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Trypanosoma cruzi-induced depressive-like behavior is independent of meningoencephalitis but responsive to parasiticide and TNF-targeted therapeutic interventions.
- Source :
-
Brain, behavior, and immunity [Brain Behav Immun] 2012 Oct; Vol. 26 (7), pp. 1136-49. Date of Electronic Publication: 2012 Jul 25. - Publication Year :
- 2012
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Abstract
- Inflammatory cytokines and microbe-borne immunostimulators have emerged as triggers of depressive behavior. Behavioral alterations affect patients chronically infected by the parasite Trypanosoma cruzi. We have previously shown that C3H/He mice present acute phase-restricted meningoencephalitis with persistent central nervous system (CNS) parasitism, whereas C57BL/6 mice are resistant to T. cruzi-induced CNS inflammation. In the present study, we investigated whether depression is a long-term consequence of acute CNS inflammation and a contribution of the parasite strain that infects the host. C3H/He and C57BL/6 mice were infected with the Colombian (type I) and Y (type II) T. cruzi strains. Forced-swim and tail-suspension tests were used to assess depressive-like behavior. Independent of the mouse lineage, the Colombian-infected mice showed significant increases in immobility times during the acute and chronic phases of infection. Therefore, T. cruzi-induced depression is independent of active or prior CNS inflammation. Furthermore, chronic depressive-like behavior was triggered only by the type I Colombian T. cruzi strain. Acute and chronic T. cruzi infection increased indoleamine 2,3-dioxygenase (IDO) expression in the CNS. Treatment with the selective serotonin reuptake inhibitor (SSRI) fluoxetine abrogated the T. cruzi-induced depressive-like behavior. Moreover, treatment with the parasiticide drug benznidazole abrogated depression. Chronic T. cruzi infection of C57BL/6 mice increased tumor necrosis factor (TNF) expression systemically but not in the CNS. Importantly, TNF modulators (anti-TNF and pentoxifylline) reduced immobility. Therefore, direct or indirect parasite-induced immune dysregulation may contribute to chronic depressive disorder in T. cruzi infection, which opens a new therapeutic pathway to be explored.<br /> (Copyright © 2012 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Antidepressive Agents, Second-Generation therapeutic use
Depression drug therapy
Depression etiology
Emotions physiology
Exploratory Behavior
Female
Fluoxetine therapeutic use
Glial Fibrillary Acidic Protein metabolism
Hindlimb Suspension psychology
Immunohistochemistry
Mice
Mice, Inbred C3H
Motor Activity physiology
Nitroimidazoles therapeutic use
Pentoxifylline therapeutic use
Phenotype
Phosphodiesterase Inhibitors therapeutic use
Psychomotor Performance physiology
Real-Time Polymerase Chain Reaction
Swimming psychology
Chagas Disease drug therapy
Chagas Disease psychology
Depression psychology
Meningoencephalitis psychology
Trypanocidal Agents therapeutic use
Trypanosoma cruzi
Tumor Necrosis Factor-alpha antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2139
- Volume :
- 26
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Brain, behavior, and immunity
- Publication Type :
- Academic Journal
- Accession number :
- 22841695
- Full Text :
- https://doi.org/10.1016/j.bbi.2012.07.009