Journal
AQUATIC TOXICOLOGY
Volume 177, Issue -, Pages 63-73Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.aquatox.2016.05.011
Keywords
Progestin; Pituitary-thyroid axis; Ex vivo organ culture; TSH; NIS; Deiodinase; Xenopus laevis
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Funding
- Leibniz Association within the Project PAKT - Effects of pharmaceutical active compounds on aquatic species [PAKT2008/203263]
- German Research Foundation (DFG) [LO 1600/2-1]
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The synthetic gestagen levonorgestrel (LNG) was previously shown to perturb thyroid hormone dependent metamorphosis in Xenopus laevis. However, so far the mechanisms underlying the anti-metamorphic effects of LNG remained unknown. Therefore, a series of in vivo and ex vivo experiments was performed to identify potential target sites of LNG action along the pituitary-thyroid axis of X. laevis tadpoles. Prometamorphic tadpoles were treated in vivo with LNG (0.01-10 nM) for 72 h and brain-pituitary and thyroid tissue was analyzed for marker gene expression. While no treatment-related changes were observed in brain-pituitary tissue, LNG treatment readily affected thyroidal gene expression in tadpoles including decreased slc5a5 and iyd mRNA expression and a strong induction of dio2 and dio3 expression. When using an ex vivo organ explant culture approach, direct effects of LNG on both pituitary and thyroid gland gene expression were detecTable Specifically, treatment of pituitary explants with 10 nM LNG strongly stimulated dio2 expression and concurrently suppressed tshb expression. In thyroid glands, ex vivo LNG treatment induced dio2 and dio3 mRNA expression in a thyrotropin-independent manner. When thyroid explants were cultured in thyrotropin-containing media, LNG caused similar gene expression changes as seen after 72 h in vivo treatment including a very strong repression of thyrotropininduced slc5a5 expression. Concerning the anti-thyroidal activity of LNG as seen under in vivo conditions, our ex vivo data provide clear evidence that LNG directly affects expression of genes important for thyroidal iodide handling as well as genes involved in negative feedback regulation of pituitary tshb expression. (C) 2016 Elsevier B.V. All rights reserved.
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