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The nutritional supply of iodine and selenium affects thyroid hormone axis related endpoints in mice

Zugehörigkeit
Department of Nutritional Physiology, Institute of Nutritional Sciences, Friedrich Schiller University Jena, Jena, Germany
Lossow, Kristina;
ORCID
0000-0003-2050-0961
Zugehörigkeit
German Federal Institute for Risk Assessment (BfR), Department 9 Experimental Toxicology and ZEBET, Unit 93 Animal Protection and Laboratory Animal Science, Germany
Renko, Kostja;
Zugehörigkeit
Department of Nutritional Physiology, Institute of Nutritional Sciences, Friedrich Schiller University Jena, Jena, Germany
Schwarz, Maria;
Zugehörigkeit
TraceAge-DFG Research Unit on Interactions of Essential Trace Elements in Healthy and Diseased Elderly, Jena, Germany
Schomburg, Lutz;
ORCID
0000-0002-4873-7488
Zugehörigkeit
German Federal Institute for Risk Assessment (BfR), Executive Office, Germany; TraceAge-DFG Research Unit on Interactions of Essential Trace Elements in Healthy and Diseased Elderly, 07743 Jena, Germany; Department of Food Chemistry, Institute of Nutritional Science, University of Potsdam, 14558 Nuthetal, Germany
Schwerdtle, Tanja;
Zugehörigkeit
Department of Nutritional Physiology, Institute of Nutritional Sciences, Friedrich Schiller University Jena, Jena, Germany
Kipp, Anna Patricia

Selenium and iodine are the two central trace elements for the homeostasis of thyroid hormones but additional trace elements such as iron, zinc, and copper are also involved. To compare the primary effects of inadequate intake of selenium and iodine on the thyroid gland, as well as the target organs of thyroid hormones such as liver and kidney, mice were subjected to an eight-week dietary intervention with low versus adequate selenium and iodine supply. Analysis of trace element levels in serum, liver, and kidney demonstrated a successful intervention. Markers of the selenium status were unaffected by the iodine supply. The thyroid gland was able to maintain serum thyroxine levels even under selenium-deficient conditions, despite reduced selenoprotein expression in liver and kidney, including deiodinase type 1. Thyroid hormone target genes responded to the altered selenium and iodine supply, whereas the iron, zinc, and copper homeostasis remained unaffected. There was a notable interaction between thyroid hormones and copper, which requires further clarification. Overall, the effects of an altered selenium and iodine supply were pronounced in thyroid hormone target tissues, but not in the thyroid gland.

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