Evidence map›Paper›PMID 32554550›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2020

Anastasia Kosenko, Shirin Moftakhar, Marcelo A Wood, Naoto Hoshi

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Kv7 Channels and Excitability Disorders.Handbook of experimental pharmacology · 2021
    Article
  6. 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

4 authors at 1 institution in 1 country.

Anastasia KosenkoDepartment of Pharmacology, University of California, Irvine, Irvine, California 92697.
Shirin MoftakharDepartment of Pharmacology, University of California, Irvine, Irvine, California 92697.
Marcelo A WoodDepartment of Neurobiology and Behavior, Center for the Neurobiology of Learning and Memory, University of California, Irvine, Irvine, California 92697.
Naoto HoshiDepartment of Pharmacology, University of California, Irvine, Irvine, California 92697 nhoshi@uci.edu.
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

The M-current is a low voltage-activated potassium current generated by neuronal Kv7 channels. A prominent role of the M-current is to a create transient increase of neuronal excitability in response to neurotransmitters through the suppression of this current. Accordingly, M-current suppression is assumed to be involved in higher brain functions including learning and memory. However, there is little evidence supporting such a role to date. To address this gap, we examined behavioral tasks to assess learning and memory in homozygous Kv7.2 knock-in mice, Kv7.2(S559A), which show reduced M-current suppression while maintaining a normal basal M-current activity in neurons. We found that Kv7.2(S559A) mice had normal object location memory and contextual fear memory, but impaired long-term object recognition memory. Furthermore, short-term memory for object recognition was intact in Kv7.2(S559A) mice. The deficit in long-term object recognition memory was restored by the administration of a selective Kv7 channel inhibitor, XE991, when delivered during the memory consolidation phase. Lastly, c-Fos induction 2 h after training in Kv7.2(S559A) mice was normal in the hippocampus, which corresponds to intact object location memory, but was reduced in the perirhinal cortex, which corresponds to impaired long-term object recognition memory. Together, these results support the overall conclusion that M-current suppression is important for memory consolidation of specific types of memories.

Indexed as

Amino Acid SequenceAnimalsFearFemaleKCNQ2 Potassium ChannelMaleMemory ConsolidationMiceMice, Inbred C57BLMice, TransgenicOdorantsRecognition, PsychologySmellKCNQ2 Potassium ChannelKCNQ2Kv7.2object location memoryobject recognition memorypotassium channelvoltage-gated channel

Identifiers

PMID32554550
PMCPMC7380971
OpenAlexW3035827471

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.