Evidence map›Paper›PMID 32631938›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2020

Developmentally Transient CB1Rs on Cerebellar Afferents Suppress Afferent Input, Downstream Synaptic Excitation, and Signaling to Migrating Neurons.

Jesse L Barnes, Claudia Mohr, Caitlin R Ritchey, Chloe M Erikson, Hiroko Shiina, David J Rossi

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 10 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

6 authors at 1 institution in 1 country.

Jesse L BarnesWashington State University, Integrative Physiology and Neuroscience, Pullman, Washington 99164.
Claudia MohrWashington State University, Integrative Physiology and Neuroscience, Pullman, Washington 99164.
Caitlin R RitcheyWashington State University, Integrative Physiology and Neuroscience, Pullman, Washington 99164.
Chloe M EriksonWashington State University, Integrative Physiology and Neuroscience, Pullman, Washington 99164.
Hiroko ShiinaWashington State University, Integrative Physiology and Neuroscience, Pullman, Washington 99164.
David J RossiWashington State University, Integrative Physiology and Neuroscience, Pullman, Washington 99164 david.rossi@wsu.edu.
Washington State University · US

Funding

NEUROSTEROID MODULATION OF ETHANOL WITHDRAWAL SEVERITYR01AA012439 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI FINN, DEBORAH A., ROSSI, DAVID J · 2000 to 2017
$4.6M
Cerebellar Contributions to Alcohol Use DisordersR01AA026078 · NIAAA · WASHINGTON STATE UNIVERSITY · PI ROSSI, DAVID J · 2017 to 2021
$1.7M
NIAAA NIH HHS R01 AA012439NIAAA NIH HHS R01 AA026078
6 · The paper itself

Abstract

The endocannabinoid system plays important roles in brain development, but mechanistic studies have focused on neuronal differentiation, migration, and synaptogenesis, with less attention to transcellular interactions that coordinate neurodevelopmental processes across developing neural networks. We determined that, in the developing rodent cerebellar cortex (of both sexes), there is a transient window when the dominant brain cannabinoid receptor, CB1R, is expressed on afferent terminals instead of output neuron Purkinje cell synapses that dominate the adult cerebellum. Activation of these afferent CB1Rs suppresses synaptic transmission onto developing granule cells, and consequently also suppresses excitation of downstream neurons in the developing cortical network, including nonsynaptic, migrating neurons. Application of a CB1R antagonist during afferent stimulation trains and depolarizing voltage steps caused a significant, sustained potentiation of synaptic amplitude. Our data demonstrate that transiently expressed afferent CB1Rs regulate afferent synaptic strength during synaptogenesis, which enables coordinated dampening of transcortical developmental signals.

Indexed as

Excitatory Postsynaptic PotentialsNeurogenesisAction PotentialsAnimalsCannabinoid Receptor AntagonistsCell MovementFemaleMaleMiceMice, Inbred C57BLNeurons, AfferentPurkinje CellsReceptor, Cannabinoid, CB1SynapsesCannabinoid Receptor AntagonistsReceptor, Cannabinoid, CB1cannabinoidcerebellumdevelopmentmarijuanamigrationTHC

Identifiers

PMID32631938
PMCPMC7406284
OpenAlexW3038267005

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.