects
dc.subject.othermetabolism
dc.subject.otherSalmonella enterica serovar Typhimurium
dc.subject.otheradult
dc.subject.otherAmes test
dc.subject.otherantigenotoxic activity
dc.subject.otherantioxidant activity
dc.subject.otherArticle
dc.subject.otherconcentration (parameters)
dc.subject.othercontrolled study
dc.subject.otherdrug activity
dc.subject.otherEscherichia coli test
dc.subject.othergenotoxicity
dc.subject.otherhuman
dc.subject.otherhuman cell
dc.subject.otherlipid peroxidation
dc.subject.othermutagen testing
dc.subject.othermutagenicity
dc.subject.othernonhuman
dc.subject.othernormal human
dc.subject.otherprotection
dc.subject.othersolvent extraction
dc.subject.otherspecies
dc.subject.otherUsnea articulata
dc.subject.otherUsnea filipendula
dc.titleGenotoxic and antigenotoxic potentials of two Usnea species
dc.typeArticle
rdl.citation.openalex14
rdl.citation.scopus16
rdl.citation.wos13
rdl.departmentCentral Research and Application Laboratories, Agri Ibrahim Cecen University, Agri, Turkey Department of Biology, Faculty of Science, Ataturk University, Erzurum, Turkey
rdl.departmentEducation Faculty, Bayburt University, Bayburt, Turkey
rdl.departmentDepartment of Biology, Faculty of Science, Fatih University, Istanbul, Turkey
rdl.departmentDepartment of Biology, Faculty of Science, Ataturk University, Erzurum, Turkey
rdl.departmentDepartment of Biology Education, Kazım Karabekir Faculty of Education, Ataturk University, Erzurum, Turkey
rdl.oa.statusgreen
rdl.oa.statuspreprint
rdl.oa.urlhttps://hdl.handle.net/20.500.12501/1025
rdl.scopus.quartileQ2
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)