Cellular and Synaptic Dysfunctions in Parkinson's Disease: Stepping out of the Striatum

Cells. 2019 Aug 29;8(9):1005. doi: 10.3390/cells8091005.

Abstract

The basal ganglia (BG) are a collection of interconnected subcortical nuclei that participate in a great variety of functions, ranging from motor programming and execution to procedural learning, cognition, and emotions. This network is also the region primarily affected by the degeneration of midbrain dopaminergic neurons localized in the substantia nigra pars compacta (SNc). This degeneration causes cellular and synaptic dysfunctions in the BG network, which are responsible for the appearance of the motor symptoms of Parkinson's disease. Dopamine (DA) modulation and the consequences of its loss on the striatal microcircuit have been extensively studied, and because of the discrete nature of DA innervation of other BG nuclei, its action outside the striatum has been considered negligible. However, there is a growing body of evidence supporting functional extrastriatal DA modulation of both cellular excitability and synaptic transmission. In this review, the functional relevance of DA modulation outside the striatum in both normal and pathological conditions will be discussed.

Keywords: GABAergic transmission; Globus pallidus; dopamine; neuronal excitability; neuronal oscillations; pacemaking; substantia nigra; subthalamic nucleus.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Dopamine / metabolism*
  • Dopaminergic Neurons / metabolism*
  • Dopaminergic Neurons / pathology
  • Globus Pallidus / metabolism*
  • Globus Pallidus / pathology
  • Humans
  • Parkinson Disease / metabolism*
  • Parkinson Disease / pathology
  • Substantia Nigra / metabolism*
  • Substantia Nigra / pathology
  • Synaptic Transmission*

Substances

  • Dopamine