Vlamings R, Visser-Vandewalle V, Koopmans G, Joosten E A J, Kozan R, Kaplan S, Steinbusch H W M, Temel Y
Department of Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands.
Neuroscience. 2007 Sep 7;148(3):815-23. doi: 10.1016/j.neuroscience.2007.06.043. Epub 2007 Jul 17.
The subthalamic nucleus (STN) plays an important role in motor and non-motor behavior in Parkinson's disease, but its involvement in gait functions is largely unknown. In this study, we investigated the role of the STN on gait in a rat model of PD using the CatWalk method. Parkinsonian rats received bilateral high frequency stimulation (HFS) with different stimulation amplitudes of the STN. Rats were rendered parkinsonian by bilateral injections of 6-hydroxydopamine (6-OHDA) into the striatum. One group of 6-OHDA animals was implanted bilaterally with stimulation electrodes at the level of the STN. Stimulations were performed at 130 Hz (frequency), 60 micros (pulse width) and varying amplitudes of 0, 3, 30 and 150 microA. Rats were evaluated in an automated quantitative gait analysis method (CatWalk method). After behavioral evaluations, rats were killed and the brains processed for histological stainings to determine the impact of the dopaminergic lesion (tyrosine hydroxylase immunohistochemistry) and the localization of the electrode tip (hematoxylin-eosin histochemistry). Results show that bilateral 6-OHDA infusion significantly decreased (70%) the number of dopaminergic cells in the substantia nigra pars compacta (SNc). Due to 6-OHDA treatment, the gait parameters changed considerably. There was a general slowness. The most pronounced effects were seen at the level of the hind paws. Due to implantation of STN electrodes the step pattern changed. STN electrical stimulation improved the general slowness but induced slowing of the forelimb movement. Furthermore, we found that HFS with a medium amplitude significantly changed speed, the so-called dynamic aspect of gait. The static features of gait were only significantly influenced with low amplitude. Remarkably, STN stimulation affected predominantly the forepaws/limbs.
丘脑底核(STN)在帕金森病的运动和非运动行为中起着重要作用,但其在步态功能中的作用在很大程度上尚不清楚。在本研究中,我们使用CatWalk方法在帕金森病大鼠模型中研究了STN对步态的作用。帕金森病大鼠接受了不同刺激幅度的双侧高频刺激(HFS)。通过向纹状体双侧注射6-羟基多巴胺(6-OHDA)使大鼠患帕金森病。一组6-OHDA动物双侧植入STN水平的刺激电极。刺激频率为130Hz,脉冲宽度为60微秒,幅度分别为0、3、30和150微安。采用自动定量步态分析方法(CatWalk方法)对大鼠进行评估。行为评估后,处死大鼠,对大脑进行组织学染色,以确定多巴胺能损伤的影响(酪氨酸羟化酶免疫组织化学)和电极尖端的定位(苏木精-伊红组织化学)。结果显示,双侧注射6-OHDA显著减少了黑质致密部(SNc)中多巴胺能细胞的数量(70%)。由于6-OHDA治疗,步态参数发生了显著变化。普遍出现行动迟缓。在后爪水平观察到最明显的影响。由于植入了STN电极,步幅模式发生了变化。STN电刺激改善了普遍的行动迟缓,但导致前肢运动减慢。此外,我们发现中等幅度的高频刺激显著改变了速度,即步态的所谓动态方面。步态的静态特征仅在低幅度刺激时受到显著影响。值得注意的是,STN刺激主要影响前爪/前肢。