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The organization of midbrain projections to the striatum in the primate: Sensorimotor-related striatum versus ventral striatum
Open accessAbstract
In order to examine the organization of nigrostriatal projections in the primate, the retrograde tracers Lucifer Yellow conjugated to dextran amines and horseradish peroxidase conjugated to wheatgerm agglutinin were injected into different regions of the dorsolateral and ventral striatum. Based on the topography of cortical inputs to the striatum, the dorsolateral striatum is associated with the motor system, and the ventral striatum is related to the limbic system. Our results indicate that although midbrain neurons projecting to the ventral and dorsolateral striatum are mostly separate, there are neurons projecting to these different striatal territories that overlap in the medial substantia nigra. The dopaminergic neurons of the ventral mesencephalon can be subdivided into dorsal and ventral tiers that include the cells of the ventral tegmental area, the substantia nigra pars compacta, and the retrorubral area. Neurons projecting to the ventral striatum are found in both the dorsal and ventral tiers. A large number of neurons occupying the medial densocellular zone of the ventral tier are labeled following injections into different regions of the ventral striatum. Neurons projecting to the sensorimotor-related striatum are derived almost exclusively from the ventral tier. Many of these neurons are located very ventrally in the substantia nigra, where clusters of neurons invade the pars reticulata. In addition, labeled neurons are found throughout the mediolateral extent of the densocellular zone of the pars compacta. Notably, neurons are labeled in the medial densocellular zone following injections into the dorsolateral and ventral striatum. Mesencephalic neurons projecting to different striatal territories are distinct in that dorsal tier neurons mainly innervate the ventral striatum, whereas the ventral columns of neurons in the ventral tier innervate the sensorimotor-related striatum. Thus, the dopaminergic regulation of the sensorimotor-related striatum and the ventral striatum may be different. However, a subgroup of dopaminergic neurons in the medial densocellular zone projects to both striatal territories. Such divergent projections may allow the substantia nigra to serve as a link, connecting different striatal territories, via their connections with the substantia nigra.
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“In contrast, a dorsomedial region (i.e., caudate) is connected with frontal and parietal association cortices”
From Contributions of the striatum to learning, motivation, and performance: an associative account (2012) · cites this paper as [1]
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“whereas the ventral striatum is connected with limbic structures, including the amygdala, hippocampus, and medial orbitofrontal and anterior cingulate cortices [1,2].”
From Contributions of the striatum to learning, motivation, and performance: an associative account (2012) · cites this paper as [1]
In the citing paper
“demonstrating that the dorsolateral region of the striatum (i.e., putamen) is primarily connected to sensory and motor cortices.”
From Contributions of the striatum to learning, motivation, and performance: an associative account (2012) · cites this paper as [1]
Citations
Cites
Dahlstroem, A., & Fuxé, K. (1964) · PubMed · Cited by 5,133
Ehringer, H., & Hornykiewicz, O. (1960) · Journal of Molecular Medicine · doi:10.1007/bf01485901 · Cited by 1,875
Neurotransmitters and neuromodulators in the basal ganglia
Graybiel, A. M. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90104-i · Cited by 1,576
Evidence for the existence of monoamine neurons in the central nervous system
Fuxé, K. (1965) · Cell and Tissue Research · doi:10.1007/bf00337069 · Cited by 1,567
The neostriatal mosaic: multiple levels of compartmental organization
Gerfen, C. R. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90355-c · Cited by 1,471
Efferent connections of the substantia nigra and ventral tegmental area in the rat
Beckstead, R. M., Domesick, V. B., & Nauta, W. J. H. (1979) · Brain Research · doi:10.1016/0006-8993(79)91001-1 · Cited by 1,293
Specificity in the projection patterns of accumbal core and shell in the rat
Heimer, L., Zahm, D. S., Churchill, L., Kalivas, P. W., & Wohltmann, C. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90202-y · Cited by 1,219
Fallon, J. H., & Moore, R. Y. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901800310 · Cited by 1,190
Cellular localization of brain monoamines.
Carlsson, A. C., FALCK, B., & Hillarp, N. ‐. (1962) · PubMed · Cited by 1,144
Lindvall, O., & Björklund, A. (1974) · PubMed · Cited by 1,131
Longitudinal topography and interdigitation of corticostriatal projections in the rhesus monkey
Selemon, L. D., & Goldman-Rakic, P. S. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-03-00776.1985 · Cited by 1,074
Central Catecholamine Neuron Systems: Anatomy and Physiology of the Dopamine Systems
Moore, R. Y., & Bloom, F. E. (1978) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.01.030178.001021 · Cited by 931
Selemon, L. D., & Goldman-Rakic, P. S. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-11-04049.1988 · Cited by 908
Kelley, A. E., Domesick, V. B., & Nauta, W. J. H. (1982) · Neuroscience · doi:10.1016/0306-4522(82)90067-7 · Cited by 888
Efferent connections and nigral afferents of the nucleus accumbens septi in the rat
Nauta, W. J. H., Smith, G. P., Faull, R. L. M., & Domesick, V. B. (1978) · Neuroscience · doi:10.1016/0306-4522(78)90041-6 · Cited by 876
Demonstration and mapping out of nigro-neostriatal dopamine neurons
Andén, N. ‐., Carlsson, A., Dahlström, A. B., Fuxé, K., Hillarp, N. ‐., & Larsson, K. (1964) · Life Sciences · doi:10.1016/0024-3205(64)90161-4 · Cited by 812
Gerfen, C. R., Herkenham, M. A., & Thibault, J. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-12-03915.1987 · Cited by 804
THE CORTICO-STRIATE PROJECTION IN THE MONKEY
Kemp, J. M., & Powell, T. P. S. (1970) · Brain · doi:10.1093/brain/93.3.525 · Cited by 798
Kelley, A. E., & Domesick, V. B. (1982) · Neuroscience · doi:10.1016/0306-4522(82)90198-1 · Cited by 746
Künzle, H. (1975) · Brain Research · doi:10.1016/0006-8993(75)90384-4 · Cited by 714
Yeterian, E. H., & Hoesen, G. W. V. (1978) · Brain Research · doi:10.1016/0006-8993(78)90059-8 · Cited by 641
An intricately patterned prefronto‐caudate projection in the rhesus monkey
Goldman, P. S., & Nauta, W. J. H. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901710305 · Cited by 509
The neurobiology of the nucleus accumbens
Bailey, P. (1982) · Neuroscience · doi:10.1016/0306-4522(82)90145-2 · Cited by 453
Jones, E. G., Coulter, J. D., Burton, H., & Porter, R. W. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901730105 · Cited by 436
The topographic order of inputs to nucleus accumbens in the rat
Phillipson, O. T., & Griffiths, A. C. (1985) · Neuroscience · doi:10.1016/0306-4522(85)90002-8 · Cited by 415
Two transpallidal pathways originating in the rat nucleus accumbens
Zahm, D. S., & Heimer, L. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903020302 · Cited by 406
The amygdalostriatal projections in the monkey. An anterograde tracing study
Russchen, F. T., Bakst, I., Amaral, D. G., & Price, J. L. (1985) · Brain Research · doi:10.1016/0006-8993(85)90530-x · Cited by 395
Flaherty, A. W., & Graybiel, A. M. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.66.4.1249 · Cited by 344
Gerfen, C. R., Baimbridge, K. G., & Thibault, J. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-12-03935.1987 · Cited by 340
Differential connections of caudate nucleus and putamen in the squirrel monkey (Saimiri sciureus)
Smith, Y., & Parent, A. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90159-4 · Cited by 334
Haber, S. N., Lynd‐Balta, E., Klein, C. M., & Groenewegen, H. J. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902930210 · Cited by 291
Self-citationMorecraft, R. J., & Hoesen, G. W. V. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903220403 · Cited by 289
Widespread corticostriate projections from temporal cortex of the rhesus monkey
Hoesen, G. W. V., Yeterian, E. H., & Lavizzo‐Mourey, R. J. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.901990205 · Cited by 264
Felten, D. L., & Sladek, J. R. (1983) · Brain Research Bulletin · doi:10.1016/0361-9230(83)90045-x · Cited by 259
Nigrostriatal and nigrothalamic fibers in the rhesus monkey
Carpenter, M. B., & Peter, P. (1972) · The Journal of Comparative Neurology · doi:10.1002/cne.901440105 · Cited by 252
Felten, D. L., & Sladek, J. R. (1982) · Brain Research Bulletin · doi:10.1016/0361-9230(82)90138-1 · Cited by 246
Organization of striatopallidal, striatonigral, and nigrostriatal projections in the macaque
Hedreen, J. C., & Delong, M. R. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903040406 · Cited by 245
Parent, A., Mackey, A., & Bellefeuille, L. D. (1983) · Neuroscience · doi:10.1016/0306-4522(83)90104-5 · Cited by 233
Somogyi, P., Bolam, J. P., Totterdell, S., & Smith, A. D. (1981) · Brain Research · doi:10.1016/0006-8993(81)90002-0 · Cited by 207
The organization of the descending ventral pallidal projections in the monkey
Haber, S., Lynd-Balta, E., & Mitchell, S. (1993) · The Journal of comparative neurology · doi:10.1002/cne.903290108 · Cited by 184
Self-citationGroenewegen, H. J., Room, P., Witter, M. P., & Lohman, A. H. M. (1982) · Neuroscience · doi:10.1016/0306-4522(82)90055-0 · Cited by 180
Groenewegen, H. J., Becker, N. E. H. M., & Lohman, A. H. M. (1980) · Neuroscience · doi:10.1016/0306-4522(80)90038-x · Cited by 179
A brainstem atlas of catecholaminergic neurons in man, using melanin as a natural marker
Bogerts, B. (1981) · Journal of Comparative Neurology · doi:10.1002/cne.901970106 · Cited by 177
Golgi centennial symposium: Perspectives in neurobiology
Eidelberg, E. (1976) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(76)90169-3 · Cited by 173
Russchen, F. T., & Price, J. L. (1984) · Neuroscience Letters · doi:10.1016/0304-3940(84)90379-3 · Cited by 167
Dopaminergic neurons expressing calbindin in normal and parkinsonian monkeys
Lavoie, B. A., & Parent, A. (1991) · Neuroreport · doi:10.1097/00001756-199110000-00012 · Cited by 165
Lynd‐Balta, E., & Haber, S. N. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903450407 · Cited by 164
Self-citationGarver, D. L., & Sladek, J. R. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901590302 · Cited by 149
Comparative morphology of the substantia nigra and ventral tegmental area in the monkey, cat and rat
POIRIER, L. J., Giguère, M., & Marchand, R. (1983) · Brain Research Bulletin · doi:10.1016/0361-9230(83)90173-9 · Cited by 142
Organization of the ascending striatal afferents in monkeys
Szabo, J. (1980) · The Journal of Comparative Neurology · doi:10.1002/cne.901890207 · Cited by 140
Hubbard, J. E., & Carlo, V. D. (1974) · The Journal of Comparative Neurology · doi:10.1002/cne.901530403 · Cited by 130
Fornix system efferent projections in the squirrel monkey: An experimental degeneration study
Poletti, C. E., & Creswell, G. F. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901750107 · Cited by 128
Immunohistochemical studies on monoamine-containing cell systems
Ho¨kfelt, T., Fuxé, K., & Goldstein, M. (1973) · Brain Research · doi:10.1016/0006-8993(73)90709-9 · Cited by 125
François, C., Percheron, G., & Yelnik, J. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90259-8 · Cited by 123
Crossroads of Limbic and Striatal Circuitry: Hypothalamo-Nigral Connections
Nauta, W. J. H., & Domesick, V. B. (1978) · Springer eBooks · doi:10.1007/978-1-4757-0716-8_6 · Cited by 121
Tanaka, C., Ishikawa, M., & Shimada, S. (1982) · Brain Research Bulletin · doi:10.1016/0361-9230(82)90139-3 · Cited by 71
Schofield, S. P. M., & Everitt, B. J. (1981) · PubMed · Cited by 60
Haber, S. N., & Groenewegen, H. J. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902900105 · Cited by 58
Self-citationA histological atlas of the macaque (Macaca, mulatta) substantia nigra in ventricular coordinates
François, C., Percheron, G., Yelnik, J., & Heyner, S. (1985) · Brain Research Bulletin · doi:10.1016/0361-9230(85)90196-0 · Cited by 53
Anterograde transport of lucifer yellow-dextran conjugate
Chang, H. T. (1991) · Brain Research Bulletin · doi:10.1016/0361-9230(91)90180-r · Cited by 21
Research works printed but not linked: 3
- Lynd-Balta, 1992, Organization of dopaminergic striatal projections in relation to peptidergic innervation of the substantia nigra in primate, Soc. Neurosci. Abstr., 18, 306
- Nagamoto, 1992, Distribution of dopamine D2 receptors in subpopulations of primate midbrain dopaminergic neurons, Soc. Neurosci. Abstr., 18, 660
- Szabo, 1979, Cellular and synaptic organization of basal ganglia, Appl. Neurophysiol., 42, 9
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Self-citationDopamine neuron systems in the brain: An update
Björklund, A., & Dunnett, S. B. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.006 · Cited by 1,777
Haber, S. N., Fudge, J. L., & McFarland, N. R. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-06-02369.2000 · Cited by 1,610
Self-citationThe primate basal ganglia: Parallel and integrative networks
Haber, S. N. (2003) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2003.10.003 · Cited by 1,479
Self-citationTwo types of dopamine neuron distinctly convey positive and negative motivational signals
Matsumoto, M., & Hikosaka, O. (2009) · Nature · doi:10.1038/nature08028 · Cited by 1,378
Metadata
- Authors
- Lynd-Balta, E., & Haber, S. N.
- Affiliations
- University of Rochester Medicine (US)
- Corresponding author
- Haber, S.N.
- ORCID
- Haber, S.N.
- Venue
- Neuroscience
- Publisher
- Elsevier BV
- Published
- 1994-04
- Volume
- 59
- Issue
- 3
- Pages
- 625-640
- ISSN
- 0306-4522 (ISSN-L)
- OpenAlex
- W2071189762
- Cited by
- 233
- References
- 60
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 3 · 2023: 3 · 2022: 8 · 2021: 7 · 2020: 7 · 2019: 9 · 2018: 4 · 2017: 11 · 2016: 11 · 2015: 4 · 2014: 14 · 2013: 6 · 2012: 12
- FWCI
- 5.24
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Neuroscience (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (NS22511, R01NS022511)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Deep Brain Stimulation and Movement Disorders
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- nigrostriatal projection, midbrain, ventral striatum, dorsolateral striatum, substantia nigra, ventral tegmental area, substantia nigra pars compacta, dopaminergic neurons, limbic system, primates
- MeSH terms
- Animals, Axonal Transport, Corpus Striatum, Fluorescent Dyes, Horseradish Peroxidase, Isoquinolines, Limbic System, Macaca mulatta, Macaca nemestrina, Mesencephalon, Neurons, Putamen, Substantia Nigra, Wheat Germ Agglutinins, Wheat Germ Agglutinin-Horseradish Peroxidase Conjugate
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