Abstract
Selenium (Se) status and individual selenoproteins are important regulators of hormonal homeostasis during development and adulthood. Because endocrine cells and organs are highly perfused and continuously involved in hormone secretion and feedback sensor function, adequate control of their redox state is required to sustain the hormone secretory machinery. Several selenoproteins contribute to this essential function, which might explain the high relative Se content in endocrine tissues. Specifically, hypothalamus-pituitary-feedback regulation is responsive to Se, and the thyroid, islets of Langerhans in the pancreas, adrenal cortex, and gonads are strongly affected by Se status. Deiodinase selenoproteins contribute to the hypothalamic control of satiety, food intake, and energy expenditure, as well as to the development and proper function of several endocrine tissues. Inadequate Se status is linked to autoimmune diseases of the thyroid, impaired insulin secretion and resistance, delayed chondrocyte differentiation, defective bone formation, and reduced gonadal function. Single-nucleotide polymorphisms of several selenoprotein genes affect nutritional Se status and several hormonal axes. An inactivating mutation of thioredoxin reductase 2 causes familial glucocorticoid deficiency. Thus, adequate Se supply is crucial for the appropriate function of the endocrine system and hormone action.
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Supported by grants of the DFG (KO 922/17-2) and Charité.
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Köhrle, J. (2016). Selenium and Endocrine Tissues. In: Hatfield, D., Schweizer, U., Tsuji, P., Gladyshev, V. (eds) Selenium. Springer, Cham. https://doi.org/10.1007/978-3-319-41283-2_33
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DOI: https://doi.org/10.1007/978-3-319-41283-2_33
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