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dc.contributor.authorPakdelmoradlou, Mina
dc.contributor.authorYuca, Hafize
dc.contributor.authorOzer, Elif Beyza
dc.contributor.authorAydin, Bilge
dc.contributor.authorAlkuyruk, Satuk Bugra
dc.contributor.authorGulsahin, Yusuf
dc.contributor.authorKaradayi, Mehmet
dc.date.accessioned2025-12-28T16:39:54Z
dc.date.available2025-12-28T16:39:54Z
dc.date.issued2025
dc.identifier.issn0033-183X
dc.identifier.issn1615-6102
dc.identifier.urihttps://doi.org/10.1007/s00709-025-02131-4
dc.identifier.urihttps://hdl.handle.net/20.500.12933/2195
dc.description.abstractOnopordum acanthium L. (Asteraceae), a traditionally used medicinal plant, was investigated for its morphological, phytochemical, and biological properties in this comprehensive study. Methanolic and aqueous extracts were prepared from different parts of the plant (root, stem, leaf, flower, and fruit) and analyzed for their phenolic composition, antioxidant, antidiabetic, anticholinesterase, antimicrobial, and genotoxic activities. LC-MS/MS analysis revealed that chlorogenic acid was most abundant in the flower (3045.38 ng/mL) and root (728.53 ng/mL) aqueous extracts, while quinic acid reached 856.27 ng/mL in the root. Quercetin, apigenin, and luteolin were also detected at significant levels. The fruit methanol extract showed the highest total phenolic (100.78 +/- 0.0015 mu g GAE/mg), flavonoid (603.67 +/- 0.0015 mu g RE/mg), and tannin (186.22 +/- 0.0015 mu g TAE/mg) contents. Antioxidant assays demonstrated notable ABTS center dot(+) (38.38 +/- 0.0042%) and DPPH center dot (28.43 +/- 0.0252%) scavenging capacities in the same extract. Regarding enzyme inhibition, the flower aqueous extract showed the strongest alpha-glucosidase inhibition (45.58%), while the fruit aqueous extract exhibited moderate alpha-amylase inhibition (26.33%). The stem methanol extract displayed the highest acetylcholinesterase inhibition (19.02%), whereas the root aqueous extract showed the highest butyrylcholinesterase inhibition (10.76%). Antimicrobial assays revealed moderate antifungal activity, particularly against Candida tropicalis (MIC = 312.5 mu g/mL), with the flower and fruit methanol extracts being the most effective. Genotoxicity assessment using Ames and Allium tests confirmed biosafety up to 5 mg/plate and 250 mg/L, respectively, except for flower extracts, which showed slight cytogenotoxicity. Overall, this study highlights O. acanthium as a promising natural source of phenolic compounds with therapeutic potential, particularly in managing oxidative stress, diabetes, and neurodegenerative disorders.
dc.description.sponsorshipTUBITAK
dc.description.sponsorshipSatuk Bugra ALKUYRUK thanks graduate program and scholarship supported by TUBITAK.
dc.language.isoen
dc.publisherSpringer Wien
dc.relation.ispartofProtoplasma
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAntidiabetic
dc.subjectAnticholinesterase
dc.subjectAsteraceae
dc.subjectLC-MS/MS
dc.subjectOnopordum acanthium
dc.titlePhytochemical riches and bioactive potential of Onopordum acanthium L. (Asteraceae) from Iran
dc.typeArticle
dc.departmentAfyonkarahisar Sağlık Bilimleri Üniversitesi
dc.identifier.doi10.1007/s00709-025-02131-4
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.department-temp[Pakdelmoradlou, Mina; Yuca, Hafize; Ozer, Elif Beyza] Ataturk Univ, Fac Pharm, Dept Pharmacognosy, Erzurum, Turkiye; [Ozer, Elif Beyza] Ondokuz Mayis Univ, Fac Pharm, Dept Pharmacognosy, Samsun, Turkiye; [Aydin, Bilge] Erzincan Binali Yildirim Univ, Fac Pharm, Dept Pharmacognosy, Erzincan, Turkiye; [Alkuyruk, Satuk Bugra] Ataturk Univ, Fac Pharm, Dept Pharmaceut Microbiol, Erzurum, Turkiye; [Alkuyruk, Satuk Bugra] Ankara Univ, Grad Sch Hlth Sci, Ankara, Turkiye; [Gulsahin, Yusuf; Karadayi, Mehmet] Ataturk Univ, Fac Sci, Dept Biol, Erzurum, Turkiye; [Goger, Gamze] Afyonkarahisar Hlth Sci Univ, Fac Pharm, Dept Pharmacognosy, Afyonkarahisar, Turkiye; [Eksi Bona, Gulnur] Istanbul Univ Cerrahpasa, Fac Pharm, Dept Pharmaceut Bot, Istanbul, Turkiye; [Bona, Mehmet] Istanbul Univ, Fac Sci, Dept Biol, Istanbul, Turkiye; [Karakaya, Songul] Ataturk Univ, Fac Pharm, Dept Pharmaceut Bot, Erzurum, Turkiye
dc.identifier.pmid41193840
dc.identifier.scopus2-s2.0-105021028048
dc.identifier.scopusqualityQ1
dc.identifier.wosWOS:001607971200001
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.snmzKA_WoS_20251227


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