Evidence map›Paper›PMID 25100608›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Rebound potentiation of inhibition in juvenile visual cortex requires vision-induced BDNF expression.

Ming Gao, Kristen R Maynard, Varun Chokshi, Lihua Song, Cara Jacobs, Hui Wang, Trinh Tran, Keri Martinowich, Hey-Kyoung Lee

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  4. Review
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  9. Review
  10. Brief Novel Visual Experience Fundamentally Changes Synaptic Plasticity in the Mouse Visual Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  11. Experience-dependent homeostasis of 'noise' at inhibitory synapses preserves information coding in adult visual cortex.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2017
    Article
  12. Article
  13. BDNF ValScientific reports · 2016
    Article
  14. Article
  15. Article
  16. Functional Role of BDNF Production from Unique Promoters in Aggression and Serotonin Signaling.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2016
    Article
  17. Brief Dark Exposure Reduces Tonic Inhibition in Visual Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  18. Article
  19. Article
  20. Effects of developmental alcohol exposure vs. intubation stress on BDNF and TrkB expression in the hippocampus and frontal cortex of neonatal rats.International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience · 2015
    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

9 authors at 4 institutions in 1 country.

Ming GaoThe Solomon H. Snyder Department of Neuroscience, The Zanvyl-Krieger Mind/Brain Institute, Johns Hopkins University, Baltimore, Maryland 21218, Department of Biology, University of Maryland, College Park, Maryland 20742.
Kristen R MaynardLieber Institute for Brain Development, Baltimore, Maryland 21205, and.
Varun ChokshiThe Solomon H. Snyder Department of Neuroscience, The Zanvyl-Krieger Mind/Brain Institute, Johns Hopkins University, Baltimore, Maryland 21218.
Lihua SongThe Solomon H. Snyder Department of Neuroscience, The Zanvyl-Krieger Mind/Brain Institute, Johns Hopkins University, Baltimore, Maryland 21218, Department of Biology, University of Maryland, College Park, Maryland 20742.
Cara JacobsDepartment of Biology, University of Maryland, College Park, Maryland 20742.
Hui WangThe Solomon H. Snyder Department of Neuroscience, The Zanvyl-Krieger Mind/Brain Institute, Johns Hopkins University, Baltimore, Maryland 21218.
Trinh TranThe Solomon H. Snyder Department of Neuroscience, The Zanvyl-Krieger Mind/Brain Institute, Johns Hopkins University, Baltimore, Maryland 21218.
Keri MartinowichLieber Institute for Brain Development, Baltimore, Maryland 21205, and Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.ORCID http://orcid.org/0000-0002-5237-0789
Hey-Kyoung LeeThe Solomon H. Snyder Department of Neuroscience, The Zanvyl-Krieger Mind/Brain Institute, Johns Hopkins University, Baltimore, Maryland 21218, Department of Biology, University of Maryland, College Park, Maryland 20742, heykyounglee@jhu.edu.
Johns Hopkins University · USAllen Institute for Brain Science · USUniversity of Maryland, College Park · USLieber Institute for Brain Development · US

Funding

Global Synpatic Plasticity Mechanisms in Visual CortexR01EY014882 · NEI · UNIV OF MARYLAND, COLLEGE PARK · PI Hey-Kyoung Lee · 2004 to 2026
$7.9M
NEI NIH HHS R01 EY014882NEI NIH HHS R01-EY14882
6 · The paper itself

Abstract

The developmental increase in the strength of inhibitory synaptic circuits defines the time window of the critical period for plasticity in sensory cortices. Conceptually, plasticity of inhibitory synapses is an attractive mechanism to allow for homeostatic adaptation to the sensory environment. However, a brief duration of visual deprivation that causes maximal change in excitatory synapses produces minimal change in inhibitory synaptic transmission. Here we examined developmental and experience-dependent changes in inhibition by measuring miniature IPSCs (mIPSCs) in layer 2/3 pyramidal neurons of mouse visual cortex. During development from postnatal day 21 (P21) to P35, GABAA receptor function changed from fewer higher-conductance channels to more numerous lower-conductance channels without altering the average mIPSC amplitude. Although a week of visual deprivation did not alter the average mIPSC amplitude, a subsequent 2 h exposure to light produced a rapid rebound potentiation. This form of plasticity is restricted to a critical period before the developmental change in GABAergic synaptic properties is completed, and hence is absent by P35. Visual experience-dependent rebound potentiation of mIPSCs is accompanied by an increase in the open channel number and requires activity-dependent transcription of brain-derived neurotrophic factor (BDNF). Mice lacking BDNF transcription through promoter IV did not show developmental changes in inhibition and lacked rebound potentiation. Our results suggest that sensory experience may have distinct functional consequences in normal versus deprived sensory cortices, and that experience-dependent BDNF expression controls the plasticity of inhibitory synaptic transmission particularly when recovering vision during the critical period.

Indexed as

Age FactorsAnimalsAnimals, NewbornBiophysicsBrain-Derived Neurotrophic FactorElectric StimulationGene Expression Regulation, DevelopmentalGlutamate DecarboxylaseInhibitory Postsynaptic PotentialsIn Vitro TechniquesMiceMice, Inbred C57BLMice, TransgenicMicroscopy, ConfocalNeural InhibitionNeuronsBrain-Derived Neurotrophic FactorGlutamate Decarboxylaseglutamate decarboxylase 2activity-dependentBDNFcritical periodmIPSCpotentiationvisual cortex

Identifiers

PMID25100608
PMCPMC4200113
OpenAlexW2134727478

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.