In Vitro Evaluation of Thymoquinone and Lycopene Supplementation on Oxidative Dna Damage and Oxidant Status in High Glucose Conditions

dc.contributor.author Dede, Semiha
dc.contributor.author Yur, Fatmagul
dc.contributor.author Taspinar, Mehmet
dc.contributor.author Cetin, Sedat
dc.contributor.author Usta, Ayse
dc.contributor.author Yuksek, Veysel
dc.date.accessioned 2025-05-10T16:57:10Z
dc.date.available 2025-05-10T16:57:10Z
dc.date.issued 2019
dc.description.abstract The present study was planned to investigate the effects of thymoquinone (TQ) and lycopene (LYC), known to possess pro-inflammatory and antioxidant properties, on oxidative DNA damage (8-hydroxy-2-cleoxyguanosine) in BHK-21 cell line treated with high glucose (FIG) and the antioxidant system. BHK-21 cell line was cultured with regular passages (5% FBS, 10% host serum, 1% L-glutamine, 1% penicillin/streptomycin - RPMI 1640, 5% CO2 and 95%, 37 degrees C incubation). MTT cell viability tests were conducted. Proliferative TQ and LYC and glucose IC50 values were determined. Control, study groups; glucose (285 mM), TQ (10 mu M), and LYC (50 mu M)) and cross groups were designed. After incubation, trypsinized cells were broken by the freeze/thaw method and analyzed. Oxidative DNA damage, TAS, TOS and OSI values were determined for the obtained samples. It was determined that 8-OHdG levels were affected by high glucose (p <= 0.05), they increased further with the administration of TQ and LYC in addition to HG. TOS and OSI values increased in all study groups when compared to the control (p <= 0.05), and TAS levels significantly decreased (p <= 0.05) with the administration of HG when compared to TQ and LYC groups. In conclusion, TQ and LYC administration in addition to high glucose exacerbated oxidative DNA damage and OSI, and decreased TAS when compared to TQ and LYC groups. The TQ and LYC dose and administration duration in addition to high glucose in the present study led to an improvement in oxidative balance in the BHK cell line. en_US
dc.description.sponsorship YuzuncuYil University Scientific Research Projects Coordination Department [2013-VF-B063] en_US
dc.description.sponsorship The present study was sponsored by the YuzuncuYil University Scientific Research Projects Coordination Department with Project no: 2013-VF-B063. en_US
dc.identifier.issn 0326-2383
dc.identifier.scopus 2-s2.0-85060953143
dc.identifier.uri https://hdl.handle.net/20.500.14720/3952
dc.language.iso en en_US
dc.publisher Colegio Farmaceuticos Provincia de Buenos Aires en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject High Glucose en_US
dc.subject In Vitro en_US
dc.subject Lycopene en_US
dc.subject Oxidative Dna Damage en_US
dc.subject Oxidative Status en_US
dc.subject Thymoquinone en_US
dc.title In Vitro Evaluation of Thymoquinone and Lycopene Supplementation on Oxidative Dna Damage and Oxidant Status in High Glucose Conditions en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.scopusid 6603709171
gdc.author.scopusid 6603102677
gdc.author.scopusid 22235844100
gdc.author.scopusid 23969941600
gdc.author.scopusid 57196420522
gdc.author.scopusid 55736672600
gdc.author.wosid Usta, Ayşe/Aai-7545-2021
gdc.author.wosid Dede, Semiha/H-5403-2013
gdc.author.wosid Taşpinar, Mehmet/Lig-3987-2024
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Dede, Semiha; Cetin, Sedat] Van YuzuncuYil Univ, Fac Vet Med, Biochem Dept, Van, Turkey; [Yur, Fatmagul] MuglaSalaKocman Univ, Fac Hlth Sci, Mugla, Turkey; [Taspinar, Mehmet] Van YuzuncuYil Univ, Fac Med, Med Biol Dept, Van, Turkey; [Usta, Ayse] Van YuzuncuYil Univ, Fac Sci, Chem Dept, Van, Turkey; [Yuksek, Veysel] Van YuzuncuYil Univ, Ozalp Vocat High Sch, Van, Turkey en_US
gdc.description.endpage 212 en_US
gdc.description.issue 1 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q4
gdc.description.startpage 209 en_US
gdc.description.volume 38 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q4
gdc.identifier.wos WOS:000458733500032
gdc.index.type WoS
gdc.index.type Scopus

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