Evidence map›Paper›PMID 32385407›Full record

ArticleScientific reports2020

Longitudinal optical imaging technique to visualize progressive axonal damage after brain injury in mice reveals responses to different minocycline treatments.

Chelsea D Pernici, Rachel K Rowe, P Timothy Doughty, Mahboubeh Madadi, Jonathan Lifshitz, Teresa A Murray

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Treating Traumatic Brain Injury with Minocycline.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Review
  3. Article
  4. Maintenance of a Lateral Fluid Percussion Injury Device.Journal of visualized experiments : JoVE · 2023
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
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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

6 authors at 4 institutions in 1 country.

Chelsea D PerniciCenter for Biomedical Engineering and Rehabilitation Sciences, Louisiana Tech University, Ruston, LA, USA.
Rachel K RoweBarrow Neurological Institute at Phoenix Children's Hospital, Phoenix, AZ, USA.
P Timothy DoughtyCenter for Biomedical Engineering and Rehabilitation Sciences, Louisiana Tech University, Ruston, LA, USA.
Mahboubeh MadadiDepartment of Marketing and Business Analytics, Lucas College of Business, San Jose State University, San Jose, CA, USA.
Jonathan LifshitzBarrow Neurological Institute at Phoenix Children's Hospital, Phoenix, AZ, USA.
Teresa A MurrayCenter for Biomedical Engineering and Rehabilitation Sciences, Louisiana Tech University, Ruston, LA, USA. bioengineer1@hotmail.com.
Louisiana Tech University · USBarrow Neurological Institute · USPhoenix Children's Hospital · USSan Jose State University · US

Funding

Direct visualization of longitudinal effects of drug therapy on white matter in diffuse injured brainR21NS090131 · NINDS · LOUISIANA TECH UNIVERSITY · PI MURRAY, TERESA ANN · 2015 to 2016
$401k
NINDS NIH HHS R21 NS090131
6 · The paper itself

Abstract

A high-resolution, three-dimensional, optical imaging technique for the murine brain was developed to identify the effects of different therapeutic windows for preclinical brain research. This technique tracks the same cells over several weeks. We conducted a pilot study of a promising drug to treat diffuse axonal injury (DAI) caused by traumatic brain injury, using two different therapeutic windows, as a means to demonstrate the utility of this novel longitudinal imaging technique. DAI causes immediate, sporadic axon damage followed by progressive secondary axon damage. We administered minocycline for three days commencing one hour after injury in one treatment group and beginning 72 hours after injury in another group to demonstrate the method's ability to show how and when the therapeutic drug exerts protective and/or healing effects. Fewer varicosities developed in acutely treated mice while more varicosities resolved in mice with delayed treatment. For both treatments, the drug arrested development of new axonal damage by 30 days. In addition to evaluation of therapeutics for traumatic brain injury, this hybrid microlens imaging method should be useful to study other types of brain injury and neurodegeneration and cellular responses to treatment.

Indexed as

AnimalsAxonsBrainBrain InjuriesDiffuse Axonal InjuryDisease Models, AnimalHumansMiceMinocyclineOptical ImagingMinocycline

Identifiers

PMID32385407
PMCPMC7210987
OpenAlexW3023676624

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.