Evidence map›Paper›PMID 25360708›Full record

ArticlePloS one2014

Molecular and genetic determinants of the NMDA receptor for superior learning and memory functions.

Stephanie Jacobs, Zhenzhong Cui, Ruiben Feng, Huimin Wang, Deheng Wang, Joe Z Tsien

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

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  6. Effect of θ–γ neural oscillation stimulation in hippocampal CA3 area on spatial cognition ability in ratsZhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2021
    Article
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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 3 institutions in 2 countries.

Stephanie JacobsBrain and Behavior Discovery Institute and Department of Neurology, Medical College of Georgia at Georgia Regents University, Augusta, Georgia, United States of America.
Zhenzhong CuiBrain and Behavior Discovery Institute and Department of Neurology, Medical College of Georgia at Georgia Regents University, Augusta, Georgia, United States of America.
Ruiben FengBrain and Behavior Discovery Institute and Department of Neurology, Medical College of Georgia at Georgia Regents University, Augusta, Georgia, United States of America.
Huimin WangShanghai Institute of Functional Genomics, East China Normal University, Shanghai, China.
Deheng WangBanna Biomedical Research Institute, Xi-Shuang-Ban-Na Prefecture, Yunnan Province, China.
Joe Z TsienBrain and Behavior Discovery Institute and Department of Neurology, Medical College of Georgia at Georgia Regents University, Augusta, Georgia, United States of America.
Discovery Institute · USAugusta University · USEast China Normal University · CN

Funding

The NR2 Subunit Motifs & Memory Enhancement in MiceR01MH060236 · NIMH · PRINCETON UNIVERSITY · PI TSIEN, JOE Z · 1999 to 2009
$3.8M
Temporal Analysis of Memory ProcessesR01AG024022 · NIA · PRINCETON UNIVERSITY · PI TSIEN, JOE Z · 2003 to 2007
$2.3M
Presenilins, Apoptosis, and Cortical DegenerationR01AG025918 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI TSIEN, JOE Z · 2005 to 2009
$1.5M
Hippocampal Network Profiles of Memory AgingR01AG034663 · NIA · AUGUSTA UNIVERSITY · PI TSIEN, JOE Z · 2009 to 2010
$996k
NIA NIH HHS AG024022NIA NIH HHS AG025918NIA NIH HHS AG034663NIA NIH HHS R01 AG024022NIA NIH HHS R01 AG025918NIA NIH HHS R01 AG034663NIMH NIH HHS MH060236NIMH NIH HHS R01 MH060236
6 · The paper itself

Abstract

The opening-duration of the NMDA receptors implements Hebb's synaptic coincidence-detection and is long thought to be the rate-limiting factor underlying superior memory. Here, we investigate the molecular and genetic determinants of the NMDA receptors by testing the "synaptic coincidence-detection time-duration" hypothesis vs. "GluN2B intracellular signaling domain" hypothesis. Accordingly, we generated a series of GluN2A, GluN2B, and GluN2D chimeric subunit transgenic mice in which C-terminal intracellular domains were systematically swapped and overexpressed in the forebrain excitatory neurons. The data presented in the present study supports the second hypothesis, the "GluN2B intracellular signaling domain" hypothesis. Surprisingly, we found that the voltage-gated channel opening-durations through either GluN2A or GluN2B are sufficient and their temporal differences are marginal. In contrast, the C-terminal intracellular domain of the GluN2B subunit is necessary and sufficient for superior performances in long-term novel object recognition and cued fear memories and superior flexibility in fear extinction. Intriguingly, memory enhancement correlates with enhanced long-term potentiation in the 10-100 Hz range while requiring intact long-term depression capacity at the 1-5 Hz range.

Indexed as

Amino Acid SequenceAnimalsBehavior, AnimalCA1 Region, HippocampalCuesElectrophysiological PhenomenaFearLong-Term PotentiationMemoryMemory, Long-TermMice, Inbred C57BLMice, TransgenicMolecular Sequence DataNeuronsProsencephalonProtein SubunitsProtein SubunitsReceptors, N-Methyl-D-Aspartate

Identifiers

PMID25360708
PMCPMC4216132
OpenAlexW2046009781

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.