Belforte J E, Pazo J H
Laboratorio de Neurofisiología, Departamento de Fisiología, Facultad de Medicina, Universidad de Buenos Aires. Paraguay 2155, Buenos Aires 1121, Argentina.
Eur J Neurosci. 2004 Jan;19(2):346-55. doi: 10.1111/j.0953-816x.2003.03125.x.
The basal ganglia, which receive a rich serotonergic innervation, have been implicated in hyperkinetic and hypokinetic disorders. Moreover, a decrease in subthalamic nucleus (STN) activity has been associated with motor hyperactivity. To address the role of subthalamic serotonergic innervation in its motor function, turning behaviour was studied in rats with stimulation of the subthalamic serotonin (5-HT) receptors by intracerebral microinjections. The intrasubthalamic administration of 5-HT induced dose-dependent contralateral turning behaviour, with a maximal effect at a dose of 2.5 microg in 0.2 microL. Similar results were observed with microinjections of other 5-HT receptor agonists: quipazine (a 5-HT2B/C/3 agonist), MK-212 (a 5-HT2B/C agonist) and m-chlorophenylbiguanidine (a 5-HT3 agonist), while microinjections of 5-HT into the zona incerta or in the previously lesioned STN were ineffective. The effect of 5-HT was blocked by coadministration of the antagonist mianserin. Stimulation of subthalamic 5-HT receptors in animals bearing a lesion of the nigrostriatal pathway did not modify the motor response, which indicates that the dopamine innervation of the nucleus is not involved in this effect. Kainic acid lesion of the substantia nigra pars reticulata (SNr) suppressed the contralateral rotations elicited by stimulation of 5-HT2B/C/3 subthalamic receptors. This suggests a role of the subthalamic-nigral pathway in the turning activity. Furthermore, the partial blockade of glutamatergic receptors in the SNr by the antagonist DNQX increased the contralateral circling elicited by stimulation of 5-HT receptors in the STN. We concluded that the activation of the 5-HT2B/C and 5-HT3 subthalamic receptors elicited contralateral turning behaviour, probably via the subthalamic-nigral pathway.
基底神经节接受丰富的血清素能神经支配,与运动亢进和运动减退性疾病有关。此外,底丘脑核(STN)活动的减少与运动多动有关。为了研究底丘脑血清素能神经支配在其运动功能中的作用,通过脑内微注射刺激底丘脑5-羟色胺(5-HT)受体,对大鼠的旋转行为进行了研究。在底丘脑内给予5-HT可诱导剂量依赖性的对侧旋转行为,在0.2微升中注射2.5微克的剂量时效果最大。用其他5-HT受体激动剂进行微注射也观察到类似结果:喹哌嗪(一种5-HT2B/C/3激动剂)、MK-212(一种5-HT2B/C激动剂)和间氯苯双胍(一种5-HT3激动剂),而将5-HT微注射到未定带或先前损伤的STN中则无效。5-HT的作用被拮抗剂米安色林共同给药所阻断。在黑质纹状体通路受损的动物中刺激底丘脑5-HT受体并没有改变运动反应,这表明该核的多巴胺神经支配不参与此效应。黑质网状部(SNr)的 kainic 酸损伤抑制了刺激底丘脑5-HT2B/C/3受体引起的对侧旋转。这表明底丘脑-黑质通路在旋转活动中起作用。此外,拮抗剂 DNQX 对 SNr 中谷氨酸能受体的部分阻断增加了刺激 STN 中5-HT受体引起的对侧转圈。我们得出结论,底丘脑5-HT2B/C和5-HT3受体的激活可能通过底丘脑-黑质通路引起对侧旋转行为。