Evidence map›Paper›PMID 31028115›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2019

Cholinergic Neurons of the Medial Septum Are Crucial for Sensorimotor Gating.

Junghee Jin, Jia Cheng, Ko-Woon Lee, Bushra Amreen, Kathryn A McCabe, Clark Pitcher, Thomas Liebmann, Paul Greengard, Marc Flajolet

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 26 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

9 authors at 1 institution in 1 country.

Junghee JinLaboratory of Molecular and Cellular Neuroscience, The Rockefeller University, New York, New York 10065.ORCID 0000-0002-1204-097X
Jia ChengLaboratory of Molecular and Cellular Neuroscience, The Rockefeller University, New York, New York 10065.ORCID 0000-0002-9639-5187
Ko-Woon LeeLaboratory of Molecular and Cellular Neuroscience, The Rockefeller University, New York, New York 10065.
Bushra AmreenLaboratory of Molecular and Cellular Neuroscience, The Rockefeller University, New York, New York 10065.
Kathryn A McCabeLaboratory of Molecular and Cellular Neuroscience, The Rockefeller University, New York, New York 10065.
Clark PitcherLaboratory of Molecular and Cellular Neuroscience, The Rockefeller University, New York, New York 10065.
Thomas LiebmannLaboratory of Molecular and Cellular Neuroscience, The Rockefeller University, New York, New York 10065.
Paul GreengardLaboratory of Molecular and Cellular Neuroscience, The Rockefeller University, New York, New York 10065.
Marc FlajoletLaboratory of Molecular and Cellular Neuroscience, The Rockefeller University, New York, New York 10065 marc.flajolet@rockefeller.edu.
Rockefeller University · US

Funding

Striatal Cell-specific Analysis of the Molecular Mechanisms of Antipsychotic DrugP50MH090963 · NIMH · ROCKEFELLER UNIVERSITY · PI NESTLER, ERIC J. · 2010 to 2014
$9.8M
NIMH NIH HHS P50 MH090963
6 · The paper itself

Abstract

Hypofunction of NMDA receptors has been considered a possible cause for the pathophysiology of schizophrenia. More recently, indirect ways to regulate NMDA that would be less disruptive have been proposed and metabotropic glutamate receptor subtype 5 (mGluR5) represents one such candidate. To characterize the cell populations involved, we demonstrated here that knock-out (KO) of mGluR5 in cholinergic, but not glutamatergic or parvalbumin (PV)-positive GABAergic, neurons reduced prepulse inhibition of the startle response (PPI) and enhanced sensitivity to MK801-induced locomotor activity. Inhibition of cholinergic neurons in the medial septum by DREADD (designer receptors exclusively activated by designer drugs) resulted in reduced PPI further demonstrating the importance of these neurons in sensorimotor gating. Volume imaging and quantification were used to compare PV and cholinergic cell distribution, density, and total cell counts in the different cell-type-specific KO lines. Electrophysiological studies showed reduced NMDA receptor-mediated currents in cholinergic neurons of the medial septum in mGluR5 KO mice. These results obtained from male and female mice indicate that cholinergic neurons in the medial septum represent a key cell type involved in sensorimotor gating and are relevant to pathologies associated with disrupted sensorimotor gating such as schizophrenia.

Indexed as

AnimalsBrainCholinergic NeuronsDizocilpine MaleateExcitatory Amino Acid AntagonistsFemaleMaleMiceMice, KnockoutMotor ActivityPatch-Clamp TechniquesPrepulse InhibitionReceptor, Metabotropic Glutamate 5Receptors, N-Methyl-D-AspartateReflex, StartleSensory GatingDizocilpine MaleateExcitatory Amino Acid AntagonistsReceptor, Metabotropic Glutamate 5Receptors, N-Methyl-D-AspartatecholinergicgatingmGluR5NMDAsensorimotor

Identifiers

PMID31028115
PMCPMC6595952
OpenAlexW2940902977

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.