Evidence map›Paper›PMID 35916383›Full record

ArticleGlia2022

Differential role of neuronal glucose and PFKFB3 in memory formation during development.

Emmanuel Cruz, Benjamin Bessières, Pierre Magistretti, Cristina M Alberini

Open access · greenAbstract read
In one paragraph

Article in Glia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  5. Article
  6. Neuron-Glial Interactions: Implications for Plasticity, Behavior, and Cognition.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Review
  7. The Astrocyte: Metabolic Hub of the Brain.Cold Spring Harbor perspectives in biology · 2024
    Review
  8. Article
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  11. Article
  12. Review
  13. 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

4 authors at 2 institutions in 2 countries.

Emmanuel CruzCenter for Neural Science, New York University, New York, New York, USA.
Benjamin BessièresCenter for Neural Science, New York University, New York, New York, USA.ORCID 0000-0003-4660-1170
Pierre MagistrettiDivision of Biological and Environmental Sciences and Engineering, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia.
Cristina M AlberiniCenter for Neural Science, New York University, New York, New York, USA.ORCID 0000-0001-7386-0018
New York University · USKing Abdullah University of Science and Technology · SA

Funding

Gene Expression in Long-Term MemoryR01MH065635 · NIMH · NEW YORK UNIVERSITY · PI CRISTINA M ALBERINI · 2002 to 2026
$7.5M
Gene Expression in Long-Term MemoryR37MH065635 · NIMH · NEW YORK UNIVERSITY · PI ALBERINI, CRISTINA M · 2013 to 2022
$5.6M
Training Systems and Integrative NeuroscienceT32MH019524 · NIMH · NEW YORK UNIVERSITY · PI KIORPES, LYNNE · 1992 to 2025
$5.2M
Astrocytic-neuronal mechanisms in memory formation and cognitive impairmentsR01MH100822 · NIMH · NEW YORK UNIVERSITY · PI ALBERINI, CRISTINA M · 2013 to 2017
$2.5M
Postdoctoral Research Training in Neurodegenerative Disorders and the Aging BrainT32AG052909 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Helen E Scharfman, THOMAS M WISNIEWSKI · 2017 to 2026
$2.5M
NIA NIH HHS T32 AG052909NIMH NIH HHS R01 MH065635NIMH NIH HHS R01 MH100822NIMH NIH HHS R37 MH065635NIMH NIH HHS T32 MH019524
6 · The paper itself

Abstract

The consumption of glucose in the brain peaks during late childhood; yet, whether and how glucose metabolism is differentially regulated in the brain during childhood compared to adulthood remains to be understood. In particular, it remains to be determined how glucose metabolism is involved in behavioral activations such as learning. Here we show that, compared to adult, the juvenile rat hippocampus has significantly higher mRNA levels of several glucose metabolism enzymes belonging to all glucose metabolism pathways, as well as higher levels of the monocarboxylate transporters MCT1 and MCT4 and the glucose transporters endothelial-GLUT1 and GLUT3 proteins. Furthermore, relative to adults, long-term episodic memory formation in juvenile animals requires significantly higher rates of aerobic glycolysis and astrocytic-neuronal lactate coupling in the hippocampus. Only juvenile but not adult long-term memory formation recruits GLUT3, neuronal 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 (PFKFB3) and more efficiently engages glucose in the hippocampus. Hence, compared to adult, the juvenile hippocampus distinctively regulates glucose metabolism pathways, and formation of long-term memory in juveniles involves differential neuronal glucose metabolism mechanisms.

Indexed as

GlucoseGlycolysisAnimalsAstrocytesChildGlucose Transporter Type 3HumansNeuronsPhosphofructokinase-2RatsGlucoseGlucose Transporter Type 3PFKFB3 protein, humanPFKFB3 protein, mousePhosphofructokinase-2developmentglucoseGLUT3hippocampuslactatememoryPFKFB3

Identifiers

PMID35916383
PMCPMC9474594
OpenAlexW4289520075

What OpenQuestion holds

Textmetadata
LicenceTDM
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.