Evidence map›Paper›PMID 23719574›Full record

ArticlePain2013

Paradoxical surrogate markers of dental injury-induced pain in the mouse.

Jennifer L Gibbs, Rochelle Urban, Allan I Basbaum

Open access · greenAbstract read
In one paragraph

Article in Pain, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Thermosensing ability of TRPC5: current knowledge and unsettled questions.The journal of physiological sciences : JPS · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Animal models in the study and treatment of orofacial pain.Journal of clinical and experimental dentistry · 2019
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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

3 authors at 1 institution in 1 country.

Jennifer L GibbsDepartment of Preventive and Restorative Dental Sciences, Division of Endodontics, UCSF School of Dentistry, San Francisco, CA, USA. jlg15@nyu.edu
Rochelle Urban
Allan I Basbaum
University of California, San Francisco · US

Funding

BRAINSTEM CONTROL OF PAIN TRANSMISSIONR01NS014627 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BASBAUM, ALLAN I. · 1985 to 2016
$3.9M
Brainstem control of pain transmissionR37NS014627 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BASBAUM, ALLAN I. · 2008 to 2014
$3.6M
Multiple Opioid Receptors and the Control of PainR01DA029204 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BASBAUM, ALLAN I. · 2011 to 2015
$1.9M
Capsaicin-sensitive primary afferent fibers and neuropathic painK23DE019461 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GIBBS, JENNIFER LYNN · 2009 to 2013
$625k
NIDA NIH HHS DA29204NIDA NIH HHS R01 DA029204NIDCR NIH HHS K23 DE019461NIDCR NIH HHS K23DE019461NINDS NIH HHS NS14627NINDS NIH HHS R01 NS014627NINDS NIH HHS R37 NS014627
6 · The paper itself

Abstract

Dental pain, including toothache, is one of the most prevalent types of orofacial pain, causing severe, persistent pain that has a significant negative effect on quality of life, including eating disturbances, mood changes, and sleep disruption. As the primary cause of toothache pain is injury to the uniquely innervated dental pulp, rodent models of this injury provide the opportunity to study neurobiological mechanisms of tissue injury-induced persistent pain. Here we evaluated behavioral changes in mice with a dental pulp injury (DPI) produced by mechanically exposing the pulp to the oral environment. We monitored the daily life behaviors of mice with DPI, including measures of eating, drinking, and movement. During the first 48 hours, the only parameter affected by DPI was locomotion, which was reduced. There was also a significant short-term decrease in the amount of weight gained by DPI animals that was not related to food consumption. As cold allodynia is frequently observed in individuals experiencing toothache pain, we tested whether mice with DPI demonstrate an aversion to drinking cold liquids using a cold-sucrose consumption test. Surprisingly, mice with DPI increased their consumption of sucrose solution, to over 150% of baseline, regardless of temperature. Both the weight loss and increased sucrose intake in the first 2 days of injury were reversed by administration of indomethacin. These findings indicate that enhanced sucrose consumption may be a reliable measure of orofacial pain in rodents, and suggest that alterations in energy expenditure and motivational behaviors are under-recognized outcomes of tooth injury.

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalBody WeightCold TemperatureDental PulpDisease Models, AnimalDrinking BehaviorFeeding BehaviorFemaleHyperalgesiaIndomethacinMaleMiceMice, Inbred C57BLMovement DisordersStatistics, NonparametricAnti-Inflammatory Agents, Non-SteroidalIndomethacinSucrose

Identifiers

PMID23719574
PMCPMC3743260
OpenAlexW2047967002

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.