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The Emergence of a Stable Neuronal Ensemble from a Wider Pool of Activated Neurons in the Dorsal Medial Prefrontal Cortex during Appetitive Learning in Mice.
Brebner, Leonie S; Ziminski, Joseph J; Margetts-Smith, Gabriella; Sieburg, Meike C; Reeve, Hayley M; Nowotny, Thomas; Hirrlinger, Johannes; Heintz, Tristan G; Lagnado, Leon; Kato, Shigeki; Kobayashi, Kazuto; Ramsey, Leslie A; Hall, Catherine N; Crombag, Hans S; Koya, Eisuke.
Afiliação
  • Brebner LS; Sussex Neuroscience, School of Psychology, University of Sussex, Falmer, BN1 9QG, United Kingdom.
  • Ziminski JJ; Sussex Neuroscience, School of Psychology, University of Sussex, Falmer, BN1 9QG, United Kingdom.
  • Margetts-Smith G; Sussex Neuroscience, School of Psychology, University of Sussex, Falmer, BN1 9QG, United Kingdom.
  • Sieburg MC; Sussex Neuroscience, School of Psychology, University of Sussex, Falmer, BN1 9QG, United Kingdom.
  • Reeve HM; Sussex Neuroscience, School of Psychology, University of Sussex, Falmer, BN1 9QG, United Kingdom.
  • Nowotny T; Sussex Neuroscience, School of Engineering and Informatics, University of Sussex, Falmer, BN1 9QJ, United Kingdom.
  • Hirrlinger J; Carl-Ludwig-Institute for Physiology, University of Leipzig, D-04103, Leipzig, Germany, and Department of Neurogenetics, Max-Planck-Institute for Experimental Medicine, D-37075, Göttingen, Germany.
  • Heintz TG; Sussex Neuroscience, School of Life Sciences, University of Sussex, Falmer, BN1 9QG, United Kingdom.
  • Lagnado L; Sussex Neuroscience, School of Life Sciences, University of Sussex, Falmer, BN1 9QG, United Kingdom.
  • Kato S; Department of Molecular Genetics, Institute of Biomedical Sciences, Fukushima Medical University School of Medicine, Fukushima 960-1295, Japan, and.
  • Kobayashi K; Department of Molecular Genetics, Institute of Biomedical Sciences, Fukushima Medical University School of Medicine, Fukushima 960-1295, Japan, and.
  • Ramsey LA; Behavioral Neuroscience Branch, Intramural Research Program/National Institute on Drug Abuse/National Institutes of Health/Department of Health and Human Services, Baltimore, Maryland 21224.
  • Hall CN; Sussex Neuroscience, School of Psychology, University of Sussex, Falmer, BN1 9QG, United Kingdom.
  • Crombag HS; Sussex Neuroscience, School of Psychology, University of Sussex, Falmer, BN1 9QG, United Kingdom.
  • Koya E; Sussex Neuroscience, School of Psychology, University of Sussex, Falmer, BN1 9QG, United Kingdom, e.koya@sussex.ac.uk.
J Neurosci ; 40(2): 395-410, 2020 01 08.
Article em En | MEDLINE | ID: mdl-31727794
Animals selectively respond to environmental cues associated with food reward to optimize nutrient intake. Such appetitive conditioned stimulus-unconditioned stimulus (CS-US) associations are thought to be encoded in select, stable neuronal populations or neuronal ensembles, which undergo physiological modifications during appetitive conditioning. These ensembles in the medial prefrontal cortex (mPFC) control well-established, cue-evoked food seeking, but the mechanisms involved in the genesis of these ensembles are unclear. Here, we used male Fos-GFP mice that express green fluorescent protein (GFP) in recently behaviorally activated neurons, to reveal how dorsal mPFC neurons are recruited and modified to encode CS-US memory representations using an appetitive conditioning task. In the initial conditioning session, animals did not exhibit discriminated, cue-selective food seeking, but did so in later sessions indicating that a CS-US association was established. Using microprism-based in vivo 2-Photon imaging, we revealed that only a minority of neurons activated during the initial session was consistently activated throughout subsequent conditioning sessions and during cue-evoked memory recall. Notably, using ex vivo electrophysiology, we found that neurons activated following the initial session exhibited transient hyperexcitability. Chemogenetically enhancing the excitability of these neurons throughout subsequent conditioning sessions interfered with the development of reliable cue-selective food seeking, indicated by persistent, nondiscriminated performance. We demonstrate how appetitive learning consistently activates a subset of neurons to form a stable neuronal ensemble during the formation of a CS-US association. This ensemble may arise from a pool of hyperexcitable neurons activated during the initial conditioning session.SIGNIFICANCE STATEMENT Appetitive conditioning endows cues associated with food with the ability to guide food-seeking, through the formation of a food-cue association. Neuronal ensembles in the mPFC control established cue-evoked food-seeking. However, how neurons undergo physiological modifications and become part of an ensemble during conditioning remain unclear. We found that only a minority of dorsal mPFC neurons activated on the initial conditioning session became consistently activated during conditioning and memory recall. These initially activated neurons were also transiently hyperexcitable. We demonstrate the following: (1) how stable neuronal ensemble formation in the dorsal mPFC underlies appetitive conditioning; and (2) how this ensemble may arise from hyperexcitable neurons activated before the establishment of cue-evoked food seeking.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Comportamento Apetitivo / Rememoração Mental / Córtex Pré-Frontal / Neurônios Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Comportamento Apetitivo / Rememoração Mental / Córtex Pré-Frontal / Neurônios Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article