Evidence map›Paper›PMID 34813859›Full record

ArticleNeuropharmacology2022

NMDA receptor-mediated synaptic transmission in prefrontal neurons underlies social memory retrieval in female mice.

Yu-Xiang Zhang, Bo Xing, Yan-Chun Li, Chun-Xia Yan, Wen-Jun Gao

Open access · greenAbstract read
In one paragraph

Article in Neuropharmacology, 2022. 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
1.1field-weighted citation impact, top 20% 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, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Roles of AMPA receptors in social behaviors.Frontiers in synaptic neuroscience · 2024
    Review
  4. Article
  5. 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

5 authors at 2 institutions in 2 countries.

Yu-Xiang ZhangDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, 19129, USA; College of Forensic Medicine, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, 710061, China.
Bo XingDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, 19129, USA.
Yan-Chun LiDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, 19129, USA.
Chun-Xia YanCollege of Forensic Medicine, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, 710061, China. Electronic address: yanchunxia@xjtu.edu.cn.
Wen-Jun GaoDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, 19129, USA. Electronic address: wg38@drexel.edu.
Drexel University · USXi'an Jiaotong University · CN

Funding

Development of NMDAR hypofunction and cognitive deficitsR01MH085666 · NIMH · DREXEL UNIVERSITY · PI GAO, WEN-JUN · 2009 to 2018
$3.8M
Corticothalamic control of social motivationR01MH131053 · NIMH · DREXEL UNIVERSITY · PI Wen-Jun Gao · 2022 to 2026
$1.9M
Role of prefrontal cortical dopamine in aggressionR21MH110678 · NIMH · DREXEL UNIVERSITY · PI GAO, WEN-JUN · 2016 to 2017
$425k
NIMH NIH HHS R01 MH085666NIMH NIH HHS R01 MH131053NIMH NIH HHS R21 MH110678
6 · The paper itself

Abstract

Social memory is the ability to discriminate familiar conspecific from the unknown ones. Prefrontal neurons are essentially required for social memory, but the mechanism associated with this regulation remains unknown. It is also unclear to what extent the neuronal representations of social memory formation and retrieval events overlap in the prefrontal cortex (PFC) and which event drives social memory strength. Here we asked these questions by using a repeated social training paradigm for social recognition in FosTRAP mice. We found that after 4 days' repeated social training, female mice developed stable social memory. Specifically, repeated social training activated more cells that were labeled with tdTomato during memory retrieval compared with the first day of memory encoding. Besides, combining TRAP with c-Fos immunostaining, we found about 30% of the FosTRAPed cells were reactivated during retrieval. Moreover, the number of retrieval-induced but not first-day encoding-induced tdTomato neurons correlates with the social recognition ratio in the prelimbic but not other subregions. The activated cells during the retrieval session also showed increased NMDA receptor-mediated synaptic transmission compared with that in non-labeled pyramidal neurons. Blocking NMDA receptors by MK-801 impaired social memory but not sociability. Therefore, our results reveal that repetitive training elevates mPFC involvement in social memory retrieval via enhancing NMDA receptor-mediated synaptic transmission, thus rendering stable social memory.

Indexed as

AnimalsFemaleMemoryMental RecallMiceMice, Inbred C57BLNeuronsPrefrontal CortexReceptors, N-Methyl-D-AspartateRecognition, PsychologySocial BehaviorSynaptic TransmissionReceptors, N-Methyl-D-AspartateFemale mouseFosTRAP mouseMemory retrievalNMDA receptorsPrefrontal cortexSocial memory

Identifiers

PMID34813859
PMCPMC8688302
OpenAlexW3217454696

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.