Sustained rescue of prefrontal circuit dysfunction by antidepressant-induced spine formation

Author:

Moda-Sava R. N.1,Murdock M. H.1ORCID,Parekh P. K.1ORCID,Fetcho R. N.1,Huang B. S.1ORCID,Huynh T. N.1ORCID,Witztum J.1ORCID,Shaver D. C.1,Rosenthal D. L.1ORCID,Alway E. J.1ORCID,Lopez K.1ORCID,Meng Y.1ORCID,Nellissen L.1,Grosenick L.12ORCID,Milner T. A.1ORCID,Deisseroth K.2ORCID,Bito H.3ORCID,Kasai H.45,Liston C.1ORCID

Affiliation:

1. Brain and Mind Research Institute, Department of Psychiatry, and Sackler Institute for Developmental Psychobiology, Weill Cornell Medicine, New York, NY 10021, USA.

2. Departments of Bioengineering and of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA 94305, USA.

3. Department of Neurochemistry, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.

4. Laboratory of Structural Physiology, Center for Disease Biology and Integrative Medicine, Faculty of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan.

5. International Research Center for Neurointelligence (WPI-IRCN), UTIAS, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan.

Abstract

Why is ketamine an antidepressant? A better understanding of the mechanisms underlying the action of antidepressants is urgently needed. Moda-Sava et al. explored a possible mode of action for the drug ketamine, which has recently been shown to help patients recover from depression (see the Perspective by Beyeler). Ketamine rescued behavior in mice that was associated with depression-like phenotypes by selectively reversing stress-induced spine loss and restoring coordinated multicellular ensemble activity in prefrontal microcircuits. The initial induction of ketamine's antidepressant effect on mouse behavior occurred independently of effects on spine formation. Instead, synaptogenesis in the prefrontal region played a critical role in nourishing these effects over time. Interventions aimed at enhancing the survival of restored synapses may thus be useful for sustaining the behavioral effects of fast-acting antidepressants. Science , this issue p. eaat8078 ; see also p. 129

Funder

National Science Foundation

National Institute of Mental Health

Simons Foundation

Whitehall Foundation

Rita Allen Foundation

KAKENHI

Japan Agency for Medical Research and Development

Ministry of Education, Culture, Sports, Science, and Technology

Hartwell Foundation

One Mind Institute

Klingenstein-Simons Fellowship in Brain Science

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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