Evidence map›Paper›PMID 9625868›Full record

ArticleThe Journal of physiology1998

Ca2+-inhibited non-inactivating K+ channels in cultured rat hippocampal pyramidal neurones.

A A Selyanko, J A Sim

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In one paragraph

Article in The Journal of physiology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 39% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. KV7/M channels mediate osmotic modulation of intrinsic neuronal excitability.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2009
    Article
  4. Neural KCNQ (Kv7) channels.British journal of pharmacology · 2009
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

A A SelyankoDepartment of Pharmacology, University College London, Gower Street, London WC1E 6BT, UK. a.selyanko@ucl.ac.uk
J A Sim
University College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

1. Whole-cell perforated-patch recording from cultured CA1-CA3 pyramidal neurones from neonatal rat hippocampus (20-22 C; [K+]o = 2.5 mM) revealed two previously recorded non-inactivating (sustained) K+ outward currents: a voltage-independent 'leak' current (Ileak) operating at all negative potentials, and, at potentials >= -60 mV, a time- and voltage-dependent 'M-current' (IK(M)). Both were inhibited by 1 mM Ba2+ or 10 microM oxotremorine-M (Oxo-M). In ruptured-patch recording using Ca2+-free pipette solution, Ileak was strongly enhanced, and was inhibited by 1 mM Ba2+ but unaffected by 0.5 mM 4-aminopyridine (4-AP), 1 mM tetraethylammonium (TEA) or 1-10 nM margatoxin. 2. Single channels underlying these currents were sought in cell-attached patch recordings. A single class of channels of conductance approximately 7 pS showing sustained activity at resting potential and above was identified. These normally had a very low open probability (Po < 0. 1), which, however, showed a dramatic and reversible increase (to about 0.9 at approximately 0 mV) following the removal of Ca2+ from the bath. Under these (Ca2+-free) conditions, single-channel Po showed both voltage-dependent and voltage-independent components on patch depolarization from resting potential. The mean activation curve was fitted by a modified Boltzmann equation. When tested, all channels were reversibly inhibited by addition of 10 microM Oxo-M to the bath solution. 3. The channels maintained their high Po in patches excised in inside-out mode into a Ca2+-free internal solution and were strongly inhibited by application of Ca2+ to the inner face of the membrane (IC50 = 122 nM); this inhibition was observed in the absence of MgATP, and therefore was direct and unrelated to channel phosphorylation/dephosphorylation. 4. Channels in patches excised in outside-out mode were blocked by 1 mM Ba2+ but were unaffected by 4-AP or TEA. 5. Channels in cell-attached patches were inhibited after single spikes, yielding inward ensemble currents lasting several hundred milliseconds. This was prevented in Ca2+-free solution, implying that it was due to Ca2+ entry. 6. The properties of these channels (block by internal Ca2+ and external Oxo-M and Ba2+, and the presence of both voltage-dependent and voltage-independent components in their Po/V relationship) show points of resemblance to those expected for channels associated with both Ileak and IK(M) components of the sustained macroscopic currents. For this reason we designate them Ksust ('sustained current') channels. Inhibition of these channels by Ca2+ entry during an action potential may account for some forms of Ca2+-dependent after-depolarization. Their high sensitivity to internal Ca2+ may provide a new, positive feedback mechanism for cell excitation operating at low (near-resting) [Ca2+]i.

Indexed as

Potassium Channel BlockersAnimalsCalciumCells, CulturedElectric ConductivityElectrophysiologyHippocampusIntracellular MembranesPotassium ChannelsPyramidal CellsRatsRats, Sprague-DawleyCalciumPotassium Channel BlockersPotassium Channels

Identifiers

PMID9625868
PMCPMC2231017
OpenAlexW1978630242

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.