Access the full text.
Sign up today, get DeepDyve free for 14 days.
F. Cerveró, A. Iggo, H. Ogawa (1976)
Nociceptor-driven dorsal horn neurones in the lumbar spinal cord of the catPain, 2
D. Trevino, E. Carstens (1975)
Confirmation of the location of spinothalamic neurons in the cat and monkey by the retrograde transport of horseradish peroxidaseBrain Research, 98
M. Réthelyi (1977)
Preterminal and terminal axon arborizations in the substantia gelatinosa of cat's spinal cordJournal of Comparative Neurology, 172
P. Burgess, E. Perl (1967)
Myelinated afferent fibres responding specifically to noxious stimulation of the skinThe Journal of Physiology, 190
P. Burgess, E. Perl (1973)
Cutaneous Mechanoreceptors and Nociceptors
H. Ralston (1979)
The fine structure of laminae I, II and III of the macaque spinal cordJournal of Comparative Neurology, 184
A. Light, R. Durkovic (1976)
Horseradish peroxidase: An improvement in intracellular staining of single, electrophysiologically characterized neuronsExperimental Neurology, 53
Margret Kennard (1954)
The course of ascending fibers in the spinal cord of the cat essential to the recognition of painful stimuliJournal of Comparative Neurology, 100
A. Brown, P. Rose, P. Snow (1977)
The morphology of hair follicle afferent fibre collaterals in the spinal cord of the catThe Journal of Physiology, 272
T. Kumazawa, T. Kumazawa, E. Perl, E. Perl, P. Burgess, P. Burgess, D. Whitehorn, D. Whitehorn (1975)
Ascending projections from marginal zone (Lamina I) neurons of the spinal dorsal hornJournal of Comparative Neurology, 162
M. Scheibel, A. Scheibel (1968)
Terminal axonal patterns in cat spinal cord. II. The dorsal horn.Brain research, 9 1
A. Brown, P. Rose, P. Snow (1978)
Morphology and organization of axon collaterals from afferent fibres of slowly adapting type I units in cat spinal cord.The Journal of Physiology, 277
T. Kumazawa, E. Perl (1977)
Primate cutaneous receptors with unmyelinated (C) fibres and their projection to the substantia gelatinosa.Journal de physiologie, 73 3
D. Price, D. Mayer (1974)
Physiological laminar organization of the dorsal horn of M. mulatta.Brain research, 79 2
I. P. Karplus, A. Kreidl (1925)
Zur Kenntnis der Schmerzleitung im Rückenmark. II, 207
D. Trevino, J. Coulter, W. Willis (1973)
Location of cells of origin of spinothalamic tract in lumbar enlargement of the monkey.Journal of neurophysiology, 36 4
T. Kumazawa, E. Perl (1978)
Excitation of marginal and substantia gelatinosa neurons in the primate spinal cord: Indications of their place in dorsal horn functional organizationJournal of Comparative Neurology, 177
J. Beal, C. Fox (1976)
Afferent fibers in the substantia gelatinosa of the adult monkey (Macaca mulatta): A Golgi StudyJournal of Comparative Neurology, 168
(1977)
Central termination of identified cutaneous afferent units with fine myelinated fibers
(1925)
Zur Kenntnis der Schmerzleitung im Ruckenmark. 11. Mitteilung
E. Carstens, D. Trevino (1978)
Anatomical and physiological properties of ipsilaterally projecting spinothalamic neurons in the second cervical segment of the cat's spinal cordJournal of Comparative Neurology, 182
E. Jankowska, J. Rastad, J. Westman (1976)
Intracellular application of horseradish peroxidase and its light and electron microscopical appearance in spinocervical tract cellsBrain Research, 105
A. Light, D. Trevino, E. Perl (1979)
Morphological features of functionally defined neurons in the marginal zone and substantia gelatinosa of the spinal dorsal hornJournal of Comparative Neurology, 186
(1968)
Some Observations on the Encoding of Somesthetic Stimuli by Receptor Populations in the Hairy Skin of Primates
J. Szentágothai (1964)
Neuronal and synaptic arrangement in the substantia gelatinosa rolandiJournal of Comparative Neurology, 122
T. Kumazawa, E. Perl (1976)
DIFFERENTIAL EXCITATION OF DORSAL HORN AND SUBSTANTIA GELATINOSA MARGINAL NEURONS BY PRIMARY AFFERENT UNITS WITH FINE (Aδ AND C) FIBERS
B. Rexed (1952)
The cytoarchitectonic organization of the spinal cord in the catJournal of Comparative Neurology, 96
T. Kumazawa, E. R. Perl (1976)
Sensory Functions of the Skin in Primates
C. Lamotte (1977)
Distribution of the tract of lissauer and the dorsal root fibers in the primate spinal cordJournal of Comparative Neurology, 172
E. Perl (1968)
Myelinated afferent fibres innervating the primate skin and their response to noxious stimuliThe Journal of Physiology, 197
T. Kumazawa, E. Perl (1977)
Primate cutaneous sensory units with unmyelinated (C) afferent fibers.Journal of neurophysiology, 40 6
J. Capowski (1978)
The Neuroscience Display ProcessorComputer, 11
M. Scheibel, Arnold Schiebel (1969)
Terminal patterns in cat spinal cord. 3. Primary afferent collaterals.Brain research, 13 3
H. Ralston, D. Ralston
The distribution of dorsal root axons in laminae I, II and III of the macaque spinal cord: A quantitative electron microscope studyJournal of Comparative Neurology, 184
A. Brown, R. Fyffe (1978)
The morphology of group Ia afferent fibre collaterals in the spinal cord of the cat.The Journal of physiology, 274
B. Christensen, E. Perl (1970)
Spinal neurons specifically excited by noxious or thermal stimuli: marginal zone of the dorsal horn.Journal of neurophysiology, 33 2
P. R. Burgess, E. R. Perl (1973)
Handbook of Sensory Physiology. Vol. 2, Somatosensory System
Kenzo Hamano, H. Mannen, N. Ishizuka (1978)
Reconstruction of trajectory of primary afferent collaterals in the dorsal horn of the cat spinal cord, using golgi‐stained serial sectionsJournal of Comparative Neurology, 181
D. Lloyd, A. Mcintyre (1950)
Dorsal column conduction of group I muscle afferent impulses and their relay through Clarke's column.Journal of neurophysiology, 13 1
A. Light, E. Perl (1979)
Reexamination of the dorsal root projection to the spinal dorsal horn including observations on the differential termination of coarse and fine fibersJournal of Comparative Neurology, 186
J. S. Hanker, P. E. Yates, C. B. Metz, A. Rustioni (1977)
A new specific, sensitive and non‐carcinogenic reagent for the demonstration of horseradish peroxidase, 9
S. Cullheim, J. Kellerth (1976)
Combined light and electron microscopic tracing of neurons, including axons and synaptic terminals, after intracellular injection of horseradish peroxidaseNeuroscience Letters, 2
P. Bessou, E. Perl (1969)
Response of cutaneous sensory units with unmyelinated fibers to noxious stimuli.Journal of neurophysiology, 32 6
D. Albe-Fessard, A. Levante, Y. Lamour (1974)
Origin of spino-thalamic tract in monkeys.Brain research, 65 3
D. Lloyd (1943)
CONDUCTION AND SYNAPTIC TRANSMISSION OF THE REFLEX RESPONSE TO STRETCH IN SPINAL CATSJournal of Neurophysiology, 6
P. Snow, P. Rose, A. Brown (1976)
Tracing axons and axon collaterals of spinal neurons using intracellular injection of horseradish peroxidase.Science, 191 4224
B. Brown, A. Brown (1967)
A quantitative study of cutaneous receptors and afferent fibres in the cat and rabbitThe Journal of Physiology, 193
A. Pearson (1952)
Role of gelatinous substance of spinal cord in conduction of pain.A.M.A. archives of neurology and psychiatry, 68 4
J. Beall, A. Applebaum, R. Foreman, W. Willis (1977)
Spinal cord potentials evoked by cutaneous afferents in the monkey.Journal of neurophysiology, 40 2
M. Réthelyi, Capowski Jj (1977)
The terminal arborization pattern of primary afferent fibers in the substantia gelatinosa of the spinal cord in the cat.Journal de physiologie, 73 3
R. Narotzky, F. Kerr (1978)
Marginal neurons of the spinal cord: Types, afferent synaptology and functional considerationsBrain Research, 139
P. Burgess, D. Petit, R. Warren (1968)
Receptor types in cat hairy skin supplied by myelinated fibers.Journal of neurophysiology, 31 6
M. Réthelyi, D. Trevino, E. Perl (1979)
Distribution of primary afferent fibers within the sacrococcygeal dorsal horn: An autoradiographic studyJournal of Comparative Neurology, 185
D. Albe-Fessard, J. Boivie, G. Grant, A. Levante (1975)
Labelling of cells in the medulla oblongata and the spinal cord of the monkey after injections of horseradish peroxidase in the thalamusNeuroscience Letters, 1
P. Sterling, H. Kuypers (1967)
Anatomical organization of the brachial spinal cord of the cat. I. The distribution of dorsal root fibers.Brain research, 4 1
(1956)
Thoracic Surgical ManagementPostgraduate Medical Journal, 32
S. Gobel, J. Binck (1977)
Degenerative changes in primary trigeminal axons and in neurons in nucleus caudalis following tooth pulp extirpations in the catBrain Research, 132
S. Kitai, J. Kocsis, R. Preston, M. Sugimori (1976)
Monosynaptic inputs to caudate neurons identified by intracellular injection of horseradish peroxidaseBrain Research, 109
W. Willis, D. Trevino, J. Coulter, R. Maunz (1974)
Responses of primate spinothalamic tract neurons to natural stimulation of hindlimb.Journal of Neurophysiology, 37
Ramón Cajal, Santiago
Histologie du système nerveux de l'homme & des vertébrés
Single primary afferent myelinated fibers from cutaneous receptors of cat and monkey were functionally identified by recording from the spinal cord with micropipettes filled with horseradish peroxidase (HRP). Relatively slowly conducting fibers (< 40 m/sec) from high threshold mechanoreceptors (mechanical nociceptors) and two types of low threshold mechanoreceptor (D‐hair and field) were selected for staining. Iontophoresis of the HRP and subsequent histochemical reaction stained the axons recorded from and their collaterals, including terminations, for several millimeters. The termination patterns in the two species proved essentially identical. Ipsilaterally, the mechanical nociceptor fibers terminated principally in the dorsal horn's marginal zone and in the ventral parts of the nucleus proprius (lamina V in the cat). Some of these nociceptors also had terminals in the midline just dorsal to the central canal, contralaterally in the marginal zone, and at the base of the opposite nucleus proprius. In contrast, the D‐hair primary afferent axons terminated in the dorsal part of the nucleus proprius overlapping into the innermost portion of the substantia gelatinosa. The field receptor fibers terminated predominantly in the middle part of the nucleus proprius. These results suggest that there is a highly specialized central projection of primary afferent endings which is related to sensory function and not to fiber diameter. The marginal zone and most dorsal parts of the substantia gelatinosa receive direct projections from cutaneous nociceptors but do not have direct input from cutaneous receptors transmitting activity initiated by innocuous stimulation.
The Journal of Comparative Neurology – Wiley
Published: Mar 15, 1980
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.