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The afferent and efferent connections of the ventromedial thalamic nucleus in the rat
Abstract
Abstract The afferent and efferent connections of the ventromedial (VM) nucleus of the thalamus in the rat were studied by experiments using the methods of retrograde cell marking by horseradish peroxidase (HRP) and anterograde fiber tracing by autoradiography. Tritiated amino acids deposited microelectrophoretically into VM label a cortical projection that is distributed to a sharply defined superficial portion of layer I of almost the entire extent of the ipsilateral neocortex. The labeling is most dense at frontal cortical levels, where fibers radiate through the deeper layers to terminate in the outer one‐quarter of layer I throughout all neocortex rostral to the genu of the corpus callosum. A lesser number of labeled fibers extends caudally in a supracallosal location to innervate parieto‐occipital cortical areas. Labeled collaterals ascend through the cortical layers to reach layer I, where grains in the superficial portion are found in a gradually decreasing rostrocaudal gradient of density that reaches the caudal pole of the hemisphere. Coronal sections at most levels contain a band of labeling in layer I that extends uninterrupted from the callosal sulcus at the midline to the banks of the rhinal sulcus laterally. Caudal retrosplenial and ventral temporal areas appear to be the only sectors of neocortex spared by the ubiquitous projection. Evidence for additional terminal distribution in deeper layers is found only in the dorsal and lateral sectors of the cortex rostral to the genu where sparsely labeled bands appear in layers III and V. The nearly exclusive distribution of VM's cortical afferents to layer I is compared and contrasted with multilaminar distributions of other “unspecific” cortical afferent fibers. HRP injected into VM labels neurons in a variety of structures at levels ranging from the frontal cortex to caudal medulla. Cell labelling in the globus pallidus, deep layers of the superior colliculus, cerebellar nuclei and the substantia nigra, pars reticulata suggest that VM is a point of convergence for several components of the extrapyramidal motor system. The nigrothalamic projection is topographic: medial and lateral districts of the pars reticulata are connected to medial and lateral districts of VM, respectively. A dorsal‐ventral association may also obtain. Cell labeling in the prefrontal cortex, the cortex along the rhinal sulcus, the lateral habenular nucleus, tegmental and medullary reticular formations, and parabrachial nuclei indicates that VM also receives projections from more heterogeneous sources.
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“The lateral habenula (LHb) is an epithalamic structure mediating communication between the forebrain and monoaminergic systems in the midbrain and hindbrain [38,39].”
From Deep brain stimulation for depression. (2022) · cites this paper as [38]
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“A receptor - mediated decreases in extracellular GABA originating from the nigrothalamic pathway in the present study and the blockade of sodium channels on all afferents in the VM originating from the globus pallidus , frontal cortex , superior col - liculus , and cerebellum ( Herkenham , 1979 ) .”
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“Re/Rh are reciprocally connected with both the CA1 subfield of the dorsal hippocampus and the mPFC (Herkenham, 1979; Vertes et al., 2006; Vertes et al., 2007) and pharmacological inactivation of Re/Rh produces performance deficits in SWM tasks (Hembrook and Mair, 2011; Hembrook et al.”
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Evidence for a GABAergic nigrothalamic pathway in the rat
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“1A; blue) act as drivers of activity by sending projections to layers III and IV of the cerebral cortex, whereas calbindin-staining matrix cells (which are more common in higher-order thalamic nuclei; Herkenham, 1979; Honjoh et al., 2018; Jones, 2001) preferentially target agranular cortices.”
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“For example, GABA neurons in the globus pallidus, substantia nigra pars reticulata, and thalamic reticular nucleus project to the dorsal thalamus, in which relay cells are CAM II kinase-a positive (Carpenter and Peter, 1972; Carpenter et al., 1975; Kim et al., 1976; Faull and Mehler, 1978; Kultas-Ilinsky et al., 1978,…”
BackgroundThe thalamo‐cortical projection of the nucleus submedius in the cat
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Afferents to Basal Forebrain Cholinergic Projection Neurons: An Update
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New Perspectives on the Organization and Evolution of Nonspecific Thalamocortical Projections
Herkenham, M. A. (1986) · Cerebral cortex · doi:10.1007/978-1-4613-2149-1_11 · Cited by 159
Neuronal connections of orbital cortex in rats: topography of cortical and thalamic afferents
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“earlier findings (Berendse and Groenewegen 1991; Herkenham 1978, 1979; Jones and Leavitt 1974; Krettek and Price 1977).”
ResultNeocortical Layer 1: an elegant solution to top-down and bottom-up integration
Schuman, B., Dellal, S., Prönneke, A., Machold, R., & Rudy, B. (2021) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-100520-012117 · Cited by 148
Thalamic and corticocortical connections of the second somatic sensory area of the mouse
Carvell, G. E., & Simons, D. J. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902650309 · Cited by 147
Edelstein, L. R., & Denaro, F. (2004) · PubMed · Cited by 146
Diffuse Cortical Projection Systems: Anatomical Organization and Role in Cortical Function
Saper, C. B. (1987) · Comprehensive physiology · doi:10.1002/cphy.cp010506 · Cited by 146
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Topographical organization of the nigrotectal projection in rat: Evidence for segregated channels
Redgrave, P., Marrow, L. P., & Dean, P. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90448-b · Cited by 143
Royce, G. J., & Mourey, R. J. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902350302 · Cited by 140
Shammah‐Lagnado, S. J., Costa, M. S. M. O., & Ricardo, J. A. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90433-3 · Cited by 138
Deniau, J., Kitai, S. T., Donoghue, J. P., & Grofová, I. (1982) · Experimental Brain Research · doi:10.1007/bf00235891 · Cited by 138
Kuramoto, E., Fujiyama, F., Nakamura, K., Tanaka, Y. R., Hioki, H., & Kaneko, T. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07481.x · Cited by 136
“Some retrograde labeling studies have shown that the deep layers of the superior colliculus and subnucleus reticularis dorsalis of the medulla send projections to the VM (Herkenham, 1979; Villanueva et al., 1998; Desbois & Villanueva, 2001).”
Background
Metadata
- Authors
- Herkenham, M.
- Affiliations
- Massachusetts Institute of Technology (US)
- Corresponding author
- Herkenham, Miles
- ORCID
- Herkenham, Miles
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1979-02
- Volume
- 183
- Issue
- 3
- Pages
- 487-517
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2000437871
- Cited by
- 477
- References
- 69
- Citations by year
- 2026: 4 · 2025: 2 · 2024: 6 · 2023: 2 · 2022: 5 · 2021: 6 · 2020: 5 · 2019: 2 · 2018: 7 · 2017: 7 · 2016: 8 · 2015: 4 · 2014: 6 · 2013: 3 · 2012: 6
- FWCI
- 15.93
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Keywords
- ventromedial thalamic nucleus, extrapyramidal system, globus pallidus, substantia nigra pars reticulata, superior colliculus, cerebellar nuclei, lateral habenula, reticular formation
- MeSH terms
- Animals, Autoradiography, Brain Mapping, Cerebral Cortex, Electrophysiology, Female, Globus Pallidus, Horseradish Peroxidase, Male, Neural Pathways, Substantia Nigra, Thalamic Nuclei, Rats
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