Why the study?
Does thyroid hormone administration increase HCN2 mRNA expression in rat hearts?
Does thyroid hormone administration increase HCN2 mRNA expression in rat hearts?
Thyroid hormone upregulates HCN2 mRNA expression in rat hearts, providing a potential molecular mechanism for its positive chronotropic effects.
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May link thyroid hormone to HCN2 upregulation in hypothyroid rat hearts; hypothesis-generating for chronotropic mechanisms, human data needed.
Thyroid hormone regulation of the cardiac pacemaker gene, the hyperpolarization-activated cyclic nucleotide-gated channel gene (HCN2), was studied in rats by Northern analysis. Thyroid hormone administration to hypothyroid rats resulted in a doubling of the HCN2/beta-actin mRNA ratio. A smaller, not statistically significant, increase in HCN2 mRNA occurred when euthyroid animals were made hyperthyroid. A single large dose of L-triiodothyronine given to hypothyroid rats caused a 4.7-fold increase in myocardial HCN2 mRNA expression level and only a 2.3-fold increase in the beta-actin mRNA level. Although the rat HCN2 promoter has not been cloned, we identified a consensus thyroid hormone response element in the promoter sequence of the human HCN2 gene. Therefore, the increase in rat HCN2 mRNA is likely due to L-triiodothyronine stimulation of HCN2 gene transcription. The results suggest that the regulation of heart rate by thyroid hormone may be explained, at least in part, by the positive effect of this hormone on HCN2 gene expression.
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Pachucki et al. (1999) studied this question.
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