Evidence map›Paper›PMID 28157737›Full record

ArticlePain2017

Spinal cord interneurons expressing the gastrin-releasing peptide receptor convey itch through VGLUT2-mediated signaling.

Bejan Aresh, Fabio B Freitag, Sharn Perry, Edda Blümel, Joey Lau, Marina C M Franck, Malin C Lagerström

Open access · hybridAbstract read
In one paragraph

Article in Pain, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
9.2field-weighted citation impact, top 2% 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

27 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. A neuropeptide code for itch.Nature reviews. Neuroscience · 2021
    Review
  10. Article
  11. Review
  12. How Do Neurons Signal Itch?Frontiers in medicine · 2021
    Review
  13. Review
  14. The Neurokinin-1 Receptor is Expressed with Gastrin-Releasing Peptide Receptor in Spinal Interneurons and Modulates Itch.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  15. Article
  16. [Pruritus-a long journey from neurophysiology to the clinic].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2020
    Review
  17. Physiology and Pathophysiology of Itch.Physiological reviews · 2020
    Review
  18. Central circuit mechanisms of itch.Nature communications · 2020
    Review
  19. Article
  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

7 authors at 2 institutions in 2 countries.

Bejan AreshDepartments of Neuroscience and.
Fabio B FreitagDepartments of Neuroscience and.
Sharn PerryDepartments of Neuroscience and.
Edda BlümelDepartments of Neuroscience and.
Joey LauMedical Cell Biology, Uppsala University, Uppsala, Sweden.
Marina C M FranckDepartments of Neuroscience and.
Malin C LagerströmDepartments of Neuroscience and.
Society for Neuroscience · USUppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Itch is a sensation that promotes the desire to scratch, which can be evoked by mechanical and chemical stimuli. In the spinal cord, neurons expressing the gastrin-releasing peptide receptor (GRPR) have been identified as specific mediators of itch. However, our understanding of the GRPR population in the spinal cord, and thus how these neurons exercise their functions, is limited. For this purpose, we constructed a Cre line designed to target the GRPR population of neurons (Grpr-Cre). Our analysis revealed that Grpr-Cre cells in the spinal cord are predominantly excitatory interneurons that are found in the dorsal lamina, especially in laminae II-IV. Application of the specific agonist gastrin-releasing peptide induced spike responses in 43.3% of the patched Grpr-Cre neurons, where the majority of the cells displayed a tonic firing property. Additionally, our analysis showed that the Grpr-Cre population expresses Vglut2 mRNA, and mice ablated of Vglut2 in Grpr-Cre cells (Vglut2-lox;Grpr-Cre mice) displayed less spontaneous itch and attenuated responses to both histaminergic and nonhistaminergic agents. We could also show that application of the itch-inducing peptide, natriuretic polypeptide B, induces calcium influx in a subpopulation of Grpr-Cre neurons. To summarize, our data indicate that the Grpr-Cre spinal cord neural population is composed of interneurons that use VGLUT2-mediated signaling for transmitting chemical and spontaneous itch stimuli to the next, currently unknown, neurons in the labeled line of itch.

Indexed as

AnimalsAnimals, NewbornCalciumFemaleGreen Fluorescent ProteinsInterneuronsMaleMembrane PotentialsMiceMice, TransgenicPain MeasurementPruritusReceptors, BombesinSeverity of Illness IndexSignal TransductionSpinal CordCalciumenhanced green fluorescent proteinGreen Fluorescent ProteinsReceptors, BombesinSlc17a6 protein, mouseVesicular Glutamate Transport Protein 2Vesicular Inhibitory Amino Acid Transport ProteinsViaat protein, mouse

Identifiers

PMID28157737
PMCPMC5402714
OpenAlexW2587377066

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.