Behavioral inhibition and impaired spatial learning and memory in hypothyroid mice lacking thyroid hormone receptor α

Jennifer Slone Wilcoxon, Gregory J. Nadolski, Jacques Samarut, Olivier Chassande, Eva E. Redei*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

82 Scopus citations


Thyroid hormone insufficiency leads to impaired neurogenesis, behavioral alterations and cognitive deficits. Thyroid hormone receptors, expressed in brain regions involved in these behaviors, mediate the effects of thyroid hormone deficiency or excess. To determine the contribution of thyroid hormone receptor alpha (TRα) in these behaviors, we examined the behavior of euthyroid as well as hypo- and hyperthyroid mice lacking all isoforms of the TRα (TRαo/o). The hypothyroxinemic TRαo/o mice demonstrated behavioral inhibition, manifested in decreased activity and increased anxiety/fear in the open field test (OFT) and increased immobility in the forced swim test (FST) compared to C57BL/6J mice. TRαo/o mice also showed learning and recall impairments in the Morris water maze (MWM), which were exaggerated by hypothyroidism in TRαo/o mice. These impairments were concurrent with increased thigmotaxis, suggesting an increased anxiety-like state of the TRαo/o mice in the MWM. Expression of genes, known to be involved in processes modulating learning and memory, such as glucocorticoid receptor (GR), growth-associated protein 43 (GAP-43) and neurogranin (RC3), were significantly decreased in the hippocampus of TRαo/o mice. GR expression was also decreased in the frontal cortex and amygdala of TRαo/o mice, indicating that expression of GR is regulated, probably developmentally, by one or more isoforms of TRα in the mouse brain. Taken together these data demonstrate behavioral alterations in the TRαo/o mice, indicating the functional role of TRα, and a delicate interaction between TRα and TRβ-regulated genes in these behaviors. Thyroid hormone-regulated genes potentially responsible for the learning deficit found in TRαo/o mice include GR, RC3 and GAP-43.

Original languageEnglish (US)
Pages (from-to)109-116
Number of pages8
JournalBehavioural Brain Research
Issue number1
StatePublished - Feb 12 2007


  • Forced swim test
  • GAP-43
  • Glucocorticoid receptor
  • Morris water maze
  • Neurogranin
  • Open field test
  • PTU
  • T4

ASJC Scopus subject areas

  • Behavioral Neuroscience


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