Evidence map›Paper›PMID 37652286›Full record

ArticleThe Journal of nutrition2023

Palmitate-Induced Inflammation and Myotube Atrophy in C2C12 Cells Are Prevented by the Whey Bioactive Peptide, Glycomacropeptide.

Naomi Mmp de Hart, Jonathan J Petrocelli, Rebekah J Nicholson, Elena M Yee, Patrick J Ferrara, Eric D Bastian, Loren S Ward, Brent L Petersen, Scott A Summers, Micah J Drummond

Open access · greenAbstract read
In one paragraph

Article in The Journal of nutrition, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
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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 1 institution in 1 country.

Naomi Mmp de HartDepartment of Nutrition and Integrative Physiology, University of Utah, Salt Lake City, UT, United States.
Jonathan J PetrocelliDepartment of Physical Therapy and Athletic Training, University of Utah, Salt Lake City, UT, United States.
Rebekah J NicholsonDepartment of Nutrition and Integrative Physiology, University of Utah, Salt Lake City, UT, United States.
Elena M YeeDepartment of Physical Therapy and Athletic Training, University of Utah, Salt Lake City, UT, United States.
Patrick J FerraraDepartment of Nutrition and Integrative Physiology, University of Utah, Salt Lake City, UT, United States.
Eric D BastianDairy West Innovation Partnerships, Twin Falls, ID, United States.
Loren S WardGlanbia Nutritionals Research, Twin Falls, ID, United States.
Brent L PetersenGlanbia Nutritionals Research, Twin Falls, ID, United States.
Scott A SummersDepartment of Nutrition and Integrative Physiology, University of Utah, Salt Lake City, UT, United States.
Micah J DrummondDepartment of Nutrition and Integrative Physiology, University of Utah, Salt Lake City, UT, United States; Department of Physical Therapy and Athletic Training, University of Utah, Salt Lake City, UT, United States. Electronic address: micah.drummond@hsc.utah.edu.
University of Utah · US

Funding

Interdisciplinary Training Program in MetabolismT32DK091317 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI SCOTT A SUMMERS · 2011 to 2026
$4.8M
The Role of Ceramides in Skeletal MuscleR01DK115824 · NIDDK · UNIVERSITY OF UTAH · PI SUMMERS, SCOTT A · 2018 to 2021
$2.6M
The Role of Ceramides in the Intestinal Stem CellR01DK131609 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI EDGAR, BRUCE ALEXANDER, SUMMERS, SCOTT A · 2021 to 2025
$2.5M
The Role of Ceramides in the Pancreatic Beta CellR01DK130296 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI HOLLAND, WILLIAM L, SUMMERS, SCOTT A · 2022 to 2025
$2.2M
Agilent 6550 QTOF system for U of UtahS10OD016232 · OD · UNIVERSITY OF UTAH · PI COX, JAMES ERIC · 2013 to 2013
$578k
Q-ToF Mass Spectrometer for the University of Utah MS and Proteomics CoreS10OD018210 · OD · UNIVERSITY OF UTAH · PI COX, JAMES ERIC · 2015 to 2015
$530k
Agilent 7200 GC/Q-TOF for the University of UtahS10OD021505 · OD · UNIVERSITY OF UTAH · PI COX, JAMES ERIC · 2016 to 2016
$401k
Elucidating the Mechanisms of Translational Approaches to Enhance Recovery of Aged MuscleF99AG073493 · NIA · UNIVERSITY OF UTAH · PI PETROCELLI, JONATHAN JOSEPH · 2021 to 2022
$72k
NIA NIH HHS F99 AG073493NIDDK NIH HHS R01 DK115824NIDDK NIH HHS R01 DK130296NIDDK NIH HHS R01 DK131609NIDDK NIH HHS T32 DK091317NIH HHS S10 OD016232NIH HHS S10 OD018210NIH HHS S10 OD021505
6 · The paper itself

Abstract

backgroundMetabolic diseases are often associated with muscle atrophy and heightened inflammation. The whey bioactive compound, glycomacropeptide (GMP), has been shown to exhibit anti-inflammatory properties and therefore may have potential therapeutic efficacy in conditions of skeletal muscle inflammation and atrophy.

objectivesThe purpose of this study was to determine the role of GMP in preventing lipotoxicity-induced myotube atrophy and inflammation.

methodsC2C12 myoblasts were differentiated to determine the effect of GMP on atrophy and inflammation and to explore its mechanism of action in evaluating various anabolic and catabolic cellular signaling nodes. We also used a lipidomic analysis to evaluate muscle sphingolipid accumulation with the various treatments. Palmitate (0.75 mM) in the presence and absence of GMP (5 μg/mL) was used to induce myotube atrophy and inflammation and cells were collected over a time course of 6-24 h.

resultsAfter 24 h of treatment, GMP prevented the palmitate-induced decrease in the myotube area and myogenic index and the increase in the TLR4-mediated inflammatory genes tumor necrosis factor-α and interleukin 1β. Moreover, phosphorylation of Erk1/2, and gene expression of myostatin, and the E3 ubiquitin ligases, FBXO32, and MuRF1 were decreased with GMP treatment. GMP did not alter palmitate-induced ceramide or diacylglycerol accumulation, muscle insulin resistance, or protein synthesis.

conclusionsIn summary, GMP prevented palmitate-induced inflammation and atrophy in C2C12 myotubes. The GMP protective mechanism of action in muscle cells during lipotoxic stress may be related to targeting catabolic signaling associated with cellular stress and proteolysis but not protein synthesis.

Indexed as

PalmitatesWheyCaseinsHumansInflammationMuscle Fibers, SkeletalMuscle, SkeletalMuscular AtrophyPeptide FragmentscaseinomacropeptideCaseinsPalmitatesPeptide FragmentsC2C12inflammationmuscle atrophyprotein breakdownwhey protein

Identifiers

PMID37652286
PMCPMC10731921
OpenAlexW4386242943

What OpenQuestion holds

Textmetadata
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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.