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      Sex Differences in Social Interaction Behavior Following Social Defeat Stress in the Monogamous California Mouse ( Peromyscus californicus)

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          Abstract

          Stressful life experiences are known to be a precipitating factor for many mental disorders. The social defeat model induces behavioral responses in rodents (e.g. reduced social interaction) that are similar to behavioral patterns associated with mood disorders. The model has contributed to the discovery of novel mechanisms regulating behavioral responses to stress, but its utility has been largely limited to males. This is disadvantageous because most mood disorders have a higher incidence in women versus men. Male and female California mice ( Peromyscus californicus) aggressively defend territories, which allowed us to observe the effects of social defeat in both sexes. In two experiments, mice were exposed to three social defeat or control episodes. Mice were then behaviorally phenotyped, and indirect markers of brain activity and corticosterone responses to a novel social stimulus were assessed. Sex differences in behavioral responses to social stress were long lasting (4 wks). Social defeat reduced social interaction responses in females but not males. In females, social defeat induced an increase in the number of phosphorylated CREB positive cells in the nucleus accumbens shell after exposure to a novel social stimulus. This effect of defeat was not observed in males. The effects of defeat in females were limited to social contexts, as there were no differences in exploratory behavior in the open field or light-dark box test. These data suggest that California mice could be a useful model for studying sex differences in behavioral responses to stress, particularly in neurobiological mechanisms that are involved with the regulation of social behavior.

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          Essential role of BDNF in the mesolimbic dopamine pathway in social defeat stress.

          Mice experiencing repeated aggression develop a long-lasting aversion to social contact, which can be normalized by chronic, but not acute, administration of antidepressant. Using viral-mediated, mesolimbic dopamine pathway-specific knockdown of brain-derived neurotrophic factor (BDNF), we showed that BDNF is required for the development of this experience-dependent social aversion. Gene profiling in the nucleus accumbens indicates that local knockdown of BDNF obliterates most of the effects of repeated aggression on gene expression within this circuit, with similar effects being produced by chronic treatment with antidepressant. These results establish an essential role for BDNF in mediating long-term neural and behavioral plasticity in response to aversive social experiences.
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            Major depressive disorder.

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              New approaches to antidepressant drug discovery: beyond monoamines.

              All available antidepressant medications are based on serendipitous discoveries of the clinical efficacy of two classes of antidepressants more than 50 years ago. These tricyclic and monoamine oxidase inhibitor antidepressants were subsequently found to promote serotonin or noradrenaline function in the brain. Newer agents are more specific but have the same core mechanisms of action in promoting these monoamine neurotransmitters. This is unfortunate, because only approximately 50% of individuals with depression show full remission in response to these mechanisms. This review summarizes the obstacles that have hindered the development of non-monoamine-based antidepressants, and provides a progress report on some of the most promising current strategies.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2011
                25 February 2011
                : 6
                : 2
                : e17405
                Affiliations
                [1]Department of Psychology, University of California Davis, Davis, California, United States of America
                University of Minnesota, United States of America
                Author notes

                Conceived and designed the experiments: BCT. Performed the experiments: NWK MCP RVL EYT ALS KKC. Analyzed the data: BCT. Contributed reagents/materials/analysis tools: MCP KKC. Wrote the paper: BCT.

                Article
                PONE-D-10-03732
                10.1371/journal.pone.0017405
                3045459
                21364768
                82b28dd2-401b-4461-87d8-479baec1a1a8
                Trainor et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 22 October 2010
                : 29 January 2011
                Page count
                Pages: 11
                Categories
                Research Article
                Biology
                Neuroscience
                Behavioral Neuroscience
                Neuroethology
                Medicine
                Endocrinology
                Neuroendocrinology
                Social and Behavioral Sciences
                Psychology
                Psychological Stress

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                Uncategorized

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