|ZFIN ID: ZDB-PUB-160808-8|
Additive effects of levonorgestrel and ethinylestradiol on brain aromatase (cyp19a1b) in zebrafish specific in vitro and in vivo bioassays
Hinfray, N., Tebby, C., Garoche, C., Piccini, B., Bourgine, G., Aït-Aïssa, S., Kah, O., Pakdel, F., Brion, F.
|Source:||Toxicology and applied pharmacology 307: 108-114 (Journal)|
|Registered Authors:||Kah, Olivier|
|Keywords:||Brain aromatase, Ethinylestradiol, Levonorgestrel, Mixture, Transgenic zebrafish, U251-MG cells|
|PubMed:||27491593 Full text @ Tox. App. Pharmacol.|
Hinfray, N., Tebby, C., Garoche, C., Piccini, B., Bourgine, G., Aït-Aïssa, S., Kah, O., Pakdel, F., Brion, F. (2016) Additive effects of levonorgestrel and ethinylestradiol on brain aromatase (cyp19a1b) in zebrafish specific in vitro and in vivo bioassays. Toxicology and applied pharmacology. 307:108-114.
ABSTRACTEstrogens and progestins are widely used in combination in human medicine and both are present in aquatic environment. Despite the joint exposure of aquatic wildlife to estrogens and progestins, very little information is available on their combined effects. In the present study we investigated the effect of ethinylestradiol (EE2) and Levonorgestrel (LNG), alone and in mixtures, on the expression of the brain specific ER-regulated cyp19a1b gene. For that purpose, recently established zebrafish-derived tools were used: (i) an in vitro transient reporter gene assay in a human glial cell line (U251-MG) co-transfected with zebrafish estrogen receptors (zfERs) and the luciferase gene under the control of the zebrafish cyp19a1b gene promoter and (ii) an in vivo bioassay using a transgenic zebrafish expressing GFP under the control of the zebrafish cyp19a1b gene promoter (cyp19a1b-GFP). Concentration-response relationships for single chemicals were modeled and used to design the mixture experiments following a ray design. The results from mixture experiments were analyzed to predict joint effects according to concentration addition and statistical approaches were used to characterize the potential interactions between the components of the mixtures (synergism/antagonism). We confirmed that some progestins could elicit estrogenic effects in fish brain. In mixtures, EE2 and LNG exerted additive estrogenic effects both in vitro and in vivo, suggesting that some environmental progestin could exert effects that will add to those of environmental (xeno-)estrogens. Moreover, our zebrafish specific assays are valuable tools that could be used in risk assessment for both single chemicals and their mixtures.