Evidence map›Paper›PMID 22031892›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2011

Highly specific role of hypocretin (orexin) neurons: differential activation as a function of diurnal phase, operant reinforcement versus operant avoidance and light level.

Ronald McGregor, Ming-Fung Wu, Grace Barber, Lalini Ramanathan, Jerome M Siegel

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

52 citing papers in PubMed, 91 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
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  7. Hypocretin/Orexin Interactions with Norepinephrine Contribute to the Opiate Withdrawal Syndrome.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  8. Article
  9. Memory Consolidation Is Similar in Waking and Sleep.Current sleep medicine reports · 2021
    Article
  10. Pleasure, addiction, and hypocretin (orexin).Handbook of clinical neurology · 2021
    Review
  11. Review
  12. Review
  13. Transgenic Archaerhodopsin-3 Expression in Hypocretin/Orexin Neurons Engenders Cellular Dysfunction and Features of Type 2 Narcolepsy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  14. Article
  15. Article
  16. Article
  17. Knockdown of hypocretin attenuates extended access of cocaine self-administration in rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Article
  18. Article
  19. Review
  20. Review
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 at 2 institutions in 1 country.

Ronald McGregorVeterans Administration Greater Los Angeles Healthcare System, Neurobiology Research (151A3), North Hills, California 91343, USA.
Ming-Fung Wu
Grace Barber
Lalini Ramanathan
Jerome M Siegel
University of California, Los Angeles · USVA Greater Los Angeles Healthcare System · US

Funding

Hypocretin Release in Disease States and BehaviorR01MH064109 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SIEGEL, JEROME M · 2001 to 2016
$7.7M
Role of hypocretin in opiate addiction and withdrawalR01DA034748 · NIDA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SIEGEL, JEROME M · 2014 to 2024
$6.3M
IMMUNOLOGICAL FACTORS IN NARCOLEPSYR37NS014610 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SIEGEL, JEROME M · 1999 to 2005
$2.0M
Unihemispheric sleep: implications for mechanisms of sleep control and function iR01NS069640 · NINDS · SEPULVEDA RESEARCH CORPORATION · PI SIEGEL, JEROME M · 2010 to 2013
$1.8M
RETICULAR FORMATION NEURONS: BEHAVIORAL STUDIESR01NS014610 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SIEGEL, JEROME M · 1985 to 2013
$1.4M
What Causes Human Narcolepsy?I01BX001753 · VA · VA GREATER LOS ANGELES HEALTHCARE SYSTEM · PI SIEGEL, JEROME M · 2013 to 2020
–
BLRD VA I01 BX001753BLRD VA IK6 BX005245NIDA NIH HHS R01 DA034748NIMH NIH HHS MH64109NIMH NIH HHS R01 MH064109NINDS NIH HHS NS069640NINDS NIH HHS NS14610NINDS NIH HHS R01 NS014610NINDS NIH HHS R01 NS069640NINDS NIH HHS R37 NS014610
6 · The paper itself

Abstract

Hypocretin (Hcrt) cell loss is responsible for narcolepsy, but Hcrt's role in normal behavior is unclear. We found that Hcrt knock-out mice were unable to work for food or water reward during the light phase. However, they were unimpaired relative to wild-type (WT) mice when working for reward during the dark phase or when working to avoid shock in the light or dark phase. In WT mice, expression of Fos in Hcrt neurons occurs only in the light phase when working for positive reinforcement. Expression was seen throughout the mediolateral extent of the Hcrt field. Fos was not expressed when expected or unexpected unearned rewards were presented, when working to avoid negative reinforcement, or when given or expecting shock, even though these conditions elicit maximal electroencephalogram (EEG) arousal. Fos was not expressed in the light phase when light was removed. This may explain the lack of light-induced arousal in narcoleptics and its presence in normal individuals. This is the first demonstration of such specificity of arousal system function and has implications for understanding the motivational and circadian consequences of arousal system dysfunction. The current results also indicate that comparable and complementary specificities must exist in other arousal systems.

Indexed as

Reinforcement, PsychologyAnalysis of VarianceAnimalsAvoidance LearningBrainCircadian RhythmConditioning, OperantDrinkingEatingElectroencephalographyElectromyographyElectroshockIntracellular Signaling Peptides and ProteinsLightMiceMice, Inbred C57BLIntracellular Signaling Peptides and ProteinsNeuropeptidesOrexins

Identifiers

PMID22031892
PMCPMC3230273
OpenAlexW2130384863

What OpenQuestion holds

Textmetadata
LicenceTDM
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.