Evidence map›Paper›PMID 30718662›Full record

ArticleScientific reports2019

Interaction between NMDA Receptor- and Endocannabinoid-Mediated Modulation of Nociceptive Synapses.

Sharleen Yuan, Brian D Burrell

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Comparative studies of endocannabinoid modulation of pain.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    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

2 authors at 1 institution in 1 country.

Sharleen YuanCenter for Brain and Behavior Research, Division of Basic Biomedical Sciences Sanford School of Medicine, University of South Dakota, Vermillion, SD, 57069, USA.
Brian D BurrellCenter for Brain and Behavior Research, Division of Basic Biomedical Sciences Sanford School of Medicine, University of South Dakota, Vermillion, SD, 57069, USA. bburrell@usd.edu.
University of South Dakota · US

Funding

Endovanilloid-Mediated Modulation and its Role in Habituation and SensitizationR01NS092716 · NINDS · UNIVERSITY OF SOUTH DAKOTA · PI BURRELL, BRIAN DONALD · 2016 to 2020
$1.4M
Role of TRPV Receptors and Endocannabinoids in Modulating Nociceptive SignalingF31NS074473 · NINDS · UNIVERSITY OF SOUTH DAKOTA · PI YUAN, SHARLEEN · 2011 to 2012
$84k
NINDS NIH HHS F31 NS074473NINDS NIH HHS R01 NS092716
6 · The paper itself

Abstract

Nociceptors, sensory neurons that detect damage or potential damage to the body, are the first stage of communicating noxious stimuli from the periphery to central nervous system (CNS). In this study, long-term potentiation (LTP) in the CNS of the medicinal leech, Hirudo verbana, was examined, taking advantage of the ability to selectively record from nociceptive synapses in this model organism. High frequency stimulation (HFS) of nociceptors produced a persistent increase in synaptic transmission and this LTP was both NMDA receptor-mediated and synapse-specific. Surprisingly, inhibition of NMDA receptors during HFS "uncovered" a persistent form of depression. This long-term depression (LTD) was mediated by the endocannabinoid 2-arachidonoyl glycerol (2-AG) acting on a TRPV (transient receptor potential vanilloid) -like channel. These observations suggest that (1) NMDA receptor mediated LTP is observed in nociceptors across both vertebrate and invertebrate phyla and (2) there may be an interaction between NMDA receptor-mediated and endocannabinoid-mediated forms of synaptic plasticity in nociceptors. Specifically, the NMDA receptor mediated processes may suppress endocannabinoid signaling. Such findings could be significant for understanding cellular mechanisms behind nociceptive sensitization and perhaps their contribution to chronic pain.

Indexed as

AnimalsElectric StimulationEndocannabinoidsLeechesLong-Term PotentiationLong-Term Synaptic DepressionModels, NeurologicalNeuronsNociceptorsReceptors, N-Methyl-D-AspartateSynapsesEndocannabinoidsReceptors, N-Methyl-D-Aspartate

Identifiers

PMID30718662
PMCPMC6361953
OpenAlexW2920947943

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.