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Biomarkers cytochrome P450 induction

Several PAHs and hydroxylated or methylated PAH derivatives induce oestrogenic or dioxin-like (antioestrogenic) effects in fish and mammalian cell lines (Santodonato, 1997 Villeneuve et al., 2002 Michallet-Ferrier et al., 2004). For instance, benz[u]anthracene and dibenz[u/2]anthracene elicit oestrogenic responses in vitro (Villeneuve et al., 2002). These two PAHs and five others may also elicit dioxin-like responses, as shown by their induction of ethoxyresorufm-D-deethylase (EROD) activity, a biomarker for cytochrome P450 lAl (Gravato Santos, 2002 Villeneuve et al., 2002). [Pg.185]

Induction of cytochrome P450 2A6 expression in humans by the carcinogenic parasite infection, opisthorchiasis viverrini. Cancer Epidemiol. Biomarkers Prev. 5, 795—800. [Pg.477]


See other pages where Biomarkers cytochrome P450 induction is mentioned: [Pg.140]    [Pg.952]    [Pg.2090]    [Pg.48]    [Pg.176]    [Pg.248]    [Pg.158]    [Pg.632]    [Pg.642]   
See also in sourсe #XX -- [ Pg.140 ]




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