Neurophysiological properties of pallidal neurons in Parkinson's disease
Djordje Sterio MD, DSc
Department of Neurology, New York University School of Medicine, Hospital for Joint Diseases, New York, NY
Search for more papers by this authorCorresponding Author
Dr. Aleksandar Berić MD, DSc
Department of Neurology, New York University School of Medicine, Hospital for Joint Diseases, New York, NY
Department of Neurology, Box 65, Hospital for Joint Diseases, 301 East 17th Street, New York, NY 10003Search for more papers by this authorMichael Dogali MD
Department of Neurosurgery, Division of Functional and Stereotactic Neurosurgery, New York University Medical Center, New York, NY
Search for more papers by this authorEnrico Fazzini DO, PhD
Department of Neurology, New York University School of Medicine, Hospital for Joint Diseases, New York, NY
Search for more papers by this authorGeorge Alfaro PhD
Department of Neurology, Hospital for Joint Diseases, New York, NY
Search for more papers by this authorOrrin Devinsky MD
Department of Neurology, New York University School of Medicine, Hospital for Joint Diseases, New York, NY
Search for more papers by this authorDjordje Sterio MD, DSc
Department of Neurology, New York University School of Medicine, Hospital for Joint Diseases, New York, NY
Search for more papers by this authorCorresponding Author
Dr. Aleksandar Berić MD, DSc
Department of Neurology, New York University School of Medicine, Hospital for Joint Diseases, New York, NY
Department of Neurology, Box 65, Hospital for Joint Diseases, 301 East 17th Street, New York, NY 10003Search for more papers by this authorMichael Dogali MD
Department of Neurosurgery, Division of Functional and Stereotactic Neurosurgery, New York University Medical Center, New York, NY
Search for more papers by this authorEnrico Fazzini DO, PhD
Department of Neurology, New York University School of Medicine, Hospital for Joint Diseases, New York, NY
Search for more papers by this authorGeorge Alfaro PhD
Department of Neurology, Hospital for Joint Diseases, New York, NY
Search for more papers by this authorOrrin Devinsky MD
Department of Neurology, New York University School of Medicine, Hospital for Joint Diseases, New York, NY
Search for more papers by this authorAbstract
Neuronal properties of the human globus pallidus (GP) are not known. Since GP is the major output of the basal ganglia, it may be involved in the pathophysiology of Parkinson's disease. We studied 12 patients with medically resistant Parkinson's disease by using single cell recording of the GP during stereotaxic pallidotomy to define neuronal firing rate and its modulation during active and passive movements. Different frequency and pattern of single cell activity was found in globus pallidus externus compared with globus pallidus internus. Discharge rates of 19% of GP cells were modulated by passive contralateral movements. Pallidal units were most often related solely to single joint movement. Different patterns of activity in relation to the two different movements of the same joint were often observed. We identified somatotopically arranged cell clusters that alter discharge rate with related movements. These findings suggest at least a partial somatotopic organization of the human GP and similarity with experimental results in both healthy and MPTP monkeys, providing a rationale for surgical or pharmacological targeting of GP for treating Parkinson's disease.
References
- 1 Lindvall O, Backlund EO, Farde L, et al. Transplantation in Parkinson's disease: two cases of adrenal medullary grafts to the putamen. Ann Neurol 1987; 22: 475–486
- 2 Lindvall O, Rehncrona S, Brundin P, et al. Human fetal dopamine neurons grafted into the striatum in two patients with severe Parkinson's disease. Arch Neurol 1989; 46: 615–631
- 3 Bakay RAE, Watts RL, Freeman A, et al. Preliminary report on adrenal-brain transplantation for parkinsonism in man. Stereotact Funct Neurosurg 1990; 54–55: 312–323
- 4 Kordower JH, Cochran E, Penn RD, Goetz CG. Putative chromaffin cell survival and enhanced host-derived TH-fiber innervation following a functional adrenal medulla autograft for Parkinson's disease. Ann Neurol 1991; 29: 405–412
- 5 Laitinen LV, Bergenheim AT, Hariz MI. Leksell's posteroventral pallidotomy in the treatment of Parkinson's disease. J Neurosurg 1992; 76: 53–61
- 6 Fazzini E, Dogali M, Eidelberg J, et al. Long-term follow-up on patients with Parkinson's disease receiving unilateral ventroposterior medial pallidotomy. Neurology 1993; 43 (suppl): S271
- 7 Gaze RM, Gillingham FJ, Kalyanaraman S, et al. Microelectrode recordings from the human thalamus. Brain 1964; 87: 691–706
- 8 Jasper HH, Bertrand G. Thalamic units involved in somatic sensation and voluntary and involuntary movements in man. In: DP Purpura, MD Yahr, eds. The thalamus. New York: Columbia University Press, 1966: 365–390
- 9 Albe-Fessard D, Afrel G, Derome P, Guilbaud G. Thalamic unit activity in man. Electroencephalogr Clin Neurophysiol 1967; 25 (suppl): 132–142
- 10 Ohye C, Narabayashi H. Activity of thalamic neurons and their receptive fields in different functional states in man. In: G Somjen, ed. Neurophysiology studied in man. Amsterdam: Excerpta Medica, 1972: 79–84
- 11 Bakay RAE, DeLong MR, Vitek JL. Posteroventral pallidotomy for Parkinson's disease. J Neurosurg 1992; 77: 487–488
- 12 DeLong MR. Activity of pallidal neurons during movement. J Neurophysiol 1971; 34: 414–427
- 13 Filion M, Tremblay L, Bedard PJ. Abnormal influences of passive limb movement on the activity of globus pallidus neurons in parkinsonian monkeys. Brain Res 1988; 444: 165–176
- 14 Richardson RT, DeLong MR. Electrophysiological studies of the functions of the nucleus basalis in primates. In: TC Napier, PW Kalivas, I Hanin, eds. The basal forebrain. New York: Plenum Press, 1991: 233–252
- 15 DeLong MR, Alexander GE, Mitchel SJ, Richardson RT. The contribution of basal ganglia to limb control. Prog Brain Res 1986; 64: 161–174
- 16 Filion M, Tremblay L, Bedard PJ. Effects of dopamine agonists on the spontaneous activity of globus pallidus neurons in monkeys with MPTP-induced parkinsonism. Brain Res 1991; 547: 152–161
- 17 Pare D, Curro'Dossi R, Steriade M. Neuronal basis of the parkinsonian resting tremor: a hypothesis and its implications for treatment. Neuroscience 1990; 35: 217–226
- 18 Lenz FA, Tasker RR, Kwan HC, et al. Single unit analysis of the human ventral thalamic nuclear group: correlation of thalamic “tremor cells” with the 3–6 Hz component of Parinsonian tremor. J Neurosci 1988; 8: 754–764
- 19 Ohye C, Saito Y, Fukamachi A, Narabayashi H. An analysis of the spontaneous rhythmic and non-rhythmic burst discharges in the human thalamus. J Neurol Sci 1974; 22: 245–259
- 20 Ohye C, Albe-Fessard D. Rhythmic discharges related to tremor in humans and monkeys. In: N Chalazonitis, M Boisson, eds. Abnormal neuronal discharges. New York: Raven Press, 1978: 37–48
- 21 Iansek R, Porter R. The monkey globus pallidus: neuronal discharge properties in relation to movement. J Physiol 1980; 301: 439–455
- 22 Hamada I, DeLong MR, Mano NI. Activity of identified wrist-related pallidal neurons during step and ramp wrist movements in the monkey. J Neurophysiol 1990; 64: 1892–1906
- 23 Nambu A, Yoshida S, Jinnai K. Projection on the motor cortex of thalamic neuron with pallidal input in the monkey. Exp Brain Res 1988; 71: 658–662
- 24 Brotchie P, Iansek R, Horne MK. Motor function of the monkey globus pallidus. Brain 1991; 114: 1667–1683
- 25 Cappa SF, Vignolo LA. Transcortical features of aphasia following left thalamic hemorrhage. Cortex 1979; 15: 121–130
- 26
Damasio AR,
Damasio H,
Rizzo M, et al.
Aphasia with nonhemorrhagic lesions in the basal ganglia and internal capsule.
Arch Neurol
1982;
39:
501–506
10.1001/archneur.1982.00510130017003 Google Scholar
- 27 Naeser MA, Alexander MP, Levine HL, et al. Aphasia with predominantly subcortical lesion sites. Arch Neurol 1982; 39: 2–14
- 28 Damasio AR, Damasio H, Chui HC. Neglect following damage to frontal lobe or basal ganglia. Neuropsychologia 1980; 18: 123–132
- 29 Watson RT, Valenstein E, Heilman KM. Thalamic neglect: possible role of the medial thalamus and nucleus reticularis in behavior. Arch Neurol 1981; 38: 501–506
- 30 Ferro J, Kertesz A, Black SE. Subcortical neglect: quantification, anatomy, and recovery. Neurology 1987; 37: 1487–1492
- 31 Wolfe GI, Ross ED. Sensory aprosodia with left hemiparesis from subcortical infarction: right hemisphere analogue of sensory-type aphasia with right hemiparesis. Arch Neurol 1987; 44: 668–671