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Volume 271, Number 30,
Issue of July 26, 1996
pp. 17635-17643
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
Phenobarbital Induction of CYP1A1 Gene Expression in
a Primary Culture of Rainbow Trout Hepatocytes
(Received for publication, March 1, 1995, and in revised form, February 23, 1996)
Marianne D.
Sadar
§
,
Roger
Ash
§
,
Johan
Sundqvist
,
Per-Erik
Olsson
and
Tommy B.
Andersson

From the Department of Zoophysiology, University of
Göteborg, S 40031 Göteborg, Sweden, the
§ Department of Biomedical Sciences, University of Bradford,
Bradford, West Yorkshire BD7 1DP, United Kingdom, and the
Department of Pharmacokinetics and Drug Metabolism, Astra
Hässle AB, S 43183 Mölndal, Sweden
In mammals, phenobarbital (PB) is an in
vivo inducer of the cytochrome P4502B (CYP2B) family, whereas in
teleosts PB induction of cytochrome P450 is unclear. We show that
teleost cytochrome P4502K1 (CYP2K1) protein levels and
7-pentoxyresorufin-O-deethylase activity were not induced
by exposure of primary cultures of rainbow trout hepatocytes to PB.
Instead, cytochrome P4501A1 (CYP1A1) gene
expression was strongly induced by PB, based upon observations of
marked increases in CYP1A1 mRNA, CYP1A1 protein, and
7-ethoxyresorufin-O-deethylase activity. In accordance with
these data we provide a temporal study employing antibodies for the
aromatic hydrocarbon (Ah) receptor that showed an increase in Ah
receptor in nuclear extracts prepared from cells exposed to PB.
Employment of the electrophoretic mobility shift assay (EMSA) showed PB
to cause activation or ``transformation'' of the Ah receptor in
nuclear extracts. Studies employing actinomycin D and cycloheximide
indicated that PB induction of CYP1A1 was regulated at both the
transcriptional and post-transcriptional levels. Nuclear run-off
experiments confirm that PB causes an increase in CYP1A1 transcription.
Inhibition of protein synthesis led to the superinduction of CYP1A1
mRNA, suggesting the regulation of teleost CYP1A1 may involve a
labile repressor protein. These findings suggest that PB induction of
the CYP1A1 gene involves the Ah receptor and is via
transcriptional activation.

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Copyright © 1996 by the American Society for Biochemistry and Molecular Biology.
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