Evidence map›Paper›PMID 18172096›Full record

ArticleInvestigative ophthalmology & visual science2008

Myogenic growth factors can decrease extraocular muscle force generation: a potential biological approach to the treatment of strabismus.

Brian C Anderson, Stephen P Christiansen, Linda K McLoon

Open access · bronzeAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2008. 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
1.6field-weighted citation impact, top 18% 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, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Neural Plasticity Following Surgical Correction of Strabismus in Monkeys.Investigative ophthalmology & visual science · 2018
    Article
  6. Establishment of an acute extraocular muscle injury model in cats.International journal of ophthalmology · 2018
    Article
  7. Article
  8. Article
  9. Effects of sequential injections of hepatocyte growth factor and insulin-like growth factor-I on adult rabbit extraocular muscle.Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus · 2012
    Article
  10. Article
  11. Expression of insulin-like growth factor 1 isoforms in the rabbit oculomotor system.Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society · 2011
    Article
  12. Article
  13. Childhood Onset Strabismus: A Neurotrophic Factor Hypothesis.Journal of binocular vision and ocular motility
    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 3 institutions in 1 country.

Brian C AndersonDepartment of Ophthalmology, University of Minnesota, 2001 6th Street SE, Minneapolis, MN 55455, USA.
Stephen P Christiansen
Linda K McLoon
Ophthalmology Associates (United States) · USPediatrics and Genetics · USUniversity of Minnesota · US

Funding

Novel Immunotoxin and IGF Therapy for StrabismusR01EY015313 · NEI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MCLOON, LINDA K., MUSTARI, MICHAEL J · 2004 to 2022
$7.6M
NEI NIH HHS EY 11375NEI NIH HHS EY 15313NEI NIH HHS R01 EY015313
6 · The paper itself

Abstract

purposeFuture pharmacologic treatment of strabismus may be optimized if drugs that are less potentially toxic to patients can be developed. Prior studies have shown that direct injection of extraocular muscles (EOMs) with insulin growth factor or fibroblast growth factor results in significant increases in the generation of EOM force. The purpose of this study was to examine the morphometric and physiological effects of direct EOM injection with the growth factors BMP4, TGFbeta1, Shh, and Wnt3A.

methodsOne superior rectus muscle of normal adult rabbits was injected with BMP4, TGFbeta1, Shh, or Wnt3A. The contralateral muscle was injected with an equal volume of saline to serve as a control. After 1 week, the animals were euthanatized, and both superior rectus muscles were removed and assayed physiologically. The muscles were stimulated at increasing frequencies to determine force generation. A separate group of treated and control superior rectus muscles were examined histologically for alterations in total muscle cross-sectional area and myosin heavy chain isoform (MyHC) composition.

resultsOne week after a single injection of BMP4, TGFbeta1, Shh, or Wnt3A, all treated muscles showed significant decreases in generation of force compared with control muscles. BMP4, TGFbeta1, Shh, and Wnt3A significantly decreased the mean myofiber cross-sectional area of fast MyHC-positive myofibers. BMP4 resulted in a conversion of fast-to-slow myofibers and a significant decrease in the percentage of developmental and neonatal MyHC-positive myofibers. Alterations in mean cross-sectional area and proportion of MyHCs were seen after injection with TGFbeta1, Shh, and Wnt3A. TGFbeta1 and BMP4 injections resulted in increased Pax7-positive satellite cells, whereas BMP4, TGFbeta1, and Wnt3A resulted in a decrease in MyoD-positive satellite cells.

conclusionsThese results suggest that, rather than using toxins or immunotoxins, a more biological approach to decrease muscle strength is possible and demonstrate the potential utility of myogenic signaling factors for decreasing EOM strength. Ongoing drug-delivery studies will elucidate means of extending treatment effect to make such agents clinically useful.

Indexed as

AnimalsBone Morphogenetic Protein 4Bone Morphogenetic ProteinsHedgehog ProteinsImmunoenzyme TechniquesInjections, IntramuscularMuscle ContractionMuscle Fibers, SkeletalMyoD ProteinMyosin Heavy ChainsOculomotor MusclesPAX7 Transcription FactorRabbitsStrabismusTransforming Growth Factor beta1Wnt3 ProteinBone Morphogenetic Protein 4Bone Morphogenetic ProteinsHedgehog ProteinsMyoD ProteinMyosin Heavy ChainsPAX7 Transcription FactorTransforming Growth Factor beta1Wnt3 ProteinWnt Proteins

Identifiers

PMID18172096
PMCPMC3039281
OpenAlexW1990628236

What OpenQuestion holds

Textmetadata
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.