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Effects of cyclopenta[ c]phenanthrene and its derivatives on zona radiata protein, ERα, and CYP1A mRNA expression in liver of rainbow trout ( Oncorhynchus mykiss Walbaum)
Despite cyclopenta-fused polycyclic aromatic hydrocarbons (CP-PAHs) have been detected in the environment, the ability of CP-PAH to induce cellular and tissue responses remains poorly characterized. In this study, xenoestrogen-associated responses (mRNA levels of estrogen receptor α, ERα, and zona r...
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Published in: | Chemico-biological interactions 2008-07, Vol.174 (1), p.60-68 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Despite cyclopenta-fused polycyclic aromatic hydrocarbons (CP-PAHs) have been detected in the environment, the ability of CP-PAH to induce cellular and tissue responses remains poorly characterized. In this study, xenoestrogen-associated responses (mRNA levels of estrogen receptor α, ERα, and
zona radiata protein,
Zrp) and xenobiotic effects (CYP1A mRNA) have been investigated in liver of juvenile rainbow trout after short-term treatment (8 and 24
h) with following compounds administered singly: cyclopenta[
c]phenanthrene (CP[
c]Ph); its derivatives, 5A-CP[
c]Ph; 5A6M-CP[
c]Ph; 5A9M-CP[
c]Ph; B[
c]Ph, a structurally similar polycyclic aromatic hydrocarbon; B[
a]P, a model CYP1A inducer; and zearalenone (ZEA), naturally occurring ligand for ER. The CYP1A mRNA expression after 24
h of exposure with CP[
c]Ph or its derivatives, except 5A9M-CP[
c]Ph, was 3–9-fold higher compared to controls (
P
<
0.05), but it was less than that caused by B[
a]P (65-fold up regulation;
P
<
0.01). Moreover, neither of the CP-PAH compounds modulated liver ERα or
Zrp mRNA levels as compared to effects associated with ZEA. Interestingly, a treatment with this ER-ligand, caused moderate but significant increase of CYP1A mRNA expression (about 2.5-fold;
P
<
0.05). The finding that ZEA is capable of acting as either estrogenic and xenobiotic compound, should be further explored in a more detailed and differently designed experiment. |
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ISSN: | 0009-2797 1872-7786 |
DOI: | 10.1016/j.cbi.2008.04.022 |