Correlation between cortical beta power and gait speed is suppressed in a parkinsonian model, but restored by therapeutic deep brain stimulation
Correlation between cortical beta power and gait speed is suppressed in a parkinsonian model, but restored by therapeutic deep brain stimulation
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帕金森病模型中皮质β功率和步态速度之间的相关性受到抑制,但通过治疗性深部脑刺激可以恢复
DOI:
10.1016/j.nbd.2018.05.013
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发表时间:
2018
影响因子:
6.1
通讯作者:
A. Dorval
中科院分区:
文献类型:
--
作者:
Christian A. Polar;Rahul Gupta;M. Lehmkuhle;A. Dorval
The motor cortex and subthalamic nucleus (STN) of patients with Parkinson's disease (PD) exhibit abnormally high levels of electrophysiological oscillations in the ~12–35 Hz beta-frequency range. Recent studies have shown that beta is partly carried forward to regulate future motor states in the healthy condition, suggesting that steady state beta power is lower when a sequence of movements occurs in a short period of time, such as during fast gait. However, whether this relationship between beta power and motor states persists upon parkinsonian onset or in response to effective therapy is unclear. Using a 6-hydroxy dopamine (6-OHDA) rat model of PD and a custom-built behavioral and neurophysiological recording system, we aimed to elucidate a better understanding of the mechanisms underlying cortical beta power and PD symptoms. In addition to elevated levels of beta oscillations, we show that parkinsonian onset was accompanied by a decoupling of movement intensity — quantified as gait speed — from cortical beta power. Although subthalamic deep brain stimulation (DBS) reduced general levels of beta oscillations in the cortex of all PD animals, the brain's capacity to regulate steady state levels of beta power as a function of movement intensity was only restored in animals with therapeutic DBS. We propose that, in addition to lowering general levels of cortical beta power, restoring the brain's ability to maintain this inverse relationship is critical for effective symptom suppression.
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影响因子:
14.5
作者:
Levy, R;Ashby, P;Dostrovsky, JO
通讯作者:
Dostrovsky, JO
影响因子:
14.5
作者:
Crowell, Andrea L.;Ryapolova-Webb, Elena S.;Starr, Philip A.
通讯作者:
Starr, Philip A.
影响因子:
16.6
作者:
Pape, Anna-Antonia;Siegel, Markus
通讯作者:
Siegel, Markus
DOI:
10.1016/j.clinph.2017.08.028
发表时间:
2017-11
期刊:
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
影响因子:
--
作者:
Neumann WJ;Staub-Bartelt F;Horn A;Schanda J;Schneider GH;Brown P;Kühn AA
通讯作者:
Kühn AA
DOI:
10.1073/pnas.97.4.1867
发表时间:
2000-02-15
影响因子:
11.1
作者:
Kopell, N;Ermentrout, GB;Traub, RD
通讯作者:
Traub, RD