Exploring Chemical Composition, Antioxidant, Enzyme Inhibitory and Cytotoxic Properties of Glaucium acutidentatum Hausskn. & Bornm. from Turkey Flora: A Novel Source of Bioactive Agents to Design Functional Applications

dc.contributor.authorYagi, Sakina
dc.contributor.authorZengin, Gokhan
dc.contributor.authorUba, Abdullahi Ibrahim
dc.contributor.authorMaciejewska-Turska, Magdalena
dc.contributor.authorSieniawska, Elwira
dc.contributor.authorSwiatek, Lukasz
dc.contributor.authorPolz-Dacewicz, Malgorzata
dc.date.accessioned2026-08-12T18:10:44Z
dc.date.issued2024
dc.departmentFırat Üniversitesi
dc.description.abstractThe present study was performed to determine the chemical constituents, cytotoxicity, antioxidant and enzyme inhibition activities of the aerial parts of Glaucium acutidentatum Hausskn. and Bornm. (family Papaveraceae). Methanolic and aqueous extracts were prepared by maceration, homogenizer-assisted extraction (HAE) and infusion. Results showed that the highest total phenolic and flavonoids contents were obtained from the methanol extracts obtained by HAE (53.22 +/- 0.10 mg GAE/g) and maceration (30.28 +/- 0.51 mg RE/g), respectively. The aporphine, beznyltetrahydroisoquinoline, and protopine types of Glaucium alkaloids have been tentatively identified. Among them, glaucine was identified in all extracts. Flavonoids, phenolic acids, coumarins, organic acids and fatty acids were also detected. Methanolic extract obtained using the HAE method displayed the highest anti-DPPH (41.42 +/- 0.62 mg TE/g), total antioxidant (1.20 +/- 0.17 mmol TE/g), Cu2+ (113.55 +/- 6.44 mg TE/g), and Fe3+ (74.52 +/- 4.74 mg TE/g) reducing properties. The aqueous extracts obtained by infusion and HAE methods exerted the best anti-ABTS (103.59 +/- 1.49 mg TE/g) and chelating (19.81 +/- 0.05 mg EDTAE/g) activities, respectively. Methanolic extract from HAE recorded the highest acetylcholinesterase (2.55 +/- 0.10 mg GALAE/g) and alpha-amylase (0.51 +/- 0.02 mmol ACAE/g) inhibition activities, while that obtained by maceration showed the best butyrylcholinesterase (3.76 +/- 0.31 mg GALAE/g) inhibition activity. Both extracts revealed the best tyrosinase inhibitory activity (25.15 +/- 1.00 and 26.79 +/- 2.36 mg KAE/g, p >= 0.05). G. acutidentatum maceration-derived aqueous extract showed selective anticancer activity against cells originating from human hypopharyngeal carcinoma. In conclusion, these findings indicated that G. acutidentatum is a promising source of alkaloids and phenolic compounds for variable pharmaceutical formulations.
dc.description.sponsorshipMedical University of Lublin (Polish Ministry of Science) [DS 28]
dc.description.sponsorshipThe research was supported by grant DS 28 from the Medical University of Lublin (Polish Ministry of Science).
dc.identifier.doi10.3390/antiox13060643
dc.identifier.issn2076-3921
dc.identifier.issue6
dc.identifier.orcid0000-0003-4773-0329
dc.identifier.orcid0000-0002-3222-184X
dc.identifier.orcid0000-0003-4113-9079
dc.identifier.orcid0000-0002-0853-108X
dc.identifier.orcid0000-0001-8225-1505
dc.identifier.orcid0000-0003-1626-680X
dc.identifier.orcid0000-0002-8857-8688
dc.identifier.pmid38929082
dc.identifier.scopus2-s2.0-85197653213
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.3390/antiox13060643
dc.identifier.urihttps://hdl.handle.net/11508/63411
dc.identifier.volume13
dc.identifier.wosWOS:001255028200001
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherMdpi
dc.relation.ispartofAntioxidants
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectGlaucium acutidentatum
dc.subjectalkaloids
dc.subjectphenols
dc.subjectantioxidant
dc.subjectenzyme inhibition
dc.subjectcytotoxicity
dc.titleExploring Chemical Composition, Antioxidant, Enzyme Inhibitory and Cytotoxic Properties of Glaucium acutidentatum Hausskn. & Bornm. from Turkey Flora: A Novel Source of Bioactive Agents to Design Functional Applications
dc.typeArticle

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