Ketamine as a Prophylactic Against Stress-Induced Depressive-like Behavior
Autor: | Josephine C. McGowan, Alain M. Gardier, Sean C. Lim, Jennifer N. Perusini, Christine A. Denny, Thu Ha Pham, René Hen, Denis J. David, Charlène Faye, Indira Mendez-David, Rebecca A. Brachman |
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Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
medicine.medical_specialty Learned helplessness medicine.disease Social defeat 03 medical and health sciences chemistry.chemical_compound 030104 developmental biology 0302 clinical medicine Endocrinology chemistry Corticosterone Anesthesia Internal medicine medicine Major depressive disorder Anxiety Ketamine medicine.symptom Psychology 030217 neurology & neurosurgery Biological Psychiatry Psychopathology Behavioural despair test medicine.drug |
Zdroj: | ResearcherID |
ISSN: | 0006-3223 |
DOI: | 10.1016/j.biopsych.2015.04.022 |
Popis: | 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. |
Databáze: | OpenAIRE |
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