2018
DOI: 10.1007/978-3-319-77812-9_3
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Potassium Channels in the Heart

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Cited by 3 publications
(3 citation statements)
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“…In cardiac tissue, K + channels include inwardly rectifying K + channels (Kir), transient outward K + channels, delayed outward rectifying K + channels, Ca 2+ -activated K + channels, and two-pore domain K + channels. They are primarily responsible for maintaining the resting potential, regulating electrical excitation, forming the peak of the AP, and repolarizing the cell ( 43 ). Any dysfunction in these channels may result in cardiac arrhythmia.…”
Section: Resultsmentioning
confidence: 99%
“…In cardiac tissue, K + channels include inwardly rectifying K + channels (Kir), transient outward K + channels, delayed outward rectifying K + channels, Ca 2+ -activated K + channels, and two-pore domain K + channels. They are primarily responsible for maintaining the resting potential, regulating electrical excitation, forming the peak of the AP, and repolarizing the cell ( 43 ). Any dysfunction in these channels may result in cardiac arrhythmia.…”
Section: Resultsmentioning
confidence: 99%
“…Several studies have demonstrated the importance of voltage-gated potassium channels in the genesis of cardiac arrhythmias [44][45][46][47][48]. Loss-of-function mutations in the K v 7.1 channel, lead to long-QT syndrome type 1 (LQTS1), which is the most frequent type of the long-QT syndromes [49].…”
Section: The Ionic Basis Of Apmentioning
confidence: 99%
“…In table 1, we present a series of characteristics of some channels of the cardiac muscle fibrocells, relating them to the specific AP phase and we indicate the documented interferences that pro-inflammatory cytokines produce on ion channels and currents. Several studies have demonstrated the importance of Voltage-Gated Potassium Channels in the genesis of cardiac arrhythmias [31][32][33][34][35]. Loss-of-function mutations in Kv the long-QT syndromes [36].…”
Section: The Ionic Basis Of Apmentioning
confidence: 99%