Skip to main content

Study M013

Study name

Webhofer C 2011

Title

Metabolite profiling of antidepressant drug action reveals novel drug targets beyond monoamine elevation

Overall design

The aim of this study was to elucidate affected biochemical pathways downstream of monoamine reuptake inhibition by interrogating metabolomic profiles in DBA/2Ola mice after chronic paroxetine treatment. GC-time of flight-mass spectrometry metabolite profiling in the hippocampus of mice after chronic paroxetine treatment was investigated. Mice were divided into 2 groups (n = 6 in each group): (1) control group and (2) paroxetine group. Mice received either paroxetine at 10 mg/kg or vehicle (tap water) twice per day by gavaging for 28 days.

Study Type

Type3;

Data available

Unavailable

Organism

Mouse; DBA/2OlaHsd mouse;

Categories of depression

Healthy individuals; Healthy individuals; Healthy individuals;

Criteria for depression

Forced swimming test

Sample size

12

Tissue

Central; Brain; Hippocampus;

Peripheral; Blood; Plasma;

Platform

MS-based; GC-MS: Agilent 6890N gas chromatograph (Agilent, Palo Alto, CA, USA) interfaced to a time-of-flight Pegasus III mass spectrometer (Leco);

PMID

22832350

DOI

10.1038/tp.2011.56

Citation

Webhofer C, Gormanns P, Tolstikov V, et al. Metabolite profiling of antidepressant drug action reveals novel drug targets beyond monoamine elevation. Transl Psychiatry 2011;1:e58.

Metabolite

myo-Inositol;

Gamma-Aminobutyric acid;

L-Valine;

L-Leucine;

L-Proline;

L-Serine;

L-Threonine;

L-Isoleucine;

L-Lactic acid;

L-Alanine;

L-Tyrosine;

D-Fructose;

D-Glucose;

Threonic acid;

Hypoxanthine;

Fumaric acid;

Fructose 6-phosphate;

Glucose 6-phosphate;

Ethanolamine;

Taurine;

Uracil;