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Status: Bibliographieeintrag

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Verfasst von:Theile, Dirk [VerfasserIn]   i
 Schmidt, Tobias Thomas [VerfasserIn]   i
 Haefeli, Walter E. [VerfasserIn]   i
 Weiß, Johanna [VerfasserIn]   i
Titel:In-vitro evaluation of chronic alcohol effects on expression of drug-metabolizing and drug-transporting proteins
Verf.angabe:Dirk Theile, Tobias T. Schmidt, Walter E. Haefeli and Johanna Weiss
E-Jahr:2013
Jahr:30 July 2013
Umfang:8 S.
Fussnoten:Gesehen am 03.02.2022
Titel Quelle:Enthalten in: Journal of pharmacy and pharmacology
Ort Quelle:Oxford : Oxford University Press, 1949
Jahr Quelle:2013
Band/Heft Quelle:65(2013), 10, Seite 1518-1525
ISSN Quelle:2042-7158
Abstract:In alcoholics without alcoholic liver disease, boosted drug elimination has been reported. However, mechanistic explanations for this phenomenon remain uncertain. In particular, data on the potential role of drug transporters are sparse.Using a well-established in-vitro model for induction of human drug-metabolizing and drug-transporting proteins, we evaluated the potency of ethanol and the major fermentation side-product isopentanol to alter expression and function of these proteins by quantitative real-time polymerase chain reaction, Western blotting and flow cytometry. P-glycoprotein (Pgp)-inhibiting properties of ethanol and isopentanol were investigated via calcein extrusion assay.Ethanol and isopentanol significantly changed expression levels of drug-metabolizing and drug-transporting proteins that normalized within 2 weeks upon withdrawal. Cytochrome P-450 2C19 and Pgp were most strongly induced. Ethanol-induced Pgp at the messenger RNA (mRNA) (twofold to eightfold) and protein level (twofold), but not at the functional level. Both compounds did not inhibit Pgp.Ethanol is demonstrated to increase mRNA and protein expression of human drug transporters such as Pgp in vitro. Withdrawal of ethanol exposure causes return to non-induced conditions within weeks. Functional consequences of increased Pgp expression in alcoholics need to be evaluated by clinical trials applying selective Pgp substrates such as digoxin.
DOI:doi:10.1111/jphp.12124
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1111/jphp.12124
 DOI: https://doi.org/10.1111/jphp.12124
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1788450817
Verknüpfungen:→ Zeitschrift

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