Evidence map›Paper›PMID 30619048›Full record

ArticleFrontiers in neurology2018

A Concomitant Muscle Injury Does Not Worsen Traumatic Brain Injury Outcomes in Mice.

Mujun Sun, Rhys D Brady, Chris van der Poel, Danielle Apted, Bridgette D Semple, Jarrod E Church, Terence J O'Brien, Stuart J McDonald, Sandy R Shultz

Abstract read
In one paragraph

Article in Frontiers in neurology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Tanshinone-IIA mediated neuroprotection by modulating neuronal pathways.Naunyn-Schmiedeberg's archives of pharmacology · 2023
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

9 authors.

Mujun SunDepartment of Medicine, The Royal Melbourne Hospital, The University of Melbourne, Melbourne, VIC, Australia.
Rhys D BradyDepartments of Neuroscience and Medicine, Central Clinical School, Monash University, Melbourne, VIC, Australia.
Chris van der PoelDepartment of Physiology, Anatomy and Microbiology, La Trobe University, Melbourne, VIC, Australia.
Danielle AptedDepartment of Physiology, Anatomy and Microbiology, La Trobe University, Melbourne, VIC, Australia.
Bridgette D SempleDepartment of Medicine, The Royal Melbourne Hospital, The University of Melbourne, Melbourne, VIC, Australia.
Jarrod E ChurchDepartment of Physiology, Anatomy and Microbiology, La Trobe University, Melbourne, VIC, Australia.
Terence J O'BrienDepartment of Medicine, The Royal Melbourne Hospital, The University of Melbourne, Melbourne, VIC, Australia.
Stuart J McDonaldDepartment of Physiology, Anatomy and Microbiology, La Trobe University, Melbourne, VIC, Australia.
Sandy R ShultzDepartment of Medicine, The Royal Melbourne Hospital, The University of Melbourne, Melbourne, VIC, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Traumatic brain injury (TBI) often involves multitrauma in which concurrent extracranial injury occurs. We previously demonstrated that a long bone fracture exacerbates neuroinflammation and functional outcomes in mice given a TBI. Whether other forms of concomitant peripheral trauma that are common in the TBI setting, such as skeletal muscle injury, have similar effects is unknown. As such, here we developed a novel mouse multitrauma model by combining a closed-skull TBI with a cardiotoxin (CTX)-induced muscle injury to investigate whether muscle injury affects TBI outcomes. Adult male mice were assigned to four groups: sham-TBI + sham-muscle injury (SHAM); sham-TBI + CTX-muscle injury (CTX); TBI + sham-muscle injury (TBI); TBI + CTX-muscle injury (MULTI). Some mice were euthanized at 24 h post-injury to assess neuroinflammation and cerebral edema. The remaining mice underwent behavioral testing after a 30-day recovery period, and were euthanized at 35 days post-injury for post-mortem analysis. At 24 h post-injury, both TBI and MULTI mice had elevated edema, increased expression of GFAP (i.e., a marker for reactive astrocytes), and increased mRNA levels of inflammatory chemokines. There was also an effect of injury on cytokine levels at 35 days post-injury. However, the TBI and MULTI mice did not significantly differ on any of the measures assessed. These initial findings suggest that a concomitant muscle injury does not significantly affect preclinical TBI outcomes. Future studies should investigate the combination of different injury models, additional outcomes, and other post-injury time points.

Indexed as

cardiotoxincytokinesneuroinflammationpolytraumaweight-drop

Identifiers

PMID30619048
PMCPMC6297867

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.