Evidence map›Paper›PMID 12665615›Full record

ArticleThe Journal of physiology2003

Localization and function of ATP and GABAA receptors expressed by nociceptors and other postnatal sensory neurons in rat.

Charalampos Labrakakis, Chi-Kun Tong, Tamily Weissman, Carole Torsney, Amy B MacDermott

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

35 citing papers in PubMed, 72 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Chloride - The Underrated Ion in Nociceptors.Frontiers in neuroscience · 2020
    Review
  8. Article
  9. Review
  10. Review
  11. Acute inflammation reveals GABAPhysiological reports · 2017
    Article
  12. Review
  13. Article
  14. Article
  15. Peripheral cardiac sympathetic hyperactivity in cardiovascular disease: role of neuropeptides.American journal of physiology. Regulatory, integrative and comparative physiology · 2013
    Review
  16. Article
  17. Article
  18. Article
  19. Presynaptic alpha2-GABAA receptors in primary afferent depolarization and spinal pain control.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    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

5 authors at 1 institution in 1 country.

Charalampos LabrakakisDepartment of Physiology and Cellular Biophysics, Columbia University, New York, NY 10032, USA. CL461@columbia.edu
Chi-Kun Tong
Tamily Weissman
Carole Torsney
Amy B MacDermott
Columbia University · US

Funding

NOCICEPTORS AND GLUTAMATE RECEPTORSR01NS040428 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MACDERMOTT, AMY B · 2000 to 2003
$1.0M
REGULATION OF TRANSMITTER RELEASE IN THE DORSAL HORNR01NS037549 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MACDERMOTT, AMY B · 1998 to 2001
$418k
NINDS NIH HHS NS 37549NINDS NIH HHS NS 40428NINDS NIH HHS R01 NS040428
6 · The paper itself

Abstract

The role of endogenous GABA and ATP in regulating transmitter release from primary afferent terminals in the superficial dorsal horn of the spinal cord is still controversial. ATP is co-released with GABA from some inhibitory dorsal horn neurons raising the possibility that ATP could act in concert with GABA to regulate transmitter release from primary afferent terminals if receptors to both transmitters are expressed there. Using electrophysiology together with immunocytochemistry, we have investigated the expression of ATP-gated P2X and GABAA receptors by identified subpopulations of dorsal root ganglion (DRG) neurons known to project primarily to the superficial dorsal horn. Expression of the heat-sensitive vanilloid receptor 1 (VR1) and sensitivity to capsaicin were used to characterize DRG neurons sensitive to noxious heat. Both P2X and GABAA receptors were expressed on the majority of DRG neurons examined. Recording compound action potentials (CAPs) from dorsal roots in the presence of muscimol, alpha,beta-methylene-ATP (alpha,beta-meATP) or capsaicin resulted in depression of CAP in the slow and medium conducting fibres, indicating cognate receptor expression on the small diameter axons. Dorsal root-evoked dorsal root potentials (DR-DRPs), reflecting depolarization of primary afferent terminals by endogenously released substances, were depressed by the GABAA receptor antagonist SR95531 and alpha,beta-meATP. These results suggest that GABAA and P2X receptors are expressed on DRG cell bodies and slow fibre axons, many of which are heat-nociceptive. These fibres project to the superficial lamina of the dorsal horn where the receptors may function to modulate transmitter release near their central terminals.

Indexed as

Age FactorsAnimalsAxonsGanglia, SpinalMembrane PotentialsNociceptorsPatch-Clamp TechniquesPosterior Horn CellsRatsReceptors, DrugReceptors, GABA-AReceptors, PresynapticReceptors, Purinergic P2Receptors, DrugReceptors, GABA-AReceptors, PresynapticReceptors, Purinergic P2

Identifiers

PMID12665615
PMCPMC2342927
OpenAlexW2126908580

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.