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Involvement of the Red Nucleus in the Compensation of Parkinsonism may Explain why Primates can develop Stable Parkinson’s Disease

  • Ingrid H.C.H.M. Philippens*
  • , Jacqueline A. Wubben
  • , Sigrid K. Franke
  • , Sam Hofman
  • , Jan A.M. Langermans
  • *Corresponding author for this work
    • Biomedical Primate Research Centre
    • Vrije Universiteit Amsterdam
    • Biomedical Primate Research Centre (BPRC)

    Research output: Contribution to journalArticleAcademicpeer-review

    Abstract

    Neurological compensatory mechanisms help our brain to adjust to neurodegeneration as in Parkinson’s disease. It is suggested that the compensation of the damaged striato-thalamo-cortical circuit is focused on the intact thalamo-rubro-cerebellar pathway as seen during presymptomatic Parkinson, paradoxical movement and sensorimotor rhythm (SMR). Indeed, the size of the red nucleus, connecting the cerebellum with the cerebral cortex, is larger in Parkinson’s disease patients suggesting an increased activation of this brain area. Therefore, the red nucleus was examined in MPTP-induced parkinsonian marmoset monkeys during the presymptomatic stage and after SMR activation by neurofeedback training. We found a reverse significant correlation between the early expression of parkinsonian signs and the size of the parvocellular part of the red nucleus, which is predominantly present in human and non-human primates. In quadrupedal animals it consists mainly of the magnocellular part. Furthermore, SMR activation, that mitigated parkinsonian signs, further increased the size of the red nucleus in the marmoset monkey. This plasticity of the brain helps to compensate for dysfunctional movement control and can be a promising target for compensatory treatment with neurofeedback technology, vibrotactile stimulation or DBS in order to improve the quality of life for Parkinson’s disease patients.

    Original languageEnglish
    Article number880
    JournalScientific Reports
    Volume9
    Issue number1
    DOIs
    Publication statusPublished - 29 Jan 2019

    Funding

    This study was supported by the EU transnational access to the research infrastructure PRIMOCID-205 of EUPRIM-Net under the EU contract 262443 of the 7th Framework Program. SF was supported by the Parkinson Vereniging (grant 2013-R02) and by a joint grant from the BPRC and Neuroscience Campus Amsterdam. We want to thank E. Remarque for the statistical evaluation of the data, F. van Hassel for preparing the figures and illustrations and the Animal Science Department of the BPRC, the veterinarians and animal caretakers specifically, for the excellent EEG surgery and for all the animal experimental support.

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Parkinson's disease

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