Evidence map›Paper›PMID 37253591›Full record

ArticleeNeuro2023

Bidirectional Modulation of Nociception by GlyT2

Neda Assareh, Caitlin Fenech, Rebecca Power, Mohammad N Uddin, Yo Otsu, Karin R Aubrey

Open access · goldAbstract read
In one paragraph

Article in eNeuro, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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  4. Review
  5. 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

6 authors at 1 institution in 1 country.

Neda AssarehPain Management Research, Kolling Institute, Royal North Shore Hospital Northern Sydney Local Health District and Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales 2065, Australia.
Caitlin FenechPain Management Research, Kolling Institute, Royal North Shore Hospital Northern Sydney Local Health District and Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales 2065, Australia.ORCID 0009-0008-1450-8856
Rebecca PowerPain Management Research, Kolling Institute, Royal North Shore Hospital Northern Sydney Local Health District and Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales 2065, Australia.ORCID 0009-0005-5756-1241
Mohammad N UddinPain Management Research, Kolling Institute, Royal North Shore Hospital Northern Sydney Local Health District and Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales 2065, Australia.
Yo OtsuPain Management Research, Kolling Institute, Royal North Shore Hospital Northern Sydney Local Health District and Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales 2065, Australia.
Karin R AubreyPain Management Research, Kolling Institute, Royal North Shore Hospital Northern Sydney Local Health District and Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales 2065, Australia karin.aubrey@sydney.edu.au.ORCID 0000-0002-1808-4041
The University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The midbrain periaqueductal gray (PAG), particularly its ventrolateral column (vlPAG), is part of a key descending pathway that modulates nociception, fear and anxiety behaviors in both humans and rodents. It has been previously demonstrated that inhibitory GABAergic neurons within the vlPAG have a major role in this nociceptive modulation. However, the PAG contains a diverse range of neuronal subtypes and the contribution of different subtypes of inhibitory neurons to nociceptive control has not been investigated. Here, we employed a chemogenetic strategy in mice that express Cre recombinase under the promotor for the glycine transporter 2 (GlyT2::cre) to modulate a novel group of glycinergic neurons within the vlPAG and then investigate their role in nociceptive control. We show that activation of GlyT2-PAG neurons enhances cold and noxious heat responses and increases locomotor activity (LMA) in both male and female mice. In contrast, inhibition of GlyT2-PAG neurons reduced nociceptive responses, while locomotor behaviors were unaffected. Our findings demonstrate that GlyT2

Indexed as

NociceptionPeriaqueductal GrayAnimalsAnxietyFearFemaleHumansMaleMiceNeuronschemogeneticsglycinergic neurotransmissionGlyT2::Cre micenociceptionsupraspinal glycinevlPAG

Identifiers

PMID37253591
PMCPMC10270318
OpenAlexW4378781441

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.