Neuronal synchronization of tonically active neurons in the striatum of normal and parkinsonian primates.

1. Previous studies indicate that tonically active neurons (TANs) are the cholinergic interneurons of the striatum and predict that their activity is synchronized. To test whether TANs do fire synchronously, and whether dopamine depletion affects their synchronization, we recorded the simultaneous activity of several TANs in the putamens of two vervet monkeys before and after 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) treatment. 2. Cross-correlation analysis revealed that most pairs of TANS (33 of 54; 61.1%) fire synchronously at +/- 60-ms delay. Correlated activity was more common between neurons with characteristic response to reward (17 of 19 pairs; 89.5%). 3. Cross-correlation study of 24 triplets of TANS showed synchronization of spiking activity of all 3 TANS in only 29.2% of cases (7 of 24 triplets). Correlated activity of two of three possible pairs was found in 25% of the cases. 4. After MPTP treatment and the development of parkinsonian symptoms, most TANS' auto- and cross-correlograms (22 of 28 units; 78.6%; and 23 of 28 pairs; 82.1%) became oscillatory. The number of correlated pairs was slightly increased (24 of 28; 85.7%). The strength of the synchronization was not significantly different from the normal values. 5. These findings support the notion that TANs function as distributed, partially overlapping synchronized networks. However, a normal dopaminergic system is not essential for synchronization of TANs; on the contrary, dopaminergic activity may even have a desynchronizing effect on the basal ganglia's system.

[1]  A. Barbeau The pathogenesis of Parkinson's disease: a new hypothesis. , 1962, Canadian Medical Association journal.

[2]  G. P. Moore,et al.  Neuronal spike trains and stochastic point processes. I. The single spike train. , 1967, Biophysical journal.

[3]  G. P. Moore,et al.  Neuronal spike trains and stochastic point processes. II. Simultaneous spike trains. , 1967, Biophysical journal.

[4]  G L Gerstein,et al.  Mutual temporal relationships among neuronal spike trains. Statistical techniques for display and analysis. , 1972, Biophysical journal.

[5]  R. Regan,et al.  DETECTION OF , 2012 .

[6]  C M Contreras,et al.  A stereotaxic brain atlas of the green monkey (Cercopithecus aethiops aethiops). , 1981, Boletin de estudios medicos y biologicos.

[7]  J. Lehmann,et al.  The striatal cholinergic interneuron: Synaptic target of dopaminergic terminals? , 1983, Neuroscience.

[8]  J. Rajkowski,et al.  Tonically discharging putamen neurons exhibit set-dependent responses. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[9]  W. J. Daunicht,et al.  An on-line spike form discriminator for extracellular recordings based on an analog correlation technique , 1986, Journal of Neuroscience Methods.

[10]  S J Kish,et al.  Biochemical pathophysiology of Parkinson's disease. , 1987, Advances in neurology.

[11]  L. Tremblay,et al.  Abnormal influences of passive limb movement on the activity of globus pallidus neurons in parkinsonian monkeys , 1988, Brain Research.

[12]  M. Delong,et al.  Parkinsonian Symptomatology An Anatomical and Physiological Analysisa a , 1988 .

[13]  W. C. Miller,et al.  Parkinsonian symptomatology. An anatomical and physiological analysis. , 1988, Annals of the New York Academy of Sciences.

[14]  O. Hikosaka,et al.  Functional properties of monkey caudate neurons. I. Activities related to saccadic eye movements. , 1989, Journal of neurophysiology.

[15]  M K Habib,et al.  Dynamics of neuronal firing correlation: modulation of "effective connectivity". , 1989, Journal of neurophysiology.

[16]  L. Tremblay,et al.  Responses of pallidal neurons to striatal stimulation in monkeys with MPTP-induced parkinsonism , 1989, Brain Research.

[17]  S. T. Kitai,et al.  Firing patterns and synaptic potentials of identified giant aspiny interneurons in the rat neostriatum , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[18]  E. Fetz,et al.  Synaptic Interactions between Cortical Neurons , 1991 .

[19]  I. Shoulson [Therapeutic strategies in Parkinson's disease]. , 1991, Archivos de neurobiologia.

[20]  Paul Antoine Salin,et al.  Spatial and temporal coherence in cortico-cortical connections: a cross-correlation study in areas 17 and 18 in the cat. , 1992, Visual neuroscience.

[21]  C. Geula,et al.  Cholinergic innervation of the human striatum, globus pallidus, subthalamic nucleus, substantia nigra, and red nucleus , 1992, The Journal of comparative neurology.

[22]  M. Ahissar,et al.  Dependence of cortical plasticity on correlated activity of single neurons and on behavioral context. , 1992, Science.

[23]  J. Bolam,et al.  Input from the frontal cortex and the parafascicular nucleus to cholinergic interneurons in the dorsal striatum of the rat , 1992, Neuroscience.

[24]  J. Wickens A Theory of the Striatum , 1993 .

[25]  Kitai St,et al.  Cholinergic and dopaminergic modulation of potassium conductances in neostriatal neurons. , 1993 .

[26]  G. Percheron,et al.  Cholinergic neurons of the rat and primate striatum are morphologically different. , 1993, Progress in brain research.

[27]  H. Bergman,et al.  The primate subthalamic nucleus. II. Neuronal activity in the MPTP model of parkinsonism. , 1994, Journal of neurophysiology.

[28]  Charles J. Wilson,et al.  Surround inhibition among projection neurons is weak or nonexistent in the rat neostriatum. , 1994, Journal of neurophysiology.

[29]  A M Graybiel,et al.  The basal ganglia and adaptive motor control. , 1994, Science.

[30]  Micaela Morelli,et al.  Modulatory functions of neurotransmitters in the striatum: ACh/dopamine/NMDA interactions , 1994, Trends in Neurosciences.

[31]  H. Bergman,et al.  Parkinsonian Tremor is Associated with Low Frequency Neuronal Oscillations in Selective Loops of the Basal Ganglia , 1994 .

[32]  A. Graybiel,et al.  Responses of tonically active neurons in the primate's striatum undergo systematic changes during behavioral sensorimotor conditioning , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[33]  A. Graybiel,et al.  Effect of the nigrostriatal dopamine system on acquired neural responses in the striatum of behaving monkeys. , 1994, Science.

[34]  Charles J. Wilson,et al.  Striatal interneurones: chemical, physiological and morphological characterization , 1995, Trends in Neurosciences.

[35]  C. Gilbert,et al.  Receptive field expansion in adult visual cortex is linked to dynamic changes in strength of cortical connections. , 1995, Journal of neurophysiology.

[36]  D. James Surmeier,et al.  Molecular and cellular mechanisms of neostriatal function , 1995 .

[37]  A. Graybiel,et al.  Temporal and spatial characteristics of tonically active neurons of the primate's striatum. , 1995, Journal of neurophysiology.

[38]  H. Bergman,et al.  Neurons in the globus pallidus do not show correlated activity in the normal monkey, but phase-locked oscillations appear in the MPTP model of parkinsonism. , 1995, Journal of neurophysiology.