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


     


J Neurophysiol 62: 834-840, 1989;
0022-3077/89 $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 Sugiura, Y.
Right arrow Articles by Hosoya, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sugiura, Y.
Right arrow Articles by Hosoya, Y.

Journal of Neurophysiology, Vol 62, Issue 4 834-840, Copyright © 1989 by APS


ARTICLES

Difference in distribution of central terminals between visceral and somatic unmyelinated (C) primary afferent fibers

Y. Sugiura, N. Terui and Y. Hosoya
Institute of Basic Medical Sciences, University of Tsukuba, Ibaraki, Japan.

1. In the guinea pig, the central projections of somatic and visceral C-afferent fibers were compared by tracing arborizations labeled through injection of Phaseolus vulgaris leucoagglutinin (PHA-L) intracellularly into single neurons of the 13th thoracic dorsal root ganglia (DRG). 2. Two of 27 somatic C-afferent neurons that responded to electrical stimulation of the 13th thoracic (subcostal) nerve (conduction velocity: 0.69 +/- 0.14 m/s, mean +/- SD) were well enough marked to allow delineation of their central processes. In both cases, the entering axon ran rostrally, giving off branches that converged on a single terminal field located in the substantia gelatinosa (lamina II) with some extension in lamina I. The terminal field in each case extended approximately 400 microns rostrocaudally and 100 microns mediolaterally. 3. Intracellular recordings were obtained from 31 afferent units that responded to electrical stimulation of the celiac ganglion. Units with onset latencies of greater than 15 ms were classified as having visceral C-afferent fibers because the shortest course from the celiac ganglion stimulation electrodes to the DRG was greater than 7 mm (i.e., a conduction velocity of less than 0.5 m/s). 4. Seven visceral C-afferent fibers were labeled well enough to follow their central trajectories. Each had a main ascending and a descending central branch. Each main branch in turn issued several collaterals that terminated in the superficial dorsal horn (laminae I and II), laminae IV, V, and X, and occasionally in the dorsal and lateral funiculi. A few collaterals reached the contralateral laminae V and X.(ABSTRACT TRUNCATED AT 250 WORDS)


This article has been cited by other articles:


Home page
Mol. Interv.Home page
D. R. Robinson and G. F. Gebhart
Inside Information: The Unique Features of Visceral Sensation
Mol. Interv., October 1, 2008; 8(5): 242 - 253.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
V. Pinto, P. Szucs, V. A. Derkach, and B. V. Safronov
Monosynaptic convergence of C- and A{delta}-afferent fibres from different segmental dorsal roots on to single substantia gelatinosa neurones in the rat spinal cord
J. Physiol., September 1, 2008; 586(17): 4165 - 4177.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
K. M. Albers, C. J. Woodbury, A. M. Ritter, B. M. Davis, and H. R. Koerber
Glial cell line-derived neurotrophic factor expression in skin alters the mechanical sensitivity of cutaneous nociceptors.
J. Neurosci., March 15, 2006; 26(11): 2981 - 2990.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
G. Kato, H. Furue, T. Katafuchi, T. Yasaka, Y. Iwamoto, and M. Yoshimura
Electrophysiological mapping of the nociceptive inputs to the substantia gelatinosa in rat horizontal spinal cord slices
J. Physiol., October 1, 2004; 560(1): 303 - 315.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. J. Chandler, J. Zhang, C. Qin, and R. D. Foreman
Spinal Inhibitory Effects of Cardiopulmonary Afferent Inputs in Monkeys: Neuronal Processing in High Cervical Segments
J Neurophysiol, March 1, 2002; 87(3): 1290 - 1302.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
A. Ito, E. Kumamoto, M. Takeda, M. Takeda, K. Shibata, H. Sagai, and M. Yoshimura
Mechanisms for Ovariectomy-Induced Hyperalgesia and Its Relief by Calcitonin: Participation of 5-HT1A-Like Receptor on C-Afferent Terminals in Substantia Gelatinosa of the Rat Spinal Cord
J. Neurosci., August 15, 2000; 20(16): 6302 - 6308.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
H. Bester, V. Chapman, J.-M. Besson, and J.-F. Bernard
Physiological Properties of the Lamina I Spinoparabrachial Neurons in the Rat
J Neurophysiol, April 1, 2000; 83(4): 2239 - 2259.
[Abstract] [Full Text] [PDF]




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