Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/22625
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKonstandi, M.en
dc.contributor.authorHarkitis, P.en
dc.contributor.authorKostakis, D.en
dc.contributor.authorMarselos, M.en
dc.contributor.authorJohnson, E. O.en
dc.contributor.authorLang, M. A.en
dc.date.accessioned2015-11-24T19:25:29Z-
dc.date.available2015-11-24T19:25:29Z-
dc.identifier.issn0024-3205-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/22625-
dc.rightsDefault Licence-
dc.subjectAnimalsen
dc.subjectBenzo(a)pyrene/pharmacologyen
dc.subjectBlotting, Westernen
dc.subjectCatecholamines/*pharmacologyen
dc.subjectCytochrome P-450 CYP2E1/*biosynthesisen
dc.subjectDown-Regulationen
dc.subjectIsoenzymesen
dc.subject*Liver/drug effects/enzymology/metabolismen
dc.subjectMaleen
dc.subjectRatsen
dc.subjectRats, Wistaren
dc.subjectReceptors, Dopamine D2/agonists/antagonists & inhibitors/*metabolismen
dc.subject*Signal Transduction/drug effectsen
dc.subjectUp-Regulationen
dc.titleD2-receptor-linked signaling pathways regulate the expression of hepatic CYP2E1en
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1016/j.lfs.2007.09.026-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/17988693-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0024320507007394/1-s2.0-S0024320507007394-main.pdf?_tid=b68603c0e82bd95c5806f1d03d49d824&acdnat=1334047718_94c6f27c37befe24eaafe70883023b17-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2008-
heal.abstractThis study investigated the role of catecholamine-related signaling pathways in the regulation of hepatic cytochrome P450 (CYP2E1). Central and peripheral catecholamine depletion with reserpine down-regulated CYP2E1. On the other hand, selective peripheral catecholamine depletion with guanethidine increased CYP2E1 apoprotein levels. Enrichment of peripheral catecholamines with adrenaline suppressed p-nitrophenol hydroxylase activity (PNP). PNP activity was also markedly suppressed by l-DOPA. Stimulation of D(2)-receptors with bromocriptine up-regulated CYP2E1, as assessed by enzyme activity and protein levels, whereas blockade of D(2)-dopaminergic receptors with sulpiride down-regulated this isozyme. These findings indicate that central and peripheral catecholamines have different effects on CYP2E1. Central catecholamines appear related to the up-regulation, whereas the role of peripheral catecholamines is clearly related to the type and location of adrenoceptors involved. D(2)-receptor-linked signaling pathways have an up-regulating effect on CYP2E1, while D(1)-receptor pathways may down-regulate this isozyme. It is worth noting that the widespread environmental pollutant benzo(alpha)pyrene (B(alpha)P) altered the modulating effect of catecholaminergic systems on CYP2E1 regulation. In particular, whereas stimulation or blockade of adrenoceptors had no effect on constitutive PNP activity, exposure to B(alpha)P modified the impact of central and peripheral catecholamines and alpha(2)-adrenoceptors on CYP2E1 expression. It appears that under the influence of B(alpha)P, alpha(2)-adrenergic receptor-linked signaling pathways increased CYP2E1 apoprotein levels. Given that a wide range of xenobiotics and clinically used drugs are activated by CYP2E1 to toxic metabolites, including the production of reactive oxygen species (ROS), it is possible that therapies challenging dopaminergic receptor- and/or alpha(2)-adrenoceptor-linked signaling pathways may alter the expression of CYP2E1, thus affecting the progress and development of several pathologies.en
heal.journalNameLife Scien
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

Files in This Item:
File Description SizeFormat 
Konstandi-2008-D2-receptor-linked s.pdf545.34 kBAdobe PDFView/Open    Request a copy


This item is licensed under a Creative Commons License Creative Commons