Evidence map›Paper›PMID 24672016›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Discharge profiles across the sleep-waking cycle of identified cholinergic, GABAergic, and glutamatergic neurons in the pontomesencephalic tegmentum of the rat.

Soufiane Boucetta, Youssouf Cissé, Lynda Mainville, Marisela Morales, Barbara E Jones

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 150 papers.

0numbers the graph read from it
0cells of the map it votes in
150citing papers in PubMed
–field-weighted citation impact
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

150 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Diverse Firing Profiles ofThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Emerging Functions of Neuromodulation during Sleep.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Review
  19. Ventral subiculum promotes wakefulness through several pathways in male mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  20. Article

90 more citing papers are in PubMed but not listed here.

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

5 authors.

Soufiane BoucettaDepartment of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Quebec H3A 2B4, Canada, and National Institute on Drug Abuse, Neuronal Networks Section, National Institutes of Health, Baltimore, Maryland 21224.
Youssouf Cissé
Lynda Mainville
Marisela Morales
Barbara E Jones

Funding

Neuronal characterization of the ventral tegmental areaZIADA000543 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI MORALES, MARISELA · 2009 to 2020
$11.8M
ROLE OF BASAL FOREBRAIN NEURONS IN SLEEP WAKE STATESR01MH060119 · NIMH · MCGILL UNIVERSITY · PI JONES, BARBARA E · 2000 to 2011
$1.5M
CIHR MOP-13458Intramural NIH HHSNIMH NIH HHS R01 MH060119NIMH NIH HHS R01 MH-60119-01A
6 · The paper itself

Abstract

Distributed within the laterodorsal tegmental and pedunculopontine tegmental nuclei (LDT and PPT), cholinergic neurons in the pontomesencephalic tegmentum have long been thought to play a critical role in stimulating cortical activation during waking (W) and paradoxical sleep (PS, also called REM sleep), yet also in promoting PS with muscle atonia. However, the discharge profile and thus precise roles of the cholinergic neurons have remained uncertain because they lie intermingled with GABAergic and glutamatergic neurons, which might also assume these roles. By applying juxtacellular recording and labeling in naturally sleeping-waking, head-fixed rats, we investigated the discharge profiles of histochemically identified cholinergic, GABAergic, and glutamatergic neurons in the LDT, SubLDT, and adjoining medial part of the PPT (MPPT) in relation to sleep-wake states, cortical activity, and muscle tone. We found that all cholinergic neurons were maximally active during W and PS in positive correlation with fast (γ) cortical activity, as "W/PS-max active neurons." Like cholinergic neurons, many GABAergic and glutamatergic neurons were also "W/PS-max active." Other GABAergic and glutamatergic neurons were "PS-max active," being minimally active during W and maximally active during PS in negative correlation with muscle tone. Conversely, some glutamatergic neurons were "W-max active," being maximally active during W and minimally active during PS in positive correlation with muscle tone. Through different discharge profiles, the cholinergic, GABAergic, and glutamatergic neurons of the LDT, SubLDT, and MPPT thus appear to play distinct roles in promoting W and PS with cortical activation, PS with muscle atonia, or W with muscle tone.

Indexed as

Action PotentialsAnimalsBiotinCell CountCircadian RhythmElectroencephalographyElectromyographyGlutamate DecarboxylaseMaleNeuronsRatsRats, Long-EvansSleepTegmentum MesencephaliVesicular Acetylcholine Transport ProteinsVesicular Glutamate Transport Protein 2BiotinGlutamate DecarboxylaseneurobiotinVesicular Acetylcholine Transport ProteinsVesicular Glutamate Transport Protein 2EEGEMGparadoxical sleepREM sleepslow-wave sleep

Identifiers

PMID24672016
PMCPMC3965793

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.