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Spike and Local Field Synchronization Between the Pedunculopontine Nucleus and Primary Motor Cortex in a Rat Model of Parkinson's Disease.

Authors :
Geng, Xiwen
Wang, Xuenan
He, Feng
Zhang, Xiao
Xie, Jinlu
Gao, Guangheng
Han, Hongyu
Yao, Xiaomeng
Zhang, Haiyan
Gao, Yunfeng
Wang, Yanan
Wang, Min
Source :
Neuroscience. Apr2019, Vol. 404, p470-483. 14p.
Publication Year :
2019

Abstract

Abstract The pedunculopontine nucleus (PPN) shows altered electrophysiological and anatomic characteristics in Parkinson's disease (PD), but little is known about the effect of 6-hydroxydopamine (6-OHDA) lesion and levodopa (L -DOPA) therapy on the relationship between spike and local field potential (LFP) activities in the PPN and motor cortex. Aiming to investigate this, synchronous spike and LFP signals in the PPN and primary motor cortex (M1) were recorded. The spike–LFP relationship was evaluated using coherence analysis, phase-lock and spike-field coherence (SFC). The results suggested that 6-OHDA lesion had a significant effect on the spike–LFP relationship between the PPN and M1 in rats under a rest or locomotion state. The significantly altered frequency bands varied across different neuron types and animal activity states. In addition, the altered coherence values between PPN spike and M1 LFP were refractory to long-term L -DOPA therapy although all other changes could be reversed by this drug treatment. All results provided evidence of the spike–LFP relationship between the PPN and M1 in PD, revealing some network mechanisms of the cortico-basal ganglia circuitry and PPN, which might be an underlying candidate for PD pathophysiology and therapy. Highlights • 6-OHDA lesion in SNc had effect on spike–LFP coherence between PPN and M1 in rats. • Distinct neuron types in PPN and M1 showed different spike–LFP coherence alteration. • In spike–LFP coherency between PPN and M1, L -DOPA has a therapeutic limitation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03064522
Volume :
404
Database :
Academic Search Index
Journal :
Neuroscience
Publication Type :
Academic Journal
Accession number :
135686313
Full Text :
https://doi.org/10.1016/j.neuroscience.2019.01.044