Jackson Jesse, Young Calvin K, Hu Bin, Bland Brian H
Department of Psychology, Behavioral Neuroscience Research Group, The University of Calgary, Calgary, Alberta, Canada T2N 1N4.
Exp Neurol. 2008 Sep;213(1):210-9. doi: 10.1016/j.expneurol.2008.06.007. Epub 2008 Jun 18.
Deep brain stimulation (DBS) of the subthalamic nucleus has been used extensively in the treatment of Parkinson's disease. However, the efficacy of such treatments on bradykinesia/akinesia remains low. DBS of the posterior hypothalamic nucleus (PH) elicits spontaneous, non-stereotypical motor behaviours. We tested the hypothesis that PH stimulation could restore movement in animals made cataleptic by the D(2) receptor antagonist haloperidol. We further hypothesized that hippocampal-striatal neural synchrony may be important in the organization of motor behaviours. Animals chronically implanted with hippocampal and striatal recording electrodes and PH stimulating electrode were tested in open field, catalepsy and active avoidance paradigms. The degree of hippocampal-striatal theta (5-10 Hz) field coherence was assessed during baseline avoidance testing and following the administration of haloperidol. Haloperidol abolished movement in open field and active avoidance tasks and increased the latency to respond in the catalepsy test. Stimulation of the PH under haloperidol reversed catalepsy. Hippocampal-striatal theta coherence was high throughout the active avoidance task in control experiments but was greatly reduced under haloperidol. PH stimulation was able to reinstate the hippocampal-striatal theta coherence while restoring task-related behaviours. These results support the hypothesis that DBS of the PH could restore motor behaviours in rats made cataleptic with haloperidol, thus providing strong support for the PH as a promising candidate for DBS in the treatment of Parkinson's disease. Furthermore, the results support the view that hippocampal-striatal theta coherence may be important for the planning and execution of goal-oriented behaviors.
丘脑底核的深部脑刺激(DBS)已被广泛用于治疗帕金森病。然而,这种治疗对运动迟缓/运动不能的疗效仍然较低。下丘脑后核(PH)的DBS会引发自发的、非刻板的运动行为。我们测试了以下假设:PH刺激可以恢复由D(2)受体拮抗剂氟哌啶醇导致僵住不动的动物的运动能力。我们进一步假设海马体-纹状体神经同步性在运动行为的组织中可能很重要。在旷场、僵住不动和主动回避范式中对长期植入海马体和纹状体记录电极以及PH刺激电极的动物进行测试。在基线回避测试期间以及给予氟哌啶醇后,评估海马体-纹状体θ(5 - 10赫兹)场相干性的程度。氟哌啶醇使旷场和主动回避任务中的运动消失,并增加了僵住不动测试中的反应潜伏期。在氟哌啶醇作用下刺激PH可逆转僵住不动状态。在对照实验中,整个主动回避任务期间海马体-纹状体θ相干性较高,但在氟哌啶醇作用下大大降低。PH刺激能够恢复海马体-纹状体θ相干性,同时恢复与任务相关的行为。这些结果支持以下假设:PH的DBS可以恢复用氟哌啶醇诱导僵住不动的大鼠的运动行为,从而为PH作为帕金森病DBS治疗的有希望的候选靶点提供了有力支持。此外,结果支持这样的观点,即海马体-纹状体θ相干性对于目标导向行为的规划和执行可能很重要。