Evidence map›Paper›PMID 32332733›Full record

ArticleNature communications2020

Stress gates an astrocytic energy reservoir to impair synaptic plasticity.

Ciaran Murphy-Royal, April D Johnston, Andrew K J Boyce, Blanca Diaz-Castro, Adam Institoris, Govind Peringod, Oliver Zhang, Randy F Stout, David C Spray, Roger J Thompson and 3 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
9.8field-weighted citation impact, top 1% 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

95 citing papers in PubMed, 155 citations in OpenAlex.

  1. Review
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  8. Cerebellar astrocytic alterations in depression.Translational psychiatry · 2026
    Article
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35 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 2 countries.

Ciaran Murphy-RoyalHotchkiss Brain Institute, Cumming School of Medicine, Department of Physiology and Pharmacology, University of Calgary, Calgary, Canada.ORCID http://orcid.org/0000-0001-7545-593X
April D JohnstonDepartment of Physiology, David Geffen School of Medicine, University of California Los Angeles, UCLA, Los Angeles, CA, USA.
Andrew K J BoyceHotchkiss Brain Institute, Cumming School of Medicine, Department of Physiology and Pharmacology, University of Calgary, Calgary, Canada.
Blanca Diaz-CastroDepartment of Physiology, David Geffen School of Medicine, University of California Los Angeles, UCLA, Los Angeles, CA, USA.
Adam InstitorisHotchkiss Brain Institute, Cumming School of Medicine, Department of Physiology and Pharmacology, University of Calgary, Calgary, Canada.
Govind PeringodHotchkiss Brain Institute, Cumming School of Medicine, Department of Physiology and Pharmacology, University of Calgary, Calgary, Canada.
Oliver ZhangHotchkiss Brain Institute, Cumming School of Medicine, Department of Physiology and Pharmacology, University of Calgary, Calgary, Canada.
Randy F StoutDepartment of Biomedical Sciences, New York Institute of Technology College of Osteopathic Medicine, Old Westbury, NY, USA.
David C SprayDominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY, USA.
Roger J ThompsonHotchkiss Brain Institute, Cumming School of Medicine, Department of Physiology and Pharmacology, University of Calgary, Calgary, Canada.
Baljit S KhakhDepartment of Physiology, David Geffen School of Medicine, University of California Los Angeles, UCLA, Los Angeles, CA, USA.
Jaideep S BainsHotchkiss Brain Institute, Cumming School of Medicine, Department of Physiology and Pharmacology, University of Calgary, Calgary, Canada.ORCID http://orcid.org/0000-0002-3634-6463
Grant R GordonHotchkiss Brain Institute, Cumming School of Medicine, Department of Physiology and Pharmacology, University of Calgary, Calgary, Canada. gordong@ucalgary.ca.ORCID http://orcid.org/0000-0002-3154-7442
University of Calgary · CAUniversity of California, Los Angeles · USAlbert Einstein College of Medicine · USNew York Institute of Technology · US

Funding

CIHR
6 · The paper itself

Abstract

Astrocytes support the energy demands of synaptic transmission and plasticity. Enduring changes in synaptic efficacy are highly sensitive to stress, yet whether changes to astrocyte bioenergetic control of synapses contributes to stress-impaired plasticity is unclear. Here we show in mice that stress constrains the shuttling of glucose and lactate through astrocyte networks, creating a barrier for neuronal access to an astrocytic energy reservoir in the hippocampus and neocortex, compromising long-term potentiation. Impairing astrocytic delivery of energy substrates by reducing astrocyte gap junction coupling with dominant negative connexin 43 or by disrupting lactate efflux was sufficient to mimic the effects of stress on long-term potentiation. Furthermore, direct restoration of the astrocyte lactate supply alone rescued stress-impaired synaptic plasticity, which was blocked by inhibiting neural lactate uptake. This gating of synaptic plasticity in stress by astrocytic metabolic networks indicates a broader role of astrocyte bioenergetics in determining how experience-dependent information is controlled.

Indexed as

Adaptation, PsychologicalAnimalsAstrocytesDisease Models, AnimalEnergy MetabolismFemaleGlucoseHippocampusHumansLactic AcidLong-Term PotentiationMaleMetabolic Networks and PathwaysMiceNeocortexNeuronsGlucoseLactic Acid

Identifiers

PMID32332733
PMCPMC7181611
OpenAlexW3018483640

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.