Yamamoto T, Uchiyama T, Sakakibara R, Taniguchi J, Kuwabara S
Department of Neurology, Chiba University Graduate School of Medicine, Chiba, Japan.
Department of Neurology, Chiba University Graduate School of Medicine, Chiba, Japan.
Neuroscience. 2014 Feb 14;259:43-52. doi: 10.1016/j.neuroscience.2013.11.034. Epub 2013 Nov 27.
Not all the mechanisms by which subthalamic nucleus deep brain stimulation (STN-DBS) alleviates parkinsonian symptoms have been clarified as yet. The levels of striatal monoamine and the subthalamic beta activity might contribute to its efficacy. However, their direct relationship is unclear. We aimed to examine the correlation between the striatal monoamine and the STN beta activity induced by STN-DBS.
Experiments were performed under urethane anesthesia in normal (n=4) and 6-hydroxydopamine hemi-lesioned Parkinson's disease (PD) model rats (n=5). STN-DBS was applied to the left STN, and local field potential (LFP) was recorded before and after STN-DBS. Striatal extracellular fluid was collected before, during, and after STN-DBS. Spectral analysis of STN-LFP was performed, and the levels of monoamine were measured.
The levels of 3-4-dihydroxyphenylacetic acid (DOPAC) were significantly decreased after the cessation of stimulation in PD model rats. The levels of none of the monoamines were significantly affected in normal rats. The STN beta power was significantly elevated after the cessation of stimulation in normal rats but was significantly decreased in PD model rats. The STN beta power and the levels of DOPAC and 5-HT was positively correlated in PD model rats, whereas the levels of dopamine and 5-HT showed positive correlation and the levels of DOPAC and Homovanillic acid (HVA) showed negative correlation in normal rats.
STN-DBS could decrease the levels of DOPAC and the STN beta power in a PD model rat. The STN beta power and the levels of striatal monoamine might be differentially correlated between normal and PD model rats.
丘脑底核深部脑刺激(STN-DBS)缓解帕金森症状的所有机制尚未完全阐明。纹状体单胺水平和丘脑底核β活性可能对其疗效有影响。然而,它们之间的直接关系尚不清楚。我们旨在研究STN-DBS诱导的纹状体单胺与丘脑底核β活性之间的相关性。
实验在乌拉坦麻醉下对正常大鼠(n = 4)和6-羟基多巴胺半侧损伤的帕金森病(PD)模型大鼠(n = 5)进行。将STN-DBS应用于左侧丘脑底核,并在STN-DBS前后记录局部场电位(LFP)。在STN-DBS前、中、后收集纹状体细胞外液。对STN-LFP进行频谱分析,并测量单胺水平。
在PD模型大鼠中,刺激停止后3,4-二羟基苯乙酸(DOPAC)水平显著降低。正常大鼠中,单胺水平均未受到显著影响。在正常大鼠中,刺激停止后丘脑底核β功率显著升高,而在PD模型大鼠中则显著降低。在PD模型大鼠中,丘脑底核β功率与DOPAC和5-羟色胺(5-HT)水平呈正相关,而在正常大鼠中,多巴胺和5-HT水平呈正相关,DOPAC和高香草酸(HVA)水平呈负相关。
STN-DBS可降低PD模型大鼠的DOPAC水平和丘脑底核β功率。正常大鼠和PD模型大鼠中,丘脑底核β功率与纹状体单胺水平的相关性可能存在差异。