The isodendritic core of the brain stem
Abstract
According to their degree of morphological specialization, the cell populations of the brain stem may be classified into three groups: isodendritic, allodendritic and idiodendritic. The isodendritic neurons, or generalized neurons, are the most frequently encountered. If one discards those isodendritic centers that by common definition are sensory or motor, an isodendritic core is left which displays very little histological variation throughout the whole extent of the brain stem. This core corresponds, with certain restrictions, to the regions that are usually regarded as reticular formation. It constitutes a continuum of overlapping dendritic fields that extends from the spinal cord to the diencephalon. In view of the similarities that exist between the histology of the isodendritic core and the relatively disorganized nervous system of the lower vertebrates, it is postulated that it represents a pool of pluripotential neurons which in the course of phylogeny have remained relatively undifferentiated and in charge of processing afferent signals of very heterogeneous origin. By contrast, the allodendritic and idiodendritic centers can be regarded as relatively specialized centers from the point of view of their dendritic morphology, connections and functions. Attention is paid to the fact that the diffuse characteristics of the isodendritic core do not necessarily entail ill‐defined physiological properties.
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Classical anatomical studies have suggested that the brainstem reticular circuitry within which the studied regions lie is undifferentiated or diffuse.
“Classical anatomical studies have suggested that brainstem reticular circuitry within which the studied regions lie is ‘undifferentiated’23 or ‘diffuse’24.”
From Predicting modular functions and neural coding of behavior from a synaptic wiring diagram (2024) · cites this paper as [24]
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Mass Action in Cerebral Function
Lashley, K. S. (1931) · Science · doi:10.1126/science.73.1888.245 · Cited by 164 · see citing works
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Mesulam, M. ‐., Mufson, E. J., Levey, A. I., & Wainer, B. H. (1983) · Journal of Comparative Neurology · doi:10.1002/cne.902140206 · Cited by 1,962 · see citing works
Ikemoto, S. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.05.004 · Cited by 1,477 · see citing works
Cortico-Basal Ganglia Reward Network: Microcircuitry
Sesack, S. R., & Grace, A. A. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.93 · Cited by 985 · see citing works
Jones, B. E., & Yang, T. (1985) · Journal of Comparative Neurology · doi:10.1002/cne.902420105 · Cited by 896 · see citing works
Consciousness without a cerebral cortex: A challenge for neuroscience and medicine
Merker, B. (2007) · Behavioral and Brain Sciences · doi:10.1017/s0140525x07000891 · Cited by 868 · see citing works
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Afferents of the ventral tegmental area in the rat-anatomical substratum for integrative functions
Geisler, S., & Zahm, D. S. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20668 · Cited by 379 · see citing works
Neuron loss in key cholinergic and aminergic nuclei in Alzheimer disease: a meta-analysis
Lyness, S. (2003) · Neurobiology of Aging · doi:10.1016/s0197-4580(02)00057-x · Cited by 240 · see citing works
The cholinergic innervation of the human cerebral cortex.
Mesulam, M.-M. (2004) · Progress in Brain Research · doi:10.1016/s0079-6123(03)45004-8 · Cited by 211 · see citing works
Mesulam, M. ‐., Hersh, L. B., Mash, D. C., & Geula, C. (1992) · Journal of Comparative Neurology · doi:10.1002/cne.903180308 · Cited by 188 · see citing works
Comparative and Evolutionary Anatomy of the Visual Cortex of the Dolphin
Morgane, P. J., Glezer, I. I., & Jacobs, M. S. (1990) · Cerebral Cortex · doi:10.1007/978-1-4615-3824-0_4 · Cited by 41 · see citing works
Predicting modular functions and neural coding of behavior from a synaptic wiring diagram
Vishwanathan, A., Sood, A., Wu, J., Ramirez, A. D., Yang, R., Kemnitz, N., Ih, D., Turner, N., Lee, K., Tartavull, I., et al. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01784-3 · Cited by 25 · see citing works
“Classical anatomical studies have suggested that brainstem reticular circuitry within which the studied regions lie is ‘undifferentiated’ 23 or ‘diffuse’ 24 .”
- Authors
- Ramón‐Moliner, E., & Nauta, W. J. H.
- Affiliations
- Université Laval (CA)
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1966-03
- Volume
- 126
- Issue
- 3
- Pages
- 311-335
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2016204025
- Cited by
- 442
- References
- 1
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 8 · 2023: 2 · 2022: 8 · 2021: 5 · 2020: 4 · 2019: 2 · 2018: 18 · 2017: 1 · 2016: 1 · 2015: 8 · 2014: 5 · 2013: 2 · 2012: 1
- FWCI
- 3.07
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Medicine › Anatomy › Medical and Biological Sciences
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroscience of respiration and sleep
- Keywords
- brainstem, reticular formation, dendritic morphology, phylogenetic evolution, lower vertebrates, spinal cord, diencephalon
- MeSH terms
- Anatomy, Comparative, Animals, Haplorhini, Brain Stem, Dendrites, Diencephalon, Biological Evolution, Fishes, Neurons, Reticular Formation, Sharks, Spinal Cord, Mice, Rats
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