Abstract
1. The responses to natural somatic stimuli of thirty-seven antidromically identified spinothalamic tract (s.t.t.) cells in Rexed's laminae VII and VIII of the lumbar spinal cord of the cat have been studied. A further twenty-eight s.t.t. cells were identified antidromically.
2. Cells were activated from sites in, or close to, one of the following locations: nucleus (n.) parafascicularis or n. centrum medianum, magnocellular part of the medial geniculate or the medial leminiscus, n. ventralis posterior medialis, n. lateralis posterior.
3. The majority (84%) of s.t.t. cells showed spontaneous discharge at 1-67 Hz.
4. Somatic stimuli excited 81% of s.t.t. cells but gave rise to inhibition of spontaneous discharge in 54% of cells. Only 8·1% of cells gave only inhibitory responses while 35·1% gave only excitatory responses and 45·9% gave both inhibitory and excitatory responses. No response could be elicited in 10·8% of cells.
5. The proportion of s.t.t. cells giving inhibitory and excitatory responses to hair movement, light touch or tap, innocuous pinch, noxious pinch, joint movement, twisting of and intense pressure on joints, flicking, palpation or deflexion of large muscles, skin cooling and warming and noxious heat are documented. Of these stimuli, only skin cooling and warming failed to produce a response in any cell.
6. Many cells showed convergence from receptors in muscles, joint and skin although 29·7% responded exclusively to innocuous cutaneous stimuli.
7. Convergence from receptors on wide, and sometimes quite separate, areas of the hind quarters was common but exclusively contralateral receptive fields were not found and for none of the above stimuli was the contralateral side more effective than the ipsilateral side.
Full text
PDF
















Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Applebaum A. E., Leonard R. B., Kenshalo D. R., Jr, Martin R. F., Willis W. D. Nuclei in which functionally identified spinothalamic tract neurons terminate. J Comp Neurol. 1979 Dec 15;188(4):575–585. doi: 10.1002/cne.901880405. [DOI] [PubMed] [Google Scholar]
- Armstrong-James M., Millar J. Carbon fibre microelectrodes. J Neurosci Methods. 1979 Oct;1(3):279–287. doi: 10.1016/0165-0270(79)90039-6. [DOI] [PubMed] [Google Scholar]
- Boivie J. The termination of the spinothalamic tract in the cat. An experimental study with silver impregnation methods. Exp Brain Res. 1971 May 26;112(4):331–353. doi: 10.1007/BF00234489. [DOI] [PubMed] [Google Scholar]
- Brown A. G., Franz D. N. Responses of spinocervical tract neurones to natural stimulation of identified cutaneous receptors. Exp Brain Res. 1969;7(3):231–249. doi: 10.1007/BF00239031. [DOI] [PubMed] [Google Scholar]
- Brown A. G., House C. R., Rose P. K., Snow P. J. The morphology of spinocervical tract neurones in the cat. J Physiol. 1976 Sep;260(3):719–738. doi: 10.1113/jphysiol.1976.sp011540. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Comans P. E., Snow P. J. Ascending projections to nucleus parafascicularis of the cat. Brain Res. 1981 Dec 28;230(1-2):337–341. doi: 10.1016/0006-8993(81)90411-x. [DOI] [PubMed] [Google Scholar]
- Craig A. D., Jr, Burton H. Spinal and medullary lamina I projection to nucleus submedius in medial thalamus: a possible pain center. J Neurophysiol. 1981 Mar;45(3):443–466. doi: 10.1152/jn.1981.45.3.443. [DOI] [PubMed] [Google Scholar]
- Dilly P. N., Wall P. D., Webster K. E. Cells of origin of the spinothalamic tract in the cat and rat. Exp Neurol. 1968 Aug;21(4):550–562. doi: 10.1016/0014-4886(68)90072-1. [DOI] [PubMed] [Google Scholar]
- Foreman R. D., Kenshalo D. R., Jr, Schmidt R. F., Willis W. D. Field potentials and excitation of primate spinothalamic neurones in response to volleys in muscle afferents. J Physiol. 1979 Jan;286:197–213. doi: 10.1113/jphysiol.1979.sp012614. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Foreman R. D., Schmidt R. F., Willis W. D. Convergence of muscle and cutaneous input onto primate spinothalamic tract neurons. Brain Res. 1977 Apr 1;124(3):555–560. doi: 10.1016/0006-8993(77)90956-8. [DOI] [PubMed] [Google Scholar]
- Fox R. E., Holloway J. A., Iggo A., Mokha S. S. Some physiological properties of spinothalamic tract neurones in the cat [proceedings]. J Physiol. 1978 Dec;285:58P–58P. [PubMed] [Google Scholar]
- Fox R. E., Holloway J. A., Iggo A., Mokha S. S. Spinothalamic neurones in the cat: some electrophysiological observations. Brain Res. 1980 Jan 20;182(1):186–190. doi: 10.1016/0006-8993(80)90843-4. [DOI] [PubMed] [Google Scholar]
- Giesler G. J., Jr, Menétrey D., Basbaum A. I. Differential origins of spinothalamic tract projections to medial and lateral thalamus in the rat. J Comp Neurol. 1979 Mar 1;184(1):107–126. doi: 10.1002/cne.901840107. [DOI] [PubMed] [Google Scholar]
- Giesler G. J., Menétrey D., Guilbaud G., Besson J. M. Lumbar cord neurons at the origin of the spinothalamic tract in the rat. Brain Res. 1976 Dec 17;118(2):320–324. doi: 10.1016/0006-8993(76)90718-6. [DOI] [PubMed] [Google Scholar]
- Hancock M. B., Foreman R. D., Willis W. D. Convergence of visceral and cutaneous input onto spinothalamic tract cells in the thoracic spinal cord of the cat. Exp Neurol. 1975 May;47(2):240–248. doi: 10.1016/0014-4886(75)90253-8. [DOI] [PubMed] [Google Scholar]
- Holloway J. A., Fox R. E., Iggo A. Projections of the spinothalamic tract to the thalamic nuclei of the cat. Brain Res. 1978 Nov 24;157(2):336–340. doi: 10.1016/0006-8993(78)90037-9. [DOI] [PubMed] [Google Scholar]
- Jones E. G., Burton H. Cytoarchitecture and somatic sensory connectivity of thalamic nuclei other than the ventrobasal complex in the cat. J Comp Neurol. 1974 Apr 15;154(4):395–432. doi: 10.1002/cne.901540404. [DOI] [PubMed] [Google Scholar]
- McCreery D. B., Bloedel J. R. Reduction of the response of cat spinothalamic neurons to graded mechanical stimuli by electrical stimulation of the lower brain stem. Brain Res. 1975 Oct 24;97(1):151–156. doi: 10.1016/0006-8993(75)90923-3. [DOI] [PubMed] [Google Scholar]
- Meyers D. E., Snow P. J. The morphology of physiologically identified deep spinothalamic tract cells in the lumbar spinal cord of the cat. J Physiol. 1982 Aug;329:373–388. doi: 10.1113/jphysiol.1982.sp014308. [DOI] [PMC free article] [PubMed] [Google Scholar]
- REXED B. A cytoarchitectonic atlas of the spinal cord in the cat. J Comp Neurol. 1954 Apr;100(2):297–379. doi: 10.1002/cne.901000205. [DOI] [PubMed] [Google Scholar]
- Trevino D. L., Carstens E. Confirmation of the location of spinothalamic neurons in the cat and monkey by the retrograde transport of horseradish peroxidase. Brain Res. 1975 Nov 7;98(1):177–182. doi: 10.1016/0006-8993(75)90518-1. [DOI] [PubMed] [Google Scholar]
- Trevino D. L., Maunz R. A., Bryan R. N., Willis W. D. Location of cells of origin of the spinothalamic tract in the lumbar enlargement of cat. Exp Neurol. 1972 Jan;34(1):64–77. doi: 10.1016/0014-4886(72)90188-4. [DOI] [PubMed] [Google Scholar]
- Willis W. D., Kenshalo D. R., Jr, Leonard R. B. The cells of origin of the primate spinothalamic tract. J Comp Neurol. 1979 Dec 15;188(4):543–573. doi: 10.1002/cne.901880404. [DOI] [PubMed] [Google Scholar]
- Willis W. D., Maunz R. A., Foreman R. D., Coulter J. D. Static and dynamic responses of spinothalamic tract neurons to mechanical stimuli. J Neurophysiol. 1975 May;38(3):587–600. doi: 10.1152/jn.1975.38.3.587. [DOI] [PubMed] [Google Scholar]
- Willis W. D., Trevino D. L., Coulter J. D., Maunz R. A. Responses of primate spinothalamic tract neurons to natural stimulation of hindlimb. J Neurophysiol. 1974 Mar;37(2):358–372. doi: 10.1152/jn.1974.37.2.358. [DOI] [PubMed] [Google Scholar]
- Yezierski R. P., Bowker R. M. A retrograde double label tracing technique using horseradish peroxidase and the fluorescent dye 4'-,6-diamidino-2-phenylindole 2HC1 (DAPI). J Neurosci Methods. 1981 Jun;4(1):53–62. doi: 10.1016/0165-0270(81)90018-2. [DOI] [PubMed] [Google Scholar]
