The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Brainstem network controlling descending drive to phrenic motoneurons in rat
Abstract
Contraction of the diaphragm is controlled by phrenic motoneurons that receive input from sources that are not fully established. Bulbospinal (second‐order) neurons projecting to phrenic motoneurons and propriobulbar (third‐order) neurons projecting to these bulbospinal neurons were investigated in rat by transsynaptic transport of the neuroinvasive pseudorabies virus. Bulbospinal neurons were located predominantly in the medullary lateral tegmental field in two functionally described regions, the ventral respiratory group and Bötzinger complex. An intervening region, the pre‐Bötzinger complex, contained essentially no phrenic premotoneu rons. Bulbospinal neurons were also located in ventral, interstitial, and ventrolateral subnuclei of the solitary tract, and gigantocellular, Kölliker‐Fuse, parabrachial, and medullary raphe nuclei. A monosynaptic pathway to phrenic motoneurons from the nucleus of the solitary tract was confirmed; monosynaptic pathways from upper cervical, spinal cord, spinal trigeminal nucleus, medial and lateral vestibular nuclei, and medial pontine tegmentum were not verified. Locations of third‐order neurons were consistent with described projections to the ventral respiratory group, from contralateral ventral respiratory group, Bötzinger complex, A5 noradrenergic cell group, and the following nuclei: solitary, raphe, Kölliker‐Fuse, parabrachial, retrotrapezoid, and paragigantocellular. Novel findings included a projection from locus coeruleus to respiratory premotoneurons and the lack of previously described pathways from area postrema and spinal trigeminal nucleus. These second‐ and third‐order neurons form the output network for diaphragm motor control which includes numerous behaviors (e. g., respiration, phonation, defecation). Of the premotoneurons, the rostral ventral respiratory group is the primary population controlling phrenic motoneurons. © 1994 Wiley‐Liss, Inc.
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Steinbusch, H. W. M. (1981) · Neuroscience · doi:10.1016/0306-4522(81)90146-9 · Cited by 2,415
Nucleus locus ceruleus: new evidence of anatomical and physiological specificity
Foote, S. L., Bloom, F. E., & Aston-Jones, G. (1983) · Physiological Reviews · doi:10.1152/physrev.1983.63.3.844 · Cited by 1,901
Chamberlin, N. L., & Saper, C. B. (1992) · Journal of Comparative Neurology · doi:10.1002/cne.903260207 · Cited by 222
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Del Negro, C. A., Funk, G. D., & Feldman, J. L. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0003-6 · Cited by 663
Self-citationParaventricular hypothalamic nucleus: Axonal projections to the brainstem
Geerling, J. C., Shin, J., Chimenti, P. C., & Loewy, A. D. (2010) · Journal of Comparative Neurology · doi:10.1002/cne.22283 · Cited by 273
Physiological basis and pharmacology of motion sickness: an update
Yates, B. J., Miller, A. D., & Lucot, J. B. (1998) · Brain Research Bulletin · doi:10.1016/s0361-9230(98)00092-6 · Cited by 230
Efferent projections of excitatory and inhibitory preBötzinger Complex neurons
Yang, C. F., & Feldman, J. L. (2018) · Journal of Comparative Neurology · doi:10.1002/cne.24415 · Cited by 167
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Holstege, G. (2014) · Progress in brain research · doi:10.1016/b978-0-444-63274-6.00020-5 · Cited by 102
Metadata
- Authors
- Dobbins, E. G., & Feldman, J. L.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1994-09
- Volume
- 347
- Issue
- 1
- Pages
- 64-86
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2045712239
- Cited by
- 483
- References
- 3
- FWCI
- 8.83
- Type
- journal article
- Language
- en
- Open access
- closed
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