Circulation Journal
Online ISSN : 1347-4820
Print ISSN : 1346-9843
ISSN-L : 1346-9843

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Effect of Carbenoxolone on Arrhythmogenesis in Rat Ventricular Muscle
Masahito MiuraTsuyoshi NaganoNaomi MuraiYuhto TaguchiTetsuya HandohMinami SatohSatoshi MiyataLawson MillerChiyohiko ShindohBruno D. Stuyvers
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Article ID: CJ-15-0401

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Abstract
Background:Connexin43 (Cx43) is a major connexin that forms gap junction (GJ) channels in the heart and is also present in the cell membrane as unopposed/non-junctional hemichannels and in the inner mitochondrial membrane. By using carbenoxolone (CBX), a blocker of Cx43, the effect of the blockade of Cx43 on Ca2+waves and triggered arrhythmias in the myocardium with non-uniform contraction was examined.Methods and Results:Trabeculae were obtained from rat hearts. Force, [Ca2+]i, and the diffusion coefficient were measured. Non-uniform contraction was produced with a 2,3-butanedione monoxime jet. Ca2+waves were induced by electrical stimulation. Inducibility of arrhythmias was estimated based on the minimal [Ca2+]oat which arrhythmias were induced. The Ca2+spark rate was measured in isolated single rat ventricular myocytes. CBX reduced the GJ permeability, whereas it did not change force and [Ca2+]itransients. CBX increased the Ca2+leak from the sarcoplasmic reticulum in trabeculae and increased the Ca2+spark rate in isolated single myocytes. CBX increased the velocity of Ca2+waves and further increased the inducibility of arrhythmias. Modulation of mitochondrial KATPchannels by diazoxide, cromakalim and 5-hydroxydecanoic acid affected the inducibility of arrhythmias increased by CBX.Conclusions:These results suggest that in diseased hearts, Cx43 plays an important role in the occurrence of triggered arrhythmias, probably under the modulation of mitochondrial KATPchannels.
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© 2015 THE JAPANESE CIRCULATION SOCIETY
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