Evidence map›Paper›PMID 26779016›Full record

ArticleFrontiers in pharmacology2015

Serotonin 2a Receptor and Serotonin 1a Receptor Interact Within the Medial Prefrontal Cortex During Recognition Memory in Mice.

Juan F Morici, Lucia Ciccia, Gaël Malleret, Jay A Gingrich, Pedro Bekinschtein, Noelia V Weisstaub

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 30 citations in OpenAlex.

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  9. Food science and biotechnology · 2017
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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 4 institutions in 3 countries.

Juan F MoriciSystems Neuroscience Group, Laboratory of Experimental Cognition and Behavior, Institute of Physiology and Biophysics, IFIBIO "Houssay," CONICET and University of Buenos Aires Medical School Buenos Aires, Argentina.
Lucia CicciaSystems Neuroscience Group, Laboratory of Experimental Cognition and Behavior, Institute of Physiology and Biophysics, IFIBIO "Houssay," CONICET and University of Buenos Aires Medical School Buenos Aires, Argentina.
Gaël MalleretLyon Neuroscience Research Center, Centre National de la Recherche Scientifique UMR 5292 - Institut National de la Santé et de la Recherche Médicale U1028 - Université Claude Bernard Lyon1 Lyon, France.
Jay A GingrichSackler Institute for Developmental Psychobiology, Columbia University, New YorkNY, USA; New York State Psychiatric InstituteNew York, NY, USA.
Pedro BekinschteinLaboratory of Memory Research and Molecular Cognition, Institute for Cell Biology and Neuroscience, CONICET and University of Buenos Aires Medical School Buenos Aires, Argentina.
Noelia V WeisstaubSystems Neuroscience Group, Laboratory of Experimental Cognition and Behavior, Institute of Physiology and Biophysics, IFIBIO "Houssay," CONICET and University of Buenos Aires Medical School Buenos Aires, Argentina.
Consejo Nacional de Investigaciones Científicas y Técnicas · ARColumbia University · USUniversidad de Buenos Aires · ARUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Episodic memory, can be defined as the memory for unique events. The serotonergic system one of the main neuromodulatory systems in the brain appears to play a role in it. The serotonin 2a receptor (5-HT2aR) one of the principal post-synaptic receptors for 5-HT in the brain, is involved in neuropsychiatric and neurological disorders associated with memory deficits. Recognition memory can be defined as the ability to recognize if a particular event or item was previously encountered and is thus considered, under certain conditions, a form of episodic memory. As human data suggest that a constitutively decrease of 5-HT2A signaling might affect episodic memory performance we decided to compare the performance of mice with disrupted 5-HT2aR signaling (htr2a (-/-)) with wild type (htr2a (+/+)) littermates in different recognition memory and working memory tasks that differed in the level of proactive interference. We found that ablation of 5-HT2aR signaling throughout development produces a deficit in tasks that cannot be solved by single item strategy suggesting that 5-HT2aR signaling is involved in interference resolution. We also found that in the absence of 5-HT2aR signaling serotonin has a deleterious effect on recognition memory retrieval through the activation of 5-HT1aR in the medial prefrontal cortex.

Indexed as

5-HT1A receptor5-HT2A receptorinterference controlrecognition memoryserotonin

Identifiers

PMID26779016
PMCPMC4688339
OpenAlexW2239049730

What OpenQuestion holds

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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.