Literature DB >> 10908123

Pacemaker oscillations in heart and brain: a key role for hyperpolarization-activated cation channels.

R Gauss1, R Seifert.   

Abstract

Rhythmic activity of single cells or multicellular networks is a common feature of all organisms. The oscillatory activity is characterized by time intervals of several seconds up to many hours. Cellular rhythms govern the beating of the heart, the swimming behavior of sperm, cycles of sleep and wakefulness, breathing, and the release of hormones. Many neurons in the brain and cardiac cells are characterized by endogenous rhythmic activity, which relies on a complex interplay between several distinct ion channels. In particular, one type of ion channel plays a prominent role in the control of rhythmic electrical activity since it determines the frequency of the oscillations. The activity of the channels is thus setting the "pace" of the oscillations; therefore, these channels are often referred to as "pacemaker" channels. Despite their obvious important physiological function, it was not until recently that genes encoding pacemaker channels have been identified. Because both hyperpolarization and cyclic nucleotides are key elements that control their activity, pacemaker channels have now been designated hyperpolarization-activated and cyclic nucleotide-gated (HCN) channels. The molecular identification of the channels and the upcoming studies on their properties in heterologous systems will certainly enhance our understanding of "pacemaking" in physiological systems. This review gives a brief insight into the physiological importance of these channels and sums up what we have learned since the first cloning of genes succeeded (for recent reviews, see also Clapham 1998; Luthi and McCormick 1998a; Biel et al. 1999; Ludwig, Zong, Hofmann, et al. 1999; Santoro and Tibbs 1999).

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Year:  2000        PMID: 10908123     DOI: 10.1081/cbi-100101057

Source DB:  PubMed          Journal:  Chronobiol Int        ISSN: 0742-0528            Impact factor:   2.877


  18 in total

1.  Postnatal development of the hyperpolarization-activated excitatory current Ih in mouse hippocampal pyramidal neurons.

Authors:  Dmitry V Vasilyev; Michael E Barish
Journal:  J Neurosci       Date:  2002-10-15       Impact factor: 6.167

Review 2.  Regulation of recombinant and native hyperpolarization-activated cation channels.

Authors:  Samuel G A Frère; Mira Kuisle; Anita Lüthi
Journal:  Mol Neurobiol       Date:  2004-12       Impact factor: 5.590

3.  Novel role of KT5720 on regulating hyperpolarization-activated cyclic nucleotide-gated channel activity and dorsal root ganglion neuron excitability.

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Journal:  DNA Cell Biol       Date:  2013-06       Impact factor: 3.311

Review 4.  General anesthesia mediated by effects on ion channels.

Authors:  Cheng Zhou; Jin Liu; Xiang-Dong Chen
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5.  A transcriptomic analysis of type I-III neurons in the bed nucleus of the stria terminalis.

Authors:  Rimi Hazra; Ji-Dong Guo; Steven J Ryan; Aaron M Jasnow; Joanna Dabrowska; Donald G Rainnie
Journal:  Mol Cell Neurosci       Date:  2011-02-17       Impact factor: 4.314

6.  Pore topology of the hyperpolarization-activated cyclic nucleotide-gated channel from sea urchin sperm.

Authors:  Paola Roncaglia; Pavel Mistrík; Vincent Torre
Journal:  Biophys J       Date:  2002-10       Impact factor: 4.033

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Review 8.  Characteristics of HCN channels and their participation in neuropathic pain.

Authors:  Yu-Qiu Jiang; Qian Sun; Hui-Yin Tu; You Wan
Journal:  Neurochem Res       Date:  2008-05-07       Impact factor: 3.996

9.  Enhanced excitability of myenteric AH neurones in the inflamed guinea-pig distal colon.

Authors:  David R Linden; Keith A Sharkey; Gary M Mawe
Journal:  J Physiol       Date:  2003-01-24       Impact factor: 5.182

10.  Dendritic HCN2 channels constrain glutamate-driven excitability in reticular thalamic neurons.

Authors:  Shui-Wang Ying; Fan Jia; Syed Y Abbas; Franz Hofmann; Andreas Ludwig; Peter A Goldstein
Journal:  J Neurosci       Date:  2007-08-08       Impact factor: 6.167

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