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[F. Cell biology-25]



             Carteolol increases hERG current and cardiac action potential


                                                     duration




                                                      Su-Hyun Jo¹˙*

          ¹Department of Physiology, Institute of Bioscience and Biotechnology, BK21 plus Graduate Program, Kangwon

                              National University College of Medicine, Chuncheon 200-701, Korea




        Carteolol is a non-selective beta blocker used to treat glaucoma. We studied the effects of carteolol on a human
        K+ channel, human ether-a-go-go-related gene (hERG), expressed in Xenopus oocytes and on action potential of

        guinea pig ventricular myocytes. The hERG encodes the pore-forming subunits of the rapidly-activating delayed

        rectifier K+ channel in the heart. Mutations in hERG reduce IKr and cause type 2 long QT syndrome, a disorder that
        predisposes individuals to life-threatening arrhythmias. Carteolol increased hERG current amplitude at the end of
        the voltage steps and hERG tail currents in a concentration-dependent manner. Carteolol did not change the value

        of V1/2 for activation curve of hERG tail current, indicating the drug did not affect activation gating. In guinea pig
        ventricular myocytes, carteolol did not change the action potential amplitude and the resting membrane potential,

        however, the drug increased the action potential duration (APD₉₀, APD₅₀, APD₂₀), showing that carteolol could
        cause arrhythmogenic effects in cardiac function.
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