Evidence map›Paper›PMID 10479678›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1999

Two types of K(+) channel subunit, Erg1 and KCNQ2/3, contribute to the M-like current in a mammalian neuronal cell.

A A Selyanko, J K Hadley, I C Wood, F C Abogadie, P Delmas, N J Buckley, B London, D A Brown

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

48 citing papers in PubMed, 132 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Evaluation of Small-Molecule Candidates as Modulators of M-Type KInternational journal of molecular sciences · 2025
    Review
  5. Cannabidiol Modulates M-Type KBiomedicines · 2023
    Article
  6. Evidence for Dual Activation ofInternational journal of molecular sciences · 2022
    Article
  7. The Effectiveness in Activating M-Type KInternational journal of molecular sciences · 2021
    Article
  8. Article
  9. Article
  10. RLN3/RXFP3 Signaling in the PVN Inhibits Magnocellular Neurons via M-like Current Activation and Contributes to Binge Eating Behavior.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Pioglitazone, a PPAR-γ Activator, Stimulates BKFrontiers in pharmacology · 2018
    Article
  18. Review
  19. Article
  20. 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

8 authors at 2 institutions in 2 countries.

A A SelyankoDepartment of Pharmacology, University College London, London, WC1E 6BT, United Kingdom.
J K Hadley
I C Wood
F C Abogadie
P Delmas
N J Buckley
B London
D A Brown
University College London · GBUniversity of Pittsburgh Medical Center · US

Funding

Wellcome Trust
6 · The paper itself

Abstract

The potassium M current was originally identified in sympathetic ganglion cells, and analogous currents have been reported in some central neurons and also in some neural cell lines. It has recently been suggested that the M channel in sympathetic neurons comprises a heteromultimer of KCNQ2 and KCNQ3 (Wang et al., 1998) but it is unclear whether all other M-like currents are generated by these channels. Here we report that the M-like current previously described in NG108-15 mouse neuroblastoma x rat glioma cells has two components, "fast" and "slow", that may be differentiated kinetically and pharmacologically. We provide evidence from PCR analysis and expression studies to indicate that these two components are mediated by two distinct molecular species of K(+) channel: the fast component resembles that in sympathetic ganglia and is probably carried by KCNQ2/3 channels, whereas the slow component appears to be carried by merg1a channels. Thus, the channels generating M-like currents in different cells may be heterogeneous in molecular composition.

Indexed as

AnimalsBenzenesulfonamidesBenzimidazolesCell DifferentiationCHO CellsCricetinaeGliomaHumansHybrid CellsIndolesKCNQ2 Potassium ChannelKCNQ3 Potassium ChannelKineticsMembrane PotentialsMiceMice, Inbred C57BLBenzenesulfonamidesBenzimidazolesIndolesKCNQ2 Potassium ChannelKCNQ2 protein, humanKcnq2 protein, ratKCNQ3 Potassium ChannelKCNQ3 protein, humanKcnq3 protein, mouseKcnq3 protein, ratlinopirdinePotassium ChannelsPotassium Channels, Voltage-GatedPyridinesReceptor, Muscarinic M1Receptors, MuscarinicSulfanilamidesWAY 123398

Identifiers

PMID10479678
PMCPMC6782456
OpenAlexW1575439657

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.