Evidence map›Paper›PMID 24528872›Full record

ArticleExperimental & translational stroke medicine2014

Forced arm use is superior to voluntary training for motor recovery and brain plasticity after cortical ischemia in rats.

Armin Schneider, Andreas Rogalewski, Oliver Wafzig, Friederike Kirsch, Norbert Gretz, Carola Krüger, Kai Diederich, Claudia Pitzer, Rico Laage, Christian Plaas and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Experimental & translational stroke medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 12% 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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
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 4 institutions in 2 countries.

Armin Schneider *SYGNIS Bioscience, Heidelberg, Germany.
Andreas Rogalewski *Neurology Department Bethel EVKB Bielefeld and Dept. of Neurology, University of Muenster, Muenster, Germany.
Oliver WafzigSYGNIS Bioscience, Heidelberg, Germany.
Friederike KirschSYGNIS Bioscience, Heidelberg, Germany.
Norbert GretzCtr. for Med. Res., Fac. for Clin. Medicine, University of Heidelberg, Mannheim, Germany.
Carola KrügerSYGNIS Bioscience, Heidelberg, Germany.
Kai DiederichNeurology Department Bethel EVKB Bielefeld and Dept. of Neurology, University of Muenster, Muenster, Germany.
Claudia PitzerSYGNIS Bioscience, Heidelberg, Germany.
Rico LaageSYGNIS Bioscience, Heidelberg, Germany.
Christian PlaasSYGNIS Bioscience, Heidelberg, Germany.
Gerhard VogtSYGNIS Bioscience, Heidelberg, Germany.
Jens Minnerup *Neurology Department Bethel EVKB Bielefeld and Dept. of Neurology, University of Muenster, Muenster, Germany.
Wolf-Rüdiger Schäbitz *Neurology Department Bethel EVKB Bielefeld and Dept. of Neurology, University of Muenster, Muenster, Germany.
Expedeon (Germany) · DEBethel University · USEvangelisches Krankenhaus Bielefeld · DEHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeBoth the immobilization of the unaffected arm combined with physical therapy (forced arm use, FAU) and voluntary exercise (VE) as model for enriched environment are promising approaches to enhance recovery after stroke. The genomic mechanisms involved in long-term plasticity changes after different means of rehabilitative training post-stroke are largely unexplored. The present investigation explored the effects of these physical therapies on behavioral recovery and molecular markers of regeneration after experimental ischemia.

methods42 Wistar rats were randomly treated with either forced arm use (FAU, 1-sleeve plaster cast onto unaffected limb at 8/10 days), voluntary exercise (VE, connection of a freely accessible running wheel to cage), or controls with no access to a running wheel for 10 days starting at 48 hours after photothrombotic stroke of the sensorimotor cortex. Functional outcome was measured using sensorimotor test before ischemia, after ischemia, after the training period of 10 days, at 3 and 4 weeks after ischemia. Global gene expression changes were assessed from the ipsi- and contralateral cortex and the hippocampus.

resultsFAU-treated animals demonstrated significantly improved functional recovery compared to the VE-treated group. Both were superior to cage control. A large number of genes are altered by both training paradigms in the ipsi- and contralateral cortex and the hippocampus. Overall, the extent of changes observed correlated well with the functional recovery obtained. One category of genes overrepresented in the gene set is linked to neuronal plasticity processes, containing marker genes such as the NMDA 2a receptor, PKC ζ, NTRK2, or MAP 1b.

conclusionsWe show that physical training after photothrombotic stroke significantly and permanently improves functional recovery after stroke, and that forced arm training is clearly superior to voluntary running training. The behavioral outcomes seen correlate with patterns and extent of gene expression changes in all brain areas examined. We propose that physical training induces a fundamental change in plasticity-relevant gene expression in several brain regions that enables recovery processes. These results contribute to the debate on optimal rehabilitation strategies, and provide a valuable source of molecular entry points for future pharmacological enhancement of recovery.

Identifiers

PMID24528872
PMCPMC3937028
OpenAlexW2114574181

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Registered trials

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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.