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dc.contributor.authorSchepetkin I.A.
dc.contributor.authorOzek G.
dc.contributor.authorOzek T.
dc.contributor.authorKirpotina L.N.
dc.contributor.authorKhlebnikov A.I.
dc.contributor.authorQuinn M.T.
dc.date.accessioned2020-07-09T20:55:05Z
dc.date.available2020-07-09T20:55:05Z
dc.date.issued2020
dc.identifier.issn2218273X
dc.identifier.urihttps://doi.org/10.3390/biom10060916
dc.identifier.urihttps://hdl.handle.net/11421/23855
dc.descriptionPubMed: 32560389en_US
dc.description.abstractHypericum L. (Hypericaceae) extracts have been used for their therapeutic effects; however, not much is known about the immunomodulatory activity of essential oils extracted from this plant. We isolated essential oils from the flowers and leaves of H. perforatum and analyzed their chemical composition and innate immunomodulatory activity. Analysis of flower (HEOFl ) versus leaf (HEOLv) essential oils using gas chromatography–mass spectrometry revealed that HEOFl was comprised mainly of monoterpenes (52.8%), with an abundance of oxygenated monoterpenes, including cis-p-menth-3-en-1,2-diol (9.1%), ?-terpineol (6.1%), terpinen-4-ol (7.4%), and limonen-4-ol (3.2%), whereas the sesquiterpenes were found in trace amounts. In contrast, HEOLv was primarily composed of sesquiterpenes (63.2%), including germacrene D (25.7%) and ?-caryophyllene (9.5%). HEOLv also contained oxygenated monoterpenes, including terpinen-4-ol (2.6%), while monoterpene hydrocarbons were found in trace amounts. Both HEOFl and HEOLv inhibited neutrophil Ca2+ mobilization, chemotaxis, and reactive oxygen species (ROS) production, with HEOLv being much more active than HEOFl . Furthermore, the pure sesquiterpenes germacrene D, ?-caryophyllene, and ?-humulene also inhibited these neutrophil responses, suggesting that these compounds represented the active components of HEOLv. Although reverse pharmacophore mapping suggested that potential protein targets of germacrene D, ?-caryophyllene, bicyclogermacrene, and ?-humulene could be PIM1 and mitogen-activated protein kinase (MAPK)-activated protein kinase 2 (MAPKAK2), a kinase binding affinity assay did not support this finding, implying that other biological targets are involved. Our results provide a cellular and molecular basis to explain at least part of the beneficial immunotherapeutic properties of the H. perforatum essential oils. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.en_US
dc.description.sponsorshipTomsk Polytechnic University Montana Agricultural Experiment Station National Institutes of Health: GM115371, GM103474 1009546en_US
dc.description.sponsorshipFunding: This research was supported in part by National Institutes of Health IDeA Program Grants GM115371 and GM103474, USDA National Institute of Food and Agriculture Hatch project 1009546, the Montana State University Agricultural Experiment Station, and the Tomsk Polytechnic University Competitiveness Enhancement Program.en_US
dc.language.isoengen_US
dc.publisherMDPI AGen_US
dc.relation.isversionof10.3390/biom10060916en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAnti-inflammatoryen_US
dc.subjectCalcium fluxen_US
dc.subjectChemotaxisen_US
dc.subjectEssential oilen_US
dc.subjectHypericum perforatumen_US
dc.subjectNeutrophilen_US
dc.subjectReactive oxygen speciesen_US
dc.subjectSesquiterpeneen_US
dc.titleChemical composition and immunomodulatory activity of hypericum perforatum essential oilsen_US
dc.typearticleen_US
dc.relation.journalBiomoleculesen_US
dc.contributor.departmentAnadolu Üniversitesien_US
dc.identifier.volume10en_US
dc.identifier.issue6en_US
dc.identifier.startpage1en_US
dc.identifier.endpage20en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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