Evidence map›Paper›PMID 22278093›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2012

Intranasally administered neuropeptide S (NPS) exerts anxiolytic effects following internalization into NPS receptor-expressing neurons.

Irina A Ionescu, Julien Dine, Yi-Chun Yen, Dominik R Buell, Leonie Herrmann, Florian Holsboer, Matthias Eder, Rainer Landgraf, Ulrike Schmidt

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.7field-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

38 citing papers in PubMed, 83 citations in OpenAlex.

  1. Trial
  2. Article
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  4. Article
  5. Review
  6. A Role for Neuropeptide S in Alcohol and Cocaine Seeking.Pharmaceuticals (Basel, Switzerland) · 2022
    Review
  7. Article
  8. Review
  9. Article
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  12. Article
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  15. Review
  16. Article
  17. Novel transmitters in brain stem vagal neurocircuitry: new players on the pitch.American journal of physiology. Gastrointestinal and liver physiology · 2018
    Review
  18. Neuropeptide S Induces Acute Anxiolysis by Phospholipase C-Dependent Signaling within the Medial Amygdala.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    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

9 authors at 2 institutions in 1 country.

Irina A IonescuMax Planck Institute of Psychiatry, Munich, Germany.
Julien Dine
Yi-Chun Yen
Dominik R Buell
Leonie Herrmann
Florian Holsboer
Matthias Eder
Rainer Landgraf
Ulrike Schmidt
Max Planck Society · DEMax Planck Institute of Psychiatry · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Experiments in rodents revealed neuropeptide S (NPS) to constitute a potential novel treatment option for anxiety diseases such as panic and post-traumatic stress disorder. However, both its cerebral target sites and the molecular underpinnings of NPS-mediated effects still remain elusive. By administration of fluorophore-conjugated NPS, we pinpointed NPS target neurons in distinct regions throughout the entire brain. We demonstrated their functional relevance in the hippocampus. In the CA1 region, NPS modulates synaptic transmission and plasticity. NPS is taken up into NPS receptor-expressing neurons by internalization of the receptor-ligand complex as we confirmed by subsequent cell culture studies. Furthermore, we tracked internalization of intranasally applied NPS at the single-neuron level and additionally demonstrate that it is delivered into the mouse brain without losing its anxiolytic properties. Finally, we show that NPS differentially modulates the expression of proteins of the glutamatergic system involved inter alia in synaptic plasticity. These results not only enlighten the path of NPS in the brain, but also establish a non-invasive method for NPS administration in mice, thus strongly encouraging translation into a novel therapeutic approach for pathological anxiety in humans.

Indexed as

Analysis of VarianceAnimalsAnti-Anxiety AgentsAnxietyCA1 Region, HippocampalCarbocyaninesCell Line, TransformedCells, CulturedDisease Models, AnimalDose-Response Relationship, DrugElectrophysiologyEvoked PotentialsGene Expression RegulationGlial Fibrillary Acidic ProteinGreen Fluorescent ProteinsHumans3-oxo-1,1-diphenyltetrahydrooxazolo(3,4-a)pyrazine-7-carboxylic acid 4-fluorobenzylamideAnti-Anxiety AgentsCarbocyaninescyanine dye 3enhanced green fluorescent proteinGlial Fibrillary Acidic ProteinGreen Fluorescent ProteinsNeurofilament ProteinsNeuropeptidesneuropeptide S, mouseOxazolidinonesPyrazinesReceptors, AMPAReceptors, NeuropeptideRhodaminesRNA, MessengerSynapsins

Identifiers

PMID22278093
PMCPMC3327839
OpenAlexW2073943499

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.