Advances in the study of NMDA receptors in depression pathogenesis and the antidepressant efficacy of their antagonists.
Mingrui Chen, Jingyan Jin, Hongsheng Bi, Yihan Zhang, Mingyuan Sun, Xiaobai Li, Yan Wang
Asian journal of psychiatry June 1, 2025 DOI: 10.1016/j.ajp.2025.104502 via PubMed
Summary
AI-generated from the abstractNMDA receptors, a type of glutamate receptor, are central to neuroplasticity and are implicated in depression, where their dysfunction can cause neuronal damage and disrupt brain adaptability. Ketamine, an NMDA receptor antagonist, rapidly alleviates severe depression and suicidal thoughts within hours by reducing NMDA receptor activity and activating the mTOR pathway, but its use is limited by side effects like hallucinations and dependency. Esketamine, an FDA-approved variant, offers improved efficacy and fewer side effects. Other NMDA-modulating compounds, including memantine and rapastinel, are under investigation. Future research should focus on NMDA receptor molecular mechanisms to develop safer, more effective, and personalized depression treatments with longer-lasting effects.
Study at a glance
| Characteristics | Review Peer reviewed |
|---|---|
| Interventions | Ketamine Esketamine Memantine Rapastinel |
| Topics | Depression |
| Keywords | Antidepressants Glutamatergic Nmda receptor antagonists Nmda receptors Depression treatment |
| Citations | 12 |
| Key finding | NMDA receptor dysfunction is a key pathological mechanism in depression, and ketamine rapidly relieves depressive symptoms by blocking NMDA receptors and activating the mTOR signaling pathway. |
Abstract
N-methyl-D-aspartate receptors (NMDA receptors) play a crucial role as ionotropic glutamate receptors in regulating neuroplasticity, learning, memory, and a range of psychiatric disorders. Studies indicate that dysfunction of NMDA receptors is a key pathological mechanism in depression, where abnormal activation can result in neuronal excitotoxicity, excessive extracellular calcium ion accumulation, and disrupted neuroplasticity. As a non-competitive NMDA receptor antagonist, ketamine quickly relieves depressive symptoms by decreasing the activity of extracellular NMDA receptors and activating the mTOR signaling pathway. The treatment can improve severe depression and suicide thoughts within hours, but its potential for hallucinations, dissociative symptoms, and dependency restricts its broader application. Esketamine has demonstrated improvements in both side effects and efficacy and has received FDA approval, while other compounds with NMDA receptor modulating functions, such as memantine and rapastinel, are also showing potential in exploration. Future studies should concentrate on the molecular mechanisms of NMDA receptors, aiming to develop safer and more effective medications, and refine treatment strategies to offer personalized choices and longer-lasting efficacy for the treatment of depression.