Evidence map›Paper›PMID 26589960›Full record

ArticleJournal of muscle research and cell motility2016

Reduced expression of MyHC slow isoform in rat soleus during unloading is accompanied by alterations of endogenous inhibitors of calcineurin/NFAT signaling pathway.

Yulia N Lomonosova, Olga V Turtikova, Boris S Shenkman

Erratum issuedAbstract read
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In one paragraph

Article in Journal of muscle research and cell motility, 2016. 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 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

20 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
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  3. Disuse-Induced Muscle Fatigue: Facts and Assumptions.International journal of molecular sciences · 2024
    Review
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  10. Review
  11. Review
  12. Article
  13. How Postural Muscle Senses Disuse? Early Signs and Signals.International journal of molecular sciences · 2020
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Yulia N LomonosovaInstitute of Biomedical Problems, Russian Academy of Sciences, 76a, Khoroshevskoye Shosse, Moscow, Russia, 123007.
Olga V TurtikovaInstitute of Biomedical Problems, Russian Academy of Sciences, 76a, Khoroshevskoye Shosse, Moscow, Russia, 123007.
Boris S ShenkmanInstitute of Biomedical Problems, Russian Academy of Sciences, 76a, Khoroshevskoye Shosse, Moscow, Russia, 123007. bshenkman@mail.ru.
Institute of Biomedical Problems · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Under muscle disuse conditions decrease of expression of MyHC of slow type, and sometimes of type IIa, as well as upregulation of expression of IIb and IId/x isoforms were observed. Through dephosphorylation and entry of NFAT molecules to the nucleus calcineurin/NFATc1 signaling pathway promotes upregulation of the slow MyHC expression. We supposed that downregulation of calcineurin pathway took place during unloading. The study was aimed to analyze the states of the myonuclear NFAT inhibitors calsarcin I (CSI) and calsarcin II (CSII) (also referred to as myozenin II and I) and GSK3β in rat soleus during hindlimb suspension (HS). Male Wistar rats were subjected to 3, 7 and 14 day of HS. We found that after 3 days of HS the content of CSII mRNA twofold increased in soleus as compared to the controls. This level was increased by more than fivefold (as compared to control) after 2 weeks of HS. The increase of CSII mRNA expression may be explained as the mechanism of stabilization of fast phenotype. We found that from the 3 day till 14 day of HS the content of MuRF-1 and MuRF-2 in the nuclear fraction fourfold to fivefold increased in HS soleus. We supposed that nuclear import of the MuRFs allows to promote CSII expression during unloading. We also observed the decline of the phosphorylated GSK3β content in the nuclear extract of the soleus tissue. Thus decline of slow MyHC expression characteristic for the unloading conditions is accompanied with the increased expression and activation of the factors known to prevent NFAT accumulation in the myonuclei.

Indexed as

AnimalsCalcineurinGlycogen Synthase Kinase 3 betaHindlimbMaleMicrofilament ProteinsMuscle ProteinsMuscle, SkeletalMyosin Heavy ChainsNFATC Transcription FactorsRatsRats, WistarSignal TransductionCalcineurinGlycogen Synthase Kinase 3 betaGsk3b protein, ratMicrofilament ProteinsMuscle ProteinsMyosin Heavy ChainsMyoz2 protein, ratNFATC Transcription FactorsCalsarcin-1,-2Hindlimb suspensionMuRF-1,-2Myosin heavy chains expression

Identifiers

PMID26589960
OpenAlexW2177309321

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.