Evidence map›Paper›PMID 25528444›Full record

ArticleMetabolism: clinical and experimental2015

Low levels of lipopolysaccharide modulate mitochondrial oxygen consumption in skeletal muscle.

Madlyn I Frisard, Yaru Wu, Ryan P McMillan, Kevin A Voelker, Kristin A Wahlberg, Angela S Anderson, Nabil Boutagy, Kyle Resendes, Eric Ravussin, Matthew W Hulver

Open access · greenAbstract read
In one paragraph

Article in Metabolism: clinical and experimental, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 51 citations in OpenAlex.

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  17. Mitochondrial Function, Obesity, and Personalized Lifestyle Medicine.Integrative medicine (Encinitas, Calif.) · 2017
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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

10 authors at 2 institutions in 1 country.

Madlyn I FrisardDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, VA, USA, 24060; The Metabolic Phenotyping Core at Virginia Tech, Blacksburg, VA, USA, 24060; Fralin Translational Obesity Research Center, Virginia Tech, Blacksburg, VA. USA, 24060.
Yaru WuDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, VA, USA, 24060.
Ryan P McMillanDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, VA, USA, 24060; The Metabolic Phenotyping Core at Virginia Tech, Blacksburg, VA, USA, 24060.
Kevin A VoelkerDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, VA, USA, 24060.
Kristin A WahlbergDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, VA, USA, 24060.
Angela S AndersonDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, VA, USA, 24060.
Nabil BoutagyDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, VA, USA, 24060; Fralin Translational Obesity Research Center, Virginia Tech, Blacksburg, VA. USA, 24060.
Kyle ResendesDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, VA, USA, 24060.
Eric RavussinJohn S McIlhenny Skeletal Muscle Physiology Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA, USA, 70808.
Matthew W HulverDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, VA, USA, 24060; The Metabolic Phenotyping Core at Virginia Tech, Blacksburg, VA, USA, 24060; Fralin Translational Obesity Research Center, Virginia Tech, Blacksburg, VA. USA, 24060. Electronic address: hulvermw@vt.edu.
Virginia Tech · USPennington Biomedical Research Center · US

Funding

Inflammatory Regulation of Lipid Accumulation in Skeletal Muscle with ObesityR01DK078765 · NIDDK · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI HULVER, MATTHEW W · 2008 to 2012
$1.7M
Inflammatory regulation of lipid accumulation in skeletal muscle with obesityR56DK078765 · NIDDK · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI HULVER, MATTHEW W · 2007 to 2007
$157k
NIDDK NIH HHS R01 DK078765NIDDK NIH HHS R01DK078765NIDDK NIH HHS R56 DK078765
6 · The paper itself

Abstract

objectiveWe have previously demonstrated that activation of toll-like receptor 4 (TLR4) in skeletal muscle results in an increased reliance on glucose as an energy source and a concomitant decrease in fatty acid oxidation under basal conditions. Herein, we examined the effects of lipopolysaccharide (LPS), the primary ligand for TLR4, on mitochondrial oxygen consumption in skeletal muscle cell culture and mitochondria isolated from rodent skeletal muscle. MATERIALS/

methodsSkeletal muscle cell cultures were exposed to LPS and oxygen consumption was assessed using a Seahorse Bioscience extracellular flux analyzer. Mice were also exposed to LPS and oxygen consumption was assessed in mitochondria isolated from skeletal muscle.

resultsAcute LPS exposure resulted in significant reductions in Carbonyl cyanide 4-(trifluoromethoxy) phenylhydrazone (FCCP)-stimulated maximal respiration (state 3u) and increased oligomycin induced state 4 (state 4O) respiration in C2C12 and human primary myotubes. These findings were observed in conjunction with increased mRNA of uncoupling protein 3 (UCP3), superoxide dismutase 2 (SOD2), and pyruvate dehydrogenase activity. The LPS-mediated changes in substrate oxidation and maximal mitochondrial respiration were prevented in the presence of the antioxidants N-acetylcysteine and catalase, suggesting a potential role of reactive oxygen species in mediating these effects. Mitochondria isolated from red gastrocnemius and quadriceps femoris muscle from mice injected with LPS also demonstrated reduced respiratory control ratio (RCR), and ADP- and FCCP-stimulated respiration.

conclusionLPS exposure in skeletal muscle alters mitochondrial oxygen consumption and substrate preference, which is absent when antioxidants are present.

Indexed as

AnimalsAntioxidantsCells, CulturedGene DosageGene ExpressionHumansLipopolysaccharidesMiceMitochondria, MuscleMuscle, SkeletalMyoblastsOxygen ConsumptionPyruvate Dehydrogenase ComplexAntioxidantsLipopolysaccharidesPyruvate Dehydrogenase ComplexC2C12 myotubesHuman primary myotubesMitochondrial oxygen consumptionReactive oxygen speciesSkeletal muscle

Identifiers

PMID25528444
PMCPMC4501015
OpenAlexW2109861589

What OpenQuestion holds

Textmetadata
LicenceTDM
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.