Neuropharmacology of Ketamine and Its Use in the Treatment of Major Depressive Disorder: A Review.
Cureus April 1, 2025 DOI: 10.7759/cureus.83244 via PubMed
Summary
AI-generated from the abstractKetamine acts as a rapid antidepressant primarily by blocking N-methyl-D-aspartate receptors, though its effects also involve monoaminergic signaling, BDNF signaling, opioid receptor agonism, and neuroinflammation. Compared to SSRIs and tricyclic antidepressants, ketamine shows greater efficacy, faster onset, and better tolerability but has a shorter duration of action and accessibility issues. In a head-to-head trial, ketamine matched electroconvulsive therapy in efficacy for non-psychotic depression while providing faster relief. Further research is needed to optimize dosing, improve accessibility, and address risks like bladder toxicity and addiction.
Study at a glance
| Characteristics | Review Peer reviewed |
|---|---|
| Intervention | Ketamine |
| Topics | Depression Ketamine Neuroplasticity |
| Keywords | Bdnf-trkb signaling Electroconvulsive therapy Glutamatergic neurotransmission Neuropharmacology |
| Citations | 1 |
| Key finding | Ketamine demonstrates greater efficacy, faster onset, and better tolerability than SSRIs and TCAs, and similar efficacy to ECT with faster relief in non-psychotic depression. |
Abstract
Depression is a common yet potentially debilitating mood disorder with complex neurobiological underpinnings, including deficiencies in monoaminergic and glutamatergic signaling, overactivity of the lateral habenula, and dysregulation of brain-derived neurotrophic factor (BDNF) signaling. Ketamine has emerged as a mechanistically novel, effective, and rapidly acting antidepressant. Ketamine's primary effects are due to N-methyl-D-aspartate receptor (NMDAR) antagonism, although hypotheses regarding the importance of its impact on monoaminergic signaling (preclinical evidence), BDNF signaling (preclinical evidence), opioid receptor agonism (preclinical evidence), and neuroinflammation (clinical evidence) have gained traction. Compared to selective serotonin reuptake inhibitors (SSRIs) and tricyclic antidepressants (TCAs), ketamine demonstrates greater efficacy, a significantly faster onset of action, and generally more tolerable side effects. However, its benefits are offset by a far shorter duration of antidepressant effects and accessibility limitations. In a head-to-head trial, compared to electroconvulsive therapy (ECT), ketamine showed similar efficacy in non-psychotic depression while providing clinically significant relief more rapidly. While promising, further research is needed to optimize ketamine's dosing regimen, enhance its accessibility, and better understand potential drawbacks such as bladder toxicity and addiction potential. Additionally, studying the mechanisms behind ketamine's antidepressant action may provide deeper insight into the neurobiology of depression.