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Synaptic priming: A framework for pharmacotherapy in depression.

Kyle A Brown, Musa I Ajibola, Gustavo C Medeiros, Todd D Gould

Neuron November 19, 2025 Peer reviewed DOI: 10.1016/j.neuron.2025.09.010 via PubMed

Summary

Ketamine, a rapid-acting antidepressant, may maintain symptom relief through a process called synaptic priming, which enhances the brain's plasticity with repeated doses. This review proposes a dosing model that optimizes therapeutic outcomes by leveraging ketamine's effects on synapses. It also suggests that the mechanisms involved in antidepressant treatments overlap with conditions related to depression, highlighting potential new treatment strategies involving other substances like psychedelics.

Study at a glance

Design review
Key finding The review presents a model where ketamine primes synapses to enhance plasticity, potentially leading to sustained antidepressant effects.

Abstract

Recent antidepressant drug development focuses on a next generation of drugs to rapidly relieve symptoms. Yet, how ketamine, the prototype rapid-acting antidepressant, maintains symptom relief days after drug elimination, and how repeated doses sustain longer-lasting therapeutic effects, remains unclear. Derived from elements of metaplasticity (synaptic priming), this review discusses a framework in which rapid-acting antidepressants prime synapses such that subsequent doses evoke stronger plasticity. Within this framework, we describe how the indirect relationship between ketamine's pharmacokinetics and sustained antidepressant pharmacodynamics reveals a dosing model (primer pharmacology) that can be harnessed to fine-tune therapeutic outcomes. This review also explores how plasticity machinery engaged by antidepressant pharmacotherapies overlaps with priming induced by contextual conditions relevant to depression (e.g., stress and psychotherapy), suggesting innovative opportunities for treatment strategies with emerging primers (e.g., psychedelics such as psilocybin). The integration of synaptic priming with primer pharmacology reveals a model to guide clinical and translational work in psychiatry.

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