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The red nucleus of the monkey

Topographic localization of somatosensory input and motor output

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Summary

The topographic organization of somatosensory input to the primate red nucleus was investigated by studying receptive fields of rubral neurons, and that of the motor output by delivering trains of microstimulating pulses to evoke movements. A receptive field was identified in 191 of 208 rubral neurons. Most neurons (172) responded to passive movement of one or two joints including digits but some (26) had a cutaneous input. Neurons in both the parvocellular (RNpc) and magnocellular (RNmc) divisions of the nucleus had receptive fields. Neurons which responded to stimulation of the forelimb were located in the dorsomedial part of the nucleus. Those responsive to stimulation of the hindlimb were in the ventrolateral part. Thin regions on the dorsal and ventrolateral borders of the nuclei, respectively, contained neurons responsive to face and tail stimulation. Within the regions representing each limb, neurons receiving an input from the extremity (hand or foot) formed a core surrounded by neurons with an input from more proximal segments. This core extended uninterrupted throughout the RNpc and RNmc.

Movements of individual limb segments including digits were readily evoked by microstimulating in the RNmc with thresholds as low as 3 μA. In most cases, movements were evoked in the direction opposite to the passive movement which drove the neurons at the stimulating site, although fibers of passage limited the analysis of the sensory input-motor output organization with stimulation. We conclude that there is topographic localization of somatosensory input and motor output in the macaque red nucleus. Furthermore, the red nucleus of monkeys contributes to the control of independent movements of limb segments including digits, although the number of axons it sends to the spinal cord is less than 1% of the number of corticospinal axons.

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References

  • Anderson M (1971) Cerebellar and cerebral inputs to physiologically identified efferent call groups in the red nucleus of the cat. Brain Res 30: 49–66

    Google Scholar 

  • Asanuma H, Hunsperger RB (1975) Functional significance of projection from the cerebellar nuclei to the motor cortex in the cat. Brain Res 98: 73–92

    Google Scholar 

  • Asanuma H, Stoney SD Jr, Abzug C (1968) Relationship between afferent input and motor outflow in cat motorsensory cortex. J Neurophysiol 31: 670–681

    Google Scholar 

  • Baldissera F, Lundberg A, Udo M (1972) Stimulation of pre- and postsynaptic elements in the red nucleus. Exp Brain Res 15: 151–167

    Google Scholar 

  • Burton JE, Onoda N (1978) Dependence of the activity of interpositus and red nucleus neurons on sensory input data generated by movement. Brain Res 52: 41–63

    Google Scholar 

  • Castiglioni AJ, Gallaway MC, Coulter JD (1978) Spinal projections from the midbrain in monkey. J Comp Neurol 178: 329–346

    Google Scholar 

  • Crevel H van, Verhaart WJC (1963a) The rate of secondary degeneration in the central nervous system. I. The pyramidal tract in the cat. J Anat 97: 429–449

    Google Scholar 

  • Crevel H van, Verhaart WJC (1963b) The “exact” origin of the pyramidal tract. A quantitative study in the cat. J Anat 97: 495–515

    Google Scholar 

  • Fanardjian VV, Manvelian IA (1978) Neuronal analysis of skin sensitivity representation in the red nucleus of the alert cat. Neuroscience 3: 109–111

    Google Scholar 

  • Ghez C (1975) Input-output relations of the red nucleus in the cat. Brain Res 98: 93–108

    Google Scholar 

  • Ghez C, Kubota K (1977) Activity of red nucleus neurons associated with a skilled forelimb movement in the cat. Brain Res 129: 383–388

    Google Scholar 

  • Ghez C, Vicario D (1978) Discharge of red nucleus neurons during voluntary muscle contraction: activity patterns and correlations with isometric force. J Physiol (Paris) 74: 283–285

    Google Scholar 

  • Grofova I, Marsala J (1959) Tvar a struktura nucleus ruber u člověika. Cesk Morfol 8: 215–237

    Google Scholar 

  • Grofova I, Marsala J (1961) Nucleus ruber kócky. Cesk Morfol 9: 209–220

    Google Scholar 

  • Hartmann-von Monakow K, Akert K, Künzle H (1979) Projections of precentral and premotor cortex to the red nucleus and other midbrain areas in Macacca fascicularis. Exp Brain Res 34: 91–105

    Google Scholar 

  • Humphrey DR, Reitz RR (1976) Cells of origin of corticorubral projections from the arm area of primate motor cortex and their synaptic actions in the red nucleus. Brain Res 110: 162–169

    Google Scholar 

  • Klüver H, Barrera E (1953) A method for the combined staining of cells and fibers in the nervous system. J Neuropathol Exp Neurol 12: 400–403

    Google Scholar 

  • Konigsmark VW, Kalyanaraman UP, Corey P, Murphy EA (1969) An evaluation of techniques in neuronal population estimate: the sixth nerve nucleus. The John Hopkins Med J 125: 146–158

    Google Scholar 

  • Kuypers HGJM, Lawrence DG (1967) Cortical projections to the red nucleus and the brain stem in the rhesus monkey. Brain Res 4: 151–188

    Article  CAS  PubMed  Google Scholar 

  • Kuypers HGJM (1964) The descending pathways to the spinal cord, their anatomy and function. In: Eccles JC, Shadé JP (eds) Progress in brain research, vol 11. Elsevier, New York, pp 172–202

    Google Scholar 

  • Larsen KD, Yumiya H (1979) Organization of the convergence in the intermediate cerebellar nuclei of somatosensory receptive fields with motor cortical evoked responses. Exp Brain Res 36: 477–489

    Google Scholar 

  • Larsen KD, Yumiya H (1980) Motor cortical modulation of feline red nucleus output: cortico-rubral and cerebellar-mediated responses. Exp Brain Res 38: 321–331

    Google Scholar 

  • Lassek AM (1948) The pyramidal tract: basic consideration of corticospinal neuron. Res Publ Assoc Res Nerv Ment Dis 27: 106–128

    Google Scholar 

  • Laursen AM, Wiesendanger M (1966) Motor deficits after transsection of a bulbar pyramid in the cat. Acta Physiol Scand 68: 118–126

    Google Scholar 

  • Lawrence DG, Kuypers HGJM (1968a) The functional organization of the motor system in the monkey. I. The effects of bilateral pyramid lesions. Brain 91: 1–14

    Google Scholar 

  • Lawrence DG, Kuypers HGJM (1968b) The functional organization of the motor system in the monkey. II. The effects of lesions of the descending brainstem pathways. Brain 91: 15–36

    CAS  PubMed  Google Scholar 

  • Lemon RN, Porter R (1976) Afferent input to movement related precentral neurons in conscious monkeys. Proc R Soc Lond [Biol] 194: 313–339

    Google Scholar 

  • Liddell EGT, Phillips CG (1944) Pyramidal section in the cat. Brain 67: 1–9

    Google Scholar 

  • Loe PR, Whitsel BL, Dreyer DA, Metz CB (1977) Body representation in ventrobasal thalamus in macaque: a single unit analysis. J Neurophysiol 40: 1339–1355

    Google Scholar 

  • Marshall C (1934) Experimental lesions of the pyramidal tract. Arch Neurol Psychiatry 32: 778–796

    Google Scholar 

  • Massion J (1967) The mammalian red nucleus. Physiol Rev 47: 359–436

    Google Scholar 

  • Miller RA, Strominger NL (1973) Efferent connections of the red nucleus in the brainstem and spinal cord of the rhesus monkey. J Comp Neurol 152: 327–346

    Google Scholar 

  • Murphy JT, Kwan HC, MacKay WA, Wong YC (1978) Spatial organization of precentral cortex in awake primates. III. Input-output coupling. J Neurophysiol 41: 1132–1139

    Google Scholar 

  • Murphy JT, Wong YC, Kwan HC (1975) Afferent-efferent linkages in motor cortex for single forelimb muscles. J Neurophysiol 38: 990–1014

    Google Scholar 

  • Nishioka S, Nakahama H (1973) Peripheral somatic activation of neurons in the cat red nucleus. J Neurophysiol 36: 296–307

    Google Scholar 

  • Pericavalle V, Santangelo F, Sapienzo S, Serapide MF, Urbano A (1978) Motor responses evoked by microstimulation of restiform body in the cat. Exp Brain Res 33: 241–255

    Google Scholar 

  • Pompeiano O, Brodal A (1957) Experimental demonstration of a somatotopical organization of rubrospinal fibers in the cat. J Comp Neurol 108: 225–252

    Google Scholar 

  • Rosén I, Asanuma H (1972) Peripheral afferent inputs to the forelimb area of the monkey motor cortex: input-output relations. Exp Brain Res 14: 257–273

    Google Scholar 

  • Russell JR, DeMeyer W (1961) The quantitative cortical origin of pyramidal axons of macacca rhesus with some remarks on the slow rate of axolysis. Neurology (Minneap) 11: 96–108

    Google Scholar 

  • Shapovalov AI, Karamjan OA, Tamarova ZA, Kurchavyi GG (1972) Cerbello-rubrospinal effects on hindlimb motoneurons in the monkey. Brain Res 47: 49–59

    Google Scholar 

  • Shinoda Y, Arnold AP, Asanuma H (1976) Spinal branching of corticospinal axons in the cat. Exp Brain Res 26: 215–234

    Google Scholar 

  • Shinoda Y, Ghez C, Arnold A (1977) Spinal branching of rubrospinal axons in the cat. Exp Brain Res 30: 203–218

    Google Scholar 

  • Soechting JF, Burton JE, Onoda N (1978) Relationship between sensory input, motor output and unit activity in interpositus and red nuclei during intentional movement. Brain Res 152: 365–379

    Google Scholar 

  • Stoney SD Jr, Thompson WD, Asanuma H (1968) Excitation of pyramidal tract cells by intracortical microstimulation: effective extent of stimulating current. J Neurophysiol 31: 659–669

    Google Scholar 

  • Strick PL (1976) Activity of ventrolateral thalamic neurons during arm movement. J Neurophysiol 39: 1032–1044

    Google Scholar 

  • Strominger NL, Truscott TC, Miller RA, Royce GJ (1978) An autoradiographic study of the rubroolivary tract in the rhesus monkey. J Comp Neurol 183: 33–46

    Google Scholar 

  • Tower SF (1940) Pyramidal lesions in the monkey. Brain 63: 36–90

    Google Scholar 

  • Wiesendanger M (1969) The pyramidal tract. Recent investigations on its morphology and function. Ergeb Physiol Biol Chem Exp 61: 72–136

    Google Scholar 

  • Wong YC, Kwan HC, MacKay WA, Murphy JT (1978) Spatial organization of precentral cortex in awake primates. I. Somatosensory inputs. J Neurophysiol 41: 1107–1119

    Google Scholar 

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Larsen, K.D., Yumiya, H. The red nucleus of the monkey. Exp Brain Res 40, 393–404 (1980). https://doi.org/10.1007/BF00236148

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