Chemical Characterization of Different Extracts from Artemisia annua and Their Antioxidant, Enzyme Inhibitory and Anti-Inflammatory Properties

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Özet

Artemisia annua L. (Asteraceae Family) is an important plant in Asia that has been used for treating different diseases, including fever due to malaria, wounds, tubercolisis, scabues, pain, convulsions, diabetes, and inflammation. In this study we aimed to evaluate the effects of different polarity extracts (hexane, dichloromethane, ethyl acetate, ethanol, ethanol/water (70 %) and water) from A. annua against the burden of inflammation and oxidative stress occurring in colon tissue exposed to LPS. In parallel, chemical composition, antiradical, and enzyme inhibition effects against α-amylase, α-glucosidase, tyrosinase, and cholinesterases were evaluated. The water extract contained the highest content of the total phenolic with 34.59 mg gallic acid equivalent (GAE)/g extract, while the hexane had the highest content of the total flavonoid (20.06 mg rutin equivalent (RE)/g extract). In antioxidant assays, the polar extracts (ethanol, ethanol/water and water) exhibited stronger radical scavenging and reducing power abilities when compared to non-polar extracts. The hexane extract showed the best AChE, tyrosinase and glucosidase inhibitory effects. All extracts revealed effective anti-inflammatory agents, as demonstrated by the blunting effects on COX-2 and TNFα gene expression. These effects seemed to be not related to the only phenolic content. However, it is worthy of interest to highlight how the higher potency against LPS-induced gene expression was shown by the water extract; thus suggesting a potential phytotherapy application in the management of clinical symptoms related to inflammatory colon diseases, although future in vivo studies are needed to confirm such in vitro and ex vivo observations.

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https://rdlopen.rawdatalibrary.net/r/munzur/2233Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1002/cbdv.202300547Yayıncı resmi DOI adresi
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AlanDeğerDil
dc.contributor.authorAcquaviva, Alessandra
dc.contributor.authorNilofar
dc.contributor.authorBouyahya, Abdelhakim
dc.contributor.authorZengin, Gokhan
dc.contributor.authorDi Simone, Simonetta Cristina
dc.contributor.authorRecinella, Lucia
dc.contributor.authorLeone, Sheila
dc.contributor.authorBrunetti, Luigi
dc.contributor.authorUba, Abdullahi Ibrahim
dc.contributor.authorCakilcioğlu, Ugur
dc.contributor.authorPolat, Rıdvan
dc.contributor.authorDarendelioglu, Ekrem
dc.contributor.authorMenghini, Luigi
dc.contributor.authorFerrante, Claudio
dc.contributor.authorLibero, Maria Loreta
dc.contributor.authorOrlando, Giustino
dc.contributor.authorChiavaroli, Annalisa
dc.date.accessioned2026-10-28T14:55:07.424663743Z
dc.date.available2026-10-28T14:55:07.424663743Z
dc.date.issued2023
dc.description.abstractArtemisia annua L. (Asteraceae Family) is an important plant in Asia that has been used for treating different diseases, including fever due to malaria, wounds, tubercolisis, scabues, pain, convulsions, diabetes, and inflammation. In this study we aimed to evaluate the effects of different polarity extracts (hexane, dichloromethane, ethyl acetate, ethanol, ethanol/water (70 %) and water) from A. annua against the burden of inflammation and oxidative stress occurring in colon tissue exposed to LPS. In parallel, chemical composition, antiradical, and enzyme inhibition effects against α-amylase, α-glucosidase, tyrosinase, and cholinesterases were evaluated. The water extract contained the highest content of the total phenolic with 34.59 mg gallic acid equivalent (GAE)/g extract, while the hexane had the highest content of the total flavonoid (20.06 mg rutin equivalent (RE)/g extract). In antioxidant assays, the polar extracts (ethanol, ethanol/water and water) exhibited stronger radical scavenging and reducing power abilities when compared to non-polar extracts. The hexane extract showed the best AChE, tyrosinase and glucosidase inhibitory effects. All extracts revealed effective anti-inflammatory agents, as demonstrated by the blunting effects on COX-2 and TNFα gene expression. These effects seemed to be not related to the only phenolic content. However, it is worthy of interest to highlight how the higher potency against LPS-induced gene expression was shown by the water extract; thus suggesting a potential phytotherapy application in the management of clinical symptoms related to inflammatory colon diseases, although future in vivo studies are needed to confirm such in vitro and ex vivo observations.
dc.identifier.articlenumbere202300547
dc.identifier.doi10.1002/cbdv.202300547
dc.identifier.eissn1612-1880
dc.identifier.issn1612-1872
dc.identifier.issue8
dc.identifier.pmid37306942
dc.identifier.scopus2-s2.0-85165011265
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/2233
dc.identifier.volume20
dc.identifier.wosWOS:001031770700001
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofChemistry and Biodiversity
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectanti-inflammatory effects
dc.subjectantioxidant effects
dc.subjectArtemisia annua
dc.subjectenzyme inhibition
dc.subjectspecialized metabolites
dc.subject.otherAnti-Inflammatory Agents
dc.subject.otherAntioxidants
dc.subject.otherArtemisia annua
dc.subject.otherEthanol
dc.subject.otherHexanes
dc.subject.otherInflammation
dc.subject.otherLipopolysaccharides
dc.subject.otherMonophenol Monooxygenase
dc.subject.otherPhenols
dc.subject.otherPlant Extracts
dc.subject.otherWater
dc.subject.otheralpha glucosidase
dc.subject.otheramylase
dc.subject.otherArtemisia annua extract
dc.subject.otherartemisin
dc.subject.othercholinesterase
dc.subject.othercyclooxygenase 2
dc.subject.otherepicatechin
dc.subject.otherflavone
dc.subject.otherflavonoid
dc.subject.otherhesperetin
dc.subject.otherinterleukin 6
dc.subject.otherinterleukin 8
dc.subject.othernaringenin
dc.subject.otherquercetin
dc.subject.otherthymol
dc.subject.othertumor necrosis factor
dc.subject.otheralcohol
dc.subject.otherantiinflammatory agent
dc.subject.otherantioxidant
dc.subject.otherhexane
dc.subject.otherlipopolysaccharide
dc.subject.othern-hexane
dc.subject.otherphenol derivative
dc.subject.otherplant extract
dc.subject.otheranimal experiment
dc.subject.otheranimal model
dc.subject.otheranimal tissue
dc.subject.otherantidiabetic activity
dc.subject.otherantiinflammatory activity
dc.subject.otherantioxidant activity
dc.subject.otherantioxidant assay
dc.subject.otherArticle
dc.subject.otherchemical composition
dc.subject.othercolitis
dc.subject.othercolon tissue
dc.subject.othercolorimetry
dc.subject.othercontrolled study
dc.subject.othercrystal structure
dc.subject.otherdisease burden
dc.subject.otherenzyme inhibition
dc.subject.othergene expression
dc.subject.otherhuman
dc.subject.otherin vitro study
dc.subject.otherin vivo study
dc.subject.othermolecular docking
dc.subject.othermouse
dc.subject.othernonhuman
dc.subject.otheroxidative stress
dc.subject.otherphytotherapy
dc.subject.otherchemistry
dc.titleChemical Characterization of Different Extracts from Artemisia annua and Their Antioxidant, Enzyme Inhibitory and Anti-Inflammatory Properties
dc.typeArticle
rdl.citation.openalex43
rdl.citation.scopus45
rdl.departmentDepartment of Pharmacy, G. d'Annunzio University of Chieti-Pescara, 66100, Chieti, Italy
rdl.departmentLaboratory of Human Pathologies Biology, Faculty of Sciences, Department of Biology, Mohammed V University in Rabat, 1014, Rabat, Morocco
rdl.departmentPhysiology and Biochemistry Laboratory, Department of Biology, Science Faculty, Selcuk University, 42130, Konya, Turkey
rdl.departmentDepartment of Molecular Biology and Genetics, Istanbul AREL University, 34537, Istanbul, Türkiye
rdl.departmentMunzur University, Pertek Sakine Genç Vocational School, Tunceli, Pertek, 62500, Turkey
rdl.departmentDepartment of Landscape Architecture, Faculty of Agriculture, Bingol University, Bingöl, 12000, Turkey
rdl.departmentDepartment of Molecular Biology and Genetic, Science and Art Faculty, Bingol University, Bingöl, 12000, Turkey
rdl.oa.statusclosed
rdl.scopus.quartileQ2
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED