An immunohistochemical and pathway tracing study of the striatopallidal organization of area X in the male zebra finch

被引:85
作者
Reiner, A
Laverghetta, AV
Meade, CA
Cuthbertson, SL
Bottjer, SW
机构
[1] Univ Tennessee, Ctr Hlth Sci, Dept Anat & Neurobiol, Memphis, TN 38163 USA
[2] Univ So Calif, Dept Biol, Los Angeles, CA 90089 USA
关键词
striatum; pallidum; songbird; basal ganglia; song learning; motor learning;
D O I
10.1002/cne.11012
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Area X is a nucleus within songbird basal ganglia that is part of the anterior forebrain song learning circuit. It receives cortical song-related input and projects to the dorsolateral medial nucleus of thalamus (DLM). We carried out single- and double-labeled immunohistochemical and pathway tracing studies in male zebra finch to characterize the cellular organization and circuitry of area X. We found that 5.4% of area X neuronal perikarya are relatively large, possess aspiny dendrites, and are rich in the pallidal neuron/striatal interneuron marker Lys8-Asn9-neurotensin8-13 (LANT6). Many of these perikarya were found to project to the DLM, and their traits suggest that they are pallidal. Area X also contained several neuron types characteristic of the striatum, including interneurons co-containing LANT6 and the striatal interneuron marker parvalbumin (2% of area X neurons), interneurons containing parvalbumin but not LANT6 (4.8%), cholinergic interneurons (1.4%), and neurons containing the striatal spiny projection neuron marker dopamine- and adenosine 3',5'-monophosphate-regulated phosphoprotein (DARPP-32) (30%). Area X was rich in substance P (SP)-containing terminals, and many ended on area X neurons projecting to the DLM with the woolly fiber morphology characteristic of striatopallidal terminals. Although SP+ perikarya were not detected in area X, prior studies suggest it is likely that SP-synthesizing neurons are present and the source of the SP+ input to area X neurons projecting to the DLM. Area X was poor in enkephalinergic fibers and perikarya. The present data support the premise that area X contains both striatal and pallidal neurons, with the striatal neurons likely to include SP+ neurons that project to the pallidal neurons. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:239 / 261
页数:23
相关论文
共 106 条
[1]   THE FUNCTIONAL-ANATOMY OF BASAL GANGLIA DISORDERS [J].
ALBIN, RL ;
YOUNG, AB ;
PENNEY, JB .
TRENDS IN NEUROSCIENCES, 1989, 12 (10) :366-375
[2]   Unilateral striatal lesions in the cat disrupt well-learned motor plans in a GO/NO-GO reaching task [J].
Aldridge, JW ;
Thompson, JF ;
Gilman, S .
EXPERIMENTAL BRAIN RESEARCH, 1997, 113 (03) :379-393
[3]   DISTRIBUTION AND RELATIVE ABUNDANCE OF NEURONS IN THE PIGEON FOREBRAIN CONTAINING SOMATOSTATIN, NEUROPEPTIDE-Y, OR BOTH [J].
ANDERSON, KD ;
REINER, A .
JOURNAL OF COMPARATIVE NEUROLOGY, 1990, 299 (03) :261-282
[4]   EXTENSIVE COOCCURRENCE OF SUBSTANCE-P AND DYNORPHIN IN STRIATAL PROJECTION NEURONS - AN EVOLUTIONARILY CONSERVED FEATURE OF BASAL GANGLIA ORGANIZATION [J].
ANDERSON, KD ;
REINER, A .
JOURNAL OF COMPARATIVE NEUROLOGY, 1990, 295 (03) :339-369
[5]   IMMUNOHISTOCHEMICAL LOCALIZATION OF DARPP-32 IN STRIATAL PROJECTION NEURONS AND STRIATAL INTERNEURONS - IMPLICATIONS FOR THE LOCALIZATION OF D1-LIKE DOPAMINE-RECEPTORS ON DIFFERENT TYPES OF STRIATAL NEURONS [J].
ANDERSON, KD ;
REINER, A .
BRAIN RESEARCH, 1991, 568 (1-2) :235-243
[6]   DIFFERENT LOCALIZATIONS OF MET-ENKEPHALIN-LIKE IMMUNOREACTIVITY IN RAT FOREBRAIN AND SPINAL-CORD USING HYDROGEN-PEROXIDE AND TRITON X-100 - LIGHT MICROSCOPIC STUDY [J].
ARLUISON, M ;
CONRATHVERRIER, M ;
TAUC, M ;
MAILLY, P ;
DELAMANCHE, IS ;
CESSELIN, F ;
BOURGOIN, S ;
HAMON, M .
BRAIN RESEARCH BULLETIN, 1983, 11 (05) :555-571
[7]  
BARBEAU A, 1986, HDB CLIN NEUROLOGY, V5, P87
[8]   FOREBRAIN LESIONS DISRUPT DEVELOPMENT BUT NOT MAINTENANCE OF SONG IN PASSERINE BIRDS [J].
BOTTJER, SW ;
MIESNER, EA ;
ARNOLD, AP .
SCIENCE, 1984, 224 (4651) :901-903
[9]   Building a bird brain: sculpting neural circuits for a learned behavior [J].
Bottjer, SW .
BIOESSAYS, 1997, 19 (12) :1109-1116
[10]  
Bottjer SW, 1997, J NEUROBIOL, V33, P602, DOI 10.1002/(SICI)1097-4695(19971105)33:5<602::AID-NEU8>3.0.CO