Injection of dexamethasone into adrenalectomized rats increased ventricular Kv1.5 mRNA approximately 50-fold and immunoreactive protein approximately 20-fold within a day.
Does dexamethasone induce Kv1.5 K+ channel gene expression in the rat heart?
Dexamethasone specifically upregulates Kv1.5 K+ channel gene expression in rat ventricle but not atrium, suggesting glucocorticoids may affect ventricular excitability.
Multiple voltage-gated K+ channels contribute to the repolarization phases of the cardiac action potential and are targets of several antiarrhythmic drugs. The Kv1.5 K+ channel gene is expressed in the heart, and heterologous expression of this gene generates a slowly inactivating K+ current. Previously, we found that glucocorticoids specifically upregulate pituitary Kv1.5 gene expression. To test whether these steroids might also induce Kv1.5 gene expression in the heart, cardiac channel mRNA and protein were measured by RNase protection assay and by immunoblotting with antibody specific for the extracellular domain of Kv1.5 polypeptide. Kv1.5 mRNA and immunoreactive protein appeared to be more abundant in rat ventricle than atrium. Reduction of endogenous glucocorticoids by adrenalectomy decreased ventricular Kv1.5 mRNA approximately 8-fold, which was estimated by using cyclophilin mRNA as an internal control. Kv1.5 immunoreactive protein also decreased approximately 6-fold. Injection of dexamethasone into adrenalectomized rats acted within a day to increase ventricular Kv1.5 mRNA and immunoreactive protein approximately 50-fold and approximately 20-fold, respectively. In contrast, atrial Kv1.5 mRNA expression was unaffected by either adrenalectomy or injection of the glucocorticoid agonist. Furthermore, dexamethasone-induced upregulation was specific for Kv1.5, since whole-heart Kv1.4 and Kv2.1 mRNA levels, as well as ventricular Kv2.1 mRNA expression, were unchanged. Thus, dexamethasone specifically upregulates Kv1.5 K+ channel gene expression in rat ventricle but not atrium. Glucocorticoids may affect excitability of ventricular myocytes and the efficacy of clinically useful drugs by changing the expression of the Kv1.5 K+ channel.
Takimoto et al. (1994) studied this question. Dexamethasone vs. Adrenalectomized rats without dexamethasone was evaluated on Ventricular Kv1.5 mRNA and immunoreactive protein levels. Injection of dexamethasone into adrenalectomized rats increased ventricular Kv1.5 mRNA approximately 50-fold and immunoreactive protein approximately 20-fold within a day.