Targeted cortical reorganization using optogenetics in non-human primates

Elife. 2018 May 29:7:e31034. doi: 10.7554/eLife.31034.

Abstract

Brain stimulation modulates the excitability of neural circuits and drives neuroplasticity. While the local effects of stimulation have been an active area of investigation, the effects on large-scale networks remain largely unexplored. We studied stimulation-induced changes in network dynamics in two macaques. A large-scale optogenetic interface enabled simultaneous stimulation of excitatory neurons and electrocorticographic recording across primary somatosensory (S1) and motor (M1) cortex (Yazdan-Shahmorad et al., 2016). We tracked two measures of network connectivity, the network response to focal stimulation and the baseline coherence between pairs of electrodes; these were strongly correlated before stimulation. Within minutes, stimulation in S1 or M1 significantly strengthened the gross functional connectivity between these areas. At a finer scale, stimulation led to heterogeneous connectivity changes across the network. These changes reflected the correlations introduced by stimulation-evoked activity, consistent with Hebbian plasticity models. This work extends Hebbian plasticity models to large-scale circuits, with significant implications for stimulation-based neurorehabilitation.

Keywords: functional connectivity; neural stimulation; neuromodulation; neuroscience; non-human primates; optogenetics; plasticity; rhesus macaque.

Publication types

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

MeSH terms

  • Animals
  • Brain Waves / physiology
  • Connectome / methods
  • Dependovirus / genetics
  • Dependovirus / metabolism
  • Electrodes, Implanted
  • Gene Expression
  • Genetic Vectors / chemistry
  • Genetic Vectors / metabolism
  • Macaca mulatta
  • Male
  • Motor Cortex / anatomy & histology
  • Motor Cortex / cytology
  • Motor Cortex / physiology*
  • Nerve Net / anatomy & histology
  • Nerve Net / cytology
  • Nerve Net / physiology*
  • Neuronal Plasticity / physiology*
  • Neurons / cytology
  • Neurons / physiology*
  • Opsins / genetics
  • Opsins / metabolism
  • Optogenetics / methods
  • Somatosensory Cortex / anatomy & histology
  • Somatosensory Cortex / cytology
  • Somatosensory Cortex / physiology*

Substances

  • Opsins