Evidence map›Paper›PMID 16373387›Full record

ArticleThe Journal of physiology2006

Expression and biophysical properties of Kv1 channels in supragranular neocortical pyramidal neurones.

D Guan, J C F Lee, T Tkatch, D J Surmeier, W E Armstrong, R C Foehring

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

54 citing papers in PubMed, 101 citations in OpenAlex.

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  14. A-type KNeuropharmacology · 2018
    Article
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  16. Celecoxib Ameliorates Seizure Susceptibility in Autosomal Dominant Lateral Temporal Epilepsy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
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  20. Review
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

D GuanDepartment of Anatomy and Neurobiology, University of Tennessee, 855 Monroe Avenue, Memphis, TN 38163, USA.
J C F Lee
T Tkatch
D J Surmeier
W E Armstrong
R C Foehring
University of Tennessee Health Science Center · USNorthwestern University · US

Funding

SYNAPTIC CONTROLOF PALLIDAL ACTIVITYP50NS047085 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SURMEIER, DALTON JAMES · 2003 to 2018
$19.2M
Slowly Inactivating K+ Channels in Pyramidal NeuronsR01NS044163 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI FOEHRING, ROBERT C, SPAIN, WILLIAM J · 2003 to 2022
$6.5M
Plasticity of Oxytocin Neurons During LactationR01HD041002 · NICHD · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI ARMSTRONG, WILLIAM E · 2001 to 2005
$1.0M
NICHD NIH HHS R01 HD041002NINDS NIH HHS NS044163NINDS NIH HHS NS047085NINDS NIH HHS P50 NS047085NINDS NIH HHS R01 NS044163
6 · The paper itself

Abstract

Potassium channels are extremely diverse regulators of neuronal excitability. As part of an investigation into how this molecular diversity is utilized by neurones, we examined the expression and biophysical properties of native Kv1 channels in layer II/III pyramidal neurones from somatosensory and motor cortex. Single-cell RT-PCR, immunocytochemistry, and whole cell recordings with specific peptide toxins revealed that individual pyramidal cells express multiple Kv1 alpha-subunits. The most abundant subunit mRNAs were Kv1.1 > 1.2 > 1.4 > 1.3. All of these subunits were localized to somatodendritic as well as axonal cell compartments. These data suggest variability in the subunit complexion of Kv1 channels in these cells. The alpha-dendrotoxin (alpha-DTX)-sensitive current activated more rapidly and at more negative potentials than the alpha-DTX-insensitive current, was first observed at voltages near action potential threshold, and was relatively insensitive to holding potential. The alpha-DTX-sensitive current comprised about 10% of outward current at steady-state, in response to steps from -70 mV. From -50 mV, this percentage increased to approximately 20%. All cells expressed an alpha-DTX-sensitive current with slow inactivation kinetics. In some cells a transient component was also present. Deactivation kinetics were voltage dependent, such that deactivation was slow at potentials traversed by interspike intervals during repetitive firing. Because of its kinetics and voltage dependence, the alpha-DTX-sensitive current should be most important at physiological resting potentials and in response to brief stimuli. Kv1 channels should also be important at voltages near threshold and corresponding to interspike intervals.

Indexed as

AnimalsDelayed Rectifier Potassium ChannelsElapid VenomsImmunohistochemistryIon Channel GatingKv1.1 Potassium ChannelKv1.2 Potassium ChannelKv1.3 Potassium ChannelKv1.4 Potassium ChannelMotor CortexNeocortexNeuronsPotassium Channel BlockersPotassium ChannelsPyramidal CellsRatsDelayed Rectifier Potassium ChannelsdendrotoxinElapid VenomsKv1.1 Potassium ChannelKv1.2 Potassium ChannelKv1.3 Potassium ChannelKv1.4 Potassium ChannelPotassium Channel BlockersPotassium ChannelsRNA, Messenger

Identifiers

PMID16373387
PMCPMC1796796
OpenAlexW2107269392

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.