Evidence map›Paper›PMID 28694434›Full record

ArticleScientific reports2017

Laquinimod treatment in the R6/2 mouse model.

Gisa Ellrichmann, Alina Blusch, Oluwaseun Fatoba, Janine Brunner, Christiane Reick, Liat Hayardeny, Michael Hayden, Dominik Sehr, Konstanze F Winklhofer, Carsten Saft and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

28 citing papers in PubMed, 51 citations in OpenAlex.

  1. Trial
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  6. Article
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  8. Review
  9. Huntington's Disease: Latest Frontiers in Therapeutics.Current neurology and neuroscience reports · 2024
    Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Non-Cell Autonomous and Epigenetic Mechanisms of Huntington's Disease.International journal of molecular sciences · 2021
    Review
  15. Article
  16. New Avenues for the Treatment of Huntington's Disease.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Article
  19. Molecular Mechanisms Underlying Muscle Wasting in Huntington's Disease.International journal of molecular sciences · 2020
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Gisa EllrichmannDepartment of Neurology, St. Josef-Hospital, Ruhr-University Bochum, Bochum, Germany. gisa.ellrichmann@rub.de.
Alina BluschCenter of Clinical Research, Ruhr-University Bochum, Bochum, Germany.
Oluwaseun FatobaCenter of Clinical Research, Ruhr-University Bochum, Bochum, Germany.
Janine BrunnerCenter of Clinical Research, Ruhr-University Bochum, Bochum, Germany.
Christiane ReickCenter of Clinical Research, Ruhr-University Bochum, Bochum, Germany.
Liat HayardenyGalmed Pharmaceuticals, Tel Aviv, Israel.
Michael HaydenTeva Pharmaceutical Industries Ltd, Tiqva, Israel.
Dominik SehrDepartment of Molecular Cell Biology, Institute of Biochemistry and Pathobiochemistry, Ruhr-University Bochum, Bochum, Germany.
Konstanze F WinklhoferDepartment of Molecular Cell Biology, Institute of Biochemistry and Pathobiochemistry, Ruhr-University Bochum, Bochum, Germany.
Carsten SaftDepartment of Neurology, St. Josef-Hospital, Ruhr-University Bochum, Bochum, Germany.
Ralf GoldDepartment of Neurology, St. Josef-Hospital, Ruhr-University Bochum, Bochum, Germany.
Ruhr University Bochum · DESt. Josef-Hospital · DEGalmed Pharmaceuticals (Israel) · ILTeva Pharmaceuticals (Israel) · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transgenic mouse model R6/2 exhibits Huntington's disease (HD)-like deficits and basic pathophysiological similarities. We also used the pheochromocytoma-12 (PC12)-cell-line-model to investigate the effect of laquinimod on metabolic activity. Laquinimod is an orally administered immunomodulatory substance currently under development for the treatment of multiple sclerosis (MS) and HD. As an essential effect, increased levels of BDNF were observed. Therefore, we investigated the therapeutic efficacy of laquinimod in the R6/2 model, focusing on its neuroprotective capacity. Weight course and survival were not influenced by laquinimod. Neither were any metabolic effects seen in an inducible PC12-cell-line model of HD. As a positive effect, motor functions of R6/2 mice at the age of 12 weeks significantly improved. Preservation of morphologically intact neurons was found after treatment in the striatum, as revealed by NeuN, DARPP-32, and ubiquitin. Biochemical analysis showed a significant increase in the brain-derived neurotrophic factor (BDNF) level in striatal but not in cortical neurons. The number of mutant huntingtin (mhtt) and inducible nitric oxide synthase (iNOS) positive cells was reduced in both the striatum and motor cortex following treatment. These findings suggest that laquinimod could provide a mild effect on motor function and striatal histopathology, but not on survival. Besides influences on the immune system, influence on BDNF-dependent pathways in HD are discussed.

Indexed as

AnimalsBiomarkersBody WeightBrain-Derived Neurotrophic FactorCell SurvivalDisease Models, AnimalEnergy MetabolismFluorescent Antibody TechniqueGene ExpressionHuntington DiseaseMiceMice, TransgenicMotor ActivityNeuronsPC12 CellsQuinolonesBiomarkersBrain-Derived Neurotrophic FactorlaquinimodQuinolones

Identifiers

PMID28694434
PMCPMC5504033
OpenAlexW2731761516

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.