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Response inhibition subprocesses and dopaminergic pathways: basal ganglia disease effects.

机译:反应抑制子过程和多巴胺能途径:基底神经节疾病的影响。

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Response inhibition is a component of executive functions, which can be divided into distinct subprocesses by means of event-related potentials (ERPs). These subprocesses are (pre)-motor inhibition and inhibition monitoring, which are probably reflected by the Nogo-N2 and Nogo-P3, respectively. Here we ask, if these subprocesses may depend on distinct basal ganglia subsystems. We examined response inhibition processes in an extended sample of young and elderly subjects, patients with Parkinson's disease (PD) and Huntington' disease (HD). This combination of groups also allow us to study whether, and to what degree, pathological basal ganglia changes and healthy aging have similar and/or different effects on these processes. We show that subprocesses of response inhibition are differentially modulated by distinct basal ganglia circuits. Processes related to (pre)-motor inhibition appear to be modulated by the nigrostriatal system, and are sensitive to aging and age-related basal ganglia diseases (i.e. PD). Parkinson's disease induces additive effects of aging and pathology. In contrast, inhibition monitoring is most likely modulated by the mesocortico-limbic dopamine system. These processes are equally affected in healthy aging and both basal ganglia diseases (i.e. PD, HD).
机译:响应抑制是执行功能的组成部分,可通过事件相关电位(ERP)将其分为不同的子过程。这些子过程是(运动前)运动抑制和抑制监测,可能分别由Nogo-N2和Nogo-P3反映出来。在这里,我们问这些子过程是否可能依赖于不同的基底神经节子系统。我们检查了年轻人和老年人,帕金森氏病(PD)和亨廷顿病(HD)患者的样本中的反应抑制过程。这些组的组合还使我们能够研究病理性基底神经节改变和健康衰老是否对这些过程产生相似和/或不同的影响,以及在何种程度上产生影响。我们表明响应抑制的子过程是由不同的基底神经节电路差异调制的。与(运动前)抑制有关的过程似乎被黑纹状体系统调节,对衰老和与年龄相关的基底神经节疾病(即PD)敏感。帕金森氏病会诱发衰老和病理的相加作用。相反,抑制监测很可能是由中眼镜-边缘多巴胺系统调节的。这些过程在健康衰老和两种基底神经节疾病(即PD,HD)中均受到同样的影响。

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