Evidence map›Paper›PMID 21687499›Full record

ArticleFrontiers in pharmacology2011

The Voltage-Sensing Domain of K(v)7.2 Channels as a Molecular Target for Epilepsy-Causing Mutations and Anticonvulsants.

Francesco Miceli, Maria Virginia Soldovieri, Fabio Arturo Iannotti, Vincenzo Barrese, Paolo Ambrosino, Maria Martire, Maria Roberta Cilio, Maurizio Taglialatela

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. A novelMolecular medicine reports · 2022
    Article
  3. HumanJournal of neurophysiology · 2022
    Article
  4. Heterozygous Deletion of Epilepsy GeneFrontiers in behavioral neuroscience · 2022
    Article
  5. Detrusor Smooth Muscle KFrontiers in physiology · 2020
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. β-Secretase BACE1 regulates hippocampal and reconstituted M-currents in a β-subunit-like fashion.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  12. Review
  13. The endocannabinoid 2-AG controls skeletal muscle cell differentiation via CB1 receptor-dependent inhibition of Kv7 channels.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  14. Review
  15. Phosphatidylinositol 4,5-bisphosphate alters pharmacological selectivity for epilepsy-causing KCNQ potassium channels.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  16. Review
  17. Article
  18. 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.

Francesco MiceliDivision of Neurology, IRCCS Bambino Gesù Children's Hospital Rome, Italy.
Maria Virginia Soldovieri
Fabio Arturo Iannotti
Vincenzo Barrese
Paolo Ambrosino
Maria Martire
Maria Roberta Cilio
Maurizio Taglialatela

Funding

Telethon GGP07125
6 · The paper itself

Abstract

Understanding the molecular mechanisms underlying voltage-dependent gating in voltage-gated ion channels (VGICs) has been a major effort over the last decades. In recent years, changes in the gating process have emerged as common denominators for several genetically determined channelopathies affecting heart rhythm (arrhythmias), neuronal excitability (epilepsy, pain), or skeletal muscle contraction (periodic paralysis). Moreover, gating changes appear as the main molecular mechanism by which several natural toxins from a variety of species affect ion channel function. In this work, we describe the pathophysiological and pharmacological relevance of the gating process in voltage-gated K(+) channels encoded by the K(v)7 gene family. After reviewing the current knowledge on the molecular mechanisms and on the structural models of voltage-dependent gating in VGICs, we describe the physiological relevance of these channels, with particular emphasis on those formed by K(v)7.2-K(v)7.5 subunits having a well-established role in controlling neuronal excitability in humans. In fact, genetically determined alterations in K(v)7.2 and K(v)7.3 genes are responsible for benign familial neonatal convulsions, a rare seizure disorder affecting newborns, and the pharmacological activation of K(v)7.2/3 channels can exert antiepileptic activity in humans. Both mutation-triggered channel dysfunction and drug-induced channel activation can occur by impeding or facilitating, respectively, channel sensitivity to membrane voltage and can affect overlapping molecular sites within the voltage-sensing domain of these channels. Thus, understanding the molecular steps involved in voltage-sensing in K(v)7 channels will allow to better define the pathogenesis of rare human epilepsy, and to design innovative pharmacological strategies for the treatment of epilepsies and, possibly, other human diseases characterized by neuronal hyperexcitability.

Indexed as

anticonvulsant drugsepilepsygatingKv7 channelsneuronal excitabilitypotassium channelsretigabinevoltage-sensing

Identifiers

PMID21687499
PMCPMC3108560

What OpenQuestion holds

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Registered trials

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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.