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Social vs. environmental stress models of depression from a behavioural and neurochemical approach
Authors:E Venzala  AL García-García  N Elizalde  RM Tordera
Institution:1. Department of Pharmacology, University of Navarra, 31080 Pamplona, Spain;2. Department of Psychiatry, Division of Integrative Neuroscience, Columbia University, NY, USA;1. Department of Psychology, University of Saskatchewan, Saskatoon, Saskatchewan S7N 5A5, Canada;2. Division of Neurology, Department of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan S7J 5B6, Canada;3. Department of Cell Biology, University of Santiago de Compostela, Santiago de Compostela 15782, Spain;1. Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY 10461, USA;2. Departamento de Psicología y Sociología, Universidad de Zaragoza, Campus Ciudad Escolar, 44003 Teruel, Spain;3. Behavioral Core Facility, Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY 10461, USA;4. Departments of Pediatrics, Neurology and Biochemistry, Vanderbilt University (VU), and VU Medical Center, Nashville, TN, USA;1. Department of Psychology, Swansea University, Singleton Park, Swansea SA2 8PP, UK;2. Center of Functionally Integrative Neuroscience, University of Aarhus, Denmark;3. INSERM 930 and University Francois-Rabelais, Tours, France;1. Department of Physiology and Pharmacology, Graduate Institute of Biomedical Sciences, Chang-Gung University, 259 Wen-Hwa 1st Road, Tao-Yuan 333, Taiwan;2. Department of Psychiatry, Chang-Gung Memorial Hospital, Tao-Yuan, Taiwan;3. Department of Biomedical Sciences, Chang Gung University, Tao-Yuan, Taiwan;1. Behavioral Neuroscience Branch, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USA;2. Department of Organismal Biology, Uppsala University, 752 36 Uppsala, Sweden;3. Department of Neurosciences, University of California, San Diego, La Jolla, CA 92093, USA;1. Department of Pharmacology & Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Bhangagarh, Guwahati 781032, Assam, India;2. Department of Pharmacology, Gauhati Medical College, Bhangagarh, Guwahati 781032, Assam, India
Abstract:Major depression is a mental disorder often preceded by exposure to chronic stress or stressful life events. Recently, animal models based on social conflict such as chronic social defeat stress (CSDS) are proposed to be more relevant to stress-induced human psychopathology compared to environmental models like the chronic mild stress (CMS). However, while CMS reproduces specifically core depressive symptoms such as anhedonia and helplessness, CSDS studies rely on the analysis of stress-induced social avoidance, addressing different neuropsychiatric disorders. Here, we study comparatively the two models from a behavioural and neurochemical approach and their possible relevance to human depression. Mice (C57BL/6) were exposed to CMS or CSDS for six weeks and ten days. Anhedonia was periodically evaluated. A battery of test applied during the fourth week after the stress procedure included motor activity, memory, anxiety, social interaction and helplessness. Subsequently, we examined glutamate, GABA, 5-HT and dopamine levels in the prefrontal cortex, hippocampus and brainstem. CMS induced a clear depressive-like profile including anhedonia, helplessness and memory impairment. CSDS induced anhedonia, hyperactivity, anxiety and social avoidance, signs also common to anxiety and posttraumatic stress disorders. While both models disrupted the excitatory inhibitory balance in the prefrontal cortex, CMS altered importantly this balance in the brainstem. Moreover, CSDS decreased dopamine in the prefrontal cortex and brainstem. We suggests that while depressive-like behaviours might be associated to altered aminoacid neurotransmission in cortical and brain stem areas, CSDS induced anxiety behaviours might be linked to specific alteration of dopaminergic pathways involved in rewarding processes.
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