Abstract
Gene expressions of cytochrome P4501A (CYP1A), aryl hydrocarbon receptor (AhR) and vitellogenin (Vg) by endocrine disruptors, benzo[α]pyrene (B[a]P) and tributyltin (TBT) were examined in cultured eel hepatocytes which were isolated from eels treated previously with B[a]P (10 mg/kg) or estradiol-17β (20 mg/kg) in vivo, and the relationship between CYP1A, AhR and Vg genes were studied. When the cultured eel hepatocytes were treated with B[a]P (10 6 10 5 M) the gene expressions of CYP1A and AhR were enhanced in a concentration-dependent manner. However, when treated with TBT (10 9 10 5 M) the gene expressions of CYP1A and AhR were suppressed at high concentrations (10 6 10 5 M), while having no effects at low concentrations (10 9 10 7 M). Gene expression of Vg was also suppressed by TBT in a concentration-dependent manner in cultured eel hepatocytes which was previously treated in vivo with estradiol-17β.
Cite
CITATION STYLE
Choi, M. S., Kwon, S. R., Choi, S. H., & Kwon, H. C. (2012). Effect of TBT and PAHs on CYP1A, AhR and Vitellogenin Gene Expression in the Japanese Eel, Anguilla japonica. Development & Reproduciton, 16(4), 289–294. https://doi.org/10.12717/dr.2012.16.4.289
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.