Evidence map›Paper›PMID 28636643›Full record

ArticlePloS one2017

Neuromuscular electrical stimulation prevents skeletal muscle dysfunction in adjuvant-induced arthritis rat.

Koichi Himori, Daisuke Tatebayashi, Keita Kanzaki, Masanobu Wada, Håkan Westerblad, Johanna T Lanner, Takashi Yamada

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Sarcopenia in Autoimmune and Rheumatic Diseases: A Comprehensive Review.International journal of molecular sciences · 2020
    Review
  5. Article
  6. 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

7 authors at 4 institutions in 2 countries.

Koichi HimoriGraduate School of Health Sciences, Sapporo Medical University, Sapporo, Japan.
Daisuke TatebayashiGraduate School of Health Sciences, Sapporo Medical University, Sapporo, Japan.
Keita KanzakiFaculty of Health and Welfare Science, Okayama Prefectural University, Soja, Okayama, Japan.
Masanobu WadaGraduate School of Integrated Arts and Sciences, Hiroshima University, Higashi Hiroshima, Japan.
Håkan WesterbladDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Johanna T LannerDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Takashi YamadaGraduate School of Health Sciences, Sapporo Medical University, Sapporo, Japan.ORCID http://orcid.org/0000-0003-1797-3880
Sapporo Medical University · JPKarolinska Institutet · SEHiroshima University · JPOkayama Prefectural University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Skeletal muscle weakness is a prominent feature in patients with rheumatoid arthritis (RA). In this study, we investigated whether neuromuscular electrical stimulation (NMES) training protects against skeletal muscle dysfunction in rats with adjuvant-induced arthritis (AIA). AIA was produced by intraarticular injection of complete Freund's adjuvant into the knees of Wistar rats. For NMES training, dorsiflexor muscles were stimulated via a surface electrode (0.5 ms pulse, 50 Hz, 2 s on/4 s off). NMES training was performed every other day for three weeks and consisted of three sets produced at three min intervals. In each set, the electrical current was set to achieve 60% of the initial maximum isometric torque and the current was progressively increased to maintain this torque; stimulation was stopped when the 60% torque could no longer be maintained. After the intervention period, extensor digitorum longus (EDL) muscles were excised and used for physiological and biochemical analyses. There was a reduction in specific force production (i.e. force per cross-sectional area) in AIA EDL muscles, which was accompanied by aggregation of the myofibrillar proteins actin and desmin. Moreover, the protein expressions of the pro-oxidative enzymes NADPH oxidase, neuronal nitric oxide synthase, p62, and the ratio of the autophagosome marker LC3bII/LC3bI were increased in AIA EDL muscles. NMES training prevented all these AIA-induced alterations. The present data suggest that NMES training prevents AIA-induced skeletal muscle weakness presumably by counteracting the formation of actin and desmin aggregates. Thus, NMES training can be an effective treatment for muscle dysfunction in patients with RA.

Indexed as

ActinsAnimalsArthritis, ExperimentalDesminElectric Stimulation TherapyMaleMicrotubule-Associated ProteinsMuscle ContractionMuscle, SkeletalNADPH OxidasesNitric Oxide Synthase Type IPeroxynitrous AcidRatsRats, WistarSequestosome-1 ProteinSuperoxide DismutaseActinsAnxa3 protein, ratDesminMicrotubule-Associated ProteinsNADPH OxidasesNitric Oxide Synthase Type IPeroxynitrous AcidSequestosome-1 ProteinSuperoxide DismutaseSuperoxide Dismutase 2

Identifiers

PMID28636643
PMCPMC5479592
OpenAlexW2701410739

What OpenQuestion holds

Textmetadata
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.