Improved workflow for mass spectrometry-based metabolomics analysis of the heart.

Cardiac metabolism GC-MS Glycogen Metabolomics adrenergic receptor cardiac metabolism gas chromatography-mass spectrometry (GC-MS) glycogen metabolomics

Journal

The Journal of biological chemistry
ISSN: 1083-351X
Titre abrégé: J Biol Chem
Pays: United States
ID NLM: 2985121R

Informations de publication

Date de publication:
28 02 2020
Historique:
received: 13 09 2019
revised: 17 01 2020
pubmed: 26 1 2020
medline: 22 10 2020
entrez: 26 1 2020
Statut: ppublish

Résumé

MS-based metabolomics methods are powerful techniques to map the complex and interconnected metabolic pathways of the heart; however, normalization of metabolite abundance to sample input in heart tissues remains a technical challenge. Herein, we describe an improved GC-MS-based metabolomics workflow that uses insoluble protein-derived glutamate for the normalization of metabolites within each sample and includes normalization to protein-derived amino acids to reduce biological variation and detect small metabolic changes. Moreover, glycogen is measured within the metabolomics workflow. We applied this workflow to study heart metabolism by first comparing two different methods of heart removal: the Langendorff heart method (reverse aortic perfusion) and

Identifiants

pubmed: 31980460
pii: S0021-9258(17)49005-3
doi: 10.1074/jbc.RA119.011081
pmc: PMC7049973
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2676-2686

Subventions

Organisme : NIA NIH HHS
ID : R01 AG066653
Pays : United States
Organisme : NHLBI NIH HHS
ID : R56 HL131782
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL131782
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA177558
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001998
Pays : United States

Informations de copyright

© 2020 Andres et al.

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Auteurs

Douglas A Andres (DA)

Department of Molecular and Cellular Biochemistry, University of Kentucky College of Medicine, Lexington, Kentucky 40536; Gill Heart and Vascular Institute, University of Kentucky College of Medicine, Lexington, Kentucky 40536; Spinal Cord and Brain Injury Research Center, University of Kentucky College of Medicine, Lexington, Kentucky 40536; Markey Cancer Center, University of Kentucky College of Medicine, Lexington, Kentucky 40536.

Lyndsay E A Young (LEA)

Department of Molecular and Cellular Biochemistry, University of Kentucky College of Medicine, Lexington, Kentucky 40536.

Sudhakar Veeranki (S)

Department of Molecular and Cellular Biochemistry, University of Kentucky College of Medicine, Lexington, Kentucky 40536; Markey Cancer Center, University of Kentucky College of Medicine, Lexington, Kentucky 40536.

Tara R Hawkinson (TR)

Department of Neuroscience, University of Kentucky, Lexington, Kentucky 40536.

Bryana M Levitan (BM)

Gill Heart and Vascular Institute, University of Kentucky College of Medicine, Lexington, Kentucky 40536; Department of Physiology, University of Kentucky College of Medicine, Lexington, Kentucky 40536.

Daheng He (D)

Department of Biostatistics, University of Kentucky College of Medicine, Lexington, Kentucky 40536.

Chi Wang (C)

Markey Cancer Center, University of Kentucky College of Medicine, Lexington, Kentucky 40536; Department of Biostatistics, University of Kentucky College of Medicine, Lexington, Kentucky 40536.

Jonathan Satin (J)

Department of Physiology, University of Kentucky College of Medicine, Lexington, Kentucky 40536.

Ramon C Sun (RC)

Markey Cancer Center, University of Kentucky College of Medicine, Lexington, Kentucky 40536; Department of Neuroscience, University of Kentucky, Lexington, Kentucky 40536. Electronic address: ramon.sun@uky.edu.

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