Phytochemical Profile and Biological Activities of the Extracts from Two Oenanthe Species (O. aquatica and O. silaifolia)

MakaleAçık ErişimScopus SJRQ1

Özet

This study presents the evaluation of biological activities and chemical profiling of Oenanthe aquatica (L.) Poir. and Oenanthe silaifolia M. Bieb. The phytochemical profile, antioxidant, enzyme inhibitory, cytotoxic and antiviral activities of the methanolic and aqueous extracts were investigated. The aqueous extract of O. aquatica possessing the highest content of phenolics (60.85 mg gallic acid equivalent/g extract), also exhibited the strongest radical scavenging potential against 2,2-diphenyl-1-picrylhydrazyl and 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (79.46 and 148.66 mg Trolox equivalent/g extract, respectively), the highest reducing ability (207.59 and 107.27 mg Trolox equivalent/g extract, for cupric reducing antioxidant capacity and ferric reducing antioxidant activity, respectively), metal chelating potential (33.91 mg ethylenediaminetetraacetic acid equivalent/g extract) and total antioxidant ability (1.60 mmol Trolox equivalent/g extract). Liquid chromatography-electrospray ionization-quadrupole time-of-flight-mass spectrometry (LC-ESI-QTOF-MS/MS) permitted tentative identification of compounds from simple organic acids, phenolic acids, coumarins, flavonoids and their glycosides in O. aquatica and O. silaifolia extracts. The methanolic extract of O. aquatica substantially depressed acetylcholinesterase (3.67 mg galantamine equivalent/g extract), tyrosinase (126.66 mg kojic acid equivalent/g extract), and α-amylase (0.83 mmol acarbose equivalent/g extract) enzymes. The methanolic extract of O. silaifolia showed highest enzymatic inhibitory property against butyrylcholinesterase, and its aqueous extract depressed α-glucosidase activity (0.26 mmol acarbose equivalent/g extract). All tested extracts exerted selective toxicity towards cancer cell lines, and the highest anticancer potential was found for O. aquatica aqueous extract on FaDu and HeLa cells with CC50 of 57.36 and 47.16 µg/mL, respectively. Significant antiviral activity against HSV-1 (HHV-1) was found for both aqueous extracts in concentrations of 1000 µg/mL, which inhibited the HSV-1 cytopathic effect (CPE) in virus infected VERO cells and reduced the virus infective titer by more than 3 log (logCCID50 /mL). This study has produced critical scientific data on O. aquatica and O. silaifolia, which are potential contenders for the development of novel phyto-pharmaceuticals.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/munzur/2590Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.3390/ph15010050Yayıncı resmi DOI adresi
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Atıflar
Scopus
15
WoS
14
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Tam Kayıt
AlanDeğerDil
dc.contributor.authorŚwiątek, Łukasz
dc.contributor.authorSieniawska, Elwira
dc.contributor.authorMahomoodally, Mohamad Fawzi
dc.contributor.authorSadeer, Nabeelah Bibi
dc.contributor.authorWojtanowski, Krzysztof Kamil
dc.contributor.authorRajtar, Barbara
dc.contributor.authorPolz-Dacewicz, Małgorzata
dc.contributor.authorPaksoy, Mehmet Yavuz
dc.contributor.authorZengin, Gokhan
dc.date.accessioned2026-10-28T14:55:34.704817909Z
dc.date.available2026-10-28T14:55:34.704817909Z
dc.date.issued2022
dc.description.abstractThis study presents the evaluation of biological activities and chemical profiling of Oenanthe aquatica (L.) Poir. and Oenanthe silaifolia M. Bieb. The phytochemical profile, antioxidant, enzyme inhibitory, cytotoxic and antiviral activities of the methanolic and aqueous extracts were investigated. The aqueous extract of O. aquatica possessing the highest content of phenolics (60.85 mg gallic acid equivalent/g extract), also exhibited the strongest radical scavenging potential against 2,2-diphenyl-1-picrylhydrazyl and 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (79.46 and 148.66 mg Trolox equivalent/g extract, respectively), the highest reducing ability (207.59 and 107.27 mg Trolox equivalent/g extract, for cupric reducing antioxidant capacity and ferric reducing antioxidant activity, respectively), metal chelating potential (33.91 mg ethylenediaminetetraacetic acid equivalent/g extract) and total antioxidant ability (1.60 mmol Trolox equivalent/g extract). Liquid chromatography-electrospray ionization-quadrupole time-of-flight-mass spectrometry (LC-ESI-QTOF-MS/MS) permitted tentative identification of compounds from simple organic acids, phenolic acids, coumarins, flavonoids and their glycosides in O. aquatica and O. silaifolia extracts. The methanolic extract of O. aquatica substantially depressed acetylcholinesterase (3.67 mg galantamine equivalent/g extract), tyrosinase (126.66 mg kojic acid equivalent/g extract), and α-amylase (0.83 mmol acarbose equivalent/g extract) enzymes. The methanolic extract of O. silaifolia showed highest enzymatic inhibitory property against butyrylcholinesterase, and its aqueous extract depressed α-glucosidase activity (0.26 mmol acarbose equivalent/g extract). All tested extracts exerted selective toxicity towards cancer cell lines, and the highest anticancer potential was found for O. aquatica aqueous extract on FaDu and HeLa cells with CC50 of 57.36 and 47.16 µg/mL, respectively. Significant antiviral activity against HSV-1 (HHV-1) was found for both aqueous extracts in concentrations of 1000 µg/mL, which inhibited the HSV-1 cytopathic effect (CPE) in virus infected VERO cells and reduced the virus infective titer by more than 3 log (logCCID50 /mL). This study has produced critical scientific data on O. aquatica and O. silaifolia, which are potential contenders for the development of novel phyto-pharmaceuticals.
dc.identifier.articlenumber50
dc.identifier.doi10.3390/ph15010050
dc.identifier.eissn1424-8247
dc.identifier.issn1424-8247
dc.identifier.issue1
dc.identifier.pmcidPMC8779323
dc.identifier.pmid35056107
dc.identifier.scopus2-s2.0-85122144572
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/2590
dc.identifier.volume15
dc.identifier.wosWOS:000757036000001
dc.language.isoen
dc.publisherMDPI
dc.relation.ispartofPharmaceuticals
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAnticancer properties
dc.subjectAntiherpetic drugs
dc.subjectEnzyme inhibition
dc.subjectOenanthe
dc.subjectOxidative stress
dc.subject.classificationChemistry, Medicinal
dc.subject.classificationPharmacology & Pharmacy
dc.subject.other1,1 diphenyl 2 picrylhydrazyl
dc.subject.other2 isopropylmalic acid
dc.subject.other2,2' azinobis(3 ethylbenzothiazoline 6 sulfonic acid)
dc.subject.otheracarbose
dc.subject.otheracetylcholinesterase
dc.subject.otheraciclovir
dc.subject.otheramylase
dc.subject.othercaffeic acid derivative
dc.subject.othercarboxylic acid
dc.subject.othercholinesterase
dc.subject.othercitric acid
dc.subject.othercoumarin derivative
dc.subject.othercupric ion
dc.subject.otherdihydroxybenzoic acid
dc.subject.otheredetic acid
dc.subject.otherferric ion
dc.subject.otherflavonoid
dc.subject.othergalantamine
dc.subject.otherglycoside
dc.subject.otherhydroxybenzoic acid
dc.subject.otherhydroxybenzoic acid glucoside
dc.subject.otherkojic acid
dc.subject.othermalic acid
dc.subject.othermetal chelate
dc.subject.othermethanol
dc.subject.othermonophenol monooxygenase
dc.subject.otherneochlorogenic acid
dc.subject.otherOenanthe aquatica extract
dc.subject.otherOenanthe silaifolia extract
dc.subject.otherphenol
dc.subject.otherphenolic acid
dc.subject.otherplant extract
dc.subject.otherplant medicinal product
dc.subject.otherscavenger
dc.subject.othertrolox C
dc.subject.otherunclassified drug
dc.subject.othervanilmandelic acid
dc.subject.otheranimal cell
dc.subject.otherantineoplastic activity
dc.subject.otherantioxidant activity
dc.subject.otherantiviral activity
dc.subject.otheraqueous solution
dc.subject.otherArticle
dc.subject.otherCC50 (cytotoxic concentration)
dc.subject.otherchemical composition
dc.subject.otherconcentration response
dc.subject.othercontrolled study
dc.subject.othercytopathogenic effect
dc.subject.otherdrug cytotoxicity
dc.subject.otherdrug determination
dc.subject.otherdrug isolation
dc.subject.otherelectrospray
dc.subject.otherenzyme inhibition
dc.subject.otherFaDu cell line
dc.subject.otherHeLa cell line
dc.subject.otherhuman
dc.subject.otherHuman alphaherpesvirus 1
dc.subject.otherhuman cell
dc.subject.otherliquid chromatography
dc.subject.othernonhuman
dc.subject.otherOenanthe
dc.subject.otherOenanthe aquatica
dc.subject.otherOenanthe silaifolia
dc.subject.otherphytochemistry
dc.subject.otherquadrupole mass spectrometry
dc.subject.othertandem mass spectrometry
dc.subject.otherVero cell line
dc.subject.othervirus infection
dc.subject.othervirus load
dc.titlePhytochemical Profile and Biological Activities of the Extracts from Two Oenanthe Species (O. aquatica and O. silaifolia)
dc.typeArticle
rdl.citation.scopus15
rdl.citation.wos14
rdl.departmentDepartment of Virology with SARS Laboratory, Medical University of Lublin, Chodzki 1, 20-093 Lublin, Poland
rdl.departmentDepartment of Natural Products Chemistry, Medical University of Lublin, Chodzki 1, 20-093 Lublin, Poland
rdl.departmentDepartment of Health Sciences, Faculty of Medicine and Health Sciences, University of Mauritius, Réduit 80837, Mauritius
rdl.departmentDepartment of Pharmacognosy with Medicinal Plants Garden, Medical University of Lublin, Chodzki 1, 20-093 Lublin, Poland
rdl.departmentMedical Documentation and Secretaryship Programme, Department of Medical Services and Techniques, Tunceli Vocational School, Munzur University, Tunceli 62000, Turkey
rdl.departmentDepartment of Biology, Science Faculty, Selcuk University, Konya 42130, Turkey
rdl.oa.statusgold
rdl.oa.statusgreen
rdl.oa.urlhttps://www.mdpi.com/1424-8247/15/1/50/pdf?version=1640943115
rdl.scopus.quartileQ1
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)