Evidence map›Paper›PMID 18199775›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2008

Cumulative activation of voltage-dependent KVS-1 potassium channels.

Patricio Rojas, Jonathan Garst-Orozco, Beravan Baban, Jose Antonio de Santiago-Castillo, Manuel Covarrubias, Lawrence Salkoff

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Oxidation of KCNB1 Potassium Channels Causes Neurotoxicity and Cognitive Impairment in a Mouse Model of Traumatic Brain Injury.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  3. Use-dependent activation of neuronal Kv1.2 channel complexes.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  4. Toxic role of K+ channel oxidation in mammalian brain.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    Article
  5. Article
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

6 authors.

Patricio RojasDepartment of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Jonathan Garst-Orozco
Beravan Baban
Jose Antonio de Santiago-Castillo
Manuel Covarrubias
Lawrence Salkoff

Funding

MOLECULAR PROPERTIES OF SUBTHRESHOLD POTASSIUM CHANNELSR01NS032337 · NINDS · THOMAS JEFFERSON UNIVERSITY · PI COVARRUBIAS, MANUEL L · 1999 to 2010
$2.8M
A COMPREHENSIVE RESOURCE BASE OF C. ELEGANS K+ CHANNELSR24RR017342 · NCRR · WASHINGTON UNIVERSITY · PI SALKOFF, LAWRENCE B · 2003 to 2007
$2.2M
Mutant Analysis of a Novel High Conductance K+ ChannelR01GM067154 · NIGMS · WASHINGTON UNIVERSITY · PI SALKOFF, LAWRENCE B · 2003 to 2006
$1.2M
NCRR NIH HHS R24 RR017342NCRR NIH HHS R24 RR017342-01NIGMS NIH HHS R01 GM067154NIGMS NIH HHS R01 GM067154-01A1NINDS NIH HHS R01 NS032337NINDS NIH HHS R01 NS032337-13
6 · The paper itself

Abstract

In this study, we reveal the existence of a novel use-dependent phenomenon in potassium channels, which we refer to as cumulative activation (CA). CA consists of an increase in current amplitude in response to repetitive depolarizing step pulses to the same potential. CA persists for up to 20 s and is similar to a phenomenon called "voltage-dependent facilitation" observed in some calcium channels. The KVS-1 K+ channel, which exhibits CA, is a rapidly activating and inactivating voltage-dependent potassium channel expressed in chemosensory and other neurons of Caenorhabditis elegans. It is unusual in being most closely related to the Shab (Kv2) family of potassium channels, which typically behave like delayed rectifier K+ channels in other species. The magnitude of CA depends on the frequency, voltage, and duration of the depolarizing step pulse. CA also radically changes the activation and inactivation kinetics of the channel, suggesting that the channel may undergo a physical modification in a use-dependent manner; thus, a model that closely simulates the behavior of the channel postulates the existence of two populations of channels, unmodified and modified. Use-dependent changes in the behavior of potassium channels, such as CA observed in KVS-1, could be involved in functional mechanisms of cellular plasticity such as synaptic depression that represent the cellular basis of learning and memory.

Indexed as

AnimalsCell Line, TransformedDose-Response Relationship, RadiationElectric StimulationHumansIon Channel GatingMembrane PotentialsMicroinjectionsOocytesPatch-Clamp TechniquesPotassium Channels, Voltage-GatedProtein Structure, TertiaryTime FactorsTransfectionXenopusPotassium Channels, Voltage-Gated

Identifiers

PMID18199775
PMCPMC2248284

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.