Evidence map›Paper›PMID 26534765›Full record

ArticlePsychopharmacology2016

Orexin A-induced enhancement of attentional processing in rats: role of basal forebrain neurons.

Kristin N Zajo, Jim R Fadel, Joshua A Burk

Open access · bronzeAbstract read
In one paragraph

Article in Psychopharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
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  6. Article
  7. Review
  8. Orexinergic System in Neurodegenerative Diseases.Frontiers in aging neuroscience · 2021
    Review
  9. Hypocretin (Orexin) Replacement Therapies.Medicine in drug discovery · 2020
    Article
  10. Review
  11. Review
  12. Decreased serum orexin A levels in drug-naive children with attention deficit and hyperactivity disorder.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2019
    Article
  13. Article
  14. Article
  15. Review
  16. 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

3 authors at 2 institutions in 1 country.

Kristin N ZajoDepartment of Psychology, College of William & Mary, Williamsburg, VA, 23187, USA.
Jim R FadelDepartment of Pharmacology, Physiology and Neuroscience, University of South Carolina School of Medicine, Columbia, SC, 29208, USA.
Joshua A BurkDepartment of Psychology, College of William & Mary, Williamsburg, VA, 23187, USA. jabur2@wm.edu.
University of South Carolina · USWilliam & Mary · US

Funding

Hypocretin/orexin modulation of cognitive correlates of brain agingR01AG050518 · NIA · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI JIM R FADEL · 2015 to 2026
$2.1M
Aging, acetylcholine and the hypothalamusR01AG030646 · NIA · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI FADEL, JIM R · 2008 to 2011
$1.2M
NIA NIH HHS AG030646NIA NIH HHS R01 AG030646NIA NIH HHS R01 AG050518
6 · The paper itself

Abstract

rationaleOrexins are neuropeptides released in multiple brain regions from neurons that originate within the lateral hypothalamus and contiguous perfornical area. The basal forebrain, a structure implicated in attentional processing, receives orexinergic inputs. Our previous work demonstrated that administration of an orexin-1 receptor antagonist, SB-334867, systemically or via infusion directly into the basal forebrain, can disrupt performance in a task that places explicit demands on attentional processing.

objectivesGiven that the orexin-1 receptor binds orexin A with high affinity, we tested whether orexin A could enhance attention in rats.

methodsAttentional performance was assessed using a task that required discrimination of variable duration visual signals from trials when no signal was presented. We also tested whether infusions of orexin A into the lateral ventricle could attenuate deficits following lesions of medial prefrontal cortical cholinergic projections that arise from the basal forebrain.

resultsInfusions of orexin A into the basal forebrain attenuated distracter-induced decreases in attentional performance. Orexin A attenuated deficits in lesioned animals when a visual distracter was presented.

conclusionThe present results support the view that orexin A can enhance attentional performance via actions in the basal forebrain and may be beneficial for some conditions characterized by attentional dysfunction due to disruption of cortical cholinergic inputs.

Indexed as

AnimalsAttentionBasal ForebrainInfusions, IntraventricularMaleNeuronsNeuropeptidesOrexinsRatsNeuropeptidesOrexinsAcetylcholineAttentionBasal forebrainHypocretinVigilance

Identifiers

PMID26534765
PMCPMC4729649
OpenAlexW1930275499

What OpenQuestion holds

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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.