Evidence map›Paper›PMID 27645822›Full record

ReviewCellular and molecular life sciences : CMLS2017

Modulation of Kv7 channels and excitability in the brain.

Derek L Greene, Naoto Hoshi

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed, 1 pooled it
6.4field-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

105 citing papers in PubMed, 1 synthesis or guideline pooled it, 173 citations in OpenAlex.

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  5. KCommunications medicine · 2026
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  9. KArchiv der Pharmazie · 2026
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45 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 1 institution in 1 country.

Derek L GreeneDepartment of Pharmacology, University of California, 360 Med Surge II, Irvine, CA, 92697, USA.
Naoto HoshiDepartment of Pharmacology, University of California, 360 Med Surge II, Irvine, CA, 92697, USA. nhoshi@uci.edu.ORCID 0000-0001-8533-0022
University of California, Irvine · US

Funding

Regulations and function of the M-channelR01NS067288 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI HOSHI, NAOTO · 2010 to 2014
$1.6M
NINDS NIH HHS R01 NS067288
6 · The paper itself

Abstract

Neuronal Kv7 channels underlie a voltage-gated non-inactivating potassium current known as the M-current. Due to its particular characteristics, Kv7 channels show pronounced control over the excitability of neurons. We will discuss various factors that have been shown to drastically alter the activity of this channel such as protein and phospholipid interactions, phosphorylation, calcium, and numerous neurotransmitters. Kv7 channels locate to key areas for the control of action potential initiation and propagation. Moreover, we will explore the dynamic surface expression of the channel modulated by neurotransmitters and neural activity. We will also focus on known principle functions of neural Kv7 channels: control of resting membrane potential and spiking threshold, setting the firing frequency, afterhyperpolarization after burst firing, theta resonance, and transient hyperexcitability from neurotransmitter-induced suppression of the M-current. Finally, we will discuss the contribution of altered Kv7 activity to pathologies such as epilepsy and cognitive deficits.

Indexed as

Action PotentialsMembrane PotentialsAnimalsBrainCalciumCalmodulinCognitive DysfunctionEpilepsyGTP-Binding Protein alpha Subunits, Gq-G11HumansKCNQ Potassium ChannelsNeuronsSignal TransductionCalciumCalmodulinGTP-Binding Protein alpha Subunits, Gq-G11KCNQ Potassium ChannelsChannel traffickingEpilepsyExcitabilityKCNQKv7M-current

Identifiers

PMID27645822
PMCPMC5243414
OpenAlexW2521115404

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.