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首页> 外文期刊>The European Journal of Neuroscience >Changes in neuronal activity of cortico-basal ganglia thalamic networks induced by acute dopaminergic manipulations in rats
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Changes in neuronal activity of cortico-basal ganglia thalamic networks induced by acute dopaminergic manipulations in rats

机译:大鼠急性多巴胺能操纵诱导的皮质基甘神经节丘脑网络神经元活性的变化

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The basal ganglia are thought to be particularly sensitive to changes in dopaminergic tone, and the realization that reduced dopaminergic signaling causes pronounced motor dysfunction is the rationale behind dopamine replacement therapy in Parkinson' disease. It has, however, proven difficult to identify which neurophysiological changes that ultimately lead to motor dysfunctions. To clarify this, we have here recorded neuronal activity throughout the cortico-basal ganglia-thalamic circuits in freely behaving rats during periods of immobility following acute dopaminergic manipulations, involving both vesicular dopamine depletion and antagonism of D1 and D2 type dopamine receptors. Synchronized and rhythmic activities were detected in the form of betaband oscillations in local field potentials and as cortical entrainment of action potentials in several basal ganglia structures. Analyses of the temporal development of synchronized oscillations revealed a spread from cortex to gradually also include deeper structures. In addition, firing rate changes involving neurons in all parts of the network were observed. These changes were typically relatively balanced within each structure, resulting in negligible net rate changes. Animals treated with D1 receptor antagonist showed a rapid onset of hypokinesia that preceded most of the neurophysiological changes, with the exception of these balanced rate changes. Parallel rate changes in functionally coupled ensembles of neurons in different structures may therefore be the first step in a cascade of neurophysiological changes underlying motor symptoms in the parkinsonian state. We suggest that balanced rate changes in distributed networks are possible mechanism of disease that should be further investigated in conditions involving dopaminergic dysfunction.
机译:基础神经节被认为对多巴胺能调节的变化特别敏感,并且降低多巴胺能信号传导导致明显的电动机功能障碍的认识是帕金森病“疾病中多巴胺替代疗法背后的理由。然而,它已经证明难以确定最终导致电动机功能障碍的神经生理学变化。为了澄清这一点,我们在急性多巴胺能操作后,在急性多巴胺能操作后的不动的情况下,在整个皮质基 - 基底神经节 - 丘脑电路中记录了神经元活动,涉及D1和D2型多巴胺受体的囊泡多巴胺耗竭和拮抗作用。在局部场势的贝卡和振荡形式中检测到同步和节奏活动,并作为几个基底神经节结构中的动作电位的皮质夹带。同步振荡的时间发育的分析显示从皮质逐渐蔓延,也包括更深的结构。此外,观察到涉及网络中所有部分中神经元的发射率变化。这些变化通常在每个结构内相对平衡,导致净率可忽略不计。用D1受体拮抗剂治疗的动物显示出在大部分神经生理学变化之前的低管开始,除了这些平衡率变化。因此,不同结构中神经元的功能耦合整合的平行速率变化可以是Parkinsonian状态下潜在的电机症状的神经生理学变化级联的第一步。我们建议分布式网络的平衡率变化是可能在涉及多巴胺能功能障碍的条件下进一步研究的疾病机制。

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