Exploration of UHPLC-ESI-QTOF-MS Profiles and the Neuroprotective, Antidiabetic, Antioxidant and Cytotoxic Effects of Extracts from Achillea maritima (L.) Ehrend. & Y.P.Guo (Asteraceae) Collected in Türkiye

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Özet

The current study investigated the chemical composition, antioxidant activity, enzyme inhibition, and cytotoxic activities of extracts from Achillea maritima, a wild medicinal plant used for various therapeutic purposes. The antioxidant activities were assayed through different assays like DPPH, ABTS, CUPRAC, FRAP, and phosphomolybdenum, whereas in enzyme inhibition studies, cholinesterase, tyrosinase, α-amylase, and α-glucosidase were assayed. Cytotoxicity studies are conducted on S17, RAW, and HepG2 to assess its selectivity and effectiveness. Chemical profiling by UHPLC-ESI-QTOF-MS revealed multiple bioactive compounds in the extracts. Polar solvents (ethanol, ethanol/water, and water) resulted in high concentrations of phenolic acids as well as chlorogenic and caffeoylquinic acids, as well as flavonoids like vicenin and apigenin. On the other, the nonpolar (hexane extract) was rich in octadecatrienoic acid hydroperoxy and hydroxyoctadecatrienic acid. Among these, the water extract contained the highest phenolic content of 32.26 mg GAE/g, while the ethyl acetate extract was the richest in flavonoids, with 7.83 mg RE/g. In the antioxidant studies, the water and ethanol/water extracts consistently display the most potent activities, thus indicating their significant free radical scavenging and metal chelation abilities. The studies on enzyme inhibitions showed remarkable BChE inhibitory activities of the ethanol extract in 12.50 mg GALAE/g, thus showing potential in managing disease conditions related to cholinesterase. Tyrosinase inhibition was significant by the ethanol extract, presenting 55.59 mg KAE/g. The ethyl acetate extract exhibited the most potent inhibitory activity against α-amylase with 0.66 mmol ACAE/g, while ethanol extract showed significant inhibition of α-glucosidase with 4.35 ACAE/g. Cytotoxicity results showed that the water extract was most effective against the HepG2 cancer cell line by reducing cell viability to 38.4% at high doses while preserving low toxicity against normal cells, as observed by high viability percentages in S17 and RAW cell lines. These results highlight the usefulness of A. maritima extracts in nutraceutical, pharmaceutical, and cosmeceutical applications.

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https://rdlopen.rawdatalibrary.net/r/munzur/1055Resmi atıflarda kullanılan kalıcı adres
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https://doi.org/10.1007/s11130-025-01314-xYayıncı resmi DOI adresi
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AlanDeğerDil
dc.contributor.authorAhmed, Shakeel
dc.contributor.authorZengin, Gokhan
dc.contributor.authorFernández-Ochoa, Álvaro
dc.contributor.authorde la Luz Cádiz-Gurrea, Maria
dc.contributor.authorLeyva-Jiménez, Francisco Javier
dc.contributor.authorElkiran, Omer
dc.contributor.authorCakilcioglu, Ugur
dc.contributor.authorAkgul, Bengusu H.
dc.contributor.authorPereira, Catarina G.
dc.contributor.authorCustódio, Luísa
dc.date.accessioned2026-10-28T14:53:51.757886885Z
dc.date.available2026-10-28T14:53:51.757886885Z
dc.date.issued2025
dc.description.abstractThe current study investigated the chemical composition, antioxidant activity, enzyme inhibition, and cytotoxic activities of extracts from Achillea maritima, a wild medicinal plant used for various therapeutic purposes. The antioxidant activities were assayed through different assays like DPPH, ABTS, CUPRAC, FRAP, and phosphomolybdenum, whereas in enzyme inhibition studies, cholinesterase, tyrosinase, α-amylase, and α-glucosidase were assayed. Cytotoxicity studies are conducted on S17, RAW, and HepG2 to assess its selectivity and effectiveness. Chemical profiling by UHPLC-ESI-QTOF-MS revealed multiple bioactive compounds in the extracts. Polar solvents (ethanol, ethanol/water, and water) resulted in high concentrations of phenolic acids as well as chlorogenic and caffeoylquinic acids, as well as flavonoids like vicenin and apigenin. On the other, the nonpolar (hexane extract) was rich in octadecatrienoic acid hydroperoxy and hydroxyoctadecatrienic acid. Among these, the water extract contained the highest phenolic content of 32.26 mg GAE/g, while the ethyl acetate extract was the richest in flavonoids, with 7.83 mg RE/g. In the antioxidant studies, the water and ethanol/water extracts consistently display the most potent activities, thus indicating their significant free radical scavenging and metal chelation abilities. The studies on enzyme inhibitions showed remarkable BChE inhibitory activities of the ethanol extract in 12.50 mg GALAE/g, thus showing potential in managing disease conditions related to cholinesterase. Tyrosinase inhibition was significant by the ethanol extract, presenting 55.59 mg KAE/g. The ethyl acetate extract exhibited the most potent inhibitory activity against α-amylase with 0.66 mmol ACAE/g, while ethanol extract showed significant inhibition of α-glucosidase with 4.35 ACAE/g. Cytotoxicity results showed that the water extract was most effective against the HepG2 cancer cell line by reducing cell viability to 38.4% at high doses while preserving low toxicity against normal cells, as observed by high viability percentages in S17 and RAW cell lines. These results highlight the usefulness of A. maritima extracts in nutraceutical, pharmaceutical, and cosmeceutical applications.
dc.description.sponsorshipTürkiye Bilimsel ve Teknolojik Araştırma Kurumu, TÜBİTAK
dc.identifier.articlenumber66
dc.identifier.doi10.1007/s11130-025-01314-x
dc.identifier.eissn1573-9104
dc.identifier.issn0921-9668
dc.identifier.issue1
dc.identifier.pmcidPMC11825534
dc.identifier.pmid39945994
dc.identifier.scopus2-s2.0-85218483489
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/1055
dc.identifier.volume80
dc.identifier.wosWOS:001448763100002
dc.language.isoen
dc.publisherSpringer
dc.relation.ispartofPlant Foods for Human Nutrition
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectA. maritima
dc.subjectAntioxidant
dc.subjectChemical profiling
dc.subjectCytotoxicity
dc.subjectEnzyme inhibition
dc.subject.otherAchillea
dc.subject.otheralpha-Amylases
dc.subject.otherAnimals
dc.subject.otherAntioxidants
dc.subject.otherChromatography, High Pressure Liquid
dc.subject.otherFlavonoids
dc.subject.otherHep G2 Cells
dc.subject.otherHumans
dc.subject.otherHypoglycemic Agents
dc.subject.otherMonophenol Monooxygenase
dc.subject.otherNeuroprotective Agents
dc.subject.otherPlant Extracts
dc.subject.otherSpectrometry, Mass, Electrospray Ionization
dc.subject.otheramylase
dc.subject.otherantidiabetic agent
dc.subject.otherantioxidant
dc.subject.otherflavonoid
dc.subject.otherneuroprotective agent
dc.subject.otherplant extract
dc.subject.otheranimal
dc.subject.otherchemistry
dc.subject.otherelectrospray mass spectrometry
dc.subject.otherHep-G2 cell line
dc.subject.otherhigh performance liquid chromatography
dc.subject.otherhuman
dc.titleExploration of UHPLC-ESI-QTOF-MS Profiles and the Neuroprotective, Antidiabetic, Antioxidant and Cytotoxic Effects of Extracts from Achillea maritima (L.) Ehrend. & Y.P.Guo (Asteraceae) Collected in Türkiye
dc.typeArticle
rdl.citation.scopus15
rdl.departmentDepartment of Biology, Science Faculty, Selcuk University, Konya, 42130, Turkey
rdl.departmentDepartment of Analytical Chemistry, Faculty of Sciences, University of Granada, Fuentenueva s/n, Granada, E- 18071, Spain
rdl.departmentREQUIMTE/LAQV, Polytechnic of Porto- School of Engineering, Rua Dr. António Bernardino de Almeida, Porto, 4249-015, Portugal
rdl.departmentDepartment of Environmental Health, Vocational School of Health Services, Sinop University, Sinop, Turkey
rdl.departmentPertek Sakine Genç Vocational School, Munzur University, Pertek, 62500, Turkey
rdl.departmentCentre of Marine Sciences (CCMAR/CIMAR LA), Faculty of Sciences and Technology, University of Algarve, Ed. 7, Campus of Gambelas, Faro, 8005-139, Portugal
rdl.oa.statushybrid
rdl.oa.statusclosed
rdl.oa.statusgreen
rdl.oa.urlhttps://link.springer.com/content/pdf/10.1007/s11130-025-01314-x.pdf
rdl.scopus.quartileQ2
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED