Punicalagin and Punicalin Suppress the Adipocyte Differentiation Through the Transcription Factors

dc.contributor.author Berkoz, M.
dc.contributor.author Yalin, S.
dc.contributor.author Yildirim, M.
dc.contributor.author Yalin, A. E.
dc.contributor.author Comelekoglu, U.
dc.date.accessioned 2025-05-10T17:10:12Z
dc.date.available 2025-05-10T17:10:12Z
dc.date.issued 2021
dc.description Comelekoglu, Ulku/0000-0001-8060-6333 en_US
dc.description.abstract Background. Pomegranate is a rich source of many polyphenolic compounds including ellagitannins (punicalagin, punicalin and others). Aim. The effects of punicalagin and punicalin on adipogenesis were investigated in this study. Materials and Methods. To examine the effect of punicalagin and punicalin on adipocyte differentiation, various concentrations of punicalagin and punicalin (2-10 mu M) were applied to differentiated 3T3-L1 cells. Glyceraldehyde-3-phosphate dehydrogenase (GPDH) activity, Oil red O staining, intracellular triglyceride levels, and gene expressions of transcription factors (Peroxisome proliferator-activated receptor-gamma (PPAR gamma), CCAAT-enhancer-binding proteins-alpha (C/EBP alpha), Sterol regulatory element-binding protein 1c (SREBP-1c)) and lipolysisassociated genes (hormone-sensitive lipase (HSL), Perilipin A, tumor necrosis factor-alpha (TNF-alpha)) were examined in order to investigate the effects of punicalagin and punicalin on adipocyte differentiation. Results. Punicalagin and punicalin applications caused a continuous decrease in cell size and intracellular triglyceride accumulation. GPDH activity and transcription gene expressions decreased significantly in groups that were applicated punicalagin and punicalin at high concentrations. Punicalagin, but not punicalin, down-regulated the expression of HSL and perilipin A and up-regulated the expression of TNF-alpha in a dose-dependent manner. In conclusion, both punicalagin and punicalin were able to inhibit the adipocyte differentiation. en_US
dc.description.sponsorship Office of Scientific Research Projects of Mersin University [2016-2-TP3-1891] en_US
dc.description.sponsorship This research was financially supported in part by the Office of Scientific Research Projects of Mersin University under Grant number (2016-2-TP3-1891). en_US
dc.identifier.doi 10.4183/aeb.2021.157
dc.identifier.issn 1841-0987
dc.identifier.issn 1843-066X
dc.identifier.scopus 2-s2.0-85125816300
dc.identifier.uri https://doi.org/10.4183/aeb.2021.157
dc.identifier.uri https://hdl.handle.net/20.500.14720/7365
dc.language.iso en en_US
dc.publisher Editura Acad Romane en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject 3T3-L1 en_US
dc.subject Adipogenesis en_US
dc.subject Punicalagin en_US
dc.subject Punicalin en_US
dc.subject Transcription Factors en_US
dc.subject Cell Differentiation en_US
dc.title Punicalagin and Punicalin Suppress the Adipocyte Differentiation Through the Transcription Factors en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Comelekoglu, Ulku/0000-0001-8060-6333
gdc.author.scopusid 12801030200
gdc.author.scopusid 8608387300
gdc.author.scopusid 57193389683
gdc.author.scopusid 56509249400
gdc.author.scopusid 6602143517
gdc.author.wosid Yldrm, Mtn/Jmp-9922-2023
gdc.author.wosid Yalın, Serap/L-7402-2017
gdc.author.wosid Comelekoglu, Ulku/E-2239-2016
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Berkoz, M.] Yuzuncu Yil Univ, Dept Biochem, Van, Turkey; [Yalin, S.; Yalin, A. E.] Mersin Univ, Fac Pharm, Dept Biochem, Mersin, Turkey; [Yildirim, M.] Tarsus Univ, Healthcare Vocat Sch, Pharm Serv Program, Tarsus, Turkey; [Comelekoglu, U.] Mersin Univ, Fac Med, Dept Biophys, Mersin, Turkey en_US
gdc.description.endpage 167 en_US
gdc.description.issue 2 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q4
gdc.description.startpage 157 en_US
gdc.description.volume 17 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q4
gdc.identifier.pmid 34925563
gdc.identifier.wos WOS:000746547000002
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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