Evidence map›Paper›PMID 25706472›Full record

ArticleNature neuroscience2015

A subcortical inhibitory signal for behavioral arrest in the thalamus.

Kristóf Giber, Marco A Diana, Viktor Plattner, Guillaume P Dugué, Hajnalka Bokor, Charly V Rousseau, Zsófia Maglóczky, László Havas, Balázs Hangya, Hendrik Wildner and 3 more

Abstract read
In one paragraph

Article in Nature neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 83 citations in OpenAlex.

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  7. Attenuating midline thalamus bursting to mitigate absence epilepsy.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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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

13 authors at 4 institutions in 4 countries.

Kristóf Giber *Laboratory of Thalamus Research, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, H-1083, Hungary.
Marco A Diana *Ecole Normale Supérieure, Institut de Biologie de l'ENS, IBENS, Paris, F-75005 France.
Viktor Plattner *Laboratory of Thalamus Research, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, H-1083, Hungary.
Guillaume P DuguéEcole Normale Supérieure, Institut de Biologie de l'ENS, IBENS, Paris, F-75005 France.
Hajnalka BokorLaboratory of Thalamus Research, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, H-1083, Hungary.
Charly V RousseauEcole Normale Supérieure, Institut de Biologie de l'ENS, IBENS, Paris, F-75005 France.
Zsófia MaglóczkyLaboratory of Cerebral Cortex Research, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, H-1083, Hungary.
László HavasDepartment of Pathology/ Department of Psychiatry St. Borbála Hospital, Tatabánya, H-2800, Hungary.
Balázs HangyaLaboratory of Cerebral Cortex Research, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, H-1083, Hungary.
Hendrik WildnerInstitute of Pharmacology and Toxicology, University of Zurich, CH-8057 Zurich, Switzerland.
Hanns Ulrich ZeilhoferInstitute of Pharmacology and Toxicology, University of Zurich, CH-8057 Zurich, Switzerland.
Stéphane DieudonnéEcole Normale Supérieure, Institut de Biologie de l'ENS, IBENS, Paris, F-75005 France.
László AcsádyLaboratory of Thalamus Research, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, H-1083, Hungary.
Centre National de la Recherche Scientifique · FRHungarian Academy of Sciences · HUUniversity of Zurich · CHÉcole Normale Supérieure - PSL · FR

Funding

Wellcome Trust 094513
6 · The paper itself

Abstract

Organization of behavior requires rapid coordination of brainstem and forebrain activity. The exact mechanisms of effective communication between these regions are presently unclear. The intralaminar thalamic nuclei (IL) probably serves as a central hub in this circuit by connecting the critical brainstem and forebrain areas. We found that GABAergic and glycinergic fibers ascending from the pontine reticular formation (PRF) of the brainstem evoked fast and reliable inhibition in the IL via large, multisynaptic terminals. This inhibition was fine-tuned through heterogeneous GABAergic and glycinergic receptor ratios expressed at individual synapses. Optogenetic activation of PRF axons in the IL of freely moving mice led to behavioral arrest and transient interruption of awake cortical activity. An afferent system with comparable morphological features was also found in the human IL. These data reveal an evolutionarily conserved ascending system that gates forebrain activity through fast and powerful synaptic inhibition of the IL.

Indexed as

Afferent PathwaysAnimalsBehavior, AnimalGABAergic NeuronsGlycineIntralaminar Thalamic NucleiMaleMiceNerve FibersNeural InhibitionOptogeneticsPatch-Clamp TechniquesPontine TegmentumReceptors, GABAReceptors, GlycineGlycineReceptors, GABAReceptors, Glycine

Identifiers

PMID25706472
PMCPMC4885661
OpenAlexW2012708985

What OpenQuestion holds

Textmetadata
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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.