Evidence map›Paper›PMID 29098797›Full record

ArticleJournal of cachexia, sarcopenia and muscle2017

Acylated ghrelin treatment normalizes skeletal muscle mitochondrial oxidative capacity and AKT phosphorylation in rat chronic heart failure.

Rocco Barazzoni, Gianluca Gortan Cappellari, Sandra Palus, Pierandrea Vinci, Giulia Ruozi, Michela Zanetti, Annamaria Semolic, Nicole Ebner, Stephan von Haehling, Gianfranco Sinagra and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Review
  3. Nutrients · 2023
    Article
  4. Ghrelin system in Alzheimer's disease.Current opinion in neurobiology · 2023
    Review
  5. Article
  6. Locomotor and respiratory muscle abnormalities in HFrEF and HFpEF.Frontiers in cardiovascular medicine · 2023
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Natural ghrelin in advanced cancer patients with cachexia, a case series.Journal of cachexia, sarcopenia and muscle · 2021
    Article
  12. Article
  13. Muscle Wasting and Sarcopenia in Heart Failure-The Current State of Science.International journal of molecular sciences · 2020
    Review
  14. Double burden of malnutrition in persons with obesity.Reviews in endocrine & metabolic disorders · 2020
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Inactivity and Skeletal Muscle Metabolism: A Vicious Cycle in Old Age.International journal of molecular sciences · 2020
    Review
  20. Sarcopaenia complicating heart failure.European heart journal supplements : journal of the European Society of Cardiology · 2019
    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

12 authors at 4 institutions in 2 countries.

Rocco BarazzoniInternal Medicine, Department of Medical, Surgical and Health Sciences-University of Trieste, Trieste, Italy.
Gianluca Gortan CappellariInternal Medicine, Department of Medical, Surgical and Health Sciences-University of Trieste, Trieste, Italy.
Sandra PalusDepartment of Cardiology & Pneumology, University Medical Center Göttingen (UMG), Göttingen, Germany.
Pierandrea VinciInternal Medicine, Department of Medical, Surgical and Health Sciences-University of Trieste, Trieste, Italy.
Giulia RuoziMolecular Medicine Laboratory, International Centre for Genetic Engineering and Biotechnology, Trieste, Italy.
Michela ZanettiInternal Medicine, Department of Medical, Surgical and Health Sciences-University of Trieste, Trieste, Italy.
Annamaria SemolicInternal Medicine, Department of Medical, Surgical and Health Sciences-University of Trieste, Trieste, Italy.
Nicole EbnerDepartment of Cardiology & Pneumology, University Medical Center Göttingen (UMG), Göttingen, Germany.
Stephan von HaehlingDepartment of Cardiology & Pneumology, University Medical Center Göttingen (UMG), Göttingen, Germany.
Gianfranco SinagraAzienda Sanitaria Universitaria Integrata di Trieste (ASUITS), Trieste, Italy.
Mauro GiaccaMolecular Medicine Laboratory, International Centre for Genetic Engineering and Biotechnology, Trieste, Italy.
Jochen SpringerDepartment of Cardiology & Pneumology, University Medical Center Göttingen (UMG), Göttingen, Germany.
Azienda Sanitaria Universitaria Integrata di Trieste · ITUniversitätsmedizin Göttingen · DEInternational Centre for Genetic Engineering and Biotechnology · ITUniversity of Trieste · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic heart failure (CHF) is associated with skeletal muscle abnormalities contributing to exercise intolerance, muscle loss, and negative impact on patient prognosis. A primary role has been proposed for mitochondrial dysfunction, which may be induced by systemic and tissue inflammation and further contribute to low insulin signalling. The acylated form of the gastric hormone ghrelin (AG) may improve mitochondrial oxidative capacity and insulin signalling in both healthy and diseased rodent models.

methodsWe investigated the impact of AG continuous subcutaneous administration (AG) by osmotic minipump (50 nmol/kg/day for 28 days) compared with placebo (P) on skeletal muscle mitochondrial enzyme activities, mitochondrial biogenesis regulators transcriptional expression and insulin signalling in a rodent post-myocardial infarction CHF model.

resultsNo statistically significant differences (NS) were observed among the three group in cumulative food intake. Compared with sham-operated, P had low mitochondrial enzyme activities, mitochondrial biogenesis regulators transcripts, and insulin signalling activation at AKT level (P < 0.05), associated with activating nuclear translocation of pro-inflammatory transcription factor nuclear factor-κB. AG completely normalized all alterations (P < 0.05 vs P, P = NS vs sham-operated). Direct AG activities were strongly supported by in vitro C2C12 myotubes experiments showing AG-dependent stimulation of mitochondrial enzyme activities. No changes in mitochondrial parameters and insulin signalling were observed in the liver in any group.

conclusionsSustained peripheral AG treatment with preserved food intake normalizes a CHF-induced tissue-specific cluster of skeletal muscle mitochondrial dysfunction, pro-inflammatory changes, and reduced insulin signalling. AG is therefore a potential treatment for CHF-associated muscle catabolic alterations, with potential positive impact on patient outcome.

Indexed as

AnimalsBiomarkersDisease Models, AnimalGene ExpressionGhrelinHeart FailureMaleMitochondria, LiverMitochondria, MuscleMuscle, SkeletalNF-kappa BOxidation-ReductionPhosphorylationProto-Oncogene Proteins c-aktRatsBiomarkersGhrelinNF-kappa BProto-Oncogene Proteins c-aktGhrelinInsulin signallingMitochondriaSkeletal muscle

Identifiers

PMID29098797
PMCPMC5700435
OpenAlexW2766816365

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.