Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/11960
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dc.contributor.authorToselli, Fen
dc.contributor.authorMatthias, Aen
dc.contributor.authorBone, Kerryen
dc.contributor.authorGillam, EMJen
dc.contributor.authorLehmann, RPen
local.source.editorEditor(s): Leandros Skaltsounis, Prokopios Magiatis, Nikolas Fokialakisen
dc.date.accessioned2013-01-31T15:24:00Z-
dc.date.issued2008-
dc.identifier.citationPlanta Medica: Journal of Medicinal Plant and Natural Product Research, 74(9), p. 921-921en
dc.identifier.issn1439-0221en
dc.identifier.issn0032-0943en
dc.identifier.urihttps://hdl.handle.net/1959.11/11960-
dc.description.abstractPreparations from Echinacea plant parts are commonly used in contemporary alternative medicine for the treatment and prevention of upper respiratory tract infections. The phytochemicals thought to be mainly responsible for the immunomodulatory properties are the alkamides found in ethanolic extracts, with the most abundant ones being the isomers N-isobutyldodeca-2E,4E,8Z,10Z-tetraenamide (compound 8) and N-isobutyldodeca-2E,4E,8Z,10E-tetraenamide (compound 9). The market for this herbal medicine and the research devoted to the study of its therapeutic effects are increasing every year. However, few studies have focused on its metabolism, which can affect its therapeutic outcomes. In this study, we evaluated which human cytochrome P450 enzymes were predominantly involved in the metabolism of Echinacea alkamides. Recombinant human cytochromes P450 and pure compounds 8 and 9 synthesized for this study were used to investigate the relative importance of each isoform in alkamide metabolism. The main metabolites were found to be the expected epoxidation, N-dealkylation and hydroxylation products, with different metabolite profiles seen for each compound. The most abundant metabolite for compound 8 was an epoxide, whereas an N-dealkylated product was dominant for compound 9. For both compounds, the major isoforms involved in the production of epoxides were P450's 1A1, 1A2 and 2A13, whereas for the N-dealkylation only P450's 1A1 and 1A2 were important. Only low concentrations of hydroxylated metabolites were seen. In summary, the relative importance of the main human xenobiotic-metabolising P450's in the metabolism of the most abundant Echinacea alkamides have been established and the metabolites formed have been identified in this study. There are no standardization requirements for the phytochemical composition of Echinacea-based products, and different Echinacea preparations are likely to contain different relative concentrations of individual alkamides. Since P450 forms differ in abundance between individuals and tissues, as well as in their importance in alkamide metabolism, variations in metabolism may have a significant influence on the therapeutic outcome of different Echinacea preparations. Further work is in progress to evaluate how metabolism may affect the bioavailability of individual alkamides for therapeutic purposes.en
dc.languageenen
dc.publisherGeorg Thieme Verlagen
dc.relation.ispartofPlanta Medica: Journal of Medicinal Plant and Natural Product Researchen
dc.titleMetabolism of Echinacea alkamides by human recombinant P450 enzymesen
dc.typeConference Publicationen
dc.relation.conferenceGA 2008: 56th Annual Meeting of the Society for Medicinal Plant Research and 7th Joint Meeting with l'Association Francaise pour l'Enseignement et la Recherche en Pharmacognosie (AFERP), American Society of Pharmacognosy (ASP), Phytochemical Society of Europe (PSE), and Italian Phytochemical Society (SIF)en
dc.identifier.doi10.1055/s-0028-1083940en
dc.subject.keywordsComplementary and Alternative Medicineen
local.contributor.firstnameFen
local.contributor.firstnameAen
local.contributor.firstnameKerryen
local.contributor.firstnameEMJen
local.contributor.firstnameRPen
local.subject.for2008110499 Complementary and Alternative Medicine not elsewhere classifieden
local.subject.seo2008860803 Human Pharmaceutical Treatments (e.g. Antibiotics)en
local.profile.schoolSchool of Healthen
local.profile.emailkbone2@une.edu.auen
local.output.categoryE3en
local.record.placeauen
local.record.institutionUniversity of New Englanden
local.identifier.epublicationsrecordpes:6380en
local.date.conference3rd - 8th August, 2008en
local.conference.placeAthens, Greeceen
local.publisher.placeGermanyen
local.identifier.runningnumberCongress Abstract SL60en
local.format.startpage921en
local.format.endpage921en
local.identifier.volume74en
local.identifier.issue9en
local.contributor.lastnameTosellien
local.contributor.lastnameMatthiasen
local.contributor.lastnameBoneen
local.contributor.lastnameGillamen
local.contributor.lastnameLehmannen
dc.identifier.staffune-id:kbone2en
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.identifier.unepublicationidune:12163en
dc.identifier.academiclevelAcademicen
local.title.maintitleMetabolism of Echinacea alkamides by human recombinant P450 enzymesen
local.output.categorydescriptionE3 Extract of Scholarly Conference Publicationen
local.conference.detailsGA 2008: 56th Annual Meeting of the Society for Medicinal Plant Research and 7th Joint Meeting with l'Association Francaise pour l'Enseignement et la Recherche en Pharmacognosie (AFERP), American Society of Pharmacognosy (ASP), Phytochemical Society of Europe (PSE), and Italian Phytochemical Society (SIF), Athens, Greece, 3rd - 8th August, 2008en
local.search.authorToselli, Fen
local.search.authorMatthias, Aen
local.search.authorBone, Kerryen
local.search.authorGillam, EMJen
local.search.authorLehmann, RPen
local.uneassociationUnknownen
local.year.published2008en
local.date.start2008-08-03-
local.date.end2008-08-08-
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