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Dopamine control of pyramidal neuron activity in the primary motor cortex via D2 receptors

机译:多巴胺通过D2受体控制初级运动皮层锥体神经元活动

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摘要

The primary motor cortex (M1) is involved in fine voluntary movements control. Previous studies have shown the existence of a dopamine (DA) innervation in M1 of rats and monkeys that could directly modulate M1 neuronal activity. However, none of these studies have described the precise distribution of DA terminals within M1 functional region nor have quantified the density of this innervation. Moreover, the precise role of DA on pyramidal neuron activity still remains unclear due to conflicting results from previous studies regarding D2 effects on M1 pyramidal neurons. In this study we assessed in mice the neuroanatomical characteristics of DA innervation in M1 using unbiased stereological quantification of DA transporter-immunostained fibers. We demonstrated for the first time in mice that DA innervates the deep layers of M1 targeting preferentially the forelimb representation area of M1. To address the functional role of the DA innervation on M1 neuronal activity, we performed electrophysiological recordings of single neurons activity in vivo and pharmacologically modulated D2 receptor activity. Local D2 receptor activation by quinpirole enhanced pyramidal neuron spike firing rate without changes in spike firing pattern. Altogether, these results indicate that DA innervation in M1 can increase neuronal activity through D2 receptor activation and suggest a potential contribution to the modulation of fine forelimb movement. Given the demonstrated role for DA in fine motor skill learning in M1, our results suggest that altered D2 modulation of M1 activity may be involved in the pathophysiology of movement disorders associated with disturbed DA homeostasis.
机译:主运动皮层(M1)参与良好的自主运动控制。先前的研究表明,大鼠和猴子的M1中存在多巴胺(DA)神经支配,可以直接调节M1神经元的活性。但是,这些研究都没有描述DA末端在M1功能区内的精确分布,也没有量化这种神经支配的密度。此外,由于先前关于D2对M1锥体神经元的影响的研究结果相互矛盾,因此DA对锥体神经元活动的确切作用仍不清楚。在这项研究中,我们使用DA转运蛋白免疫染色纤维的无偏立体学定量评估了M1中DA神经支配的神经解剖学特征。我们首次在小鼠中证明DA支配M1的深层,优先靶向M1的前肢代表区域。为了解决DA神经支配对M1神经元活性的功能作用,我们进行了体内单个神经元活性的电生理记录和药理调节的D2受体活性。喹吡罗对局部D2受体的激活增强了锥体神经元的峰值发射速率,而峰值发射模式没有变化。总而言之,这些结果表明,M1中的DA神经支配可以通过D2受体激活来增加神经元活动,并暗示对精细前肢运动的调节有潜在作用。鉴于DA在M1的精细运动技能学习中的作用已得到证实,我们的结果表明M2活性的D2调节改变可能与与DA动态平衡相关的运动障碍的病理生理有关。

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