Evidence map›Paper›PMID 26866650›Full record

ArticleRedox report : communications in free radical research2017

Molecular hydrogen alleviates motor deficits and muscle degeneration in mdx mice.

Satoru Hasegawa, Mikako Ito, Mayu Fukami, Miki Hashimoto, Masaaki Hirayama, Kinji Ohno

Open access · bronzeAbstract read
In one paragraph

Article in Redox report : communications in free radical research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
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  6. Review
  7. Hydrogen water alleviates obliterative airway disease in mice.General thoracic and cardiovascular surgery · 2020
    Article
  8. Article
  9. Article
  10. Hydrogen: A Novel Option in Human Disease Treatment.Oxidative medicine and cellular longevity · 2020
    Review
  11. Antioxidants Attenuate Oxidative Stress-Induced Hidden Blood Loss in Rats.Turkish journal of haematology : official journal of Turkish Society of Haematology · 2017
    Article
  12. 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 1 institution in 1 country.

Satoru Hasegawaa Division of Neurogenetics , Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine , Japan.
Mikako Itoa Division of Neurogenetics , Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine , Japan.
Mayu Fukamib Department of Pathophysiological Laboratory Sciences , Nagoya University Graduate School of Medicine , Japan.
Miki Hashimotob Department of Pathophysiological Laboratory Sciences , Nagoya University Graduate School of Medicine , Japan.
Masaaki Hirayamab Department of Pathophysiological Laboratory Sciences , Nagoya University Graduate School of Medicine , Japan.
Kinji Ohnoa Division of Neurogenetics , Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine , Japan.
Nagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveDuchenne muscular dystrophy (DMD) is a devastating muscle disease caused by a mutation in DMD encoding dystrophin. Oxidative stress accounts for dystrophic muscle pathologies in DMD. We examined the effects of molecular hydrogen in mdx mice, a model animal for DMD.

methodsThe pregnant mother started to take supersaturated hydrogen water (>5 ppm) ad libitum from E15.5 up to weaning of the offspring. The mdx mice took supersaturated hydrogen water from weaning until age 10 or 24 weeks when they were sacrificed.

resultsHydrogen water prevented abnormal body mass gain that is commonly observed in mdx mice. Hydrogen improved the spontaneous running distance that was estimated by a counter-equipped running-wheel, and extended the duration on the rota-rod. Plasma creatine kinase activities were decreased by hydrogen at ages 10 and 24 weeks. Hydrogen also decreased the number of central nuclei of muscle fibers at ages 10 and 24 weeks, and immunostaining for nitrotyrosine in gastrocnemius muscle at age 24 weeks. Additionally, hydrogen tended to increase protein expressions of antioxidant glutathione peroxidase 1, as well as anti-apoptotic Bcl-2, in skeletal muscle at age 10 weeks. DISCUSSION: Although molecular mechanisms of the diverse effects of hydrogen remain to be elucidated, hydrogen potentially improves muscular dystrophy in DMD patients.

Indexed as

AnimalsBlotting, WesternDisease Models, AnimalDystrophinFemaleHydrogenMiceMice, Inbred C57BLMice, Inbred mdxMuscle, SkeletalMuscular Dystrophy, DuchenneOxidative StressReal-Time Polymerase Chain ReactionDystrophinHydrogenDuchenne muscular dystrophymdx mouseMolecular hydrogenMuscle degenerationOxidative stress

Identifiers

PMID26866650
PMCPMC6837388
OpenAlexW2256053799

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.