Effect of chronic restraint stress on sociability in mice
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    Abstract:

    Objective To investigate the effect of chronic restraint stress on sociability in mice. Method Chronic restraint stress was applied to establish stress depression model. The mice were individually housing and restrained for 4 h per day in a 50 mL polypropylene conical tube with ventilation holes. This daily restraint was repeated for 35 consecutive days. The sucrose preference test was applied to evaluate the model. The social approach-avoidance test was used to assess the effect of chronic restraint stress on sociability. Results The sucrose intake was significantly reduced in chronic restraint stress model compared with the control mice (P < 0.01). The control group investigated the social stimulus (stranger cage)significantly longer than the object stimulus(empty cage), thereby demonstrating normal social preference. The model group showed a decrease (sniffing time and frequency)in social investigation (P < 0.05,P < 0.01, vs the control group). The chronic restraint stress group did not demonstrate social preference. The preference index in chronic restraint stress model (ratio time sniffing stranger vs. empty cage) was significantly lower compared with the control mice (P < 0.01). Conclusion The chronic restraint stress showed social avoidance in sociability test.

    Reference
    [1] 孙秀萍, 李腾飞, 石哲, 等. 人参总皂苷和远志总苷配伍对小鼠抗抑郁作用[J]. 中国比较医学杂志, 2012,(06):30-36.
    [2] Yan H, Cao X, Das M, et al. Behavioral animal models of depression[J]. Neurosci Bull. 2010, (4):327-337.
    [3] Belzung C, Lemoine M. Criteria of validity for animal models of psychiatric disorders: focus on anxiety disorders and depression[J]. Biol Mood Anxiety Disord. 2011,(1):9.
    [4] Park JY, Kim TK, Choi J, et al. Implementation of a Two-dimensional Behavior Matrix to Distinguish Individuals with Differential Depression States in a Rodent Model of Depression[J]. Exp Neurobiol. 2014, (3):215-223.
    [5] Leem YH, Yoon SS, Kim YH, et al. Disrupted MEK/ERK signaling in the medial orbital cortex and dorsal endopiriform nuclei of the prefrontal cortex in a chronic restraint stress mouse model of depression[J]. Neurosci Lett. 2014,(580):163-168.
    [6] Han A, Sung Y-B, Chung S-Y, et al. Possible additional antidepressant-like mechanism of sodium butyrate: Targeting the hippocampus. Neuropharmacology[J]. 2014, (0):292-302.
    [7] Garcia-Garcia AL, Elizalde N, Matrov D, et al. Increased Vulnerability to Depressive-Like Behavior of Mice with Decreased Expression of VGLUT1. Biological Psychiatry[J]. 2009,(3):275-282.
    [8] Lukas M, Toth I, Reber SO, et al. The neuropeptide oxytocin facilitates pro-social behavior and prevents social avoidance in rats and mice. Neuropsychopharmacology. 2011;36(11):2159-2168.
    [9] Cheng Y, Rodriguiz RM, Murthy SR, et al. Neurotrophic factor-alpha1 prevents stress-induced depression through enhancement of neurogenesis and is activated by rosiglitazon[J]e. Mol Psychiatry. 2014.
    [10] Kessler RC, Berglund P, Demler O, et al. The epidemiology of major depressive disorder: results from the National Comorbidity Survey Replication (NCS-R) [J]. JAMA. 2003,(23):3095-3105.
    [11] Brielmaier J, Senerth JM, Silverman JL, et al. Chronic desipramine treatment rescues depression-related, social and cognitive deficits in Engrailed-2 knockout mice [J]. Genes Brain Behav. 2014,(3):286-298.
    [12] Van der Kooij, M.A., M.Fantin,et al.Impaired hippocampal neuroligin-2 function by chronic stress of synthetic peptide treatment is tinked to social deficits and increased aggression.Neuropsy chopharmacology,2014(5):1148-1158.
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  • Revised:March 02,2015
  • Online: April 22,2015
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