Evidence map›Paper›PMID 26507644›Full record

ArticleJournal of physiology and biochemistry2015

Targeted delivery of HGF to the skeletal muscle improves glucose homeostasis in diet-induced obese mice.

Viviana Sanchez-Encinales, Irene Cozar-Castellano, Adolfo Garcia-Ocaña, Germán Perdomo

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of physiology and biochemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Therapeutic Angiogenesis Using HGF Plasmid.Annals of vascular diseases · 2020
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. 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

4 authors at 3 institutions in 2 countries.

Viviana Sanchez-EncinalesResearch Unit, University Hospital "Puerta del Mar", Cádiz, Spain.
Irene Cozar-CastellanoResearch Unit, University Hospital "Puerta del Mar", Cádiz, Spain.
Adolfo Garcia-OcañaDiabetes, Obesity and Metabolism Institute, The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, Atran 5 Box 1152, 1 Gustave L. Levy Place, New York, NY, 10029, USA. adolfo.garcia-ocana@mssm.edu.
Germán PerdomoResearch Unit, University Hospital "Puerta del Mar", Cádiz, Spain. perdomogm@yahoo.com.
Hospital Universitario Puerta del Mar · ESChild Health and Development Institute · USInstituto de Biomedicina y Genética Molecular de Valladolid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocyte growth factor (HGF) is a cytokine that increases glucose transport ex vivo in skeletal muscle. The aim of this work was to decipher the impact of whether conditional overexpression of HGF in vivo could improve glucose homeostasis and insulin sensitivity in mouse skeletal muscle. Following tetracyclin administration, muscle HGF levels were augmented threefold in transgenic mice (SK-HGF) compared to control mice without altering plasma HGF levels. In conditions of normal diet, SK-HGF mice showed no differences in body weight, plasma triglycerides, blood glucose, plasma insulin and glucose tolerance compared to control mice. Importantly, obese SK-HGF mice exhibited improved whole-body glucose tolerance independently of changes in body weight or plasma triglyceride levels compared to control mice. This effect on glucose homeostasis was associated with significantly higher (∼80%) levels of phosphorylated protein kinase B in muscles from SK-HGF mice compared to control mice. In conclusion, muscle expression of HGF counteracts obesity-mediated muscle insulin resistance and improves glucose tolerance in mice.

Indexed as

AnimalsBlood GlucoseDiet, High-FatGene TargetingGlucoseHepatocyte Growth FactorHomeostasisInsulinLipid MetabolismMaleMice, Inbred C57BLMice, TransgenicMuscle, SkeletalObesityTranscriptional ActivationBlood GlucoseGlucoseHepatocyte Growth FactorHGF protein, mouseInsulinHepatocyte growth factorInsulin resistanceObesitySkeletal muscle

Identifiers

PMID26507644
OpenAlexW1834630481

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.