Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/51290
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dc.contributor.authorMiloğlu, F.D.-
dc.contributor.authorAkpınar, A.-
dc.contributor.authorGüven, L.-
dc.contributor.authorDemirkaya, A.K.-
dc.contributor.authorGündoğdu, Gülşah-
dc.contributor.authorNalcı, K.A.-
dc.contributor.authorHacımuftuoğlu, A.-
dc.date.accessioned2023-06-13T19:15:41Z-
dc.date.available2023-06-13T19:15:41Z-
dc.date.issued2023-
dc.identifier.issn1534-7346-
dc.identifier.urihttps://doi.org/10.1177/15347346211016693-
dc.identifier.urihttps://hdl.handle.net/11499/51290-
dc.description.abstractWound is tissue damage that occurs in the skin. Helichrysum species (Altınotu) are rich in phenolic compounds used in traditional medicine for wound healing. The main component in their flower head (capitulum) is phenolic compounds. The present study investigates the proliferative, oxidative stress, and wound healing properties of the methanolic extract of Helichrysum plicatum subsp. pseudoplicatum capitulum on a human dermal fibroblast (HDF) cell line in this study. H plicatum subsp. pseudoplicatum capitulums were collected in Erzurum, Turkey (altitude 1950 m), dried, pulverized, and extracted with methanol. Firstly, total phenolic contents were determined and secondly, the proliferative effect, oxidative stress activities, and wound healing effects on HDF cells were evaluated by the cell proliferation kit (XTT) test, total antioxidant status (TAS), and total oxidant status (TOS) commercial kits, and the scratch experiment by taking microscopic images of the cells at 0, 12, 18, and 24 h, respectively. Total phenolic content was found to be 142.00 ± 0.73 mg gallic acid equivalent per gram (GAE/g) extract. The capitulum extract has a proliferative effect at 0.5 to 10 µg/mL concentrations according to the XTT test results. It was observed that TAS levels significantly increased in the plant extract at the concentration ranges 1 to 10 µg/mL (P <.01). About 1 to 5 µg/mL plant extract started to increase cell migration at the 12 h and significantly closed the wound area at the 24 h. At the doses between 1 to 5 μg/mL, it has the most substantial effect on both cell viability and antioxidant effect, and wound healing was found to be in this concentration range. These findings suggested that the H plicatum subsp. pseudoplicatum capitulum is a valuable source of phenolic content with important antioxidant activity at wound healing and it was concluded that the capitulum extract accelerates wound healing by increasing cell migration in low doses. © The Author(s) 2021.en_US
dc.language.isoenen_US
dc.publisherSAGE Publications Inc.en_US
dc.relation.ispartofInternational Journal of Lower Extremity Woundsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectcell cultureen_US
dc.subjectH plicatum subsp. pseudoplicatumen_US
dc.subjecthuman dermal fibroblast cellen_US
dc.subjectwound healingen_US
dc.subjectdermatological agenten_US
dc.subjectHelichrysum plicatum Subsp.pseudoplicatum extracten_US
dc.subjectplant extracten_US
dc.subjectunclassified drugen_US
dc.subjectantioxidanten_US
dc.subjectmethanolen_US
dc.subjectplant extracten_US
dc.subjectantioxidant activityen_US
dc.subjectArticleen_US
dc.subjectcell migrationen_US
dc.subjectcell proliferationen_US
dc.subjectcell viabilityen_US
dc.subjectcolorimetryen_US
dc.subjectcontrolled studyen_US
dc.subjectfluorescence microscopyen_US
dc.subjectHelichrysumen_US
dc.subjecthumanen_US
dc.subjecthuman cellen_US
dc.subjectin vitro studyen_US
dc.subjectoxidative stressen_US
dc.subjectskin fibroblasten_US
dc.subjectskin injuryen_US
dc.subjectspectrophotometryen_US
dc.subjectwound healingen_US
dc.subjectwound healing assayen_US
dc.subjectXTT assayen_US
dc.subjectfibroblasten_US
dc.subjectmetabolismen_US
dc.subjectAntioxidantsen_US
dc.subjectFibroblastsen_US
dc.subjectHelichrysumen_US
dc.subjectHumansen_US
dc.subjectMethanolen_US
dc.subjectPlant Extractsen_US
dc.subjectWound Healingen_US
dc.titleEvaluation the Effects of Helichrysum plicatum Subsp. pseudoplicatum on an In-Vitro Wound Model Using Human Dermal Fibroblast Cellsen_US
dc.typeArticleen_US
dc.identifier.volume22en_US
dc.identifier.issue2en_US
dc.identifier.startpage401en_US
dc.identifier.endpage408en_US
dc.departmentPamukkale Universityen_US
dc.identifier.doi10.1177/15347346211016693-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid55695677700-
dc.authorscopusid57223632988-
dc.authorscopusid56780361300-
dc.authorscopusid57204791685-
dc.authorscopusid55320972800-
dc.authorscopusid57201260597-
dc.authorscopusid6602395368-
dc.identifier.pmid33989073en_US
dc.identifier.scopus2-s2.0-85105949717en_US
dc.institutionauthor-
dc.identifier.scopusqualityQ3-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.03. Basic Medical Sciences-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
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