Evidence map›Paper›PMID 26445495›Full record

ArticlePloS one2015

Downhill Running-Based Overtraining Protocol Improves Hepatic Insulin Signaling Pathway without Concomitant Decrease of Inflammatory Proteins.

Alisson L da Rocha, Bruno C Pereira, José R Pauli, Dennys E Cintra, Claudio T de Souza, Eduardo R Ropelle, Adelino S R da Silva

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. NADEuropean journal of nutrition · 2020
    Article
  10. Article
  11. Article
  12. 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 1 country.

Alisson L da RochaPostgraduate Program in Rehabilitation and Functional Performance, RibeirãoPreto Medical School, USP, RibeirãoPreto, São Paulo, Brazil.
Bruno C PereiraPostgraduate Program in Rehabilitation and Functional Performance, RibeirãoPreto Medical School, USP, RibeirãoPreto, São Paulo, Brazil.
José R PauliSport Sciences Course, Faculty of Applied Sciences, State University of Campinas, Limeira, São Paulo, Brazil.
Dennys E CintraSport Sciences Course, Faculty of Applied Sciences, State University of Campinas, Limeira, São Paulo, Brazil.
Claudio T de SouzaExercise Biochemistry and Physiology Laboratory Postgraduate Program in Health Sciences, Health Sciences Unit, University of Far Southern Santa Catarina, Criciúma, Santa Catarina, Brazil.
Eduardo R RopelleSport Sciences Course, Faculty of Applied Sciences, State University of Campinas, Limeira, São Paulo, Brazil.
Adelino S R da SilvaPostgraduate Program in Rehabilitation and Functional Performance, RibeirãoPreto Medical School, USP, RibeirãoPreto, São Paulo, Brazil; School of Physical Education and Sport of RibeirãoPreto, University of São Paulo, RibeirãoPreto, São Paulo, Brazil.
Universidade Estadual de Campinas (UNICAMP) · BRClinics Hospital of Ribeirão Preto · BRUniversidade de São Paulo · BRUniversidade do Sul de Santa Catarina · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of this study was to verify the effects of overtraining (OT) on insulin, inflammatory and gluconeogenesis signaling pathways in the livers of mice. Rodents were divided into control (CT), overtrained by downhill running (OTR/down), overtrained by uphill running (OTR/up) and overtrained by running without inclination (OTR). Rotarod, incremental load, exhaustive and grip force tests were used to evaluate performance. Thirty-six hours after a grip force test, the livers were extracted for subsequent protein analyses. The phosphorylation of insulin receptor beta (pIRbeta), glycogen synthase kinase 3 beta (pGSK3beta) and forkhead box O1 (pFoxo1) increased in OTR/down versus CT. pGSK3beta was higher in OTR/up versus CT, and pFoxo1 was higher in OTR/up and OTR versus CT. Phosphorylation of protein kinase B (pAkt) and insulin receptor substrate 1 (pIRS-1) were higher in OTR/up versus CT and OTR/down. The phosphorylation of IκB kinase alpha and beta (pIKKalpha/beta) was higher in all OT protocols versus CT, and the phosphorylation of stress-activated protein kinases/Jun amino-terminal kinases (pSAPK-JNK) was higher in OTR/down versus CT. Protein levels of peroxisome proliferator-activated receptor-gamma coactivator 1alpha (PGC-1alpha) and hepatocyte nuclear factor 4alpha (HNF-4alpha) were higher in OTR versus CT. In summary, OTR/down improved the major proteins of insulin signaling pathway but up-regulated TRB3, an Akt inhibitor, and its association with Akt.

Indexed as

RunningSignal TransductionAnimalsCell Cycle ProteinsGluconeogenesisInflammationInsulinLiverMaleMiceMice, Inbred C57BLPhosphorylationProto-Oncogene Proteins c-aktReceptor, InsulinCell Cycle ProteinsInsulinProto-Oncogene Proteins c-aktReceptor, InsulinTRB3 protein, mouse

Identifiers

PMID26445495
PMCPMC4596708
OpenAlexW1892020720

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.