4.5 Article

Ursolic acid abrogates depressive-like behavior and hippocampal pro-apoptotic imbalance induced by chronic unpredictable stress

Journal

METABOLIC BRAIN DISEASE
Volume 36, Issue 3, Pages 437-446

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11011-020-00658-4

Keywords

Apoptosis; Depression; Fluoxetine; Stress; Ursolic acid

Funding

  1. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) [310113/2017-2, 150082/2018-5]
  2. Coordenacao de Aperfeicoamento de Pessoal de Ensino Superior (CAPES)

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The study demonstrates that ursolic acid has antidepressant-like effects in mice exposed to chronic unpredictable stress (CUS), and this effect may be associated with the modulation of Bcl-2/Bax expression in the hippocampus. Fluoxetine showed similar antidepressant effects as ursolic acid, preventing CUS-induced behavioral changes. However, the mechanisms by which ursolic acid exerts its antidepressant effects may differ from traditional antidepressants like fluoxetine.
Emerging evidence has shown that ursolic acid exerts antidepressant-like effects, however, its ability to elicit an antidepressant-like response in rodents subjected to stress model that mimics behavioral and neurochemical alterations found in depression remains to be determined. Thus, this study investigated the possible antidepressant-like effect of ursolic acid in mice subjected to chronic unpredictable stress (CUS) for 14 days, and whether this effect could be associated with the modulation of serum corticosterone levels and hippocampal Bcl-2/Bax mRNA expression. Our results indicated that CUS induced a depressive-like behavior, as demonstrated by an increase in the immobility time and latency to first grooming in the tail suspension test and splash test, respectively. Conversely, the repeated administration of ursolic acid (0.1 mg/kg, p.o.) or fluoxetine (10 mg/kg, p.o.) in the last 7 days of CUS completely prevented CUS-induced behavioral alterations, suggesting an antidepressant-like effect. Additionally, CUS significantly increased the mRNA expression of Bax (pro-apoptosis marker), but not Bcl-2 (anti-apoptosis marker) in the hippocampus. Moreover, reduced hippocampal mRNA expression of Bcl-2/Bax ratio was detected in CUS-exposed mice. Ursolic acid, but not fluoxetine, prevented CUS-induced increase in the expression of Bax, but both ursolic acid and fluoxetine prevented CUS-induced reduction on Bcl-2/Bax ratio. Furthermore, neither CUS nor treatments with ursolic acid or fluoxetine altered serum corticosterone levels. Our study unveils the ability of ursolic acid to prevent the depressive-like behavior induced by stress and the modulation of Bcl-2/Bax expression could be associated with this response.

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