Evidence map›Paper›PMID 21666672›Full record

ArticleNature neuroscience2011

KCNQ5 channels control resting properties and release probability of a synapse.

Hai Huang, Laurence O Trussell

Abstract read
In one paragraph

Article in Nature neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

64 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
  2. Article
  3. CRISPR/Cas9-mediatedFrontiers in physiology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Phosphatidylinositol 4,5-bisphosphate activation mechanism of human KCNQ5.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Glial KCNQ KNeuron · 2024
    Article
  12. A Developmental Switch in Cholinergic Mechanisms of Modulation in the Medial Nucleus of the Trapezoid Body.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  13. Article
  14. Cholinergic modulation in the vertebrate auditory pathway.Frontiers in cellular neuroscience · 2024
    Review
  15. Regulation of Neurotransmitter Release by KAdvances in neurobiology · 2023
    Article
  16. Article
  17. HumanJournal of neurophysiology · 2022
    Article
  18. Review
  19. KCNQ Channels Enable Reliable Presynaptic Spiking and Synaptic Transmission at High Frequency.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  20. Gain of function due to increased opening probability by twoProceedings of the National Academy of Sciences of the United States of America · 2022
    Article

4 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Hai HuangOregon Hearing Research Center, Oregon Health and Science University, Portland, Oregon, USA. huanghai@ohsu.edu
Laurence O Trussell
Oregon Health & Science University · USVollum Institute · US

Funding

Synaptic mechanisms in the auditory system (Administrative Supplement)R01DC004450 · NIDCD · OREGON HEALTH & SCIENCE UNIVERSITY · PI LAURENCE O TRUSSELL · 1999 to 2026
$10.6M
Regulation of synaptic amino acid receptors (Administrative Supplement)R01NS028901 · NINDS · UNIVERSITY OF WISCONSIN MADISON · PI TRUSSELL, LAURENCE O · 1991 to 2019
$4.3M
Regulation of synaptic amino acid receptorsR37NS028901 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI TRUSSELL, LAURENCE O · 2004 to 2010
$2.7M
NIDCD NIH HHS DC004450NIDCD NIH HHS R01 DC004450NINDS NIH HHS NS028901NINDS NIH HHS R01 NS028901
6 · The paper itself

Abstract

Little is known about which ion channels determine the resting electrical properties of presynaptic membranes. In recordings made from the rat calyx of Held, a giant mammalian terminal, we found resting potential to be controlled by KCNQ (Kv7) K(+) channels, most probably KCNQ5 (Kv7.5) homomers. Unlike most KCNQ channels, which are activated only by depolarizing stimuli, the presynaptic channels began to activate just below the resting potential. As a result, blockers and activators of KCNQ5 depolarized or hyperpolarized nerve terminals, respectively, markedly altering resting conductance. Moreover, the background conductance set by KCNQ5 channels, together with Na(+) and hyperpolarization-activated and cyclic nucleotide-gated (HCN) channels, determined the size and time course of the response to subthreshold stimuli. Signaling pathways known to directly affect exocytic machinery also regulated KCNQ5 channels, and increase or decrease of KCNQ5 channel activity controlled release probability through alterations in resting potential. Thus, ion channel determinants of presynaptic resting potential also control synaptic strength.

Indexed as

ProbabilityAnimalsAnimals, NewbornAnthracenesBrain StemCyclic Nucleotide-Gated Cation ChannelsElectric StimulationEnzyme InhibitorsExcitatory Postsynaptic PotentialsExocytosisHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsIn Vitro TechniquesKCNQ Potassium ChannelsMembrane PotentialsMicroscopy, ConfocalPatch-Clamp Techniques10,10-bis(4-pyridinylmethyl)-9(10H)-anthracenoneAnthracenesCyclic Nucleotide-Gated Cation ChannelsEnzyme InhibitorsHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsKcnq5 protein, ratKCNQ Potassium ChannelsmargatoxinPotassium Channel BlockersPotassium ChannelsScorpion Venoms

Identifiers

PMID21666672
PMCPMC3133966
OpenAlexW2010185947

What OpenQuestion holds

Textmetadata
LicenceTDM
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.