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Study M182

Study name

Banasr M 2010

Title

Glial pathology in an animal model of depression: reversal of stress-induced cellular, metabolic and behavioral deficits by the glutamate-modulating drug riluzole

Overall design

This study investigates changes in glial function occurring in the rat prefrontal cortex (PFC) after chronic unpredictable stress (CUS), a rodent model of depression. Furthermore, we analyzed the effects of riluzole, a Food and Drug Administration-approved drug for the treatment of amyotrophic laterosclerosis, known to modulate glutamate release and facilate glutamate uptake, on CUS-induced glial dysfunction and depressive-like behaviors. Rats were divided into the following 4 groups (n = 8 in each group): (1) control group, (2) CUS group, (3) riluzole group (riluzole treatment at the dose of 4 mg/kg i.p), and (4) CUS + riluzole group (stressor plus riluzole treatment at the dose of 4 mg/kg i.p). Animals were first exposed to CUS for 15 days, and then were administered with riluzole daily for 21 days with continued CUS procedure. Plasma and cortical extracts were analyzed using 1H-NMR with or without 13C decoupling.

Study Type

Type1;

Type2;

Type3;

Data available

Unavailable

Organism

Rat; Sprague-Dawley rat;

Categories of depression

Animal model; Chronic mild stress model; Chronic mild stress model;

Healthy individuals; Healthy individuals; Healthy individuals;

Criteria for depression

Sucrose preference test, active avoidance test

Sample size

32

Tissue

Peripheral; Blood; Plasma;

Central; Brain; Prefrontal cortex;

Platform

NMR; NMR: Bruker AVANCE spectrometer (Bruker Instruments);

PMID

18825147

DOI

10.1038/mp.2008.106

Citation

Banasr M, Chowdhury GM, Terwilliger R, et al. Glial pathology in an animal model of depression: reversal of stress-induced cellular, metabolic and behavioral deficits by the glutamate-modulating drug riluzole. Mol Psychiatry 2010;15(5):501-11.

Metabolite

Gamma-Aminobutyric acid;

L-Glutamic acid;

L-Glutamine;