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Study M844

Study name

Tian JS 2022

Title

Stable isotope-resolved metabolomics studies on corticosteroid-induced PC12 cells: a strategy for evaluating glucose catabolism in an in vitro model of depression

Overall design

The aim of this study was to research the glucose catabolism of the corticosterone-induced PC12 cell damage model of depression by combining traditional metabolomics technology with stable isotope-resolved metabolomics. PC12 cells were divided into the no treatment control group (control group) and the corticosterone group (CORT group). The control group of PC12 cells was added 10 mL of 1640 medium, and the corticosterone group was added 10 mL of 1640 medium containing 250 uM corticosterone. After 24 h of incubation, three samples per group were used for metabonomic analysis.

Study Type

Type1;

Data available

Unavailable

Organism

Rat; Rat;

Categories of depression

Animal model; Other animal model; Other animal model;

Criteria for depression

Not reported

Sample size

6

Tissue

Central; Brain; PC12 cell;

Platform

MS-based; LC-MS: Thermo Dionex UltiMate 3000 high-performance liquid chromatograph with Thermo Q Exactive HF hybrid quadrupole-Orbitrap mass spectrometer (Thermo Fisher Scientific., Germany);

PMID

34699232

DOI

10.1021/acs.jproteome.1c00516

Citation

Tian JS, Wu WZ, Liu SB, et al. Stable isotope-resolved metabolomics studies on corticosteroid-induced PC12 cells: a strategy for evaluating glucose catabolism in an in vitro model of depression. J Proteome Res. 2022 Mar 4;21(3):788-797.

Metabolite

N-Acetyl-L-aspartic acid;

L-Tryptophan;

L-Leucine;

L-Proline;

L-Glutamic acid;

L-Serine;

L-Methionine;

L-Lactic acid;

L-Alanine;

L-Aspartic acid;

D-Glucose;

Hypoxanthine;

Fumaric acid;

Taurine;

Pyruvic acid;

4-Hydroxybutyric acid;

4-Hydroxyproline;

L-Malic acid;

Adenine;

Glycerol 3-phosphate;

Homocysteine;

Trans-Hexa-dec-2-enoic acid;

4-Oxoproline;