Evidence map›Paper›PMID 19108746›Full record

ArticleMolecular pain2008

Altered ATP release and metabolism in dorsal root ganglia of neuropathic rats.

Yoshizo Matsuka, Takeshi Ono, Hirotate Iwase, Somsak Mitrirattanakul, Kevin S Omoto, Ting Cho, Yan Yan N Lam, Bradley Snyder, Igor Spigelman

Open access · goldAbstract read
In one paragraph

Article in Molecular pain, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Photobiomodulation and vitamin B treatment alleviate both thermal and mechanical orofacial pain in rats.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2023
    Article
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  7. Article
  8. The inflammasome as a target for pain therapy.British journal of anaesthesia · 2016
    Review
  9. Article
  10. Article
  11. Article
  12. Progress in Sympathetically Mediated Pathological Pain.Journal of anesthesia and perioperative medicine · 2015
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Differential expression and pharmacology of native P2X receptors in rat and primate sensory neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    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 1 institution in 3 countries.

Yoshizo MatsukaDivision of Oral Biology & Medicine, School of Dentistry, University of California, Los Angeles, CA, USA. matsuka@md.okayama-u.ac.jp
Takeshi Ono
Hirotate Iwase
Somsak Mitrirattanakul
Kevin S Omoto
Ting Cho
Yan Yan N Lam
Bradley Snyder
Igor Spigelman
University of California, Los Angeles · US

Funding

Physiology of ATP Release in Chronic PainK08DE014573 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MATSUKA, YOSHIZO · 2002 to 2005
$497k
NIDCR NIH HHS DE14573NIDCR NIH HHS K08 DE014573
6 · The paper itself

Abstract

backgroundAdenosine 5'-triphosphate (ATP) has a ubiquitous role in metabolism and a major role in pain responses after tissue injury. We investigated the changes in basal and KCl-evoked ATP release from rat dorsal root ganglia (DRG) after peripheral neuropathy induction by unilateral sciatic nerve entrapment (SNE).

resultsAfter SNE, rats develop long-lasting decreases in ipsilateral hindpaw withdrawal thresholds to mechanical and thermal stimulation. At 15-21 days after neuropathy induction, excised ipsilateral L4-L5 DRG display significantly elevated basal extracellular ATP levels compared to contralateral or control (naive) DRG. However, KCl-evoked ATP release is no longer observed in ipsilateral DRG. We hypothesized that the differential SNE effects on basal and evoked ATP release could result from the conversion of extracellular ATP to adenosine with subsequent activation of adenosine A1 receptors (A1Rs) on DRG neurons. Adding the selective A1R agonist, 2-chloro-N(6)-cyclopentyladenosine (100 nM) significantly decreased basal and evoked ATP release in DRG from naïve rats, indicating functional A1R activation. In DRG ipsilateral to SNE, adding a selective A1R antagonist, 8-cyclopentyl-1,3-dipropylxanthine (30 nM), further increased basal ATP levels and relieved the blockade of KCl-evoked ATP release suggesting that increased A1R activation attenuates evoked ATP release in neurons ipsilateral to SNE. To determine if altered ATP release was a consequence of altered DRG metabolism we compared O(2) consumption between control and neuropathic DRG. DRG ipsilateral to SNE consumed O(2) at a higher rate than control or contralateral DRG.

conclusionThese data suggest that peripheral nerve entrapment increases DRG metabolism and ATP release, which in turn is modulated by increased A1R activation.

Indexed as

Adenosine TriphosphateAnimalsBehavior, AnimalGanglia, SpinalMaleOxygen ConsumptionPeripheral Nervous System DiseasesPotassium ChlorideRatsRats, Sprague-DawleyReceptors, Purinergic P1Sciatic NerveAdenosine TriphosphatePotassium ChlorideReceptors, Purinergic P1

Identifiers

PMID19108746
PMCPMC2630978
OpenAlexW2153132454

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.