Evidence map›Paper›PMID 31226353›Full record

ArticleMetabolism: clinical and experimental2019

Peroxisomal gene and protein expression increase in response to a high-lipid challenge in human skeletal muscle.

Tai-Yu Huang, Donghai Zheng, Robert C Hickner, Jeffrey J Brault, Ronald N Cortright

Open access · greenAbstract read
In one paragraph

Article in Metabolism: clinical and experimental, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

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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

5 authors at 1 institution in 2 countries.

Tai-Yu HuangDepartment of Kinesiology, East Carolina University, Greenville, NC, United States of America.
Donghai ZhengDepartment of Kinesiology, East Carolina University, Greenville, NC, United States of America; Diabetes and Obesity Institute, East Carolina University, Greenville, NC, United States of America.
Robert C HicknerDepartment of Kinesiology, East Carolina University, Greenville, NC, United States of America; Department of Physiology, East Carolina University, Greenville, NC, United States of America; Diabetes and Obesity Institute, East Carolina University, Greenville, NC, United States of America; College of Human Sciences, Florida State University, Tallahassee, FL, United States of America; School of Health Sciences, University of KwaZulu-Natal, Westville, South Africa.
Jeffrey J BraultDepartment of Kinesiology, East Carolina University, Greenville, NC, United States of America; Department of Physiology, East Carolina University, Greenville, NC, United States of America; Diabetes and Obesity Institute, East Carolina University, Greenville, NC, United States of America.
Ronald N CortrightDepartment of Kinesiology, East Carolina University, Greenville, NC, United States of America; Department of Physiology, East Carolina University, Greenville, NC, United States of America; Department of Surgery, East Carolina University, Greenville, NC, United States of America; Diabetes and Obesity Institute, East Carolina University, Greenville, NC, United States of America. Electronic address: cortrightr@ecu.edu.
East Carolina University · US

Funding

CELLULAR ENERGETICS AS A REGULATOR OF MUSCLE MASS AND MITOCHONDRIAL CONTENT DURING MUSCLE ATROPHYR01AR070200 · NIAMS · INDIANA UNIVERSITY INDIANAPOLIS · PI BRAULT, JEFFREY J · 2017 to 2021
$1.6M
NADPH Oxidase and Microvascular Dysfunction in ObesityR15HL113854 · NHLBI · FLORIDA STATE UNIVERSITY · PI HICKNER, ROBERT C · 2013 to 2018
$884k
NHLBI NIH HHS R15 HL113854NIAMS NIH HHS R01 AR070200
6 · The paper itself

Abstract

Peroxisomes are essential for lipid metabolism and disruption of liver peroxisomal function results in neonatal death. Little is known about how peroxisomal content and activity respond to changes in the lipid environment in human skeletal muscle (HSkM).

aimsWe hypothesized and tested that increased peroxisomal gene/protein expression and functionality occur in HSkM as an adaptive response to lipid oversupply. MATERIALS AND

methodsHSkM biopsies, derived from a total of sixty-two subjects, were collected for 1) examining correlations between peroxisomal proteins and intramyocellular lipid content (IMLC) as well as between peroxisomal functionality and IMLC, 2) assessing peroxisomal gene expression in response to acute- or 7-day high fat meal (HFM), and in human tissue derived primary myotubes for 3) treating with high fatty acids to induce peroxisomal adaptions. IMLC were measured by both biochemical analyses and fluorescent staining. Peroxisomal membrane protein PMP70 and biogenesis gene (PEX) expression were assessed using western blotting and realtime qRT-PCR respectively. 1-

results1) Under fasting conditions, HSkM tissue demonstrated a significant correlation (P ≪ 0.05) between IMCL and the peroxisomal biogenesis factor 19 (PEX19) protein as well as between lipid content and palmitate and lignocerate complete oxidation. 2) Similarly, post-HFM, additional PEX genes (Pex19, PEX11A, and PEX5) were significantly (P ≪ 0.05) upregulated. 3) Increments in PMP70, carnitine octanoyl transferase (CrOT), PGC-1α, and ERRα mRNA were observed post-fatty acid incubation in HSkM cells. PMP70 protein was significantly (P ≪ 0.05) elevated 48-h post lipid treatment.

conclusionsThese results are the first to associate IMLC with peroxisomal gene/protein expression and function in HSkM suggesting an adaptive role for peroxisomes in lipid metabolism in this tissue.

Indexed as

Diet, High-FatAdolescentAdultATP-Binding Cassette TransportersBiopsyFatty AcidsFemaleGene ExpressionHumansLipid MetabolismMaleMiddle AgedMitochondria, MuscleMuscle Fibers, SkeletalMuscle, SkeletalPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaABCD3 protein, humanATP-Binding Cassette TransportersFatty AcidsPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPHEX Phosphate Regulating Neutral EndopeptidasePHEX protein, humanPPARGC1A protein, humanHuman primary myotubesLignoceric acid oxidationLipotoxicityMitochondrial β-oxidationObesity

Identifiers

PMID31226353
PMCPMC7031862
OpenAlexW2950248656

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.