4.5 Article

THE EFFECTS OF SOCIAL DEFEAT ON BEHAVIOR AND DOPAMINERGIC MARKERS IN MICE

Journal

NEUROSCIENCE
Volume 288, Issue -, Pages 167-177

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2014.12.043

Keywords

social defeat; behavioral tests; dopamine D-1 receptors; dopamine D2 receptors; dopamine and cyclic adenosine 3 ',5 '-monophosphate-regulated phosphoprotein-32 (DARPP-32)

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Funding

  1. Basic Science Research Program through the National Research Foundation of Korea - Ministry of Education, Science and Technology - South Korea [2012-0007635]

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The present study investigated the effects of chronic social defeat stress on several behavioral parameters, and the expression of dopaminergic markers, i.e., dopamine D-1 receptors (D1Rs), dopamine D2 receptors (D2Rs), and dopamine and cyclic adenosine 3',5'-monophosphate-regulated phosphoprotein-32 (DARPP-32), in the prefrontal cortex (PFC), amygdala (AMY), and hippocampus (HIP) of mouse brains. After 10 days of social defeat stress, the defeated mice were divided into two groups: one group underwent a series of behavioral tests. The other group was sacrificed on the 11th day and tissue samples were collected for Western blotting. The behavioral tests comprised tests of locomotion, light/dark preference, social interaction, as well as the novel object recognition test (NORT), Morris water maze, and forced swimming test (FST). We measured the expression of D1Rs, D2Rs, total DARPP-32, phospho-Thr34 or Thr75-DARPP-32 using Western blotting. The defeated mice showed increased anxiety- and depression-like behaviors, and impaired cognition. No significant differences in D1Rs and D2Rs expression were shown between defeated and control mice in any area studied. A significantly increased expression in total DARPP-32, and phospho-DARPP-32 was observed in the PFC or AMY of defeated mice. These data suggest that alterations in dopaminergic markers may be involved in anxiety-and depression-like behaviors, and cognitive impairment induced by social defeat stress. (C) 2015 IBRO. Published by Elsevier Ltd. All rights reserved.

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