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      Long-Lasting Visuo-Vestibular Mismatch in Freely-Behaving Mice Reduces the Vestibulo-Ocular Reflex and Leads to Neural Changes in the Direct Vestibular Pathway

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          Abstract

          Calibration of the vestibulo-ocular reflex (VOR) depends on the presence of visual feedback. However, the cellular mechanisms associated with VOR modifications at the level of the brainstem remain largely unknown. A new protocol was designed to expose freely behaving mice to a visuo-vestibular mismatch during a 2-week period. This protocol induced a 50% reduction of the VOR. In vivo pharmacological experiments demonstrated that the VOR reduction depends on changes located outside the flocculus/paraflocculus complex. The cellular mechanisms associated with the VOR reduction were then studied in vitro on brainstem slices through a combination of vestibular afferent stimulation and patch-clamp recordings of central vestibular neurons. The evoked synaptic activity demonstrated that the efficacy of the synapses between vestibular afferents and central vestibular neurons was decreased. In addition, a long-term depression protocol failed to further decrease the synapse efficacy, suggesting that the VOR reduction might have occurred through depression-like mechanisms. Analysis of the intrinsic membrane properties of central vestibular neurons revealed that the synaptic changes were supplemented by a decrease in the spontaneous discharge and excitability of a subpopulation of neurons. Our results provide evidence that a long-lasting visuo-vestibular mismatch leads to changes in synaptic transmission and intrinsic properties of central vestibular neurons in the direct VOR pathway. Overall, these results open new avenues for future studies on visual and vestibular interactions conducted in vivo and in vitro.

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          A theory of cerebellar cortex.

          D. Marr (1969)
          1. A detailed theory of cerebellar cortex is proposed whose consequence is that the cerebellum learns to perform motor skills. Two forms of input-output relation are described, both consistent with the cortical theory. One is suitable for learning movements (actions), and the other for learning to maintain posture and balance (maintenance reflexes).2. It is known that the cells of the inferior olive and the cerebellar Purkinje cells have a special one-to-one relationship induced by the climbing fibre input. For learning actions, it is assumed that:(a) each olivary cell responds to a cerebral instruction for an elemental movement. Any action has a defining representation in terms of elemental movements, and this representation has a neural expression as a sequence of firing patterns in the inferior olive; and(b) in the correct state of the nervous system, a Purkinje cell can initiate the elemental movement to which its corresponding olivary cell responds.3. Whenever an olivary cell fires, it sends an impulse (via the climbing fibre input) to its corresponding Purkinje cell. This Purkinje cell is also exposed (via the mossy fibre input) to information about the context in which its olivary cell fired; and it is shown how, during rehearsal of an action, each Purkinje cell can learn to recognize such contexts. Later, when the action has been learnt, occurrence of the context alone is enough to fire the Purkinje cell, which then causes the next elemental movement. The action thus progresses as it did during rehearsal.4. It is shown that an interpretation of cerebellar cortex as a structure which allows each Purkinje cell to learn a number of contexts is consistent both with the distributions of the various types of cell, and with their known excitatory or inhibitory natures. It is demonstrated that the mossy fibre-granule cell arrangement provides the required pattern discrimination capability.5. The following predictions are made.(a) The synapses from parallel fibres to Purkinje cells are facilitated by the conjunction of presynaptic and climbing fibre (or post-synaptic) activity.(b) No other cerebellar synapses are modifiable.(c) Golgi cells are driven by the greater of the inputs from their upper and lower dendritic fields.6. For learning maintenance reflexes, 2(a) and 2(b) are replaced by2'. Each olivary cell is stimulated by one or more receptors, all of whose activities are usually reduced by the results of stimulating the corresponding Purkinje cell.7. It is shown that if (2') is satisfied, the circuit receptor --> olivary cell --> Purkinje cell --> effector may be regarded as a stabilizing reflex circuit which is activated by learned mossy fibre inputs. This type of reflex has been called a learned conditional reflex, and it is shown how such reflexes can solve problems of maintaining posture and balance.8. 5(a), and either (2) or (2') are essential to the theory: 5(b) and 5(c) are not absolutely essential, and parts of the theory could survive the disproof of either.
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            A theory of cerebellar function

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              Beyond parallel fiber LTD: the diversity of synaptic and non-synaptic plasticity in the cerebellum.

              In recent years, it has become clear that motor learning, as revealed by associative eyelid conditioning and adaptation of the vestibulo-ocular reflex, contributes to the well-established cerebellar functions of sensorimotor integration and control. Long-term depression of the parallel fiber-Purkinje cell synapse (which is often called 'cerebellar LTD') is a cellular phenomenon that has been suggested to underlie these forms of learning. However, it is clear that parallel fiber LTD, by itself, cannot account for all the properties of cerebellar motor learning. Here we review recent electrophysiological experiments that have described a rich variety of use-dependent plasticity in cerebellum, including long-term potentiation (LTP) and LTD of excitatory and inhibitory synapses, and persistent modulation of intrinsic neuronal excitability. Finally, using associative eyelid conditioning as an example, we propose some ideas about how these cellular phenomena might function and interact to endow the cerebellar circuit with particular computational and mnemonic properties.
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                Author and article information

                Journal
                eNeuro
                eNeuro
                eneuro
                eneuro
                eNeuro
                eNeuro
                Society for Neuroscience
                2373-2822
                16 January 2017
                27 February 2017
                Jan-Feb 2017
                : 4
                : 1
                : ENEURO.0290-16.2017
                Affiliations
                [1 ]Center for Neurophysics, Physiology, Pathology, CNRS UMR 8119, Université Paris Descartes , Sorbonne Paris Cité, Paris, France
                [2 ]INRIA Grenoble, Rhône-Alpes, Laboratoire Jean Kuntzmann, UMR 5224 , France
                [3 ]Cognition and Action Group, CNRS UMR 8257, Université Paris Descartes , Sorbonne Paris Cité, Paris, France
                Author notes

                The authors declare no competing financial interests.

                Author contributions: J.C. and M.B. designed research; J.C., F.F.D.B., E.I., D.E., L.R., and M.B. performed research; J.C., F.F.D.B., E.I., L.R., L.E.M., and M.B. analyzed data; J.C., F.F.D.B., E.I., D.E., L.E.M., P.-P.V., and M.B. wrote the paper.

                This research was supported by the Centre National de la Recherche Scientifique and the University Paris Descartes. EI and MB receive support from the Centre National des Etudes Spatiales. JC and MB receive support from the French ANR-13-CESA-0005-02. FFB and MB receive support from the French ANR-15-CE32-0007.

                Correspondence should be addressed to M. Beraneck. Center for Neurophysics, Physiology, Pathology, CNRS UMR 8119, 45 rue des St-Pères 75270, Université Paris Descartes, Paris, France. E-mail: mathieu.beraneck@ 123456parisdescartes.fr .
                Author information
                http://orcid.org/0000-0002-6916-4631
                http://orcid.org/0000-0003-2722-0532
                Article
                eN-NWR-0290-16
                10.1523/ENEURO.0290-16.2017
                5354632
                28303261
                31eade5e-ffd1-46bf-a836-7e8a9208285f
                Copyright © 2017 Carcaud et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 26 September 2016
                : 5 January 2017
                : 10 January 2017
                Page count
                Figures: 7, Tables: 2, Equations: 2, References: 89, Pages: 17, Words: 12710
                Funding
                Funded by: Centre National d'Etudes Spatiales (CNES)
                Award ID: 501100002830
                Award ID: DAR n{degree sign} 4800000860
                Funded by: Centre National de la Recherche Scientifique (CNRS)
                Award ID: 501100004794
                Funded by: Agence Nationale pour la Recherche (ANR)
                Award ID: ANR-13-CESA-0005-02
                Funded by: Université Paris Descartes
                Funded by: Agence National pour le Recherche (ANR)
                Award ID: ANR-15-CE32-0007
                Categories
                5
                New Research
                Integrative Systems
                Custom metadata
                January/February 2017

                multisensory,neuronal excitability,reflex,synaptic plasticity,vestibular neurons,vor

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