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The cognitive neuroscience of ketamine in major depression.

Sara Costi, Chloe Wigg, Erdem Pulcu, Susannah E Murphy, Catherine J Harmer

Brain : a journal of neurology June 30, 2025 DOI: 10.1093/brain/awaf242 via PubMed

Summary

AI-generated from the abstract

Ketamine, long used as an anesthetic, was first identified in 2000 as a fast-acting antidepressant. A single dose alleviates depressive symptoms, including anhedonia, within hours, and effects last for days. Research in animals indicates ketamine rapidly influences brain regions involved in punishment and reward processing, reverses negative affective biases in memories, and promotes stress resilience. Translating these findings to humans is ongoing, with emerging evidence suggesting similar mechanisms in healthy volunteers and patients. Clinical use is limited by acute side effects and unknown long-term safety. Understanding ketamine's mechanisms may guide development of safer rapid-acting antidepressants.

Study at a glance

Characteristics Review Peer reviewed
Intervention Ketamine
Topics Depression Ketamine
Keywords Fast-acting antidepressant Ketamine treatment Ketamine therapy Ketamine medication Ketamine drug
Citations 3
Key finding Ketamine rapidly alleviates depressive symptoms including anhedonia within hours, with effects lasting days, and preclinical evidence suggests it influences punishment- and reward-related brain systems and reverses negative affective biases.

Abstract

Ketamine's potential as a rapid-acting antidepressant was first identified in 2000, despite its long-standing use as an anesthetic agent. Clinically, ketamine alleviates depressive symptoms, including the difficult to treat symptom of anhedonia, within hours, with the effects of a single dose lasting for days. Since then, research has focused on uncovering the mechanisms underlying its rapid antidepressant effects in both humans and animal models. While its molecular and cellular effects have been extensively characterized, its impact on cognitive and neuropsychological mechanisms - potential mediators of its clinical efficacy - remains an area of ongoing investigation. Preclinical studies suggest that ketamine rapidly influences the lateral habenula (involved in punishment processing) and fronto-striatal (reward) systems, reverses negative affective biases in established memories, and promotes long-term stress resilience. Translating these findings to human models is crucial, and emerging evidence suggests that ketamine engages similar mechanisms in healthy volunteer and patient groups. However, its clinical application is constrained by acute side effects and an unknown long-term safety profile. Further research into ketamine's mechanisms of action will be essential to inform the development of novel, safer, and more accessible rapid-acting antidepressants.

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