4.4 Article

Propagation of beta/gamma rhythms in the cortico-basal ganglia circuits of the parkinsonian rat

Journal

JOURNAL OF NEUROPHYSIOLOGY
Volume 119, Issue 5, Pages 1608-1628

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/jn.00629.2017

Keywords

basal ganglia; connectivity; local field potential; Parkinson's disease; synchronization

Funding

  1. Medical Research Council UK [UU138197109, MC_UU_12020/5, MC_UU_12024/2, MC_UU_21024/1]
  2. Parkinson's UK [G-0806]
  3. Engineering Research Council UK [EPSRC EP/F500351/1, EP/N007050/1]
  4. University College London Hospitals Biomedical Research Centre
  5. Wellcome Trust [539208]
  6. MRC [MC_UU_12024/1, MC_UU_12024/2, MC_UU_12020/5] Funding Source: UKRI

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Much of the motor impairment associated with Parkinson's disease is thought to arise from pathological activity in the networks formed by the basal ganglia (BG) and motor cortex. To evaluate several hypotheses proposed to explain the emergence of pathological oscillations in parkinsonism, we investigated changes to the directed connectivity in BG networks following dopamine depletion. We recorded local field potentials (LFPs) in the cortex and basal ganglia of rats rendered parkinsonian by injection of 6-hydroxydopamine (6-OHDA) and in dopamine-intact controls. We performed systematic analyses of the networks using a novel tool for estimation of directed interactions (nonparametric directionality, NPD). We used a conditioned version of the NPD analysis that reveals the dependence of the correlation between two signals on a third reference signal. We find evidence of the dopamine dependency of both low-beta (14-20 Hz) and high-beta/low-gamma (20-40 Hz) directed network interactions. Notably, 6-OHDA lesions were associated with enhancement of the cortical hyperdirect connection to the subthalamic nucleus (STN) and its feedback to the cortex and striatum. We find that pathological beta synchronization resulting from 6-OHDA lesioning is widely distributed across the network and cannot be located to any individual structure. Furthermore, we provide evidence that high-beta/gamma oscillations propagate through the striatum in a pathway that is independent of STN. Rhythms at high beta/gamma show susceptibility to conditioning that indicates a hierarchical organization compared with those at low beta. These results further inform our understanding of the substrates for pathological rhythms in salient brain networks in parkinsonism. NEW & NOTEWORTHY We present a novel analysis of electrophysiological recordings in the cortico-basal ganglia network with the aim of evaluating several hypotheses concerning the origins of abnormal brain rhythms associated with Parkinson's disease. We present. evidence for changes in the directed connections within the network may arise.

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