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      Action of the Noradrenergic System on Adult-Born Cells Is Required for Olfactory Learning in Mice

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          Abstract

          We have previously shown that an experience-driven improvement in olfactory discrimination (perceptual learning) requires the addition of newborn neurons in the olfactory bulb (OB). Despite this advance, the mechanisms which govern the selective survival of newborn OB neurons following learning remain largely unknown. We propose that activity of the noradrenergic system is a critical mediator providing a top-down signal to control the selective survival of newly born cells and support perceptual learning.

          In adult mice, we used pharmacological means to manipulate the noradrenergic system and neurogenesis and to assess their individual and additive effects on behavioral performance on a perceptual learning task. We then looked at the effects of these manipulations on regional survival of adult-born cells in the OB. Finally, using confocal imaging and electrophysiology, we investigated potential mechanisms by which noradrenaline could directly influence the survival of adult-born cells.

          Consistent with our hypotheses, direct manipulation of noradrenergic transmission significantly effect on adult-born cell survival and perceptual learning. Specifically, learning required both the presence of adult-born cell and noradrenaline. Finally, we provide a mechanistic link between these effects by showing that adult-born neurons receive noradrenergic projections and are responsive to noradrenaline.

          Based upon these data we argue that noradrenergic transmission is a key mechanism selecting adult-born neurons during learning and demonstrate that top-down neuromodulation acts on adult-born neuron survival to modulate learning performance.

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          Author and article information

          Journal
          J Neurosci
          J. Neurosci
          jneuro
          jneurosci
          J. Neurosci
          The Journal of Neuroscience
          Society for Neuroscience
          0270-6474
          1529-2401
          14 March 2012
          : 32
          : 11
          : 3748-3758
          Affiliations
          [1] 1INSERM U1028, CNRS, UMR5292, Lyon Neuroscience Research Center, University Lyon 1, F-69000, France,
          [2] 2Department of Psychiatry, Weill Cornell Medical College, New York, New York 10021, and
          [3] 3Department of Neuroscience, Brown University, Providence, Rhode Island 02912
          Author notes
          Correspondence should be addressed to Nathalie Mandairon, INSERM U1028, CNRS UMR 5292, Lyon Neuroscience Research Center, 50 Avenue Tony Garnier, F-69007 Lyon, France. nathalie.mandairon@ 123456olfac.univ-lyon1.fr

          Author contributions: M.M.M. and N.M. designed research; M.M.M., N.K., J.S., and N.M. performed research; M.M.M., K.B., N.K., A.D., and N.M. analyzed data; M.M., K.B., A.D., and N.M. wrote the paper.

          *K.B. and N.K. contributed equally.

          Article
          PMC6703441 PMC6703441 6703441 3761315
          10.1523/JNEUROSCI.6335-11.2012
          6703441
          22423095
          7c15fe9b-0e2a-4cfe-b117-ab531943cce1
          Copyright © 2012 the authors 0270-6474/12/323748-11$15.00/0
          History
          : 20 December 2011
          : 23 January 2012
          Categories
          Articles
          Behavioral/Systems/Cognitive

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