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Sub-chronic Administration of Rimonabant Causes Loss of Antidepressive Activity and Decreases Doublecortin Immunoreactivity in the Mouse Hippocampus. Neuroscience letters [Neurosci Lett] Journal article

 
TitleSub-chronic Administration of Rimonabant Causes Loss of Antidepressive Activity and Decreases Doublecortin Immunoreactivity in the Mouse Hippocampus.
Author(s)Lee S, Kim DH, Yoon SH, Ryu JH 
InstitutionDepartment of Life and Nanopharmaceutical Sciences, College of Pharmacy, Kyung Hee University, Hoeki-dong, Dongdaemoon-Ku, Seoul 130-701, Korea; Kyung Hee East-West Pharmaceutical Research Institute, College of Pharmacy, Kyung Hee University, Hoeki-dong, Dongdaemoon-Ku, Seoul 130-701, Korea.
SourceNeurosci Lett 2009 Oct 8.
AbstractRimonabant is a cannabinoid receptor 1 antagonist, and is used to treat anorexia and obesity. However, it has been suggested that rimonabant may act as a depressant. In the present study, we investigated the depressive effects of rimonabant using behavioral and biochemical methods. A single treatment with rimonabant (10mg/kg, p.o) reduced immobility duration in the forced swimming test (FST) to a level similar to that observed for the tricyclic antidepressant, imipramine (15mg/kg, i.p.). However, mice treated with rimonabant for 2 weeks did not show any significant reductions in immobility duration versus vehicle-treated controls. To investigate why the antidepressant effect of rimonabant disappeared after extended treatment, we carried out 5-bromo-2-deoxyuridine (BrdU) and doublecortin (DCX) immunohistochemistry assay. Numbers of BrdU-immunoreactive cells were not significantly changed after administering rimonabant (10mg/kg, p.o) for 2 weeks in the hippocampal dentate gyrus (DG), but interestingly, numbers of DCX-immunopositive cells in the DG were significantly reduced after 2 weeks of rimonabant treatment at doses of 1 or 10mg/kg/day compared with vehicle-treated controls (P < 0.05). These results suggest that sub-chronic treatments with rimonabant inhibit cell proliferation in DG, and that a lack of antidepressive activity may be related to a reduction in cell proliferation in this region.
LanguageENG
Pub Type(s)JOURNAL ARTICLE
PubMed ID19819298
  
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