Evidence map›Paper›PMID 27807032›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2016

NR2A-Containing NMDARs in the Prefrontal Cortex Are Required for Working Memory and Associated with Age-Related Cognitive Decline.

Joseph A McQuail, B Sofia Beas, Kyle B Kelly, Kailey L Simpson, Charles J Frazier, Barry Setlow, Jennifer L Bizon

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

49 citing papers in PubMed, 80 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Joseph A McQuailDepartment of Neuroscience, College of Medicine.
B Sofia BeasDepartment of Neuroscience, College of Medicine.
Kyle B KellyDepartment of Pharmacodynamics, College of Pharmacy.
Kailey L SimpsonDepartment of Neuroscience, College of Medicine.
Charles J FrazierDepartment of Pharmacodynamics, College of Pharmacy.
Barry SetlowDepartment of Neuroscience, College of Medicine.
Jennifer L BizonDepartment of Neuroscience, College of Medicine, bizonj@ufl.edu.
University of Florida · US

Funding

Neural Mechanisms of Cognitive Decline in AgingR01AG029421 · NIA · UNIVERSITY OF FLORIDA · PI BIZON, JENNIFER LYNN · 2007 to 2018
$3.1M
Molecular and physiological determinants of age-related working memory declineF32AG051371 · NIA · UNIVERSITY OF FLORIDA · PI MCQUAIL, JOSEPH ALOYSIUS · 2015 to 2017
$173k
NIA NIH HHS F32 AG051371NIA NIH HHS R01 AG029421
6 · The paper itself

Abstract

Working memory, the ability to temporarily maintain representational knowledge, is a foundational cognitive process that can become compromised in aging and neuropsychiatric disease. NMDA receptor (NMDAR) activation in prefrontal cortex (PFC) is necessary for the pyramidal neuron activity believed to enable working memory; however, the distinct biophysical properties and localization of NMDARs containing NR2A and NR2B subunits suggest unique roles for NMDAR subtypes in PFC neural activity and working memory. Experiments herein show that working memory depends on NR2A- but not NR2B-NMDARs in PFC of rats and that NR2A-NMDARs mediate the majority of evoked NMDAR currents on layer 2/3 PFC pyramidal neurons. Moreover, attenuated expression of the NR2A but not the NR2B subunit in PFC associates with naturally occurring working memory impairment in aged rats. Finally, NMDAR currents and working memory are enhanced in aged rats by promoting activation of the NR2A-enriched synaptic pool of PFC NMDARs. These results implicate NR2A-NMDARs in normal working memory and suggest novel treatment strategies for improving working memory in cognitive disorders. SIGNIFICANCE STATEMENT: Working memory, the ability to hold information "in mind," requires persistent activity of pyramidal neurons in prefrontal cortex (PFC) mediated by NMDA receptor (NMDAR) activation. NMDAR loss in PFC may account for working memory impairments in aging and psychiatric disease. Our studies demonstrate that NMDARs containing the NR2A subunit, but not the NR2B subunit, are required for working memory and that loss of NR2A predicts severity of age-related working memory impairment. The importance of NR2A to working memory is likely due its abundant contribution to pyramidal neuron activity and location at synaptic sites in PFC. This information is useful in designing new therapies to treat working memory impairments by enhancing the function of NR2A-containing NMDARs.

Indexed as

AgingAnimalsCognitive DysfunctionConditioning, OperantExcitatory Amino Acid AntagonistsMaleMemory DisordersMemory, Short-TermPatch-Clamp TechniquesPrefrontal CortexPyramidal CellsRatsRats, Inbred F344Receptors, N-Methyl-D-AspartateSerineSignal TransductionExcitatory Amino Acid AntagonistsNR2B NMDA receptorReceptors, N-Methyl-D-AspartateSerineagingcognitionNMDA receptorprefrontal cortexratworking memory

Identifiers

PMID27807032
PMCPMC5157101
OpenAlexW2547648483

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.