Evidence map›Paper›PMID 28874448›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2017

Glycinergic Input to the Mouse Basal Forebrain Cholinergic Neurons.

Zsuzsanna Bardóczi, Balázs Pál, Áron Kőszeghy, Tamás Wilheim, Masahiko Watanabe, László Záborszky, Zsolt Liposits, Imre Kalló

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.5field-weighted citation impact, top 42% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. GlyNAC (Glycine andAntioxidants (Basel, Switzerland) · 2022
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Glycinergic Input to the Mouse Basal Forebrain Cholinergic Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    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

8 authors at 5 institutions in 3 countries.

Zsuzsanna BardócziLaboratory of Endocrine Neurobiology, Institute of Experimental Medicine, HAS, 1083, Budapest, Hungary.
Balázs PálDepartment of Physiology, Faculty of Medicine, University of Debrecen, 4032, Debrecen, Hungary.
Áron KőszeghyDepartment of Physiology, Faculty of Medicine, University of Debrecen, 4032, Debrecen, Hungary.
Tamás WilheimLaboratory of Endocrine Neurobiology, Institute of Experimental Medicine, HAS, 1083, Budapest, Hungary.
Masahiko WatanabeDepartment of Anatomy, Hokkaido University School of Medicine, Sapporo 060-8638, Japan.ORCID 0000-0001-5037-7138
László ZáborszkyCenter for Molecular and Behavioral Neuroscience, Rutgers, Newark, New Jersey 07102, and.
Zsolt LipositsLaboratory of Endocrine Neurobiology, Institute of Experimental Medicine, HAS, 1083, Budapest, Hungary.
Imre KallóLaboratory of Endocrine Neurobiology, Institute of Experimental Medicine, HAS, 1083, Budapest, Hungary, kallo@koki.hu.ORCID 0000-0003-3412-4100
Pázmány Péter Catholic University · HUUniversity of Debrecen · HUHokkaido University · JPRutgers, The State University of New Jersey · USSemmelweis University · HU

Funding

AFFERENT REGULATION OF CHOLINERGIC FOREBRAIN NEURONSR01NS023945 · NINDS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI ZABORSZKY, LASZLO · 1986 to 2019
$6.5M
NINDS NIH HHS R01 NS023945
6 · The paper itself

Abstract

The basal forebrain (BF) receives afferents from brainstem ascending pathways, which has been implicated first by Moruzzi and Magoun (1949) to induce forebrain activation and cortical arousal/waking behavior; however, it is very little known about how brainstem inhibitory inputs affect cholinergic functions. In the current study, glycine, a major inhibitory neurotransmitter of brainstem neurons, and gliotransmitter of local glial cells, was tested for potential interaction with BF cholinergic (BFC) neurons in male mice. In the BF, glycine receptor α subunit-immunoreactive (IR) sites were localized in choline acetyltransferase (ChAT)-IR neurons. The effect of glycine on BFC neurons was demonstrated by bicuculline-resistant, strychnine-sensitive spontaneous IPSCs (sIPSCs; 0.81 ± 0.25 × 10

Indexed as

AnimalsBicucullineCholine O-AcetyltransferaseCholinergic NeuronsFemaleGlycineGlycine AgentsGlycine Plasma Membrane Transport ProteinsInhibitory Postsynaptic PotentialsMaleMiceNeurogliaProsencephalonStrychnineSynapsesBicucullineCholine O-AcetyltransferaseGlycineGlycine AgentsGlycine Plasma Membrane Transport ProteinsStrychnineaxospinousbasal forebraincholinergicglycineglycine transportersynapse

Identifiers

PMID28874448
PMCPMC5618268
OpenAlexW2752695536

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.