4.7 Article

Ketamine as a Prophylactic Against Stress-Induced Depressive-like Behavior

Journal

BIOLOGICAL PSYCHIATRY
Volume 79, Issue 9, Pages 776-786

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2015.04.022

Keywords

Depression; Ketamine; Mice; PTSD; Stress; Stress resilience

Funding

  1. National Institute of Child Health and Human Development Grant [T32HD07430]
  2. Lundbeck and the Brain & Behavior Research Foundation
  3. Agence Nationale pour la Recherche SAMENTA [ANR-12-SAMA-0007]
  4. Hope for Depression Research Foundation
  5. National Institutes of Health [T32 MH015174-36, DP5 OD017908-01]
  6. National Alliance for Research on Schizophrenia and Depression Young Investigator Grant from the Brain & Behavior Research Foundation
  7. New York Stem Cell Science [N13S-006]
  8. [R37 MH068542]
  9. [R01 AG043688]
  10. Agence Nationale de la Recherche (ANR) [ANR-12-SAMA-0007] Funding Source: Agence Nationale de la Recherche (ANR)

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BACKGROUND: Stress exposure is one of the greatest risk factors for psychiatric illnesses like major depressive disorder and posttraumatic stress disorder. However, not all individuals exposed to stress develop affective disorders. Stress resilience, the ability to experience stress without developing persistent psychopathology, varies from individual to individual. Enhancing stress resilience in at-risk populations could potentially protect against stress-induced psychiatric disorders. Despite this fact, no resilience-enhancing pharmaceuticals have been identified. METHODS: Using a chronic social defeat (SD) stress model, learned helplessness (LH), and a chronic corticosterone (CORT) model in mice, we tested if ketamine could protect against depressive-like behavior. Mice were administered a single dose of saline or ketamine and then 1 week later were subjected to 2 weeks of SD, LH training, or 3 weeks of CORT. RESULTS: SD robustly and reliably induced depressive-like behavior in control mice. Mice treated with prophylactic ketamine were protected against the deleterious effects of SD in the forced swim test and in the dominant interaction test. We confirmed these effects in LH and the CORT model. In the LH model, latency to escape was increased following training, and this effect was prevented by ketamine. In the CORT model, a single dose of ketamine blocked stress-induced behavior in the forced swim test, novelty suppressed feeding paradigm, and the sucrose splash test. CONCLUSIONS: These data show that ketamine can induce persistent stress resilience and, therefore, may be useful in protecting against stress-induced disorders.

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