Evidence map›Paper›PMID 23630592›Full record

ArticlePloS one2013

Vivo-morpholinos induced transient knockdown of physical activity related proteins.

David P Ferguson, Emily E Schmitt, J Timothy Lightfoot

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. 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
2.1field-weighted citation impact, top 14% 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, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Optochemical Control of Biological Processes in Cells and Animals.Angewandte Chemie (International ed. in English) · 2018
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Differential skeletal muscle proteome of high- and low-active mice.Journal of applied physiology (Bethesda, Md. : 1985) · 2014
    Article
  12. Morpholino treatment improves muscle function and pathology of Pitx1 transgenic mice.Molecular therapy : the journal of the American Society of Gene Therapy · 2014
    Article
  13. 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 2 institutions in 1 country.

David P FergusonDepartment of Health and Kinesiology, Texas A&M University, College Station, Texas, United States of America. davidpferguson13@gmail.com
Emily E Schmitt
J Timothy Lightfoot
Texas A&M University · USTexas A&M University System · US

Funding

GENETIC FACTORS RESPONSIBLE FOR EXERCISE ENDURANCER01AR050085 · NIAMS · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI LIGHTFOOT, J TIMOTHY · 2005 to 2009
$1.6M
NIAMS NIH HHS AR050085NIAMS NIH HHS R01 AR050085
6 · The paper itself

Abstract

Physical activity is associated with disease prevention and overall wellbeing. Additionally there has been evidence that physical activity level is a result of genetic influence. However, there has not been a reliable method to silence candidate genes in vivo to determine causal mechanisms of physical activity regulation. Vivo-morpholinos are a potential method to transiently silence specific genes. Thus, the aim of this study was to validate the use of Vivo-morpholinos in a mouse model for voluntary physical activity with several sub-objectives. We observed that Vivo-morpholinos achieved between 60-97% knockdown of Drd1-, Vmat2-, and Glut4-protein in skeletal muscle, the delivery moiety of Vivo-morpholinos (scramble) did not influence physical activity and that a cocktail of multiple Vivo-morpholinos can be given in a single treatment to achieve protein knockdown of two different targeted proteins in skeletal muscle simultaneously. Knocking down Drd1, Vmat2, or Glut4 protein in skeletal muscle did not affect physical activity. Vivo-morpholinos injected intravenously alone did not significantly knockdown Vmat2-protein expression in the brain (p = 0.28). However, the use of a bradykinin analog to increase blood-brain-barrier permeability in conjunction with the Vivo-morpholinos significantly (p = 0.0001) decreased Vmat2-protein in the brain with a corresponding later over-expression of Vmat2 coincident with a significant (p = 0.0016) increase in physical activity. We conclude that Vivo-morpholinos can be a valuable tool in determining causal gene-phenotype relationships in whole animal models.

Indexed as

Gene Knockdown TechniquesAnimalsGlucose Transporter Type 4MaleMiceMice, Inbred C57BLMorpholinosMotor ActivityMuscle, SkeletalNucleus AccumbensOrgan SpecificityReceptors, Dopamine D1RunningVesicular Monoamine Transport ProteinsGlucose Transporter Type 4MorpholinosReceptors, Dopamine D1Slc18a2 protein, mouseSlc2a4 protein, mouseVesicular Monoamine Transport Proteins

Identifiers

PMID23630592
PMCPMC3632599
OpenAlexW1985974825

What OpenQuestion holds

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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.