JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 70: 1911-1936, 1993;
0022-3077/93 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Jacquin, M. F.
Right arrow Articles by Panneton, W. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Jacquin, M. F.
Right arrow Articles by Panneton, W. M.

Journal of Neurophysiology, Vol 70, Issue 5 1911-1936, Copyright © 1993 by APS


ARTICLES

Morphology and topography of identified primary afferents in trigeminal subnuclei principalis and oralis

M. F. Jacquin, W. E. Renehan, R. W. Rhoades and W. M. Panneton
Department of Anatomy and Neurobiology, St. Louis University School of Medicine, Missouri 63104.

1. Intra-axonal recording, receptive field mapping, horseradish peroxidase injection, cytochrome oxidase staining, and computer-assisted reconstruction/morphometric methods were used to elucidate the structure and topography of trigeminal primary afferent collaterals in the normal adult rat. Prior studies focused on trigeminal brain stem subnuclei interpolaris and caudalis. This work is extended here to the remaining 2 subnuclei, principalis (PrV) and oralis (SpVo), where collaterals from 66 axons in 37 adult rats were studied. In nine rats, three to five axons were stained for within-nucleus comparisons of different fibers. Quantitative analyses were restricted to vibrissa sensitive fibers. 2. All of the axons conducted rapidly with small, low-threshold receptive fields. The majority responded to vibrissa deflection (n = 47); the remainder responded to guard hair deflection; gentle pressure applied to hairy skin, glabrous skin, lingual mucosa, or an incisor; or jaw movement. All descended in the trigeminal sensory root where some bifurcated into ascending and descending branches. Each well-stained fiber gave rise to transversely oriented collaterals in PrV and SpVo. 3. Within PrV and SpVo, fibers with differing adaptation properties and receptive fields had indistinguishable collateral morphologies. Arbors from single axons were rostrocaudally discontinuous, small relative to collaterals in subnuclei interpolaris and caudalis, circumscribed and topographically organized in a manner consistent with cytochrome oxidase and bulk-labeled primary afferent staining patterns. In SpVo and caudal PrV, the map is inverted with the nose pointing medially. In rostral PrV, the map turns 90 degrees such that the nose points dorsally. 4. Axons had different quantitative properties along the rostrocaudal axis of the trigeminal brain stem complex. Whereas arbors subtended similar transverse areas throughout PrV and SpVo, collaterals in the rostral third of PrV had a relatively low bouton density. Arbors in the caudal two thirds of PrV had the highest bouton density. Arbors in SpVo tended to be more variable in size and shape than those of caudal PrV, and their bouton numbers were significantly lower than in PrV. 5. In PrV, arbors were largely confined to somatotopically corresponding cytochrome oxidase patches, precluding significant overlap of neighboring whisker projections. In SpVo, termination sites were not as strictly confined and numerous examples of within- and between-row overlap were obtained for whisker afferents in cases where multiple axons were stained.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
Brief BioinformHome page
A. N. Pavlov, V. A. Makarov, E. Mosekilde, and O. V. Sosnovtseva
Application of wavelet-based tools to study the dynamics of biological processes
Brief Bioinform, December 1, 2006; 7(4): 375 - 389.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
L.-J. Lee, F.-S. Lo, and R. S. Erzurumlu
NMDA Receptor-Dependent Regulation of Axonal and Dendritic Branching
J. Neurosci., March 2, 2005; 25(9): 2304 - 2311.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. Deschenes, E. Timofeeva, and P. Lavallee
The Relay of High-Frequency Sensory Signals in the Whisker-to-Barreloid Pathway
J. Neurosci., July 30, 2003; 23(17): 6778 - 6787.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
B. S. Minnery and D. J. Simons
Response Properties of Whisker-Associated Trigeminothalamic Neurons in Rat Nucleus Principalis
J Neurophysiol, January 1, 2003; 89(1): 40 - 56.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. L. Kwan, J. A. Demaro, J. W. Hu, M. F. Jacquin, and B. J. Sessle
C-Fiber Depletion Alters Response Properties of Neurons in Trigeminal Nucleus Principalis
J Neurophysiol, February 1, 1999; 81(2): 435 - 446.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online