Parkinson Department, Marienhospital Kevelaer, Basilikastr. 55, 47612 Kevelaer, Germany.
J Neural Transm (Vienna). 2010 Dec;117(12):1359-69. doi: 10.1007/s00702-010-0454-z. Epub 2010 Nov 16.
The article presents the hypothesis that nigrostriatal dopamine may regulate movement by modulation of tone and contraction in skeletal muscles through a concentration-dependent influence on the postsynaptic D1 and D2 receptors on the follow manner: nigrostriatal axons innervate both receptor types within the striatal locus somatotopically responsible for motor control in agonist/antagonist muscle pair around a given joint. D1 receptors interact with lower and D2 receptors with higher dopamine concentrations. Synaptic dopamine concentration increases immediately before movement starts. We hypothesize that increasing dopamine concentrations stimulate first the D1 receptors and reduce muscle tone in the antagonist muscle and than stimulate D2 receptors and induce contraction in the agonist muscle. The preceded muscle tone reduction in the antagonist muscle eases the efficient contraction of the agonist. Our hypothesis is applicable for an explanation of physiological movement regulation, different forms of movement pathology and therapeutic drug effects. Further, this hypothesis provides a theoretical basis for experimental investigation of dopaminergic motor control and development of new strategies for treatment of movement disorders.
本文提出了一个假设,即黑质纹状体多巴胺可能通过对突触后 D1 和 D2 受体的浓度依赖性影响来调节运动,方式如下:黑质纹状体轴突在纹状体部位内支配两种受体类型,这些受体在给定关节周围的运动控制中具有特定的躯体定位作用,负责运动控制。D1 受体与较低浓度的多巴胺相互作用,而 D2 受体与较高浓度的多巴胺相互作用。突触多巴胺浓度在运动开始前立即增加。我们假设,多巴胺浓度的增加首先刺激 D1 受体,降低拮抗剂肌肉的肌肉张力,然后刺激 D2 受体,诱导激动剂肌肉收缩。拮抗剂肌肉的先前肌肉张力降低有助于激动剂的有效收缩。我们的假设适用于对生理运动调节、不同形式的运动病理学和治疗药物效应的解释。此外,该假设为多巴胺能运动控制的实验研究以及运动障碍治疗新策略的发展提供了理论基础。