Summary of Study ST001665

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 PR001070. The data can be accessed directly via it's Project DOI: 10.21228/M8D12Q This work is supported by NIH grant, U2C- DK119886.

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Study IDST001665
Study TitleBranched-chain alpha-ketoacids are preferentially reaminated and activate protein synthesis in the rat heart
Study SummaryBranched-chain amino acids (BCAA) and their cognate α-ketoacids (BCKA) are elevated in an array of cardiometabolic diseases. Here we demonstrate that the major metabolic fate of uniformly-13C-labeled α-ketoisovalerate ([U-13C]KIV) in the heart is reamination to valine. Activation of cardiac branched-chain α-ketoacid dehydrogenase (BCKDH) by treatment with the BCKDH kinase inhibitor, BT2, does not impede the strong flux of [U-13C]KIV to valine.
Institute
Duke University
Last NameWalejko
First NameJacquelyn
Address300 N Duke St
Emailjacquelyn.walejko@duke.edu
Phone9194792304
Submit Date2021-01-26
Analysis Type DetailGC-MS
Release Date2021-02-17
Release Version1
Jacquelyn Walejko Jacquelyn Walejko
https://dx.doi.org/10.21228/M8D12Q
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Combined analysis:

Analysis ID AN002717
Analysis type MS
Chromatography type GC
Chromatography system Agilent 7890B
Column Agilent HP5-MS (30m x 0.25mm, 0.25 um)
MS Type EI
MS instrument type Single quadrupole
MS instrument name Agilent 5977A
Ion Mode UNSPECIFIED
Units Concentration of 13C (uM)

MS:

MS ID:MS002514
Analysis ID:AN002717
Instrument Name:Agilent 5977A
Instrument Type:Single quadrupole
MS Type:EI
MS Comments:Masshunter used for data acquisition and processing.
Ion Mode:UNSPECIFIED
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