• Made available online as an Accepted Preprint 6 January 2011
  • Accepted Preprint first posted online on 6 January 2011

Effects of cortisol and thyroid hormone on peripheral outer ring deiodination and osmoregulatory parameters in the Senegalese sole (Solea senegalensis)

  1. Peter H M Klaren1
  1. 1Department of Animal Physiology, Institute for Water and Wetland Research, Faculty of Science, Radboud University Nijmegen, Heyendaalseweg 135, 6525 AJ Nijmegen, The Netherlands
    2Departamento de Biología, Facultad de Ciencias del Mar y Ambientales, Universidad de Cádiz, 11510 Puerto Real, Cádiz, Spain
    3Instituto de Zoología, Facultad de Ciencias, Universidad Austral de Chile, Casilla 567, 5090000 Valdivia, Chile
  1. (Correspondence should be addressed to F J Arjona at Department of Animal Physiology, Institute for Water and Wetland Research, Faculty of Science, Radboud University Nijmegen; Email: f.arjona{at}science.ru.nl)

Abstract

The thyroid gland in fish mainly secretes the thyroid prohormone 3,5,3′,5′-tetraiodothyronine (T4), and extrathyroidal outer ring deiodination (ORD) of the prohormone to 3,5,3′-triiodothyronine (T3) is pivotal in thyroid hormone economy. Despite its importance in thyroid hormone metabolism, factors that regulate ORD are still largely unresolved in fish. In addition, the osmoregulatory role of T3 is still a controversial issue in teleosts. In this study, we investigated the regulation of the ORD pathway by cortisol and T3 in different organs (liver, kidney, and gills) of Solea senegalensis and the involvement of T3 in the control of branchial and renal Na+, K+-ATPase activity, a prime determinant of the hydromineral balance in teleosts. Animals were treated with i.p. slow-release coconut oil implants containing cortisol or T3. Hepatic and renal ORD activities were up-regulated in cortisol-injected animals. T3-treated fish showed a prominent decrease in plasma-free T4 levels, whereas ORD activities did not change significantly. Branchial and renal Na+, K+-ATPase activities were virtually unaffected by T3, but were transiently up-regulated by cortisol. We conclude that cortisol regulates local T3 bioavailability in S. senegalensis via ORD in an organ-specific manner. Unlike T3, cortisol appears to be directly implicated in the up-regulation of branchial and renal Na+, K+-ATPase activities.

  • Received in final form 6 December 2010
  • Accepted 5 January 2011
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