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

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Özet

The 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 α-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.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/munzur/2037Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.3390/antiox13060643Yayıncı resmi DOI adresi
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Scopus
13
OpenAlex
13
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Tam Kayıt
AlanDeğerDil
dc.contributor.authorYagi, Sakina
dc.contributor.authorZengin, Gokhan
dc.contributor.authorUba, Abdullahi Ibrahim
dc.contributor.authorMaciejewska-Turska, Magdalena
dc.contributor.authorSieniawska, Elwira
dc.contributor.authorŚwiątek, Łukasz
dc.contributor.authorRajtar, Barbara
dc.contributor.authorBahşi, Muammer
dc.contributor.authorGuler, Osman
dc.contributor.authorDall’Acqua, Stefano
dc.contributor.authorPolz-Dacewicz, Małgorzata
dc.date.accessioned2026-10-28T14:54:51.721827130Z
dc.date.available2026-10-28T14:54:51.721827130Z
dc.date.issued2024
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 α-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.sponsorshipUniwersytet Medyczny w Lublinie, UML
dc.description.sponsorshipMinisterstwo Edukacji i Nauki, MNiSW
dc.identifier.articlenumber643
dc.identifier.doi10.3390/antiox13060643
dc.identifier.eissn2076-3921
dc.identifier.issn2076-3921
dc.identifier.issue6
dc.identifier.pmcidPMC11200578
dc.identifier.pmid38929082
dc.identifier.scopus2-s2.0-85197653213
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/2037
dc.identifier.volume13
dc.identifier.wosWOS:001255028200001
dc.language.isoen
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.relation.ispartofAntioxidants
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectalkaloids
dc.subjectantioxidant
dc.subjectcytotoxicity
dc.subjectenzyme inhibition
dc.subjectGlaucium acutidentatum
dc.subjectphenols
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
rdl.citation.openalex13
rdl.citation.scopus13
rdl.departmentDepartment of Botany, Faculty of Science, University of Khartoum, Khartoum 11115, Sudan
rdl.departmentLAE, INRAE, Université de Lorraine, F-54000 Nancy, France
rdl.departmentPhysiology and Biochemistry Laboratory, Department of Biology, Science Faculty, Selcuk University, Konya 42130, Turkey
rdl.departmentDepartment of Molecular Biology and Genetics, Istanbul AREL University, Istanbul 34537, Turkey
rdl.departmentDepartment of Pharmacognosy with Medicinal Plant Garden, Medical University of Lublin, 20-093 Lublin, Poland
rdl.departmentDepartment of Natural Products Chemistry, Medical University of Lublin, 20-093 Lublin, Poland
rdl.departmentDepartment of Virology with Viral Diagnostics Laboratory, Medical University of Lublin, 20-093 Lublin, Poland
rdl.departmentDepartment of Primary Education, Faculty of Education, Fırat University, Elazıg 23119, Turkey
rdl.departmentPertek Sakine Genç Vocational School, Munzur University, Tunceli 62500, Turkey
rdl.departmentDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, 35131 Padua, Italy
rdl.oa.statusgold
rdl.oa.statusclosed
rdl.oa.statusgreen
rdl.oa.urlhttps://www.mdpi.com/2076-3921/13/6/643/pdf?version=1716622539
rdl.scopus.quartileQ1
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED