Abstract
The posterior wall of the central sulcus in forelimb area of SI has been expolred with extracellular micro-electrodes in baboons lightyl anaesthetized with nitrous oxide and sodium thiopentone. 2. The excitatory responses of 130 single units to low intensity electrical stimulation of the deep radial (muscle) and the superficial radial (cutaneous) nerves have been investigated. 3. Units that responded only to muscle nerve stimulation were located in area 3a but overlapped into area 3b. Units that responded only to cutaneous nerve stimulation were found mainly in area 3b but a number occurred in area 3a. Units that responded to both muscle and nerve stimuli (convergent units) were found throughout area 3a and the rostral part of area 3b. 4. Latency analyses of all three response groups revealed a single population of units responding to low threshold muscle nerve stimulation (mean latency 8.5 msec), and both early and late populations responding to low threshold cutaneous nerve stimulation (mean latencies 9.5 and 13.6 msec respectively). A number of the convergent units had very similar latencies for both inputs. 5. Electrical stimulation within area 3a deminstrated a projection from areas 1 and 3b to area 3a; such a pathway may provide a route for excitation of the late skin population which was found mainly in area 3a. 6. In area 3a units commonly responded to light touch, local pressure or deep pressure but only rarely to movement of hairs. A number of the convergent units responded to natural stimulation of cutaneous receptors.
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- ADEY W. R., PORTER R., CARTER I. D. Temporal dispersion in cortical afferent volleys as a factor in perception; an evoked potential study of deep somatic sensibility in the monkey. Brain. 1954;77(2):325–344. doi: 10.1093/brain/77.2.325. [DOI] [PubMed] [Google Scholar]
- BURNS B. D., ROBSON J. G. 'Weightless' micro-electrodes for recording extracellular unit action potentials from the central nervous system. Nature. 1960 Apr 16;186:246–247. doi: 10.1038/186246a0. [DOI] [PubMed] [Google Scholar]
- Brown A. G., Gordon G., Kay R. H. A study of single axons in the cat's medial lemniscus. J Physiol. 1974 Jan;236(1):225–246. doi: 10.1113/jphysiol.1974.sp010432. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Burchfiel J. L., Duffy F. H. Muscle afferent input to single cells in primate somatosensory cortex. Brain Res. 1972 Oct 13;45(1):241–246. doi: 10.1016/0006-8993(72)90231-4. [DOI] [PubMed] [Google Scholar]
- Dreyer D. A., Schneider R. J., Metz C. B., Whitsel B. L. Differential contributions of spinal pathways to body representation in postcentral gyrus of Macaca mulatta. J Neurophysiol. 1974 Jan;37(1):119–145. doi: 10.1152/jn.1974.37.1.119. [DOI] [PubMed] [Google Scholar]
- ELDRED E., HAGBARTH K. E. Facilitation and inhibition of gamma efferents by stimulation of certain skin areas. J Neurophysiol. 1954 Jan;17(1):59–65. doi: 10.1152/jn.1954.17.1.59. [DOI] [PubMed] [Google Scholar]
- Eccles R. M., Phillips C. G., Chien-Ping W. Motor innervation, motor unit organization and afferent innervation of m. extensor digitorum communis of the baboon's forearm. J Physiol. 1968 Sep;198(1):179–192. doi: 10.1113/jphysiol.1968.sp008600. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GORDON G., JUKES M. G. DUAL ORGANIZATION OF THE EXTEROCEPTIVE COMPONENTS OF THE CAT'S GRACILE NUCLEUS. J Physiol. 1964 Sep;173:263–290. doi: 10.1113/jphysiol.1964.sp007456. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goodwin G. M., McCloskey D. I., Matthews P. B. The contribution of muscle afferents to kinaesthesia shown by vibration induced illusions of movement and by the effects of paralysing joint afferents. Brain. 1972;95(4):705–748. doi: 10.1093/brain/95.4.705. [DOI] [PubMed] [Google Scholar]
- HUNT C. C., McINTYRE A. K. An analysis of fibre diameter and receptor characteristics of myelinated cutaneous afferent fibres in cat. J Physiol. 1960 Aug;153:99–112. doi: 10.1113/jphysiol.1960.sp006521. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jones E. G., Powell T. P. Connexions of the somatic sensory cortex of the rhesus monkey. 3. Thalamic connexions. Brain. 1970;93(1):37–56. doi: 10.1093/brain/93.1.37. [DOI] [PubMed] [Google Scholar]
- Jones E. G., Powell T. P. Connexions of the somatic sensory cortex of the rhesus monkey. I. Ipsilateral cortical connexions. Brain. 1969;92(3):477–502. doi: 10.1093/brain/92.3.477. [DOI] [PubMed] [Google Scholar]
- MOUNTCASTLE V. B., DAVIES P. W., BERMAN A. L. Response properties of neurons of cat's somatic sensory cortex to peripheral stimuli. J Neurophysiol. 1957 Jul;20(4):374–407. doi: 10.1152/jn.1957.20.4.374. [DOI] [PubMed] [Google Scholar]
- MOUNTCASTLE V. B. Modality and topographic properties of single neurons of cat's somatic sensory cortex. J Neurophysiol. 1957 Jul;20(4):408–434. doi: 10.1152/jn.1957.20.4.408. [DOI] [PubMed] [Google Scholar]
- MOUNTCASTLE V. B., POWELL T. P. Central nervous mechanisms subserving position sense and kinesthesis. Bull Johns Hopkins Hosp. 1959 Oct;105:173–200. [PubMed] [Google Scholar]
- MOUNTCASTLE V. B., POWELL T. P. Neural mechanisms subserving cutaneous sensibility, with special reference to the role of afferent inhibition in sensory perception and discrimination. Bull Johns Hopkins Hosp. 1959 Oct;105:201–232. [PubMed] [Google Scholar]
- Mountcastle V. B., Talbot W. H., Sakata H., Hyvärinen J. Cortical neuronal mechanisms in flutter-vibration studied in unanesthetized monkeys. Neuronal periodicity and frequency discrimination. J Neurophysiol. 1969 May;32(3):452–484. doi: 10.1152/jn.1969.32.3.452. [DOI] [PubMed] [Google Scholar]
- OSCARSSON O., ROSEN I. PROJECTION TO CEREBRAL CORTEX OF LARGE MUSCLE-SPINDLE AFFERENTS IN FORELIMB NERVES OF THE CAT. J Physiol. 1963 Dec;169:924–945. doi: 10.1113/jphysiol.1963.sp007305. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Oscarsson O., Rosén I. Short-latency projections to the cat's cerebral cortex from skin and muscle afferents in the contralateral forelimb. J Physiol. 1966 Jan;182(1):164–184. doi: 10.1113/jphysiol.1966.sp007816. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Oscarsson O., Rosén I., Sulg I. Organization of neurones in the cat cerebral cortex that are influenced from group I muscle afferents. J Physiol. 1966 Mar;183(1):189–210. doi: 10.1113/jphysiol.1966.sp007860. [DOI] [PMC free article] [PubMed] [Google Scholar]
- POWELL T. P., MOUNTCASTLE V. B. Some aspects of the functional organization of the cortex of the postcentral gyrus of the monkey: a correlation of findings obtained in a single unit analysis with cytoarchitecture. Bull Johns Hopkins Hosp. 1959 Sep;105:133–162. [PubMed] [Google Scholar]
- POWELL T. P., MOUNTCASTLE V. B. The cytoarchitecture of the postcentral gyrus of the monkey Macaca mulatta. Bull Johns Hopkins Hosp. 1959 Sep;105:108–131. [PubMed] [Google Scholar]
- Paul R. L., Merzenich M., Goodman H. Representation of slowly and rapidly adapting cutaneous mechanoreceptors of the hand in Brodmann's areas 3 and 1 of Macaca mulatta. Brain Res. 1972 Jan 28;36(2):229–249. doi: 10.1016/0006-8993(72)90732-9. [DOI] [PubMed] [Google Scholar]
- Phillips C. G., Powell T. P., Wiesendanger M. Projection from low-threshold muscle afferents of hand and forearm to area 3a of baboon's cortex. J Physiol. 1971 Sep;217(2):419–446. doi: 10.1113/jphysiol.1971.sp009579. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ROSE J. E. The cellular structure of the auditory region of the cat. J Comp Neurol. 1949 Dec;91(3):409-39, incl 5 pl. doi: 10.1002/cne.900910305. [DOI] [PubMed] [Google Scholar]
- Rosén I. Functional organization of group I activated neurones in the cuneate nucleus of the cat. Brain Res. 1967 Dec;6(4):770–772. doi: 10.1016/0006-8993(67)90133-3. [DOI] [PubMed] [Google Scholar]
- Schwarz D. W., Deecke L., Fredrickson J. M. Cortical projection of group I muscle afferents to areas 2, 3a, and the vestibular field in the rhesus monkey. Exp Brain Res. 1973 Jul 30;17(5):516–526. doi: 10.1007/BF00234865. [DOI] [PubMed] [Google Scholar]
- Schwarz D. W., Fredrickson J. M. Tactile direction sensitivity of area 2 oral neurons in the rhesus monkey cortex. Brain Res. 1971 Apr 2;27(2):397–401. doi: 10.1016/0006-8993(71)90270-8. [DOI] [PubMed] [Google Scholar]
- Werner G., Whitsel B. L. Topology of the body representation in somatosensory area I of primates. J Neurophysiol. 1968 Nov;31(6):856–869. doi: 10.1152/jn.1968.31.6.856. [DOI] [PubMed] [Google Scholar]
- Whitsel B. L., Roppolo J. R., Werner G. Cortical information processing of stimulus motion on primate skin. J Neurophysiol. 1972 Sep;35(5):691–717. doi: 10.1152/jn.1972.35.5.691. [DOI] [PubMed] [Google Scholar]

