Evidence map›Paper›PMID 20021438›Full record

ReviewCurrent molecular pharmacology2008

TRPV1: on the road to pain relief.

Andrés Jara-Oseguera, Sidney A Simon, Tamara Rosenbaum

2 registry-linked trialsOpen access · bronzeAbstract readReview
In one paragraph

Review in Current molecular pharmacology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 101 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 12% 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.

NCT03515720 nacompletednot on this mapstarted 2018, after this paper: background citation

Effectiveness of Neuroprolotherapy With Home Physical Therapy Against Isolated Physical Therapy for the Treatment of Patellar Chondromalacia

TypeinterventionalSponsorInstituto Mexicano del Seguro SocialRan2018 to 2020Enrolled50ConditionsChondromalacia PatellaeArmsProlotherapy
NCT03899246 phase1completednot on this mapstarted 2019, after this paper: background citation

Safety and Feasibility of High-Dose Topical Capsaicin for the Treatment of Neuropathic Pain in Pediatric Sickle Cell Disease

TypeinterventionalSponsorChildren's Hospital of MichiganRan2019 to 2020Enrolled10ConditionsNeuropathic Pain, Sickle Cell DiseaseArmsEight Percent Topical Capsaicin
3 · Its place in the literature

Who cites it

101 citing papers in PubMed, 1 synthesis or guideline pooled it, 195 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. A novel role for TRPV1 in macrophage giant cell formation.bioRxiv : the preprint server for biology · 2026
    Article
  7. Review
  8. Article
  9. Review
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  11. Molecular dynamics simulation of thermal activation of human TRPV1.Molecular biology research communications · 2026
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article

41 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 2 countries.

Andrés Jara-OsegueraDepartamento de Biofísica, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico.
Sidney A Simon
Tamara Rosenbaum
Universidad Nacional Autónoma de México · MXDuke University · US

Funding

TRP and AQP Channels: Modulation of Function, Raft Location by Membrane LipidsR01GM027278 · NIGMS · DUKE UNIVERSITY · PI MC INTOSH, THOMAS J. · 1985 to 2012
$4.6M
MODULATION OF TASTE RESPONSES BY THE TRIGEMINAL SYSTEMR01DC001065 · NIDCD · DUKE UNIVERSITY · PI SIMON, SIDNEY A · 1991 to 2010
$3.1M
NIDCD NIH HHS DC-01065NIDCD NIH HHS R01 DC001065NIGMS NIH HHS GM27278NIGMS NIH HHS R01 GM027278
6 · The paper itself

Abstract

Historically, drug research targeted to pain treatment has focused on trying to prevent the propagation of action potentials in the periphery from reaching the brain rather than pinpointing the molecular basis underlying the initial detection of the nociceptive stimulus: the receptor itself. This has now changed, given that many receptors of nociceptive stimuli have been identified and/or cloned. Transient Receptor Potential (TRP) channels have been implicated in several physiological processes such as mechanical, chemical and thermal stimuli detection. Ten years after the cloning of TRPV1, compelling data has been gathered on the role of this channel in inflammatory and neuropathic states. TRPV1 activation in nociceptive neurons, where it is normally expressed, triggers the release of neuropeptides and transmitters resulting in the generation of action potentials that will be sent to higher CNS areas where they will often be perceived as pain. Its activation also will evoke the peripheral release of pro-inflammatory compounds that may sensitize other neurons to physical, thermal or chemical stimuli. For these reasons as well as because its continuous activation causes analgesia, TRPV1 has become a viable drug target for clinical use in the management of pain. This review will provide a general picture of the physiological and pathophysiological roles of the TRPV1 channel and of its structural, pharmacological and biophysical properties. Finally, it will provide the reader with an overall view of the status of the discovery of potential therapeutic agents for the management of chronic and neuropathic pain.

Indexed as

Action PotentialsAntipruriticsHumansPainTRPV Cation ChannelsAntipruriticsTRPV1 protein, humanTRPV Cation Channels

Identifiers

PMID20021438
PMCPMC2802457
OpenAlexW2123815407

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.