Summary of Study ST004231

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR002669. The data can be accessed directly via it's Project DOI: 10.21228/M8NN9R This work is supported by NIH grant, U2C- DK119886. See: https://www.metabolomicsworkbench.org/about/howtocite.php

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Study IDST004231
Study TitleMetabolomic studies of H9c2 cells samples
Study SummaryCardiomyocyte differentiation is a complex process involving significant metabolic remodeling, but its impact on cellular redox state and cell damage remains poorly understood. Using metabolomic, biophysical, and biochemical approaches, we characterized, in vitro, the metabolic shift of differentiating cardiomyocytes and its implications for oxidative damage. We found that differentiating cardiomyocytes undergo a broad metabolic reprogramming from a glycolytic to an oxidative state, marked by increased activity in key pathways, including malate-aspartate shuttle, glutathione metabolism, and tricarboxylic acid cycle. This metabolic transition was associated with mitochondrial enlargement and increased reactive oxygen species (ROS) production. Intriguingly, despite ROS increase, differentiated cells maintained similar levels of DNA damage as cardiomyoblasts and were more resistant to a H₂O₂ challenge. Our findings suggest that metabolic adaptations during cardiomyocyte differentiation enhance their capacity to mitigate oxidative stress damage, providing an adaptive avenue that enables cardiomyocyte survival upon exposure to a rich oxygen environment.
Institute
University of Campinas
Last NameAmaral
First NameAlan
AddressRua Josué de Castro, s/n - Cidade Universitária, Campinas - SP, 13083-970
Emaila228197@dac.unicamp.br
Phone+5527996413870
Submit Date2025-09-16
Raw Data AvailableYes
Raw Data File Type(s)cdf
Analysis Type DetailGC-MS
Release Date2025-09-29
Release Version1
Alan Amaral Alan Amaral
https://dx.doi.org/10.21228/M8NN9R
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Combined analysis:

Analysis ID AN007046
Chromatography ID CH005349
MS ID MS006743
Analysis type MS
Chromatography type GC
Chromatography system Agilent 5975C
Column Agilent HP5-MS (30m x 0.25mm, 0.25 um)
MS Type EI
MS instrument type Single quadrupole
MS instrument name Agilent 5975C
Ion Mode POSITIVE
Units Normalized Intensity (a.u.)
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