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      Increasing adult hippocampal neurogenesis is sufficient to improve pattern separation

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          Abstract

          Adult hippocampal neurogenesis is a unique form of neural circuit plasticity that results in the generation of new neurons in the dentate gyrus (DG) throughout life 1, 2. Adult-born neurons exhibit heightened synaptic plasticity during their maturation 3 and can account for up to ten percent of the entire granule cell population 4. Moreover, levels of adult hippocampal neurogenesis are elevated by interventions associated with beneficial effects on cognition and mood such as learning 5, environmental enrichment 6, exercise 6 and chronic antidepressant treatment 710. Together, these properties of adult neurogenesis suggest that it may be harnessed to improve hippocampal functions. However, despite a substantial number of studies demonstrating that adult-born neurons are necessary for mediating specific cognitive functions 11 and some of the behavioural effects of antidepressants 810, 12, 13, it is unknown whether increasing adult hippocampal neurogenesis is sufficient to improve cognition and mood. Here we show that inducible genetic expansion of the population of adult-born neurons by enhancing their survival improves performance in a specific cognitive task in which an animal must distinguish between two similar contexts. Mice with increased adult hippocampal neurogenesis show normal object recognition, spatial learning, contextual fear conditioning and extinction learning but are more efficient in differentiating between overlapping contextual representations, suggestive of enhanced pattern separation. Furthermore, stimulation of adult hippocampal neurogenesis, when combined with an intervention such as voluntary exercise, produces a robust increase in exploratory behaviour. In contrast, increasing adult hippocampal neurogenesis, on its own, does not produce an anxiolytic or antidepressant-like behavioural response. Together, our findings suggest that strategies designed to specifically increase adult hippocampal neurogenesis, by targeting cell death of adult-born neurons or other means, may have therapeutic potential for reversing impairments in pattern separation such as that seen during normal aging 14, 15.

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          Most cited references30

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          Neural consequences of environmental enrichment.

          Neuronal plasticity is a central theme of modern neurobiology, from cellular and molecular mechanisms of synapse formation in Drosophila to behavioural recovery from strokes in elderly humans. Although the methods used to measure plastic responses differ, the stimuli required to elicit plasticity are thought to be activity-dependent. In this article, we focus on the neuronal changes that occur in response to complex stimulation by an enriched environment. We emphasize the behavioural and neurobiological consequences of specific elements of enrichment, especially exercise and learning.
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            Neurogenesis-dependent and -independent effects of fluoxetine in an animal model of anxiety/depression.

            Understanding the physiopathology of affective disorders and their treatment relies on the availability of experimental models that accurately mimic aspects of the disease. Here we describe a mouse model of an anxiety/depressive-like state induced by chronic corticosterone treatment. Furthermore, chronic antidepressant treatment reversed the behavioral dysfunctions and the inhibition of hippocampal neurogenesis induced by corticosterone treatment. In corticosterone-treated mice where hippocampal neurogenesis is abolished by X-irradiation, the efficacy of fluoxetine is blocked in some, but not all, behavioral paradigms, suggesting both neurogenesis-dependent and -independent mechanisms of antidepressant action. Finally, we identified a number of candidate genes, the expression of which is decreased by chronic corticosterone and normalized by chronic fluoxetine treatment selectively in the hypothalamus. Importantly, mice deficient in one of these genes, beta-arrestin 2, displayed a reduced response to fluoxetine in multiple tasks, suggesting that beta-arrestin signaling is necessary for the antidepressant effects of fluoxetine.
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              Distinct morphological stages of dentate granule neuron maturation in the adult mouse hippocampus.

              Adult neurogenesis in the dentate gyrus may contribute to hippocampus-dependent functions, yet little is known about when and how newborn neurons are functional because of limited information about the time course of their connectivity. By using retrovirus-mediated gene transduction, we followed the dendritic and axonal growth of adult-born neurons in the mouse dentate gyrus and identified distinct morphological stages that may indicate different levels of connectivity. Axonal projections of newborn neurons reach the CA3 area 10-11 d after viral infection, 5-6 d before the first spines are formed. Quantitative analyses show that the peak of spine growth occurs during the first 3-4 weeks, but further structural modifications of newborn neurons take place for months. Moreover, the morphological maturation is differentially affected by age and experience, as shown by comparisons between adult and postnatal brains and between housing conditions. Our study reveals the key morphological transitions of newborn granule neurons during their course of maturation.
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                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                0028-0836
                1476-4687
                18 January 2011
                3 April 2011
                28 April 2011
                28 October 2011
                : 472
                : 7344
                : 466-470
                Affiliations
                [1 ] Departments of Neuroscience and Psychiatry, Columbia University
                [2 ] Department of Pharmacology, Columbia University
                [3 ] Division of Integrative Neuroscience, New York 10025, USA
                [4 ] The New York State Psychiatric Institute, New York 10025, USA
                [5 ] The Robert F. Furchgott Center for Neural and Behavioural Science, Departments of Physiology and Pharmacology and Neurology, State University of New York, Downstate Medical Center, New York 11203, USA
                Author notes
                Correspondence and requests for materials should be addressed to A.S. ( as2619@ 123456columbia.edu ) or R.H. ( rh95@ 123456columbia.edu )
                Article
                nihpa263528
                10.1038/nature09817
                3084370
                21460835
                a26fcc2a-89f0-465b-a16f-d288528d63f7

                Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms

                History
                Funding
                Funded by: National Institute of Mental Health : NIMH
                Award ID: R01 MH091844-03 ||MH
                Funded by: National Institute of Mental Health : NIMH
                Award ID: R01 MH091844-02 ||MH
                Funded by: National Institute of Mental Health : NIMH
                Award ID: R01 MH091844-01 ||MH
                Funded by: National Institute of Mental Health : NIMH
                Award ID: K99 MH086615-02 ||MH
                Funded by: National Institute of Mental Health : NIMH
                Award ID: K08 MH079088-05 ||MH
                Funded by: National Institute of Mental Health : NIMH
                Award ID: K08 MH079088-04 ||MH
                Funded by: National Institute of Mental Health : NIMH
                Award ID: K08 MH079088-03S1 ||MH
                Funded by: National Institute of Mental Health : NIMH
                Award ID: K08 MH079088-03 ||MH
                Funded by: National Institute of Mental Health : NIMH
                Award ID: K08 MH079088-02 ||MH
                Funded by: National Institute of Mental Health : NIMH
                Award ID: K08 MH079088-01 ||MH
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