The antidepressant potential of (2R,6R)-hydroxynorketamine: A detailed review of pre-clinical findings.
Isis Koutrouli, Kristýna Mazochová, Rachel R Horsley
European journal of pharmacology July 15, 2025 DOI: 10.1016/j.ejphar.2025.177604 via PubMed
Summary
AI-generated from the abstractA selective review of preclinical rodent studies suggests that (2R,6R)-hydroxynorketamine ((2R,6R)-HNK), a metabolite of ketamine, reduces behavioral despair, anhedonia, anxiety, and social avoidance in both stressed and non-stressed animals. Antidepressant effects appear rapidly (within 30 minutes) and last up to 21 days at doses between 5 and 125 mg/kg. However, some studies failed to find significant effects at doses below 40 mg/kg, particularly in models with pre-induced depression. No major adverse effects were reported, though side-effect data were limited. The authors conclude that (2R,6R)-HNK shows promise as a next-generation antidepressant but requires further research on long-term safety and mechanisms.
Study at a glance
| Characteristics | Selective review Peer reviewed |
|---|---|
| Population | Rodents |
| Interventions | (2R 6R)-hydroxynorketamine |
| Dose | 5 and 125 mg/kg |
| Duration | Up to 21 days |
| Topics | Depression |
| Keywords | Behavioral despair Hydroxynorketamine Learned helplessness Pre-clinical Depression treatment |
| Citations | 4 |
| Key finding | (2R,6R)-HNK reduces behavioral despair, anhedonia, anxiety, and social avoidance in rodent models, with rapid and lasting effects, though some studies show no benefit at lower doses in depressed animals. |
Abstract
Depression affects hundreds of millions globally, and in 2019, esketamine, an S-enantiomer of ketamine, was approved for treatment-resistant depression (TRD). While effective, esketamine carries risks, including abuse potential and adverse effects even at low doses. As a result, ketamine's metabolite, (2R,6R)-hydroxynorketamine ((2R,6R)-HNK), has garnered attention for its potential antidepressant effects without these drawbacks. This selective review evaluates preclinical behavioral evidence for (2R,6R)-HNK's antidepressant properties, focusing on rodent studies that used established depression models. Results showed that (2R,6R)-HNK reduced behavioral despair, anhedonia, anxiety, and social avoidance in both stressed and non-stressed rodents. Antidepressant effects were observed at doses between 5 and 125 mg/kg, with rapid onset (30 min) and long-lasting effects (up to 21 days). However, some studies failed to demonstrate significant antidepressant effects at doses below 40 mg/kg, often in models with pre-induced depression. No significant adverse effects were reported, but data on side effects were limited. In conclusion, (2R,6R)-HNK shows promise as a next-generation antidepressant. However, further research is needed to fully understand its long-term safety and mechanisms, and to determine its advantages over existing treatments like esketamine, particularly for TRD patients.