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      Animal models of major depression: drawbacks and challenges

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          Abstract

          Major depression is a leading contributor to the global burden of disease. This situation is mainly related to the chronicity and/or recurrence of the disorder, and to poor response to antidepressant therapy. Progress in this area requires valid animal models. Current models are based either on manipulating the environment to which rodents are exposed (during the developmental period or adulthood) or biological underpinnings (i.e. gene deletion or overexpression of candidate genes, targeted lesions of brain areas, optogenetic control of specific neuronal populations, etc.). These manipulations can alter specific behavioural and biological outcomes that can be related to different symptomatic and pathophysiological dimensions of major depression. However, animal models of major depression display substantial shortcomings that contribute to the lack of innovative pharmacological approaches in recent decades and which hamper our capabilities to investigate treatment-resistant depression. Here, we discuss the validity of these models, review putative models of treatment-resistant depression, major depression subtypes and recurrent depression. Furthermore, we identify future challenges regarding new paradigms such as those proposing dimensional rather than categorical approaches to depression.

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          Mechanisms and functional implications of adult neurogenesis.

          The generation of new neurons is sustained throughout adulthood in the mammalian brain due to the proliferation and differentiation of adult neural stem cells. In this review, we discuss the factors that regulate proliferation and fate determination of adult neural stem cells and describe recent studies concerning the integration of newborn neurons into the existing neural circuitry. We further address the potential significance of adult neurogenesis in memory, depression, and neurodegenerative disorders such as Alzheimer's and Parkinson's disease.
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            Depression: a new animal model sensitive to antidepressant treatments.

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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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                Author and article information

                Contributors
                + 33 2 47 36 69 94 , catherine.belzung@univ-tours.fr
                Journal
                J Neural Transm (Vienna)
                J Neural Transm (Vienna)
                Journal of Neural Transmission
                Springer Vienna (Vienna )
                0300-9564
                1435-1463
                4 October 2019
                4 October 2019
                2019
                : 126
                : 11
                : 1383-1408
                Affiliations
                [1 ]GRID grid.12366.30, ISNI 0000 0001 2182 6141, UMR 1253, iBrain, Université de Tours, Inserm, ; Tours, France
                [2 ]GRID grid.12366.30, ISNI 0000 0001 2182 6141, UMR 1253, iBrain, UFR Sciences et Techniques, ; Parc Grandmont, 37200 Tours, France
                Author information
                http://orcid.org/0000-0001-6095-5974
                Article
                2084
                10.1007/s00702-019-02084-y
                6815270
                31584111
                7fe35d9f-73ba-4b16-83de-0ec148195748
                © The Author(s) 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 25 June 2019
                : 17 September 2019
                Categories
                Psychiatry and Preclinical Psychiatric Studies - Review Article
                Custom metadata
                © Springer-Verlag GmbH Austria, part of Springer Nature 2019

                depression,antidepressant,treatment-resistant depression,animal models,validity

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