Evidence map›Paper›PMID 28928640›Full record

ArticleFrontiers in systems neuroscience2017

HDAC3 Inhibitor RGFP966 Modulates Neuronal Memory for Vocal Communication Signals in a Songbird Model.

Mimi L Phan, Mark M Gergues, Shafali Mahidadia, Jorge Jimenez-Castillo, David S Vicario, Kasia M Bieszczad

Open access · goldAbstract read
In one paragraph

Article in Frontiers in systems neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

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  18. The discovery of novel HDAC3 inhibitors via virtual screening and in vitro bioassay.Journal of enzyme inhibition and medicinal chemistry · 2018
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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

6 authors at 1 institution in 1 country.

Mimi L PhanDepartment of Psychology, Behavioral & Systems Neuroscience, Rutgers, The State University of New JerseyNew Brunswick, NJ, United States.
Mark M GerguesDepartment of Psychology, Behavioral & Systems Neuroscience, Rutgers, The State University of New JerseyNew Brunswick, NJ, United States.
Shafali MahidadiaDepartment of Psychology, Behavioral & Systems Neuroscience, Rutgers, The State University of New JerseyNew Brunswick, NJ, United States.
Jorge Jimenez-CastilloDepartment of Psychology, Behavioral & Systems Neuroscience, Rutgers, The State University of New JerseyNew Brunswick, NJ, United States.
David S VicarioDepartment of Psychology, Behavioral & Systems Neuroscience, Rutgers, The State University of New JerseyNew Brunswick, NJ, United States.
Kasia M BieszczadDepartment of Psychology, Behavioral & Systems Neuroscience, Rutgers, The State University of New JerseyNew Brunswick, NJ, United States.
Rutgers, The State University of New Jersey · US

Funding

Molecular epigenetics of auditory memory and cortical plasticityR03DC014753 · NIDCD · RUTGERS, THE STATE UNIV OF N.J. · PI BIESZCZAD, KASIA · 2015 to 2017
$455k
NIDCD NIH HHS R03 DC014753
6 · The paper itself

Abstract

Epigenetic mechanisms that modify chromatin conformation have recently been under investigation for their contributions to learning and the formation of memory. For example, the role of enzymes involved in histone acetylation are studied in the formation of long-lasting memories because memory consolidation requires gene expression events that are facilitated by an open state of chromatin. We recently proposed that epigenetic events may control the entry of specific sensory features into long-term memory by enabling transcription-mediated neuronal plasticity in sensory brain areas. Histone deacetylases, like HDAC3, may thereby regulate the specific sensory information that is captured for entry into long-term memory stores (Phan and Bieszczad, 2016). To test this hypothesis, we used an HDAC3-selective inhibitor (RGFP966) to determine whether its application after an experience with a sound stimulus with unique acoustic features could contribute to the formation of a memory that would assist in mediating its later recognition. We gave adult male zebra finches limited exposure to unique conspecific songs (20 repetitions each, well below the normal threshold to form long-term memory), followed by treatment with RGFP966 or vehicle. In different groups, we either made multi-electrode recordings in the higher auditory area NCM (caudal medial nidopallidum), or determined expression of an immediate early gene,

Indexed as

electrophysiologyepigeneticsgene expressionlateralizationmemoryNCMstimulus specific adaptation (SSA)

Identifiers

PMID28928640
PMCPMC5591857
OpenAlexW2752991971

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.