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Sökning: L773:1872 7786 OR L773:0009 2797 > (2000-2004) > Metabolic fate of t...

Metabolic fate of the Ah receptor ligand 6-formylindolo[3,2-b]carbazole

Bergander, Linda (författare)
Wincent, Emma (författare)
Stockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi
Rannug, Agneta (författare)
Karolinska Institutet
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Foroozesh, Maryam (författare)
Alworth, William (författare)
Rannug, Ulf (författare)
Stockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi
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 (creator_code:org_t)
Elsevier BV, 2004
2004
Engelska.
Ingår i: Chemico-Biological Interactions. - : Elsevier BV. - 0009-2797. ; 149:2-3, s. 151-164
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The physiological role of the aryl hydrocarbon receptor (AhR), a member of the basic helix-loop-helix PER-ARNT-SIM (PAS) transcription factor family is not known. We have suggested that the AhR is involved in light signaling through binding of photoproducts with high AhR affinity. This suggestion is based on (i) the high AhR affinity of the tryptophan photoproduct formylindolo[3,2-b]carbazole (FICZ), (ii) the induction of rapid and transient expression of AhR-regulated genes by FICZ and by extracts of UV-irradiated tryptophan as well as (iii) the fact that light induces the AhR-regulated cytochrome P450s CYP1A1, CYP1B1 and CYP2S1. The transient mRNA expression caused by light and tryptophan photoproducts suggests that the biotransformation enzymes induced by AhR activation take part in a metabolic degradation of the natural AhR ligand. This study aimed at identifying the involvement of phase I and phase II enzymes in the metabolic degradation of FICZ. A cytochrome P450-dependent metabolism of FICZ giving rise to preferentially mono- and di-hydroxylated derivatives has earlier been reported. In the present study, rat and human hepatic S9 mixes were employed together with specific enzyme inhibitors and cofactors. Compared to the Aroclor-induced rat liver S9, the non-induced rat liver S9 and the human liver S9 caused a more complex metabolite profile of FICZ. The CYP1A1 enzyme was confirmed to be the most important enzyme for the first step in the metabolism. CYP1A2 was found to have overlapping specificity with CYP1A1 being able to form the same major metabolites although with different kinetics. CYP1B1 turned out to be preferentially involved in the further metabolism of dihydroxylated metabolites. Microsomal epoxide hydrolase, and as yet not identified forms of sulphotransferases and glucuronosyltransferases were also found to take part in the metabolic degradation of FICZ. Thus, tryptophan photoproducts fit into a model in which the ligand-activated AhR signaling is autoregulated by the induced metabolic enzymes.

Nyckelord

Animals
Aroclor 1254/metabolism
Carbazoles/*metabolism/toxicity
Chromatography; High Pressure Liquid
Cytochrome P-450 Enzyme System/antagonists & inhibitors/*metabolism
Enzyme Inhibitors/pharmacology
Humans
Indoles/*metabolism/toxicity
Male
Microsomes; Liver/enzymology/*metabolism
Rats
Rats; Sprague-Dawley
Receptors; Aryl Hydrocarbon/*metabolism
Tryptophan/metabolism

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