Evidence map›Paper›PMID 25972184›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

Activation of Metabotropic Glutamate Receptor 7 Is Required for Induction of Long-Term Potentiation at SC-CA1 Synapses in the Hippocampus.

Rebecca Klar, Adam G Walker, Dipanwita Ghose, Brad A Grueter, Darren W Engers, Corey R Hopkins, Craig W Lindsley, Zixiu Xiang, P Jeffrey Conn, Colleen M Niswender

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Overexpression of mGluMolecular neurobiology · 2025
    Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Discovery ofACS medicinal chemistry letters · 2023
    Article
  10. Article
  11. Article
  12. Development and profiling of mGluBioorganic & medicinal chemistry letters · 2022
    Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Phenotypic profiling of mGluGenes, brain, and behavior · 2020
    Article
  19. Review
  20. 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

10 authors at 3 institutions in 3 countries.

Rebecca KlarDepartment of Pharmacology, Vanderbilt Center for Neuroscience Drug Discovery.ORCID http://orcid.org/0000-0001-5650-1187
Adam G WalkerDepartment of Pharmacology, Vanderbilt Center for Neuroscience Drug Discovery.
Dipanwita GhoseDepartment of Anesthesiology.
Brad A GrueterDepartment of Anesthesiology, Department of Molecular Physiology and Biophysics, and Department of Psychiatry, Vanderbilt University Medical Center, Nashville, Tennessee 37232, and.
Darren W EngersDepartment of Pharmacology, Vanderbilt Center for Neuroscience Drug Discovery.
Corey R HopkinsDepartment of Pharmacology, Vanderbilt Center for Neuroscience Drug Discovery, Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37232.ORCID http://orcid.org/0000-0001-9194-4784
Craig W LindsleyDepartment of Pharmacology, Vanderbilt Center for Neuroscience Drug Discovery, Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37232.
Zixiu XiangDepartment of Pharmacology, Vanderbilt Center for Neuroscience Drug Discovery.
P Jeffrey ConnDepartment of Pharmacology, Vanderbilt Center for Neuroscience Drug Discovery, Jeff.Conn@vanderbilt.edu Colleen.Niswender@vanderbilt.edu.
Colleen M NiswenderDepartment of Pharmacology, Vanderbilt Center for Neuroscience Drug Discovery, Jeff.Conn@vanderbilt.edu Colleen.Niswender@vanderbilt.edu.
Center for Discovery · USVanderbilt University · USInstitute of Molecular Biology and Biophysics · RU

Funding

Research Project: Sensory and Multisensory Contributions to AutismU54HD083211 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DYKENS, ELISABETH MAY · 2015 to 2019
$7.1M
FUNCTIONS OF METABOTROPIC GLUTAMATE RECEPTOR SUBTYPESR01NS031373 · NINDS · VANDERBILT UNIVERSITY · PI CONN, P JEFFREY · 1993 to 2025
$6.2M
Functions of Metabotropic Glutamate Receptor SubtypesR37NS031373 · NINDS · VANDERBILT UNIVERSITY · PI CONN, P JEFFREY · 2014 to 2020
$3.5M
Metabotropic Glutamate Receptors in the Basal GangliaR21NS078262 · NINDS · VANDERBILT UNIVERSITY · PI NISWENDER, COLLEEN M · 2012 to 2013
$421k
Howard Hughes Medical InstituteNICHD NIH HHS U54 HD083211NINDS NIH HHS R01 NS031373NINDS NIH HHS R21 NS078262NINDS NIH HHS R37 NS031373
6 · The paper itself

Abstract

Of the eight metabotropic glutamate (mGlu) receptor subtypes, only mGlu7 is expressed presynaptically at the Schaffer collateral (SC)-CA1 synapse in the hippocampus in adult animals. Coupled with the inhibitory effects of Group III mGlu receptor agonists on transmission at this synapse, mGlu7 is thought to be the predominant autoreceptor responsible for regulating glutamate release at SC terminals. However, the lack of mGlu7-selective pharmacological tools has hampered direct testing of this hypothesis. We used a novel, selective mGlu7-negative allosteric modulator (NAM), ADX71743, and a newly described Group III mGlu receptor agonist, LSP4-2022, to elucidate the role of mGlu7 in modulating transmission in hippocampal area CA1 in adult C57BL/6J male mice. Interestingly, although mGlu7 agonists inhibit SC-CA1 EPSPs, we found no evidence for activation of mGlu7 by stimulation of SC-CA1 afferents. However, LSP4-2022 also reduced evoked monosynaptic IPSCs in CA1 pyramidal cells and, in contrast to its effect on SC-CA1 EPSPs, ADX71743 reversed the ability of high-frequency stimulation of SC afferents to reduce IPSC amplitudes. Furthermore, blockade of mGlu7 prevented induction of LTP at the SC-CA1 synapse and activation of mGlu7 potentiated submaximal LTP. Together, these data suggest that mGlu7 serves as a heteroreceptor at inhibitory synapses in area CA1 and that the predominant effect of activation of mGlu7 by stimulation of glutamatergic afferents is disinhibition, rather than reduced excitatory transmission. Furthermore, this mGlu7-mediated disinhibition is required for induction of LTP at the SC-CA1 synapse, suggesting that mGlu7 could serve as a novel therapeutic target for treatment of cognitive disorders.

Indexed as

AnimalsCA1 Region, HippocampalCA3 Region, HippocampalChannelrhodopsinsElectric StimulationExcitatory Amino Acid AgonistsExcitatory Amino Acid AntagonistsHippocampusInhibitory Postsynaptic PotentialsInterneuronsIn Vitro TechniquesLong-Term PotentiationMaleMiceMice, Inbred C57BLMice, TransgenicChannelrhodopsinsExcitatory Amino Acid AgonistsExcitatory Amino Acid Antagonistsmetabotropic glutamate receptor 7ParvalbuminsReceptors, Metabotropic GlutamateglutamatehippocampusLTPmGlumGlu7mGlur7

Identifiers

PMID25972184
PMCPMC4429158
OpenAlexW1724700858

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.