Evidence map›Paper›PMID 15634779›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2005

Direct and indirect inhibition by catecholamines of hypocretin/orexin neurons.

Ying Li, Anthony N van den Pol

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

53 citing papers in PubMed, 124 citations in OpenAlex.

  1. Article
  2. Nucleus of the solitary tract regulation of cue-induced appetitive behaviors via midbrain dopamine neurons.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  3. Hypothalamic control of arousal.Reviews in endocrine & metabolic disorders · 2026
    Review
  4. Article
  5. The NaeLife · 2024
    Article
  6. The NabioRxiv : the preprint server for biology · 2023
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. The Dual Hypocretin Receptor Antagonist Almorexant is Permissive for Activation of Wake-Promoting Systems.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2016
    Article
  15. Review
  16. The Neurobiology of Sleep and Wakefulness.The Psychiatric clinics of North America · 2015
    Review
  17. Orexin-A enhances feeding in male rats by activating hindbrain catecholamine neurons.American journal of physiology. Regulatory, integrative and comparative physiology · 2015
    Article
  18. Article
  19. Article
  20. 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

2 authors at 1 institution in 1 country.

Ying LiDepartment of Neurosurgery, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
Anthony N van den Pol
Yale University · US

Funding

Cytomegalovirus in the BrainR01AI048854 · NIAID · YALE UNIVERSITY · PI VAN DEN POL, ANTHONY N · 2001 to 2010
$3.8M
Hypocretin NeuronsR01NS041454 · NINDS · YALE UNIVERSITY · PI VAN DEN POL, ANTHONY N · 2002 to 2010
$2.9M
NPY DEPRESSION OF HIPPOCAMPAL EPILEPSYR01NS037788 · NINDS · YALE UNIVERSITY · PI VAN DEN POL, ANTHONY N · 1999 to 2002
$909k
NIAID NIH HHS AI/NS48854NINDS NIH HHS NS37788NINDS NIH HHS NS41454NINDS NIH HHS R01 NS037788NINDS NIH HHS R01 NS041454
6 · The paper itself

Abstract

Hypothalamic hypocretin enhances arousal, similar to the actions of norepinephrine (NE). The physiological actions of NE were examined in hypocretin neurons identified by selective green fluorescent protein expression in transgenic mouse hypothalamic slices using whole-cell recording. NE induced an outward current, inhibited spike frequency, and hyperpolarized hypocretin neurons dose dependently. Similar actions were evoked by the selective alpha2 adrenergic agonist clonidine. The alpha2 antagonist idazoxan increased spike frequency, suggesting tonic NE-mediated inhibition. The NE-induced current was inwardly rectified, and the reversal potential was dependent on external potassium concentration; it was blocked by barium in the bath and by GTP-gamma-S in the pipette, suggesting activation of a G-protein inward rectifying K+ (GIRK) current. NE and clonidine decreased calcium currents evoked by depolarizing voltage steps. The selective alpha1 adrenergic agonist phenylephrine had no effect on membrane potential but did increase IPSC frequency; miniature IPSC frequency was also increased, in some cells without any effect on amplitude, suggesting a facilitative presynaptic action at alpha1 receptors on GABAergic axons that innervate hypocretin neurons. NE therefore inhibits hypocretin neurons directly through two mechanisms: activation of a GIRK current, depression of calcium currents, and indirectly through increased inhibitory GABA input. Similar to NE, dopamine and epinephrine reduced or blocked spikes and, in the presence of TTX, showed direct hyperpolarizing actions. The action of dopamine was blocked by the D2 receptor antagonist eticlopride, whereas a D1/5 antagonist had no effect. These data suggest that catecholamines evoke strong inhibitory actions on hypocretin neurons and suggest negative feedback from catecholamine cells that may be excited by hypocretin.

Indexed as

Action PotentialsAdrenergic alpha-AgonistsAgingAnimalsCalcium ChannelsCatecholaminesClonidineG Protein-Coupled Inwardly-Rectifying Potassium ChannelsHypothalamusIntracellular Signaling Peptides and ProteinsMembrane PotentialsMiceMice, TransgenicNeural InhibitionNeuronsNeuropeptidesAdrenergic alpha-AgonistsCalcium ChannelsCatecholaminesClonidineG Protein-Coupled Inwardly-Rectifying Potassium ChannelsIntracellular Signaling Peptides and ProteinsNeuropeptidesNorepinephrineOrexin ReceptorsOrexinsPhenylephrinePotassium Channels, Inwardly RectifyingReceptors, AdrenergicReceptors, G-Protein-CoupledReceptors, Neuropeptide

Identifiers

PMID15634779
PMCPMC6725201
OpenAlexW1984459245

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.