Ketamine and the neurobiology of depression: Toward next-generation rapid-acting antidepressant treatments

Author:

Krystal John H.123ORCID,Kaye Alfred P.13,Jefferson Sarah13,Girgenti Matthew J.13,Wilkinson Samuel T.12,Sanacora Gerard12,Esterlis Irina13ORCID

Affiliation:

1. Department of Psychiatry, Yale School of Medicine, New Haven, CT 06511

2. Psychiatry and Behavioral Health Services, Yale-New Haven Hospital, New Haven, CT 06510

3. Clinical Neuroscience Division, National Center for Posttraumatic Stress Disorder, Veterans Affairs Connecticut Healthcare System, West Haven, CT 06516

Abstract

Ketamine has emerged as a transformative and mechanistically novel pharmacotherapy for depression. Its rapid onset of action, efficacy for treatment-resistant symptoms, and protection against relapse distinguish it from prior antidepressants. Its discovery emerged from a reconceptualization of the neurobiology of depression and, in turn, insights from the elaboration of its mechanisms of action inform studies of the pathophysiology of depression and related disorders. It has been 25 y since we first presented our ketamine findings in depression. Thus, it is timely for this review to consider what we have learned from studies of ketamine and to suggest future directions for the optimization of rapid-acting antidepressant treatment.

Funder

VA | National Center for PTSD, U.S. Department of Veterans Affairs

Yale | YSM | Yale Center for Clinical Investigation, Yale School of Medicine

HHS | NIH | National Institute of Mental Health

American Foundation for Suicide Prevention

Janssen Pharmaceuticals

Oui Therapeutics

Freedom Biosciences

Nancy Taylor Foundation

Sage Therapeutics

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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