Evidence map›Paper›PMID 33692389›Full record

ArticleScientific reports2021

Loss of retinoid X receptor gamma subunit impairs group 1 mGluR mediated electrophysiological responses and group 1 mGluR dependent behaviors.

Chirag Upreti, Caitlin M Woodruff, Xiao-Lei Zhang, Michael J Yim, Zhen-Yu Zhou, Andrew M Pagano, Dina S Rehanian, Deqi Yin, Eric R Kandel, Patric K Stanton and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 41% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Activity-dependent modulation of neuronal KThe Journal of biological chemistry · 2022
    Article
  4. Review
  5. 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

11 authors at 2 institutions in 1 country.

Chirag UpretiDepartment of Cell Biology and Anatomy, New York Medical College, Valhalla, NY, 10595, USA.
Caitlin M WoodruffDepartment of Neuroscience, Columbia University, 3227 Broadway, New York, NY, 10027, USA.
Xiao-Lei ZhangDepartment of Cell Biology and Anatomy, New York Medical College, Valhalla, NY, 10595, USA.
Michael J YimDepartment of Neuroscience, Columbia University, 3227 Broadway, New York, NY, 10027, USA.
Zhen-Yu ZhouDepartment of Cell Biology and Anatomy, New York Medical College, Valhalla, NY, 10595, USA.
Andrew M PaganoDepartment of Neuroscience, Columbia University, 3227 Broadway, New York, NY, 10027, USA.
Dina S RehanianDepartment of Pathology and Cell Biology, Columbia University, 630 West 168thStreet, New York, NY, 10032, USA.
Deqi YinDepartment of Neuroscience, Columbia University, 3227 Broadway, New York, NY, 10027, USA.
Eric R KandelDepartment of Neuroscience, Columbia University, 3227 Broadway, New York, NY, 10027, USA.
Patric K StantonDepartment of Cell Biology and Anatomy, New York Medical College, Valhalla, NY, 10595, USA.
Russell E NichollsDepartment of Pathology and Cell Biology, Columbia University, 630 West 168thStreet, New York, NY, 10032, USA. rn95@columbia.edu.
Columbia University · USNew York Medical College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Retinoid X receptors are members of the nuclear receptor family that regulate gene expression in response to retinoic acid and related ligands. Group 1 metabotropic glutamate receptors are G-protein coupled transmembrane receptors that activate intracellular signaling cascades in response to the neurotransmitter, glutamate. These two classes of molecules have been studied independently and found to play important roles in regulating neuronal physiology with potential clinical implications for disorders such as depression, schizophrenia, Parkinson's and Alzheimer's disease. Here we show that mice lacking the retinoid X receptor subunit, RXRγ, exhibit impairments in group 1 mGluR-mediated electrophysiological responses at hippocampal Schaffer collateral-CA1 pyramidal cell synapses, including impaired group 1 mGluR-dependent long-term synaptic depression (LTD), reduced group 1 mGluR-induced calcium release, and loss of group 1 mGluR-activated voltage-sensitive currents. These animals also exhibit impairments in a subset of group 1 mGluR-dependent behaviors, including motor performance, spatial object recognition, and prepulse inhibition. Together, these observations demonstrate convergence between the RXRγ and group 1 mGluR signaling pathways that may function to coordinate their regulation of neuronal activity. They also identify RXRγ as a potential target for the treatment of disorders in which group 1 mGluR signaling has been implicated.

Indexed as

Long-Term Synaptic DepressionSignal TransductionAnimalsCA1 Region, HippocampalMiceMice, KnockoutPyramidal CellsReceptors, Metabotropic GlutamateRetinoid X Receptor gammaSynapsesmetabotropic glutamate receptor type 1Receptors, Metabotropic GlutamateRetinoid X Receptor gamma

Identifiers

PMID33692389
PMCPMC7946894
OpenAlexW3134574903

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.