Evidence map›Paper›PMID 20015699›Full record

ArticleThe journal of pain2010

Spinal nerve ligation in mouse upregulates TRPV1 heat function in injured IB4-positive nociceptors.

Daniel Vilceanu, Prisca Honore, Quinn H Hogan, Cheryl L Stucky

Open access · greenAbstract read
In one paragraph

Article in The journal of pain, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.2field-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

39 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Neuropathic pain; what we know and what we should do about it.Frontiers in pain research (Lausanne, Switzerland) · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Oxaliplatin Depolarizes the IB4Frontiers in molecular neuroscience · 2021
    Article
  12. Article
  13. Physiology and Pathophysiology of Itch.Physiological reviews · 2020
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. Molecular and cellular mechanisms that initiate pain and itch.Cellular and molecular life sciences : CMLS · 2015
    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

4 authors at 2 institutions in 1 country.

Daniel VilceanuDepartment of Cell Biology, Medical College of Wisconsin, Milwaukee, Wisconsin 53226-0509, USA.
Prisca Honore
Quinn H Hogan
Cheryl L Stucky
Medical College of Wisconsin · USAbbott (United States) · US

Funding

FUNCTIONAL ANALYSIS OF DISTINCT NOCICEPTOR POPULATIONSR01NS040538 · NINDS · MEDICAL COLLEGE OF WISCONSIN · PI STUCKY, CHERYL LOUISE · 2000 to 2019
$6.2M
NINDS NIH HHS NS40538NINDS NIH HHS R01 NS040538
6 · The paper itself

Abstract

unlabelledPeripheral nerve injury leads to neuropathic pain, but the underlying mechanisms are not clear. The TRPV1 channel expressed by nociceptors is one receptor for noxious heat and inflammatory molecules. Lumbar 4 (L4) spinal nerve ligation (SNL) in mice induced persistent heat hyperalgesia 4 to 10 days after injury. The heat hypersensitivity was completely reversed by the TRPV1 antagonist A-425619. Furthermore, DRG neurons were isolated from the injured L4 ganglia or adjacent L3 ganglia 4 to 10 days after L4 SNL. Whole-cell patch-clamp recordings were performed and heat stimuli (22 degrees C to 50 degrees C/3 s) were applied to the soma. Neurons were classified by soma size and isolectin-B4 (IB4) binding. Among directly injured L4 neurons, SNL increased the percentage of small-diameter IB4-positive neurons that were heat-sensitive from 13% (naive controls) to 56% and conversely decreased the proportion of small IB4-negative neurons that were heat-sensitive from 66% (naive controls) to 34%. There was no change in IB4 binding in neurons from the injured ganglia. Surprisingly, in neurons from the adjacent L3 ganglia, SNL had no effect on the heat responsiveness of either IB4-positive or negative small neurons. Also, SNL had no effect on heat responses in medium-large-diameter neurons from either the injured or adjacent ganglia. PERSPECTIVE: TRPV1 function is upregulated in IB4-positive sensory neurons, and TRPV1 is responsible for the behavioral heat hypersensitivity in the spinal nerve ligation model. Because IB4-positive neurons may contribute to the emotional perception of pain, TRPV1 antagonists, targeting both sensory and affective pain components, could have broad analgesic effects.

Indexed as

AnimalsCells, CulturedDisease Models, AnimalGanglia, SpinalHot TemperatureIsoquinolinesLectinsLumbar VertebraeMaleMiceMice, Inbred C57BLMice, KnockoutNeuralgiaNociceptorsPeripheral Nervous System AgentsRandom Allocation1-isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-ureaIsoquinolinesLectinsPeripheral Nervous System AgentsTRPV1 protein, mouseTRPV Cation ChannelsUrea

Identifiers

PMID20015699
PMCPMC2879455
OpenAlexW2069220320

What OpenQuestion holds

Textmetadata
LicenceTDM
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.