“…However, it is well documented that, in hyperthyroid states, type-2 deiodinase (D2) activity is decreased in pituitary, central nervous system, and brown adipose tissue (Bates et al 1999, Schneider et al 2001, Volpato & Nunes 2001. Moreover, in the early postnatal life, changes in the expression of TH receptor isoforms are taking place, under TH control (Kaplan & Yaskoski 1981, Silva & Larsen 1982, Bradley et al 1992, Santini et al 1999, which interferes with the pattern of GH gene response to T3 observed in adult rats, in which the adult isoforms predominate. Furthermore, in the NP, the a-2 isoform of TR (TRa 2) is highly expressed, which prevents, in a certain degree, the binding of other TR isoforms (TRa 1, b1, and b2) to the DNA-binding domain (DBD) of the T3 target genes (Bradley et al 1992), and taking into account that T3-binding domain is missing in the TRa 2, this might prevent, in some way, the impact of TH on the expression of many genes in this period of development, in which the patterns of gene expression that will persist in adult life is being settled (Csaba & Nagy 1985).…”