PubMed · 2012 · 48 citations · 50 references
MedicinePharmacologyPsychiatryNeurochemistryNeuropharmacologyPsychopharmacologyAntidepressant PharmacologyAntidepressant PharmacotherapyNeurochemical PharmacologyPsychostimulant PharmacologyAntidepressant MedicationsGlutathione ReductionLipid Peroxidation MarkersLipopolysaccharide-induced DamageOxidative Stress InjuryReduced GlutathioneSelective Serotonin Reuptake Inhibitor TreatmentTricyclic Antidepressant Therapy
The administration of lipopolysaccharide increased oxidative stress in brain and liver; it increased brain MDA by 36.1 and liver MDA by 159.8 %. GSH decreased by 34.1 % and 64.8 % and nitric oxide increased by 78.7 % and 103.8 % in brain and liver, respectively. In brain, MDA decreased after the administration of sertraline and by the lower dose of fluoxetine or fluvoxamine, but increased after the higher dose of imipramine. Reduced glutathione increased after sertraline, fluvoxamine and the lower dose of fluoxetine or imipramine. Nitric oxide decreased by sertraline, fluoxetine, fluvoxamine and by the lower dose of imipramine. In the liver, all drugs decreased MDA and increased GSH level. Nitric oxide is decreased by sertraline, fluvoxamine and by the lower dose of fluoxetine or imipramine. It is concluded that, during mild systemic inflammatory illness induced by peripheral bacterial endotoxin injection, the SSRIs fluoxetine, sertraline and fluvoxamine reduced, while the TCA impiramine increased oxidative stress induced in the brain. The SSRIs as well as imipramine reduced oxidative stress due to lipopolysaccharide in liver tissue.
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