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  • Oral presentation
  • Open Access

Synchronization of the parkinsonian globus pallidus by gap junctions

  • 1, 2Email author,
  • 1,
  • 2, 3 and
  • 1
BMC Neuroscience201415 (Suppl 1) :O17

https://doi.org/10.1186/1471-2202-15-S1-O17

  • Published:

Keywords

  • Globus Pallidus
  • Electrical Coupling
  • Dopamine Depletion
  • Synaptic Coupling
  • External Globus Pallidus

The mechanisms for the emergence and transmission of synchronized oscillations in Parkinson’s disease (PD) still remain debated. In a previous publication [1], we argue that the external globus pallidus (GPe) has a crucial role in desynchronising and synchronizing the basal ganglia. While neural activity of the healthy GPe shows almost no correlations between pairs of neurons, prominent synchronization in the β frequency band arises after dopamine depletion. Intrinsic factors of the GPe, in particular its internal connections, could be take major roles in this synchronisation process.

We introduce pallidal gap junctional coupling as a possible mechanism for synchronization of the GPe after dopamine depletion. In a confocal imaging study, we show the presence of the neural gap junction protein Cx36 in the human GPe, including a possible remodeling process in PD patients. Dopamine has been shown to down-regulate the conductance of gap junctions in different regions of the brain [2, 3], making dopamine depletion a possible candidate for increased influence of gap junctional coupling in PD.

To see what effect electrical coupling in the GPe could have, we incorporate gap junctions in a small conductance-based model of the basal ganglia. In both GPe and GPi, gap junctional coupling has clear effects on synchrony. Especially numerous coupling with sufficient strength in the GPe is able to synchronize the whole basal ganglia. Next, we focus on dynamics inside the GPe. Phase-response curve analysis is used to describe the susceptibility of GPe neurons to synchronize with input, depending on electrical coupling to other GPe neurons. Additionally, we simulate the effect of gap junctions on synchrony in a larger network of the GPe, including biologically realistic cell models and inhibitory synaptic coupling.

Conclusions

We hypothesize that strong gap junctional coupling in the GPe disturbs the self-desynchronization in this nucleus and leads to long-range synchronization. Pallidal gap junctions, which are potentially modulated by dopamine, could be a powerful trigger of synchrony in Parkinson's disease. We stress that also gap junctions in other nuclei such as the striatum may play important roles.

Authors’ Affiliations

(1)
Applied Analysis, MIRA Institute of Biomedical Technology and Technical Medicine, University of Twente, 7500AE Enschede, The Netherlands
(2)
Biomedical Signals and Systems, MIRA Institute of Biomedical Technology and Technical Medicine, University of Twente, 7500AE Enschede, The Netherlands
(3)
Biophysics, Donders Institute for Brain, Cognition and Behavior, Radboud University, Nijmegen, The Netherlands

References

  1. Schwab BC, Heida T, Zhao Y, Marani E, van Gils SA, van Wezel RJA: Synchrony in Parkinson's disease: Importance of intrinsic properties of the external pallidal segment. Front Syst Neurosci. 2013, 7 (60): 1-7. 10.3389/fnsys.2013.00060.Google Scholar
  2. McHahon DG, Knapp AG, Dowling JE: Horizontal cell gap junctions: single-channel conductance and modulation by dopamine. Proceedings of the National Academy of Sciences. 1989, 86 (19): 7639-7643. .View ArticleGoogle Scholar
  3. Onn SP, Grace AA: Alterations in electrophysiological activity and dye coupling of striatal spiny and aspiny neurons in dopamine-denervated rat striatum recorded in vivo. Synapse. 1999, 33 (1): 1-15. .View ArticlePubMedGoogle Scholar

Copyright

© Schwab et al; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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