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Anatomically segregated basal ganglia pathways allow parallel behavioral modulation

In the basal ganglia (BG), anatomically segregated and topographically-organized feedforward circuits are thought to modulate multiple behaviors in parallel. Although topographically-arranged BG circuits have been described, the extent to which these relationships are maintained across the BG output...

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Autores principales: Lee, Jaeeon, Wang, Wengang, Sabatini, Bernardo L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606600/
https://www.ncbi.nlm.nih.gov/pubmed/32989293
http://dx.doi.org/10.1038/s41593-020-00712-5
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author Lee, Jaeeon
Wang, Wengang
Sabatini, Bernardo L.
author_facet Lee, Jaeeon
Wang, Wengang
Sabatini, Bernardo L.
author_sort Lee, Jaeeon
collection PubMed
description In the basal ganglia (BG), anatomically segregated and topographically-organized feedforward circuits are thought to modulate multiple behaviors in parallel. Although topographically-arranged BG circuits have been described, the extent to which these relationships are maintained across the BG output nuclei and in downstream targets is unclear. Here, using focal transsynaptic anterograde tracing, we show that the motor-action related topographical organization of the striatum is preserved in all BG output nuclei. The topography is also maintained downstream of the BG and in multiple parallel closed loops that provide striatal input. Furthermore, focal activation of two distinct striatal regions induce either licking or turning, consistent with the structure of projections to targets outside the BG. Our results confirm the parallel model of BG function, and suggest that the integration and competition of information relating to different behavior occurs largely outside of the BG.
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spelling pubmed-76066002021-03-28 Anatomically segregated basal ganglia pathways allow parallel behavioral modulation Lee, Jaeeon Wang, Wengang Sabatini, Bernardo L. Nat Neurosci Article In the basal ganglia (BG), anatomically segregated and topographically-organized feedforward circuits are thought to modulate multiple behaviors in parallel. Although topographically-arranged BG circuits have been described, the extent to which these relationships are maintained across the BG output nuclei and in downstream targets is unclear. Here, using focal transsynaptic anterograde tracing, we show that the motor-action related topographical organization of the striatum is preserved in all BG output nuclei. The topography is also maintained downstream of the BG and in multiple parallel closed loops that provide striatal input. Furthermore, focal activation of two distinct striatal regions induce either licking or turning, consistent with the structure of projections to targets outside the BG. Our results confirm the parallel model of BG function, and suggest that the integration and competition of information relating to different behavior occurs largely outside of the BG. 2020-09-28 2020-11 /pmc/articles/PMC7606600/ /pubmed/32989293 http://dx.doi.org/10.1038/s41593-020-00712-5 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Lee, Jaeeon
Wang, Wengang
Sabatini, Bernardo L.
Anatomically segregated basal ganglia pathways allow parallel behavioral modulation
title Anatomically segregated basal ganglia pathways allow parallel behavioral modulation
title_full Anatomically segregated basal ganglia pathways allow parallel behavioral modulation
title_fullStr Anatomically segregated basal ganglia pathways allow parallel behavioral modulation
title_full_unstemmed Anatomically segregated basal ganglia pathways allow parallel behavioral modulation
title_short Anatomically segregated basal ganglia pathways allow parallel behavioral modulation
title_sort anatomically segregated basal ganglia pathways allow parallel behavioral modulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606600/
https://www.ncbi.nlm.nih.gov/pubmed/32989293
http://dx.doi.org/10.1038/s41593-020-00712-5
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