Matrix-biased excitatory and inhibitory inputs to the striatum involving external segment of the globus pallidus.

阅读:2
作者:Karube Fuyuki, Kobayashi Kenta, Fujiyama Fumino
INTRODUCTION: The external segment of the globus pallidus (GPe) is traditionally viewed as a relay nucleus within the indirect basal ganglia pathway. However, a subpopulation of GPe neurons projects directly to the striatum, raising questions about their compartmental and cell-type-specific targeting. METHODS: To address this issue, we employed neural tracing and ex vivo whole-cell patch-clamp recordings with optogenetics using adeno-associated viral vectors in rats. Anatomical observations and intersectional labeling techniques were applied to examine spatial relationships of projections among the striatum, GPe, and ventral thalamus. RESULTS: GPe axons exhibited a strong bias toward the matrix compartment of the striatum. This biased projection originated from both subthalamic nucleus-targeting and striatum-targeting GPe neurons. In contrast, striatal projections to the GPe arose from both matrix and striosome compartments. Optogenetic stimulation of GPe axons elicited inhibitory postsynaptic currents in medium spiny neurons (MSNs) and cholinergic interneurons (CINs) in the matrix compartment. Cesium-based recordings indicated distal synaptic contacts in MSNs. Anatomical data also revealed proximal appositions of GPe axons to CIN somata and dendrites. Excitatory inputs from motor cortical areas and ventral thalamic nuclei also preferentially targeted the matrix. Furthermore, optogenetic stimulation of ventral thalamic axons elicited excitatory postsynaptic currents in GPe neurons. Intersectional labeling revealed substantial overlap between striatal neurons and axons of GPe neurons, both of which were innervated by the same population of ventral thalamic neurons. DISCUSSION: These findings suggest that convergent cortical and thalamic excitation of both the striatum and GPe may induce feedforward inhibition within the striatal matrix, particularly onto CINs. This mechanism may contribute to the fine-tuning of striatal output in motor-related basal ganglia circuits.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。