Neurochemistry and circuit organization of the lateral spiriform nucleus of birds: A uniquely nonmammalian direct pathway component of the basal ganglia

Author:

Reiner Anton1ORCID,Medina Loreta23,Abellan Antonio23,Deng Yunping1,Toledo Claudio A. B.4,Luksch Harald5,Vega‐Zuniga Tomas56,Riley Nell B.7,Hodos William7,Karten Harvey J.8

Affiliation:

1. Department of Anatomy and Neurobiology The University of Tennessee Health Science Center Memphis Tennessee USA

2. Department of Experimental Medicine Universitat de Lleida Lleida Spain

3. Laboratory of Evolutionary and Developmental Neurobiology Lleida's Institute for Biomedical Research‐Dr. Pifarré Foundation (IRBLleida) Lleida Catalonia Spain

4. Neuroscience Research Nucleus Universidade Cidade de Sao Paulo Sao Paulo Brazil

5. School of Life Sciences Technische Universität München Freising‐Weihenstephan Germany

6. Institute of Science and Technology Austria Klosterneuburg Austria

7. Department of Psychology University of Maryland College Park California USA

8. Department of Neurosciences University of California San Diego San Diego California USA

Abstract

AbstractWe 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.

Funder

National Institutes of Health

Publisher

Wiley

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3