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Chronic Treatment with the IDO1 Inhibitor 1-Methyl-D-Tryptophan Minimizes the Behavioural and Biochemical Abnormalities Induced by Unpredictable Chronic Mild Stress in Mice - Comparison with Fluoxetine. | LitMetric

AI Article Synopsis

  • The study used a model of stress-induced depression in mice to show that chronic mild stress leads to behavioral changes and alterations in the kynurenine pathway, affecting glutamatergic neurotransmission.
  • Treatment with the IDO1 inhibitor 1-methyl-D-tryptophan and the antidepressant fluoxetine partially reversed these biochemical changes and improved behavior in mice exposed to stress.
  • Both treatments were found to reduce levels of proinflammatory cytokines, indicating that their therapeutic effects might arise from anti-inflammatory processes, suggesting that targeting the kynurenine pathway could help alleviate depressive-like symptoms.

Article Abstract

We demonstrated that confronting mice to the Unpredictable Chronic Mild Stress (UCMS) procedure-a validated model of stress-induced depression-results in behavioural alterations and biochemical changes in the kynurenine pathway (KP), suspected to modify the glutamatergic neurotransmission through the imbalance between downstream metabolites such as 3-hydroxykynurenine, quinolinic and kynurenic acids. We showed that daily treatment with the IDO1 inhibitor 1-methyl-D-tryptophan partially rescues UCMS-induced KP alterations as does the antidepressant fluoxetine. More importantly we demonstrated that 1-methyl-D-tryptophan was able to alleviate most of the behavioural changes resulting from UCMS exposure. We also showed that both fluoxetine and 1-methyl-D-tryptophan robustly reduced peripheral levels of proinflammatory cytokines in UCMS mice suggesting that their therapeutic effects might occur through anti-inflammatory processes. KP inhibition might be involved in the positive effects of fluoxetine on mice behaviour and could be a relevant strategy to counteract depressive-like symptoms.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5102430PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0164337PLOS

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