Literature DB >> 15534822

Optical mapping of propagation changes induced by elevated extracellular potassium ion concentration in genetically altered mouse hearts.

Bonnie B Punske1, Stefano Rossi, Philip Ershler, Isaac Rasmussen, E Dale Abel.   

Abstract

UNLABELLED: Diabetes is associated with high rates of cardiovascular disease and sudden death. Therefore, dissecting specific mechanisms, such as the effects of impaired insulin signaling on cardiac electrophysiology may lead to better diagnosis and treatment. Lack of insulin receptors in mouse myocytes has been shown to reduce repolarizing potassium currents and prolong action potential duration. We hypothesized that these changes would manifest as rate-related effects on electrical propagation in the intact heart. This study employed optical mapping to characterize propagation changes in intact mouse hearts with cardiomyocyte-restricted knock out of insulin receptors (CIRKO).
METHODS: Fluorescent signals emitted from excited Di-4-ANEPPS in isolated Langendorff perfused mouse hearts were recorded from the left ventricular epicardium using an 8 by 8 photo diode array. The study included hearts from 8 CIRKO mice and 8 wild type (WT) littermate controls. Hearts were stimulated from the right atrium or the left ventricle at basic cycle lengths ranging from 160 to 280 ms under normal conditions and then after 5 minutes of perfusion with elevated potassium ion concentration (9.4 mM).
RESULTS: None of the 8 CIRKO hearts maintained regular responses to atrial stimulation at the 160 ms cycle length under normal conditions; however, all of the WT hearts were captured at this rate. Total activation time for a 4 mm by 4 mm area was longer for CIRKO hearts when compared with WT. Average epicardial conduction velocity was slower for the CIRKO when compared to WT. Propagation delay due to the presence of high [K+]e was significant in both CIRKO and WT mice, but significantly longer for the CIRKO hearts.
CONCLUSIONS: These results show that in addition to reducing repolarization currents, impaired myocardial insulin signaling leads to impaired electrical impulse propagation particularly at increased heart rates. These data suggest a link between impaired myocardial insulin signaling and the increased risk of arrhythmia and sudden death in patients with diabetes.

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Year:  2004        PMID: 15534822     DOI: 10.1016/j.jelectrocard.2004.08.037

Source DB:  PubMed          Journal:  J Electrocardiol        ISSN: 0022-0736            Impact factor:   1.438


  4 in total

1.  Reduced Na⁺ current density underlies impaired propagation in the diabetic rabbit ventricle.

Authors:  Catherine L Stables; Hassan Musa; Aditi Mitra; Sandesh Bhushal; Makarand Deo; Guadalupe Guerrero-Serna; Sergey Mironov; Manuel Zarzoso; Karen L Vikstrom; William Cawthorn; Sandeep V Pandit
Journal:  J Mol Cell Cardiol       Date:  2014-01-09       Impact factor: 5.000

Review 2.  Cardiac conduction in isolated hearts of genetically modified mice--Connexin43 and salts.

Authors:  Sharon A George; Steven Poelzing
Journal:  Prog Biophys Mol Biol       Date:  2015-11-25       Impact factor: 3.667

3.  The absence of insulin signaling in the heart induces changes in potassium channel expression and ventricular repolarization.

Authors:  Angelica Lopez-Izquierdo; Renata O Pereira; Adam R Wende; Bonnie B Punske; E Dale Abel; Martin Tristani-Firouzi
Journal:  Am J Physiol Heart Circ Physiol       Date:  2013-12-27       Impact factor: 4.733

Review 4.  New Molecular Insights of Insulin in Diabetic Cardiomyopathy.

Authors:  Francisco Westermeier; Jaime A Riquelme; Mario Pavez; Valeria Garrido; Ariel Díaz; Hugo E Verdejo; Pablo F Castro; Lorena García; Sergio Lavandero
Journal:  Front Physiol       Date:  2016-04-12       Impact factor: 4.566

  4 in total

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