Heterogeneity and standardization of Phase II metabolism in cultured cells. (Articolo in rivista)

Type
Label
  • Heterogeneity and standardization of Phase II metabolism in cultured cells. (Articolo in rivista) (literal)
Anno
  • 2009-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1159/000218189 (literal)
Alternative label
  • Biasutto L.; Marotta E.; De Marchi U.; Beltramello S.; Bradaschia A.; Garbisa S.; Zoratti M.; Paradisi C. (2009)
    Heterogeneity and standardization of Phase II metabolism in cultured cells.
    in Cellular physiology and biochemistry
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Biasutto L.; Marotta E.; De Marchi U.; Beltramello S.; Bradaschia A.; Garbisa S.; Zoratti M.; Paradisi C. (literal)
Pagina inizio
  • 425 (literal)
Pagina fine
  • 430 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://content.karger.com/produktedb/produkte.asp?DOI=10.1159/000218189 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 23 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
  • 6 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 4-6 (literal)
Note
  • Scopu (literal)
  • ISI Web of Science (WOS) (literal)
  • PubMe (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Biasutto L; De Marchi U; Beltramello S; Bradaschia A.; Garbisa S.; Zoratti M: Dip. di Scienze Biomediche Sperimentali, Università di Padova Marotta E; Paradisi C: Dip. di Scienze Chimiche, Università di Padova Zoratti M: IN - Padova (literal)
Titolo
  • Heterogeneity and standardization of Phase II metabolism in cultured cells. (literal)
Abstract
  • Caco-2 cells are widely used for transepithelial transport and metabolism studies. We analysed the metabolites produced from quercetin (Q) during transport of this flavonoid across Caco-2 monolayers and by plastic-adhering cells. We found that the pattern of Phase II metabolic activity varies markedly depending on the particular cell clone, age of the cell culture, and stressful treatment such as freezing/thawing. Prolonged culturing and stress cause a decrease of \"detoxifying\" conjugating activity. This can be re-established by growing the cells with a low concentration of the transport/metabolism substrate for a few days. We suggest this metabolism-activating procedure be used to make studies with these cells more readily comparable. (literal)
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