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Antidepressant Drugs: MAOIs and Other Agents

Atypical antidepressants, including bupropion (Wellbutrin), mirtazapine (Remeron), nefazodone (Serzone), trazodone (Desyrel), and vilazodone (Viibryd), offer unique mechanisms of action. Bupropion weakly inhibits dopamine and norepinephrine reuptake, aiding depression treatment and smoking cessation, with a low risk of sexual dysfunction. Mirtazapine enhances serotonin and norepinephrine neurotransmission, leading to sedation, increased appetite, and weight gain. As a result, it helps treat...
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Related Experiment Video

Updated: Jul 5, 2026

Vagus Nerve Stimulation As an Adjunctive Neurostimulation Tool in Treatment-resistant Depression
04:29

Vagus Nerve Stimulation As an Adjunctive Neurostimulation Tool in Treatment-resistant Depression

Published on: January 7, 2019

Psychostimulants for depression.

M Candy1, L Jones, R Williams

  • 1Royal Free & University College Medicial School, Marie Curie Palliative Care Research Unit, Hampstead Campus, Rowland Hill Street, London, UK, NW3 2PF. b.candy@medsch.ucl.ac.uk

The Cochrane Database of Systematic Reviews
|April 22, 2008
PubMed
Summary
This summary is machine-generated.

Psychostimulants (PS) show short-term effectiveness in reducing depression symptoms, but clinical significance requires further study. More high-quality trials are needed to confirm findings and assess long-term effects and safety.

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Last Updated: Jul 5, 2026

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Area of Science:

  • Psychiatry
  • Pharmacology
  • Clinical Trials

Background:

  • Depression is a prevalent, debilitating, and costly condition with suboptimal treatment outcomes.
  • Current first-line antidepressant therapies present challenges for moderate to severe depression.
  • Psychostimulants (PS) have been investigated for depression treatment, necessitating a systematic review.

Purpose of the Study:

  • To systematically evaluate the effectiveness of psychostimulants (PS) in treating depression.
  • To assess the adverse events associated with PS use in depression.

Main Methods:

  • A systematic search of multiple databases (e.g., Cochrane, MEDLINE, EMBASE) was conducted.
  • Included were randomized controlled trials (RCTs) of adults diagnosed with depression, comparing PS to placebo or active treatments.
  • Data extraction and quality assessment were performed independently; meta-analysis was used for comparable trials.

Main Results:

  • Twenty-four RCTs of generally low quality were identified, evaluating five different PS.
  • Oral PS as monotherapy significantly reduced short-term depressive symptoms compared to placebo (SMD -0.87).
  • PS were generally well-tolerated in the short term, but tolerance and dependence were under-evaluated.

Conclusions:

  • Evidence suggests short-term efficacy of PS in reducing depression symptoms, though clinical significance remains uncertain.
  • Larger, high-quality trials with extended follow-up are required.
  • Further research should investigate optimal PS, clinical situations, and long-term safety profiles.