Quercetin, quercetin glycosides and taxifolin differ in their ability to induce AhR activation and cyp1a1 expression in HepG2 cells

Phytotherapy Research

Volumn 26, Issue 11, 2012, Pages 1746-1752

  Vrba, Jiri ^a   Kren, Vladimir ^b   Vacek, Jan ^a   Papouskova, Barbora ^a   Ulrichova, Jitka ^a  

^a PALACKÝ UNIVERSITY   (Czech Republic)

^b INSTITUTE OF MICROBIOLOGY   (Czech Republic)

Author keywords

aryl hydrocarbon receptor; CYP1A1; glycoside; metabolism; quercetin; taxifolin

Indexed keywords

2,3,7,8 TETRACHLORODIBENZO PARA DIOXIN; CYTOCHROME P450 1A1; ISOQUERCITRIN; MESSENGER RNA; QUERCETIN; RUTOSIDE; TAXIFOLIN;

ARTICLE; CELL STRAIN HEPG2; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG EXPOSURE; DRUG MECHANISM; DRUG STRUCTURE; ENZYME ACTIVITY; ENZYME INDUCTION; ENZYME REGULATION; GENE EXPRESSION; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; INCUBATION TIME; PROTEIN EXPRESSION; RECEPTOR UPREGULATION; REPORTER GENE; TRANSCRIPTION INITIATION;

CYTOCHROME P-450 CYP1A1; GLUCOSIDES; HEP G2 CELLS; HUMANS; QUERCETIN; RECEPTORS, ARYL HYDROCARBON; RUTIN;

EID: 84867847900     PISSN: 0951418X     EISSN: 10991573     Source Type: Journal    
DOI: 10.1002/ptr.4637     Document Type: Article

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