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This version published online on May 8, 2008
Endocrinology, doi:10.1210/en.2008-0350
A more recent version of this article appeared on August 1, 2008
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Submitted on March 13, 2008
Accepted on April 30, 2008

Thyroid hormone action in the adult brain: Gene expression profiling of the effects of single and multiple doses of Triiodo-L-thyronine in the rat striatum

Diego Diez, Carmen Grijota-Martinez, Patrizia Agretti, Giuseppina De Marco, Massimo Tonacchera, Aldo Pinchera, Gabriella Morreale de Escobar, Juan Bernal*, and Beatriz Morte*

Instituto de Investigaciones Biomédicas, CSIC-UAM, 28029 Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), ISCIII, Madrid, Spain; Department of Endocrinology and Metabolism, Centro Eccellenza AmbiSEN, University of Pisa, Pisa, Italy

* To whom correspondence should be addressed. E-mail: jbernal{at}iib.uam.es or bmorte{at}iib.uam.es.

Thyroid hormones have profound effects on mood and behaviour, but the molecular basis of thyroid hormone action in the adult brain is relatively unknown. In particular, few thyroid hormone dependent genes have been identified in the adult brain despite extensive work carried out on the developing brain. In this work we have performed global analysis of gene expression in the adult rat striatum in search for genomic changes taking place after administration of triiodothyronine (T3) to hypothyroid rats. The hormone was administered in two different schedules: i) a single, large dose of 25 ug/100 g body weight (SD), or ii) 1.5 ug/100 g body weight once daily for 5 days (RD). Twenty four hours after the single or the last of multiple doses, gene expression in the striatum was analyzed using Codelink microarrays. SD caused up-regulation of 149 genes and down-regulation of 88 genes. RD caused up-regulation of 18 genes and down-regulation of 1 gene. The results were confirmed by hybridization to AffymetrixTM microarrays and by TaqMan PCR. Among the genes identified are genes involved in circadian regulation and in the regulation of signalling pathways in the striatum. These results suggest that thyroid hormone is involved in regulation of striatal physiology at multiple control points. In addition, they may explain the beneficial effects of large doses of thyroid hormone in bipolar disorders.


Key words: microarrays • hypothyroidism • thyroidectomy • thyroid hormone treatment • caudate nucleus • bipolar depression • nuclear receptors







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