3
Views
0
CrossRef citations to date
0
Altmetric
Original Article

Peripheral and Spinal Inputs to Physiologically Identified Thalamic and Nonthalamic Relay Neurons in Cat Cuneate Nucleus

Pages 253-268 | Published online: 10 Jul 2009

References

  • Andersen P., Eccles J. C., Schmidt R. F., Yokota T. Identification of relay cells and interneurons in the cuneate nucleus. J. Neuro‐physiol. 1964; 27: 1080–1095
  • Berman A. L. The Brain Stem of the Cat: A Cytoarchitectonic Atlas with Stereotaxic Coordinates. University of Wisconsin Press, Madison 1968
  • Blum P., Bromberg M. B., Whitehorn D. Population analysis of single units in the cuneate nucleus of the cat. Exp. Neurol. 1975; 48: 57–78
  • Bowsher D. Place and modality analysis in caudal reticular formation. J. Physiol. (Lond.) 1970; 209: 473–486
  • Bromberg M. B., Burnham J. A., Towe A. L. Doubly projecting neurons of the dorsal column nuclei. Neurosci. Lett. 1981; 25: 215–220
  • Bromberg M. B., Whitehorn D. Myelinated fiber types in the superficial radial nerve of the cat and their central projections. Brain Res. 1974; 78: 157–163
  • Brodal A. Reticulo‐cerebellar connections in the cat. J. Comp. Neurol. 1953; 98: 113–154
  • Bull M. S., Berkley K. J. Differences in the neurons that project from the dorsal column nuclei to the diencephalon, pretectum, and tectum in the cat. Somatosens. Res. 1984; 1: 281–300
  • Burton H., Loewy A. D. Projections to the spinal cord from medullary somatosensory relay nuclei. J. Comp. Neurol. 1977; 173: 773–792
  • Cesa‐Bianchi M. G., Sotgiu M. L. Control by brain stem reticular formation of sensory transmission in Burdach nucleus: Analysis of single units. Brain Res. 1969; 13: 129–139
  • Cheek M. D., Rustioni A., Trevino D. L. Dorsal column nuclei projections to the cerebellar cortex in cats as revealed by the use of the retrograde transport of horseradish peroxidase. J. Comp. Neurol. 1975; 164: 31–46
  • Cooke J. D., Larson B., Oscarsson O., Sjölund B. Origin and termination of cuneocerebellar tract. Exp. Brain Res. 1971a; 13: 339–358
  • Cooke J. D., Larson B., Oscarsson O., Sjölund B. Organization of afferent connections to cuneocerebellar tract. Exp. Brain Res. 1971b; 13: 359–377
  • Craig A. D. Spinal and medullary input to the lateral cervical nucleus. J. Comp. Neurol. 1978; 181: 729–744
  • Dart A. M., Gordon G. Some properties of spinal connections of the cat's dorsal column nuclei which do not involve the dorsal columns. Brain Res. 1973; 58: 61–68
  • Dykes R. W., Rasmusson D. D., Rehman N. B. Submodality segregation and receptive‐field sequences in cuneate, gracile, and external cuneate nuclei of the cat. J. Neurophysiol. 1982; 47: 389–416
  • Ellis L. C., Diorio J. P., Rustioni A. Thalamic projecting neurons in the feline nucleus cuneatus: A combined horseradish peroxidase and high voltage electron microscopic study. J. Neurocytol. 1982; 11: 3–17
  • Ellis L. C., Rustioni A. A correlative HRP, Golgi, and EM study of the intrinsic organization of the feline dorsal column nuclei. J. Comp. Neurol. 1981; 197: 341–367
  • Ennever J. A., Towe A. L. Response of somatosensory cerebral neurons to stimulation of dorsal and dorsolateral spinal funiculi. Exp. Neurol. 1974; 43: 124–142
  • Gordon G., Grant G. Dorsolateral spinal afferents to some medullary sensory nuclei: An anatomical study in the cat. Exp. Brain Res. 1982; 46: 12–23
  • Gordon G., Jukes M. G. M. Dual organization of the exteroceptive components of the cat's gracile nucleus. J. Physiol. (Lond.) 1964; 173: 263–290
  • Golovchinsky V. Patterns of responses of neurons in cuneate nucleus to controlled mechanical stimulation of cutaneous velocity receptors in the cat. J. Neurophysiol. 1980; 43: 1673–1699
  • Hand P., van Winkle T. The efferent connections of the feline nucleus cuneatus. J Comp. Neur. 1977; 171: 83–110
  • Harris F. A. Population analysis of somatosensory thalamus in the cat. Nature 1970; 225: 559–562
  • Horch K. W., Tuckett R. P., Burgess P. R. A key to the classification of cutaneous mechanoreceptors. J. Invest. Dermatol. 1977; 69: 75–82
  • Jabbur S. J., Baker M. A., Towe A. L. Wide‐field neurons in thalamic nucleus ventralis posterolateralis of the cat. Exp. Neurol. 1972; 36: 213–238
  • Jabbur S. J., Banna N. R. Widespread cutaneous inhibition in dorsal column nuclei. J. Neurophysiol. 1970; 33: 616–624
  • Jundi A. S., Saadé N. E., Banna N. R., Jabbur S. J. Modification of transmission in the cuneate nucleus by raphe and periaqueductal gray stimulation. Brain Res. 1982; 250: 349–352
  • Kuypers H. G. J. M., Tuerk J. D. The distribution of the cortical fibers within the nuclei cuneatus and gracilis in the cat. J. Anat. 1964; 98: 143–162
  • Nyberg G., Blomqvist A. The termination of forelimb nerves in the feline cuneate nucleus demonstrated by the transganglionic transport method. Brain Res. 1982; 248: 209–222
  • Rosén I. Afferent connexions to group I activated cells in the main cuneate nucleus of the cat. J. Physiol. (Lond.) 1969; 205: 209–236
  • Rosén I., Sjölund B. Organization of group I activated cells in the main and external cuneate nuclei of the cat: Identification of muscle receptors. Exp. Brain Res. 1973; 16: 221–237
  • Rustioni A. Non‐primary afferents to the cuneate nucleus in the brachial dorsal funiculus of the cat. Brain Res. 1974; 75: 247–259
  • Rustioni A., Kaufman A. B. Identification of cells of origin of non‐primary afferents to the dorsal column nuclei of the cat. Exp. Brain Res. 1977; 27: 1–14
  • Rustioni A., Molenaar I. Dorsal column nuclei afferents in the lateral funiculus of the cat: Distribution pattern and absence of sprouting after chronic deafferentation. Exp. Brain Res. 1975; 23: 1–12
  • Saadé N. E., Jabbur S. J. Interactions of ventral tract and dorsal column inputs into the cat cuneate nucleus. Brain Res. 1984; 299: 178–181
  • Saadé N. E., Jabbur S. J., Banna N. R. Interactions of isolated dorsal column and ventral spinal ascending volleys on single neurons in the postcruciate cortex (SmI) of the cat. Brain Res. 1980; 201: 446–451
  • Saadé N. E., Salibi N. A., Banna N. R., Towe A. L., Jabbur S. J. Spinal input pathways affecting the medullary gigantocellular reticular nucleus. Exp. Neurol. 1983; 80: 582–600
  • Sotgiu M. L., Margnelli M. Electrophysiological identification of pontomedullary reticular neurons directly projecting into dorsal column nuclei. Brain Res. 1976; 103: 443–453
  • Sotgiu M. L., Marini G. Reticulocuneate projections as revealed by horseradish peroxidase axonal transport. Brain Res. 1977; 128: 341–345
  • Towe A. L., Harding G. W. Extracellular microelectrode sampling bias. Exp. Neurol. 1970; 29: 366–381
  • Towe A. L., Tyner C. F., Nyquist J. K. Facilitatory and inhibitory modulation of wide‐field neuron activity in postcruciate cerebral cortex of the domestic cat. Exp. Neurol. 1976; 50: 734–756
  • Uddenberg N. Functional organization of long, second‐order afferents in the dorsal funiculus. Exp. Brain Res. 1968; 4: 377–382
  • Whitehorn D., Morse R. W., Towe A. L. Role of the spinocervical tract in production of the primary cortical response evoked by forepaw stimulation. Exp. Neurol. 1969; 25: 349–364

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.