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灵长类动物外侧苍白球功能障碍诱发的行为障碍II. 解剖学研究。

Behavioural disorders induced by external globus pallidus dysfunction in primates II. Anatomical study.

作者信息

François Chantal, Grabli David, McCairn Kevin, Jan Caroline, Karachi Carine, Hirsch Etienne-C, Féger Jean, Tremblay Léon

机构信息

Neurologie et Thérapeutique expérimentale, INSERM U289, Hôpital de la Salpêtrière, Paris, France.

出版信息

Brain. 2004 Sep;127(Pt 9):2055-70. doi: 10.1093/brain/awh239. Epub 2004 Aug 3.

Abstract

The anatomical organization of the basal ganglia supports their involvement in movement and behavioural disorders. Thus dyskinesia, attention deficit with or without hyperactivity, and stereotyped behaviour can be induced by microinjections of bicuculline, a GABAergic antagonist, into different parts of the external globus pallidus (GPe) in monkeys. The aim of the present study was to determine the anatomo-functional circuits inside the basal ganglia which are specifically related to each of these behavioural changes. For that, axonal tracers were injected in the same pallidal sites where abnormal behaviours have previously been obtained by bicuculline microinjections. The labelling was mapped in the different basal ganglia and matched with the topography of the cortico-striato-pallidal projections already reported in the literature and with the distribution of calbindin immunoreactivity. Our results first show that the pallidal sites related to dyskinesia, attention deficit with or without hyperactivity, and stereotyped behaviour, were respectively in motor, associative and limbic territories, defined as weak, moderate and intensive calbindin immunoreactivity. The same relationship was observed between the distribution of the labelling in the different basal ganglia after tracer injections performed in these different pallidal sites and the anatomo-functional territories. Thus regarding the origin of the circuits within the striatum, tracer injections performed in the dyskinesia site labelled neurons located in the posterior sensorimotor putamen, those performed in the hyperactivity and/or attention deficit labelled neurons in the laterodorsal putamen and caudate nucleus, regions corresponding to associative and anterior motor territories, while those performed in the stereotyped behaviour site labelled neurons in the ventral limbic striatum. Regarding the GPe output on the basal ganglia, the different circuits also appeared underlined by different anatomo-functional territories, even if a partial overlap exists. Each of these anatomical circuits systematically involves both the internal globus pallidus (GPi) and the substantia nigra pars reticulata (SNr) but, whereas movement circuit is mainly related to the GPi, stereotyped behaviour is mainly related to the SNr. Additionally, subregions of the subthalamic nucleus were also systematically involved, depending on the movement or behavioural disorder produced. These results demonstrate that distinct circuits involving different anatomo-functional territories of the basal ganglia, with partial overlap, participate in different behavioural disorders in monkeys. It seems likely that these neuronal circuits are involved in pathologies like Tourette's syndrome, attention deficit/hyperactivity disorders and obsessional compulsive troubles. This study provides the basis for further researches with a therapeutical viewpoint.

摘要

基底神经节的解剖结构支持其参与运动和行为障碍。因此,通过向猴子外侧苍白球(GPe)的不同部位微量注射GABA能拮抗剂荷包牡丹碱,可诱发运动障碍、伴有或不伴有多动的注意力缺陷以及刻板行为。本研究的目的是确定基底神经节内与这些行为变化各自具体相关的解剖功能回路。为此,将轴突示踪剂注射到先前通过荷包牡丹碱微量注射获得异常行为的相同苍白球部位。对标记物在不同基底神经节中的分布进行绘图,并与文献中已报道的皮质-纹状体-苍白球投射的地形图以及钙结合蛋白免疫反应性的分布相匹配。我们的结果首先表明,与运动障碍、伴有或不伴有多动的注意力缺陷以及刻板行为相关的苍白球部位分别位于运动、联合和边缘区域,其定义为钙结合蛋白免疫反应性弱、中度和强。在这些不同的苍白球部位进行示踪剂注射后,不同基底神经节中标记物的分布与解剖功能区域之间也观察到了相同的关系。因此,关于纹状体内回路的起源,在运动障碍部位进行示踪剂注射标记的神经元位于后感觉运动性壳核,在多动和/或注意力缺陷部位进行注射标记的神经元位于背外侧壳核和尾状核,这些区域对应于联合和前运动区域,而在刻板行为部位进行注射标记的神经元位于腹侧边缘纹状体。关于GPe对基底神经节的输出,即使存在部分重叠,不同的回路也似乎由不同的解剖功能区域所突显。这些解剖回路中的每一个都系统地涉及内侧苍白球(GPi)和黑质网状部(SNr),但是,运动回路主要与GPi相关,而刻板行为主要与SNr相关。此外,视所产生的运动或行为障碍不同,丘脑底核的亚区域也系统地涉及其中。这些结果表明,涉及基底神经节不同解剖功能区域且有部分重叠的不同回路参与了猴子的不同行为障碍。这些神经元回路似乎可能参与了诸如妥瑞氏综合征、注意力缺陷/多动障碍和强迫性障碍等病理过程。本研究为从治疗角度进行进一步研究提供了基础。

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