Evidence map›Paper›PMID 25245401›Full record

ArticleThe journal of pain2014

Sensitization of group III and IV muscle afferents in the mouse after ischemia and reperfusion injury.

Jessica L Ross, Luis F Queme, Aaron T Shank, Renita C Hudgins, Michael P Jankowski

Open access · greenAbstract read
In one paragraph

Article in The journal of pain, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

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  12. Frontiers in neuroscience · 2021
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  14. A dual role for peripheral GDNF signaling in nociception and cardiovascular reflexes in the mouse.Proceedings of the National Academy of Sciences of the United States of America · 2020
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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 2 institutions in 1 country.

Jessica L RossDepartment of Anesthesia, Division of Pain Management, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH
Luis F Queme
Aaron T Shank
Renita C Hudgins
Michael P Jankowski
Cincinnati Children's Hospital Medical Center · USUniversity of Cincinnati · US

Funding

Mechanisms of Muscle Afferent Sensitization after IschemiaR01AR064551 · NIAMS · CINCINNATI CHILDRENS HOSP MED CTR · PI JANKOWSKI, MICHAEL P · 2013 to 2017
$1.6M
NIAMS NIH HHS R01 AR064551NIAMS NIH HHS R01AR064551-01A1
6 · The paper itself

Abstract

unlabelledIschemic myalgia is a unique type of muscle pain in the patient population. The role that discrete muscle afferent subpopulations play in the generation of pain during ischemic events, however, has yet to be determined. Using 2 brachial artery occlusion models to compare prolonged ischemia or transient ischemia with reperfusion of the muscles, we found that both injuries caused behavioral decrements in grip strength, as well as increased spontaneous pain behaviors. Using our ex vivo forepaw muscles, median and ulnar nerves, dorsal root ganglion, and spinal cord recording preparation, we found after both prolonged and transient ischemia that there was a significant increase in the number of afferents that responded to both noxious and non-noxious chemical (lactate, adenosine triphosphate, varying pH) stimulation of the muscles compared to uninjured controls. However, we found an increase in firing to heat stimuli specifically in muscle afferents during prolonged ischemia, but a distinct increase in afferent firing to non-noxious chemicals and decreased mechanical thresholds after transient ischemia. The unique changes in afferent function observed also corresponded with distinct patterns of gene expression in the dorsal root ganglia. Thus, the development of ischemic myalgia may be generated by unique afferent-based mechanisms during prolonged and transient ischemia. PERSPECTIVE: This study analyzed the response properties of thinly myelinated group III and unmyelinated group IV muscle afferents during prolonged and transient ischemia in addition to pain behaviors and alterations in DRG gene expression in the mouse. Results suggest that mechanisms of pain generation during prolonged ischemia may be different from ischemia/reperfusion.

Indexed as

Action PotentialsAdenosine TriphosphateAnimalsDisease Models, AnimalForelimbGanglia, SpinalHot TemperatureHydrogen-Ion ConcentrationIschemiaLactic AcidMedian NerveMiceMuscle, SkeletalMuscle StrengthMyalgiaNeurons, AfferentAdenosine TriphosphateLactic Acid

Identifiers

PMID25245401
PMCPMC4302035
OpenAlexW2025743750

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.