4.5 Article

Dysfunction of Serotonergic and Dopaminergic Neuronal Systems in the Antidepressant-Resistant Impairment of Social Behaviors Induced by Social Defeat Stress Exposure as Juveniles

Journal

INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY
Volume 21, Issue 9, Pages 837-846

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ijnp/pyy038

Keywords

social defeat stress; juvenile; adolescent; social behaviors; monoaminergic neuronal system

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan [24590219, 26460240, 16K08421, 17H04252]
  2. Japan Agency for Medical Research and development, AMED
  3. Adaptable and Seamless Technology Transfer Program Through Target-driven R&D, Japan Science and Technology Agency [AS251Z03018]
  4. Meijo University Research Institute grant
  5. Smoking Research Foundation Grant for Biomedical Research
  6. Grants-in-Aid for Scientific Research [17H04252, 17H00512] Funding Source: KAKEN

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Background: Extensive studies have been performed on the role of monoaminergic neuronal systems in rodents exposed to social defeat stress as adults. In the present study, we investigated the role of monoaminergic neuronal systems in the impairment of social behaviors induced by social defeat stress exposure as juveniles. Methods: Juvenile, m ale C57BL/6J mice were exposed to social defeat stress for 10 consecutive days. From 1 day after the last stress exposure, desipramine, sertraline, and aripiprazole were administered for 15 days. Social behaviors were assessed at 1 and 15 days after the last stress exposure. Monoamine turnover was determined in specific regions of the brain in the m ice exposed to the stress. Results: Stress exposure as juveniles induced the impairment of social behaviors in adolescent mice. In mice that showed impairment of social behaviors, turnover of serotonin and dopamine, but not noradrenaline, was decreased in specific brain regions.Acute and repeated administration of desipramine,sertraline,and aripiprazole failed to attenuate the impairment of social behaviors, whereas repeated administration of a combination of sertraline and aripiprazole showed additive attenuating effects. Conclusions: These findings suggest that social defeat stress exposure as juveniles induces the treatment-resistant impairment of social behaviors in adolescents through dysfunction in the serotonergic and dopaminergic neuronal systems. The combination of sertraline and aripiprazole may be used as a new treatment strategy for treatment-resistant stress-related psychiatric disorders in adolescents with adverse juvenile experiences.

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