Hameleers Rob, Blokland Arjan, Steinbusch Harry W M, Visser-Vandewalle Veerle, Temel Yasin
Department of Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, P.O. Box 616, 6200 MD Maastricht, The Netherlands.
Behav Brain Res. 2007 Dec 11;185(1):65-7. doi: 10.1016/j.bbr.2007.07.011. Epub 2007 Jul 17.
Intervening with serotonergic neurotransmission can have profound effects on mobility. For instance, the peripheral administration of the 5-HT(2A/C) agonist, 2,5-dimethoxy-4-iodoamphetamine (DOI), changes the locomotor activity substantially. Locomotor activity is classically linked to the basal ganglia, in which the subthalamic nucleus (STN) plays a pivotal role. In this study, we tested the hypothesis that deep brain stimulation (DBS) of the STN modulates DOI-induced hypomobility. Rats were implanted with stimulating electrodes at the level of the STN and were tested in an open field (OF) task in various conditions (stimulation on/off, in combination with DOI treatment). We found that DOI administration (i.p.) reduced the behavioural activity of the animals and that STN HFS reversed these effects. This study provides the first evidence that the therapeutic effect of STN HFS may also be mediated by a 5-HT-dependent mechanism.
干预血清素能神经传递会对运动能力产生深远影响。例如,外周给予5-HT(2A/C)激动剂2,5-二甲氧基-4-碘苯丙胺(DOI)会显著改变运动活性。运动活性传统上与基底神经节有关,其中丘脑底核(STN)起关键作用。在本研究中,我们测试了以下假设:对STN进行深部脑刺激(DBS)可调节DOI诱导的运动减少。将大鼠植入STN水平的刺激电极,并在各种条件下(刺激开启/关闭,结合DOI治疗)在旷场(OF)任务中进行测试。我们发现腹腔注射DOI会降低动物的行为活性,而STN高频刺激(HFS)可逆转这些效应。本研究首次证明STN HFS的治疗效果也可能由5-羟色胺依赖性机制介导。