Evidence map›Paper›PMID 11850450›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2002

Activation of central terminal vanilloid receptor-1 receptors and alpha beta-methylene-ATP-sensitive P2X receptors reveals a converged synaptic activity onto the deep dorsal horn neurons of the spinal cord.

Terumasa Nakatsuka, Hidemasa Furue, Megumu Yoshimura, Jianguo G Gu

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2002. 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
2.8field-weighted citation impact, top 8% 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, 97 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. TRPs and pain.Seminars in immunopathology · 2016
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. TRP channels and analgesia.Life sciences · 2013
    Review
  13. Article
  14. Review
  15. Article
  16. Endogenous purinergic control of bladder activity via presynaptic P2X3 and P2X2/3 receptors in the spinal cord.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2010
    Article
  17. Article
  18. 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

4 authors at 2 institutions in 2 countries.

Terumasa NakatsukaMcKnight Brain Institute of the University of Florida and Division of Neuroscience, Department of Oral Surgery, College of Dentistry, University of Florida, Gainesville, Florida 32610, USA.
Hidemasa Furue
Megumu Yoshimura
Jianguo G Gu
Kyushu University · JPUniversity of Florida · US

Funding

ATP P2X RECEPTORS AND NOCICEPTIVE TRANSMISSIONR01NS038254 · NINDS · UNIVERSITY OF FLORIDA · PI GU, JIANGUO · 1999 to 2002
$662k
NINDS NIH HHS NS38254
6 · The paper itself

Abstract

Using a spinal cord slice preparation and patch-clamp recordings from spinal cord dorsal horn neurons, we examined excitatory and inhibitory circuits connecting to lamina V neurons after the activation of afferent central terminal vanilloid receptor-1 (VR1) receptors and P2X receptors. We found that single neurons in lamina V often received excitatory inputs from two chemically defined afferent pathways. One of these pathways was polysynaptic from capsaicin-sensitive afferent terminals. In this pathway the capsaicin-sensitive afferent input first activated interneurons in superficial laminas, and then the excitatory activity was transmitted onto lamina V neurons. The second excitatory input was monosynaptic from alpha(beta)m-ATP-sensitive/capsaicin-insensitive afferent terminals. Both capsaicin-sensitive and alpha(beta)m-ATP-sensitive/capsaicin-insensitive pathways also recruited polysynaptic inhibitory inputs to lamina V neurons. Furthermore, we demonstrated that simultaneous activation of both capsaicin-sensitive afferent pathways and alpha(beta)m-ATP-sensitive/capsaicin-insensitive pathways could generate a temporal summation of excitatory inputs onto single lamina V neurons. These convergent pathways may provide a mechanism of sensory integration for two chemically defined sensory inputs and may have implications in different sensory states.

Indexed as

Purinergic P2 Receptor AntagonistsAction PotentialsAdenosine TriphosphateAgingAnimalsCapsaicinElectric StimulationExcitatory Postsynaptic PotentialsGanglia, SpinalGlycine AgentsIn Vitro TechniquesNerve NetNeural InhibitionNeural PathwaysNeurons, AfferentPatch-Clamp TechniquesAdenosine Triphosphatealpha,beta-methyleneadenosine 5'-triphosphateCapsaicinGlycine AgentsPurinergic P2 Receptor AntagonistsReceptors, DrugReceptors, Purinergic P2Receptors, Purinergic P2XTetrodotoxin

Identifiers

PMID11850450
PMCPMC6757570
OpenAlexW1912302639

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.