Evidence map›Paper›PMID 25231380›Full record

ArticleJournal of proteome research2015

Metabolomic analysis of akt1-mediated muscle hypertrophy in models of diet-induced obesity and age-related fat accumulation.

Kian-Kai Cheng, Yuichi Akasaki, Emmanuelle Lecommandeur, Ross T Lindsay, Steven Murfitt, Kenneth Walsh, Julian L Griffin

Open access · greenAbstract read
In one paragraph

Article in Journal of proteome research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Frontiers in pharmacology · 2021
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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 3 institutions in 4 countries.

Kian-Kai ChengDepartment of Biochemistry and Cambridge Systems Biology Centre, University of Cambridge , Cambridge CB2 1GA, United Kingdom.
Yuichi Akasaki
Emmanuelle Lecommandeur
Ross T Lindsay
Steven Murfitt
Kenneth Walsh
Julian L Griffin
University of Cambridge · GBBoston University · USKagoshima University · JP

Funding

Redox regulation in Endothelial Progenitor CellsP01HL081587 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WALSH, KENNETH · 2005 to 2015
$21.5M
Muscle loss and metabolic dysfunction associated with agingR01AG034972 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WALSH, KENNETH · 2010 to 2014
$1.6M
Paracrine Regulation of Heart FailureR01HL116591 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WALSH, KENNETH · 2013 to 2016
$1.6M
Mitochondrial dynamics and cardiac remodelingR01HL120160 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WALSH, KENNETH · 2013 to 2016
$1.6M
Medical Research Council MC_UP_A090_1006Medical Research Council UD99999906NHLBI NIH HHS HL081587NHLBI NIH HHS HL116591NHLBI NIH HHS HL120160NHLBI NIH HHS P01 HL081587NHLBI NIH HHS R01 HL120160NIA NIH HHS AG034972NIA NIH HHS R01 AG034972Wellcome Trust 093148/Z/10/Z
6 · The paper itself

Abstract

Akt1 is a serine/threonine kinase that promotes cell growth and survival. Previously, Akt1 activation in a double transgenic (DTG) mouse model fed a high-fat/high-sucrose (HF/HS) diet was found to promote type IIb muscle growth and to lead to a significant reduction in obesity. Here, we have used metabolomics to examine the metabolic perturbations in blood serum and liver and gastrocnemius tissues of the DTG mice. Multivariate statistics highlighted consistent metabolic changes in gastrocnemius muscle following Akt1 activation, which included significant reductions of serine and histidine-containing dipeptides (anserine and carnosine), in addition to increased concentrations of phosphorylated sugars. In addition, Akt1-mediated regression in obesity could be associated with increased glycolysis in gastrocnemius muscle as well as increased gluconeogenesis, glycogenolysis, and ketogenesis in the liver. In old DTG animals, Akt1 activation was found to improve glucose metabolism and confer a beneficial effect in the regression of age-related fat accumulation. This study identifies metabolic changes induced by Akt1-mediated muscle growth and demonstrates a cross-talk between distant organs that leads to a regression of fat mass. The current findings indicate that agents that promote Akt1 induction in muscle have utility in the regression of obesity.

Indexed as

Age FactorsAnimalsChromatography, LiquidEnzyme ActivationGas Chromatography-Mass SpectrometryLiverMagnetic Resonance SpectroscopyMass SpectrometryMetabolomicsMiceMice, TransgenicMultivariate AnalysisMuscle, SkeletalObesityProto-Oncogene Proteins c-aktAkt1 protein, mouseProto-Oncogene Proteins c-aktmetabonomicsobesityProtein kinase Btype 2 diabetes

Identifiers

PMID25231380
PMCPMC4286153
OpenAlexW2035788688

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.