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Neurochemistry and circuit organization of the lateral spiriform nucleus of birds: A uniquely nonmammalian direct pathway component of the basal ganglia.
Reiner, Anton; Medina, Loreta; Abellan, Antonio; Deng, Yunping; Toledo, Claudio A B; Luksch, Harald; Vega-Zuniga, Tomas; Riley, Nell B; Hodos, William; Karten, Harvey J.
Afiliação
  • Reiner A; Department of Anatomy and Neurobiology, The University of Tennessee Health Science Center, Memphis, Tennessee, USA.
  • Medina L; Department of Experimental Medicine, Universitat de Lleida, Lleida, Spain.
  • Abellan A; Laboratory of Evolutionary and Developmental Neurobiology, Lleida's Institute for Biomedical Research-Dr. Pifarré Foundation (IRBLleida), Lleida, Catalonia, Spain.
  • Deng Y; Department of Experimental Medicine, Universitat de Lleida, Lleida, Spain.
  • Toledo CAB; Laboratory of Evolutionary and Developmental Neurobiology, Lleida's Institute for Biomedical Research-Dr. Pifarré Foundation (IRBLleida), Lleida, Catalonia, Spain.
  • Luksch H; Department of Anatomy and Neurobiology, The University of Tennessee Health Science Center, Memphis, Tennessee, USA.
  • Vega-Zuniga T; Neuroscience Research Nucleus, Universidade Cidade de Sao Paulo, Sao Paulo, Brazil.
  • Riley NB; School of Life Sciences, Technische Universität München, Freising-Weihenstephan, Germany.
  • Hodos W; School of Life Sciences, Technische Universität München, Freising-Weihenstephan, Germany.
  • Karten HJ; Institute of Science and Technology Austria, Klosterneuburg, Austria.
J Comp Neurol ; 532(5): e25620, 2024 May.
Article em En | MEDLINE | ID: mdl-38733146
ABSTRACT
We used diverse methods to characterize the role of avian lateral spiriform nucleus (SpL) in basal ganglia motor function. Connectivity analysis showed that SpL receives input from globus pallidus (GP), and the intrapeduncular nucleus (INP) located ventromedial to GP, whose neurons express numerous striatal markers. SpL-projecting GP neurons were large and aspiny, while SpL-projecting INP neurons were medium sized and spiny. Connectivity analysis further showed that SpL receives inputs from subthalamic nucleus (STN) and substantia nigra pars reticulata (SNr), and that the SNr also receives inputs from GP, INP, and STN. Neurochemical analysis showed that SpL neurons express ENK, GAD, and a variety of pallidal neuron markers, and receive GABAergic terminals, some of which also contain DARPP32, consistent with GP pallidal and INP striatal inputs. Connectivity and neurochemical analysis showed that the SpL input to tectum prominently ends on GABAA receptor-enriched tectobulbar neurons. Behavioral studies showed that lesions of SpL impair visuomotor behaviors involving tracking and pecking moving targets. Our results suggest that SpL modulates brainstem-projecting tectobulbar neurons in a manner comparable to the demonstrated influence of GP internus on motor thalamus and of SNr on tectobulbar neurons in mammals. Given published data in amphibians and reptiles, it seems likely the SpL circuit represents a major direct pathway-type circuit by which the basal ganglia exerts its motor influence in nonmammalian tetrapods. The present studies also show that avian striatum is divided into three spatially segregated territories with differing connectivity, a medial striato-nigral territory, a dorsolateral striato-GP territory, and the ventrolateral INP motor territory.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Gânglios da Base / Vias Neurais Limite: Animals Idioma: En Revista: J Comp Neurol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Gânglios da Base / Vias Neurais Limite: Animals Idioma: En Revista: J Comp Neurol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos