Literature DB >> 9831910

Use-dependent block of Ih in mouse dorsal root ganglion neurons by sinus node inhibitors.

A Raes1, G Van de Vijver, M Goethals, P P van Bogaert.   

Abstract

1. The sinus node inhibitors UL FS 49 and DK-AH 269 reduce heart rate by slowing diastolic depolarization rate in the sino-atrial (SA) node, which might originate from the use-dependent blockade of a hyperpolarization-activated current If. A hyperpolarization-activated current Ih, which is present in many types of neurons, is similar to If. We studied the effects of these drugs on Ih in cultured mouse dorsal root ganglion (DRG) neurons. 2. With the whole-cell patch-clamp technique use-dependent block of Ih was observed. The steady-state block following a voltage-clamp pulse train (1-s steps from -38 to -108 mV applied at 0.5 Hz) was dependent on drug concentration and showed an apparent Kd of 0.1 and 0.79 microM with DK AH 269 and UL-FS 49 respectively. 3. The rate of block increased linearly with drug concentration. The rate of recovery from block was, however, much slower compared to cardiac tissue. 4. There was no significant effect of UL-FS 49 on the activation curve. 5. At high concentrations of UL-FS 49 a clear association of the drug with the open channel was observed. 6. When the cell was stimulated at a frequency of 3 Hz, a distinct hyperpolarization was observed in the presence of extracellular Cs+ or when Ih was blocked with UL-FS 49, but not in the absence of Cs+ and UL-FS 49. 7. These results indicate that Ih protects the cell against hyperpolarizations and subsequent inexcitability. The action of the drugs on the hyperpolarization-activated current in cardiac and neuronal tissue show some similarities; however, some pronounced differences indicate that different subtypes of the channel might exist.

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Year:  1998        PMID: 9831910      PMCID: PMC1571028          DOI: 10.1038/sj.bjp.0702153

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  6 in total

1.  Assessing the role of Ih channels in synaptic transmission and mossy fiber LTP.

Authors:  Vivien Chevaleyre; Pablo E Castillo
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-01       Impact factor: 11.205

2.  HCN2 channels: a permanent open state and conductance changes.

Authors:  François Pittoors; Pierre Paul Van Bogaert
Journal:  J Membr Biol       Date:  2014-11-13       Impact factor: 1.843

3.  The hyperpolarization-activated channel HCN4 is required for the generation of pacemaker action potentials in the embryonic heart.

Authors:  Juliane Stieber; Stefan Herrmann; Susanne Feil; Jana Löster; Robert Feil; Martin Biel; Franz Hofmann; Andreas Ludwig
Journal:  Proc Natl Acad Sci U S A       Date:  2003-12-01       Impact factor: 11.205

4.  Characterization of the human HCN1 channel and its inhibition by capsazepine.

Authors:  Catherine H Gill; Andrew Randall; Stewart A Bates; Kerstin Hill; Davina Owen; Phil M Larkman; William Cairns; Shahnaz P Yusaf; Paul R Murdock; Paul J L M Strijbos; Andrew J Powell; Christopher D Benham; Ceri H Davies
Journal:  Br J Pharmacol       Date:  2004-09-06       Impact factor: 8.739

5.  Local anaesthetics block hyperpolarization-activated inward current in rat small dorsal root ganglion neurones.

Authors:  Ulrike Bischoff; Michael E Bräu; Werner Vogel; Gunter Hempelmann; Andrea Olschewski
Journal:  Br J Pharmacol       Date:  2003-08       Impact factor: 8.739

6.  Blocker state dependence and trapping in hyperpolarization-activated cation channels: evidence for an intracellular activation gate.

Authors:  K S Shin; B S Rothberg; G Yellen
Journal:  J Gen Physiol       Date:  2001-02       Impact factor: 4.086

  6 in total

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