Weinberger Moran, Mahant Neil, Hutchison William D, Lozano Andres M, Moro Elena, Hodaie Mojgan, Lang Anthony E, Dostrovsky Jonathan O
Department of Physiology, Med Sci Building 3302, 1 King's College Circle, University of Toronto, Toronto, Ontario M5S 1A8, Canada.
J Neurophysiol. 2006 Dec;96(6):3248-56. doi: 10.1152/jn.00697.2006. Epub 2006 Sep 27.
Recent studies suggest that beta (15-30 Hz) oscillatory activity in the subthalamic nucleus (STN) is dramatically increased in Parkinson's disease (PD) and may interfere with movement execution. Dopaminergic medications decrease beta activity and deep brain stimulation (DBS) in the STN may alleviate PD symptoms by disrupting this oscillatory activity. Depth recordings from PD patients have demonstrated beta oscillatory neuronal and local field potential (LFP) activity in STN, although its prevalence and relationship to neuronal activity are unclear. In this study, we recorded both LFP and neuronal spike activity from the STN in 14 PD patients during functional neurosurgery. Of 200 single- and multiunit recordings 56 showed significant oscillatory activity at about 26 Hz and 89% of these were coherent with the simultaneously recorded LFP. The incidence of neuronal beta oscillatory activity was significantly higher in the dorsal STN (P = 0.01) and corresponds to the significantly increased LFP beta power recorded in the same region. Of particular interest was a significant positive correlation between the incidence of oscillatory neurons and the patient's benefit from dopaminergic medications, but not with baseline motor deficits off medication. These findings suggest that the degree of neuronal beta oscillatory activity is related to the magnitude of the response of the basal ganglia to dopaminergic agents rather than directly to the motor symptoms of PD. The study also suggests that LFP beta oscillatory activity is generated largely within the dorsal portion of the STN and can produce synchronous oscillatory activity of the local neuronal population.
近期研究表明,帕金森病(PD)患者丘脑底核(STN)中的β(15 - 30Hz)振荡活动显著增强,可能会干扰运动执行。多巴胺能药物可降低β活动,而STN深部脑刺激(DBS)可能通过破坏这种振荡活动来缓解PD症状。PD患者的深度记录显示STN中存在β振荡神经元和局部场电位(LFP)活动,但其发生率以及与神经元活动的关系尚不清楚。在本研究中,我们在功能神经外科手术期间记录了14例PD患者STN的LFP和神经元放电活动。在200次单单位和多单位记录中,56次显示在约26Hz处有显著振荡活动,其中89%与同时记录的LFP相干。背侧STN中神经元β振荡活动的发生率显著更高(P = 0.01),且与同一区域记录到的LFPβ功率显著增加相对应。特别值得关注的是,振荡神经元的发生率与患者从多巴胺能药物中获得的益处之间存在显著正相关,但与未用药时的基线运动缺陷无关。这些发现表明,神经元β振荡活动的程度与基底神经节对多巴胺能药物的反应强度有关,而非直接与PD的运动症状相关。该研究还表明,LFPβ振荡活动主要在STN的背侧部分产生,并可产生局部神经元群体的同步振荡活动。