Literature DB >> 8815800

Myocardial potassium channels: electrophysiological and molecular diversity.

D M Barry1, J M Nerbonne.   

Abstract

Myocardial K+ currents function to control resting membrane potentials, the heights and durations of action potentials, and refractoriness and automaticity. They are important targets for the actions of transmitters and hormones or drugs known, or postulated, to modulate cardiac functioning. A variety of K+ currents that subserve these functions have now been identified in myocardial cells isolated from different species, as well as in cells isolated from different regions of the heart in the same species. These currents include the voltage-gated K+ types, such as the transient outward (Ito) and delayed rectifier (IK) currents, as well as the inwardly rectifying currents, IK1, IK(ACh), and IK(ATP). The physiological and functional properties of the various K+ currents/channels expressed in different myocardial cell types are the focus of this review. Advances made in cloning K+ channel subunits of the Kv, eag, Kir, and IsK families are discussed, and progress made in identifying the K+ channel subunits expressed in the mammalian myocardium is summarized. The relationships between the various cloned K+ channel subunits and the functional K+ channels characterized electrophysiologically in myocardial cells are explored.

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Year:  1996        PMID: 8815800     DOI: 10.1146/annurev.ph.58.030196.002051

Source DB:  PubMed          Journal:  Annu Rev Physiol        ISSN: 0066-4278            Impact factor:   19.318


  44 in total

1.  Heteromeric assembly of Kv2.1 with Kv9.3: effect on the state dependence of inactivation.

Authors:  D Kerschensteiner; M Stocker
Journal:  Biophys J       Date:  1999-07       Impact factor: 4.033

Review 2.  Molecular basis of functional voltage-gated K+ channel diversity in the mammalian myocardium.

Authors:  J M Nerbonne
Journal:  J Physiol       Date:  2000-06-01       Impact factor: 5.182

3.  State-dependent barium block of wild-type and inactivation-deficient HERG channels in Xenopus oocytes.

Authors:  M Weerapura; S Nattel; M Courtemanche; D Doern; N Ethier; T Hebert
Journal:  J Physiol       Date:  2000-07-15       Impact factor: 5.182

4.  Molecular correlates of the calcium-independent, depolarization-activated K+ currents in rat atrial myocytes.

Authors:  E Bou-Abboud; J M Nerbonne
Journal:  J Physiol       Date:  1999-06-01       Impact factor: 5.182

5.  Inactivation and recovery in Kv1.4 K+ channels: lipophilic interactions at the intracellular mouth of the pore.

Authors:  Glenna C L Bett; Randall L Rasmusson
Journal:  J Physiol       Date:  2003-11-07       Impact factor: 5.182

6.  A model of the interaction between N-type and C-type inactivation in Kv1.4 channels.

Authors:  Glenna C L Bett; Isidore Dinga-Madou; Qinlian Zhou; Vladimir E Bondarenko; Randall L Rasmusson
Journal:  Biophys J       Date:  2011-01-05       Impact factor: 4.033

7.  Dispersion of repolarization and refractoriness are determinants of arrhythmia phenotype in transgenic mice with long QT.

Authors:  Barry London; Linda C Baker; Polina Petkova-Kirova; Jeanne M Nerbonne; Bum-Rak Choi; Guy Salama
Journal:  J Physiol       Date:  2006-11-16       Impact factor: 5.182

8.  Excitation-contraction coupling in Na+-Ca2+ exchanger knockout mice: reduced transsarcolemmal Ca2+ flux.

Authors:  Christian Pott; Kenneth D Philipson; Joshua I Goldhaber
Journal:  Circ Res       Date:  2005-11-17       Impact factor: 17.367

9.  Molecular identification of Kvalpha subunits that contribute to the oxygen-sensitive K+ current of chemoreceptor cells of the rabbit carotid body.

Authors:  Diego Sanchez; Jose R López-López; M Teresa Pérez-García; Gloria Sanz-Alfayate; Ana Obeso; Maria D Ganfornina; Constancio Gonzalez
Journal:  J Physiol       Date:  2002-07-15       Impact factor: 5.182

10.  Arrhythmia phenotype in mouse models of human long QT.

Authors:  Guy Salama; Linda Baker; Robert Wolk; Jacques Barhanin; Barry London
Journal:  J Interv Card Electrophysiol       Date:  2009-01-16       Impact factor: 1.900

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