Published Online
on August 18, 2008

A more recent version of this article appeared on September 2, 2008

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Submitted on December 5, 2007
Accepted on June 11, 2008

Feedback Remodeling of Cardiac Potassium Current Expression. A Novel Potential Mechanism for Control of Repolarization Reserve

Ling Xiao BSc, Jiening Xiao PhD, Xiaobin Luo MSc, Huixian Lin PhD, Zhiguo Wang PhD, and Stanley Nattel MD^*

From the Department of Medicine, Montreal Heart Institute and Université de Montréal (L.X., J.X., X.L., H.L., Z.W., S.N.), and Department of Pharmacology and Therapeutics, McGill University (L.X., S.N.), Montreal, Quebec, Canada.

^* To whom correspondence should be addressed. E-mail: stanley.nattel{at}icm-mhi.org.

Background—Inhibition of individual K⁺ currents causes functionally based compensatory increases in other K⁺ currents that minimize changes in action potential duration, a phenomenon known as repolarization reserve. The possibility that sustained K⁺ channel inhibition may induce remodeling of ion current expression has not been tested. Accordingly, we assessed the effects of sustained inhibition of one K⁺ current on various other cardiac ionic currents.

Methods and Results—Adult canine left ventricular cardiomyocytes were incubated in primary culture and paced at a physiological rate (1 Hz) for 24 hours in the presence or absence of the highly selective rapid delayed-rectifier K⁺ current (I_Kr) blocker dofetilide (5 nmol/L). Sustained dofetilide exposure led to shortened action potential duration and increased repolarization reserve (manifested as a reduced action potential duration–prolonging response to I_Kr blockade). These repolarization changes were accompanied by increased slow delayed-rectifier (I_Ks) density, whereas I_Kr, transient-outward (I_to), inward-rectifier (I_K1), L-type Ca²⁺ (I_CaL), and late Na⁺ current remained unchanged. The mRNA expression corresponding to KvLQT1 and minK (real-time polymerase chain reaction) was unchanged, but their protein expression (Western blot) was increased, suggesting posttranscriptional regulation. To analyze possible mechanisms, we quantified the muscle-specific microRNA subtypes miR-133a and miR-133b, which can posttranscriptionally regulate and repress KvLQT1 protein expression without affecting mRNA expression. The expression levels of miR-133a and miR-133b were significantly decreased in cells cultured in dofetilide compared with control, possibly accounting for KvLQT1 protein upregulation.

Conclusions—Sustained reductions in I_Kr may lead to compensatory upregulation of I_Ks through posttranscriptional upregulation of underlying subunits, likely mediated (at least partly) by microRNA changes. These results suggest that feedback control of ion channel expression may influence repolarization reserve.

Key words: action potentials • electrocardiography • electrophysiology • long-QT syndrome • microRNAs • potassium channels

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Circulation 2008 118: 979-980. [Extract] [Full Text]

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