Evidence map›Paper›PMID 37363910›Full record

ArticlePloS one2023

Evaluation of tarsal injuries in C57BL/6J male mice.

Brenda L Kick, Laura Anderson, Rosalinda Doty, Christine Wooley, Meaghan Dyer, Torrian Green, Veronica Knickerbocker, Zoe Brown, Samantha Loeber, Janine Wotton and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 90% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

13 authors at 2 institutions in 1 country.

Brenda L KickComparative Medicine and Quality, The Jackson Laboratory, Bar Harbor, Maine, United States of America.ORCID 0000-0001-9577-5922
Laura AndersonCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Rosalinda DotyComparative Medicine and Quality, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Christine WooleyCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Meaghan DyerCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Torrian GreenCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Veronica KnickerbockerCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Zoe BrownCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Samantha LoeberDepartment of Surgical Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, Wisconsin, United States of America.
Janine WottonCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Bonnie LyonsComparative Medicine and Quality, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Linda WatermanComparative Medicine and Quality, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Zoë BichlerCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Jackson Laboratory · USUniversity of Wisconsin–Madison · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tarsal joint abnormalities have been observed in aged male mice on a C57BL background. This joint disease consists of calcaneal displacement, inflammation, and proliferation of cartilage and connective tissue, that can progress to ankylosis of the joint. While tarsal pathology has been described previously in C57BL/6N substrains, as well as in STR/ort and B10.BR strain, no current literature describes this disease occurring in C57BL/6J mice. More importantly the behavioral features that may result from such a change to the joint have yet to be evaluated. This condition was observed in older male mice of the C57BL/6J lineage, around the age of 20 weeks or older, at a frequency of 1% of the population. To assess potential phenotypic sequela, this study sought to evaluate body weight, frailty assessment, home cage wheel running, dynamic weight bearing, and mechanical allodynia with and without the presence of pain relief with morphine. Overall mice with tarsal injuries had significantly higher frailty scores (p< 0.05) and weighed less (p<0.01) compared to unaffected mice. Affected mice had greater overall touch sensitivity (p<0.05) and they placed more weight on their forelimbs (p<0.01) compared to their hind limbs. Lastly, when housed with a running wheel, affected mice ran for a shorter length of time (p<0.01) but tended to run a greater distance within the time they did run (p<0.01) compared to unaffected mice. When tested just after being given morphine, the affected mice performed more similarly to unaffected mice, suggesting there is a pain sensation to this disease process. This highlights the importance of further characterizing inbred mouse mutations, as they may impact research programs or specific study goals.

Indexed as

FrailtyMotor ActivityAnimalsMaleMiceMice, Inbred C57BLMorphinePainMorphine

Identifiers

PMID37363910
PMCPMC10292699
OpenAlexW4382139212

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.