Basal ganglia circuits and thalamocortical outputse

Handbook of Tourette's Syndrome and Related Tic and Behavioral Disorders, Second Edition

Volumn , Issue , 2004, Pages 253-272

  Mink, Jonathan W ^a  

^a UNIVERSITY OF ROCHESTER SCHOOL OF MEDICINE AND DENTISTRY   (United States)

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EID: 33745609967     PISSN: None     EISSN: None     Source Type: Book    
DOI: None     Document Type: Chapter

References (88)

1. Denny-Brown D, Yanagisawa N. The role of the basal ganglia in the initiation of movement. In: Yahr MD, ed. The Basal Ganglia. New York: Raven Press, 1976:115–149.
2. Penney JB, Young AB. Speculations on the functional anatomy of basal ganglia disorders. Annu Rev Neurosci 1983; 6:73–94.
3. Leckman J, Cohen D. Tourette’s Syndrome—Tics, Obsessions, Compulsions: Developmental Psychopathology and Clinical Care. New York: John Wiley & Sons, 1999:584.
4. Mink JW. Basal ganglia dysfunction in Tourette’s syndrome: a new hypothesis. Pediatr Neurol 2001; 25:190–198.
5. Albin RL, Young AB, Penney JB. The functional anatomy of basal ganglia disorders. Trends Neurosci 1989; 12:366–375.
6. DeLong MR. Primate models of movement disorders of basal ganglia origin. Trends Neurosci 1990; 13:281–285.
7. Mink JW. The basal ganglia: focused selection and inhibition of competing motor programs. Prog Neurobiol 1996; 50:381–425.
8. Redgrave P, Prescott T, Gurney K. The basal ganglia: a vertebrate solution to the selection problem? Neuroscience 1999; 89:1009–1023.
9. Mink J. The basal ganglia and involuntary movements: impaired inhibition of competing motor patterns. Arch Neurol 2003; 60:1365–1368.
10. Kemp JM, Powell TPS. The corticostriate projection in the monkey. Brain 1970; 93:525–546.
11. Russchen F, Bakst I, Amaral D, Price J. The amygdalostriatal projections in the monkey. An anterograde tracing study. Brain Res 1985; 329:241–257.
12. Fudge J, Kunishio K, Walsh C, Richard D, Haber S. Amygdaloid projections to ventromedial striatal subterritories in the primate. Neuroscience 2002; 110: 257–275.
13. Cherubini E, Herrling PL, Lanfumey L, Stanzione P. Excitatory amino acids in synaptic excitation of rat striatal neurones in vitro. J Physiol 1988; 400:677–690.
14. Bouyer JJ, Park DH, Joh TH, Pickel VM. Chemical and structural analysis of the relation between cortical inputs and tyrosine hydroxylase-containing terminals in rat neostriatum. Brain Res 1984; 302:267–275.
15. Alexander GE, DeLong MR, Strick PL. Parallel organization of functionally segregated circuits linking basal ganglia and cortex. Annu Rev Neurosci 1986; 9:357–381.
16. Wilson CJ, Groves PM. Fine structure and synaptic connections of the common spiny neuron of the rat neostriatum: a study employing intracellular injection of horseradish peroxidase. J Comp Neurol 1980; 194:599–614.
17. Selemon LD, Goldman-Rakic PS. Longitudinal topography and interdigitation of corticostriatal projections in the rhesus monkey. J Neurosci 1985; 5:776–794.
18. Flaherty AW, Graybiel AM. Corticostriatal transformations in the primate somatosensory system. Projections from physiologically mapped body-part representations. J Neurophysiol 1991; 66:1249–1263.
19. Graybiel AM, Aosaki T, Flaherty AW, Kimura M. The basal ganglia and adaptive motor control. Science 1994; 265:1826–1831.
20. Lapper SR, Bolam JP. Input from the frontal cortex and the parafascicular nucleus to cholinergic interneurons in the dorsal striatum of the rat. Neuroscience 1992; 51:533–545.
21. Sadikot AF, Parent A, Francois C. Efferent connections of the centromedian and parafascicular thalamic nuclei in the squirrel monkey: a PHA-L study of subcortical projections. J Comp Neurol 1992; 315:137–159.
22. McFarland NR, Haber SN. Organization of thalamostriatal terminals from the ventral motor nuclei in the macaque. J Comp Neurol 2001; 429:321–336.
23. Izzo PN, Bolam JP. Cholinergic synaptic input to different parts of spiny striatonigral neurons in the rat. J Comp Neurol 1988; 269:219–234.
24. Penny GR, Afsharpour S, Kitai ST. The glutamate decarboxylase-, leucine enkephalin-, methionine enkephalin- and substance P-immunoreactive neurons in the neostriatum of the rat and cat: evidence for partial population overlap. Neuroscience 1986; 17:1011–1045.
25. Bolam JP, Hanley JJ, Booth PA, Bevan MD. Synaptic organisation of the basal ganglia. J Anat 2000; 196:527–542.
26. Carpenter MB. Anatomy of the corpus striatum and brain stem integrating systems. In: Brooks VB, ed. Handbook of Physiology: The Nervous System. Bethesda, MD: American Physiological Society, 1981:947–995.
27. Lavoie B, Parent A. Immunohistochemical study of the serotoninergic innervations of the basal ganglia in the squirrel monkey. J Comp Neurol 1990; 299: 1–16.
28. Sibley DR, Monsma FJ. Molecular biology of dopamine receptors. Trends Pharmacol Sci 1992; 13:61–69.
29. Surmeier DJ, Reiner A, Levine MS, Ariano MA. Are neostriatal dopamine receptors co-localized? Trends Neurosci 1993; 16:299–305.
30. Hernandez-Lopez S, Bargas J, Surmeier DJ, Reyes A, Galarraga E. D1receptor activation enhances evoked discharge in neostriatal medium spiny neurons by modulating an L-type Ca2+ conductance. J Neurosci 1997; 17:3334–3342.
31. Ribak CE, Vaughn JE, Roberts E. The GABA neurons and their axon terminals in rat corpus striatum as demonstrated by GAD immunocytochemistry. J Comp Neurol 1979; 187:261–283.
32. Graybiel AM. Neurotransmitters and neuromodulators in the basal ganglia. Trends Neurosci 1990; 13:244–254.
33. Gerfen CR, Engber TM, Mahan LC, Susel Z, Chase TN, Monsma FJ, Sibley DR. D1 and D2 dopamine receptor regulated gene expression of striatonigral and striatopallidal neurons. Science 1990; 250:1429–1432.
34. Gerfen CR, Young WS III. Distribution of striatonigral and striatopallidal peptidergic neurons in both patch and matrix compartments: an in situ hybridization histochemistry and fluorescent retrograde tracing study. Brain Res 1988; 460:161–167.
35. Graybiel AM, Ragsdale CW. Histochemically distinct compartments in the striatum of human, monkey and cat demonstrated by acetylcholinesterase staining. Proc Natl Acad Sci USA 1978; 75:5723–5726.
36. Gerfen CR. The neostriatal mosaic: multiple levels of compartmental organization in the basal ganglia. Annu Rev Neurosci 1992; 15:285–320.
37. Graybiel AM, Ragsdale CW, Yoneika ES, Elde RP. An immunohistochemical study of enkephalins and other neuropeptides in the striatum of the cat with evidence that the opiate peptides are arranged to form mosaic patterns in register with striosomal compartments visible with acetylcholinesterase staining. Neuroscience 1981; 6:377–397.
38. Rouzaire-Dubois B, Scarnati E. Pharmacological study of the cortical-induced excitation of subthalamic nucleus neurons in the rat: evidence for amino acids as putative neurotransmitters. Neuroscience 1987; 21:429–440.
39. Fujimoto K, Kita H. Response characteristics of subthalamic neurons to the stimulation of the sensorimotor cortex in the rat. Brain Res 1993; 609:185–192.
40. Hartmann-von Monakow K, Akert K, Kunzle H. Projections of the precentral motor cortex and other cortical areas of the frontal lobe to the subthalamic nucleus in the monkey. Exp Brain Res 1978; 33:395–403.
41. Kita H, Chang HT, Kitai ST. Pallidal inputs to subthalamus: intracellular analysis. Brain Res 1983; 264:255–265.
42. Rinvik E, Ottersen OP. Terminals of subthalamonigral fibres are enriched with glutamate-like immunoreactivity: an electron microscopic, immunogold analysis in the cat. J Chem Neuroanat 1993; 6:19–30.
43. Brotchie JM, Crossman AR. D-[³H]Aspartate and [14C]GABA uptake in the basal ganglia of rats following lesions in the subthalamic region suggest a role for excitatory amino acid but not GABA-mediated transmission in subthalamic nucleus efferents. Exp Neurol 1991; 113:171–181.
44. Parent A, Smith Y, Filion M, Dumas J. Distinct afferents to internal and external pallidal segments in the squirrel monkey. Neurosci Lett 1989; 96:140– 144.
45. Nambu A, Takada M, Inase M, Tokuno H. Dual somatotopical representations in the primate subthalamic nucleus: evidence for ordered but reversed body-map transformations from the primary motor cortex and the supplementary motor area. J Neurosci 1996; 16:2671–2683.
46. DeLong MR, Crutcher MD, Georgopoulos AP. Primate globus pallidus and subthalamic nucleus: functional organization. J Neurophysiol 1985; 53:530– 543.
47. Maurice N, Deniau J, Glowinski J, Thierry A. Relationships between the prefrontal cortex and the basal ganglia in the rat: physiology of the cortico-subthalamic circuits. J Neurosci 1998; 18:9539–9546.
48. Percheron G, Yelnik J, Francois C. A Golgi analysis of the primate globus pallidus. III. Spatial organization of the striato–pallidal complex. J Comp Neurol 1984; 227:214–227.
49. Francois C, Yelnik J, Percheron G. Golgi study of the primate substantia nigra. II. Spatial organization of dendritic arborizations in relation to the cytoarchitectonic boundaries and to the striatonigral bundle. J Comp Neurol 1987; 265: 473–493.
50. Penney JB, Young AB. GABA as the pallidothalamic neurotransmitter: implications for basal ganglia function. Brain Res 1981; 207:195–199.
51. Rye DB, Lee HJ, Saper CB, Wainer BH. Medullary and spinal efferents of the pedunculopontine tegmental nucleus and adjacent mesopontine tegmentum in the rat. J Comp Neurol 1988; 269:315–341.
52. Parent A, De Bellefeuille L. Organization of efferent projections from the internal segment of globus pallidus in primate as revealed by fluorescence retrograde labelling method. Brain Res 1982; 245:201–213.
53. Francois C, Percheron G, Yelnik J, Tande D. A topographic study of the course of nigral axons and of the distribution of pallidal axonal endings in the centre median–parafascicular complex of macaques. Brain Res 1988; 473:181–186.
54. Georgopoulos AP, DeLong MR, Crutcher MD. Relation between parameters of step-tracking movements and single cell discharge in the globus pallidus and subthalamic nucleus of the behaving monkey. J Neurosci 1983; 3:1586–1598.
55. Middleton FA, Strick PL. Anatomical evidence for cerebellar and basal ganglia involvement in higher cognitive function. Science 1994; 266:458–461.
56. Hoover JE, Strick PL. Multiple output channels in the basal ganglia. Science 1993; 259:819–821.
57. Alexander GE, Crutcher MD. Functional architecture of basal ganglia circuits: neural substrates of parallel processing. Trends Neurosci 1990; 13:266–271.
58. Bolam JP, Smith Y. The striatum and the globus pallidus send convergent synaptic inputs onto single cells in the entopeduncular nucleus of the rat: a double anterograde labelling study combined with postembedding immunocytochemistry for GABA. J Comp Neurol 1992; 321:456–476.
59. Bevan MD, Booth PA, Eaton SA, Bolam JP. Selective innervation of neostriatal interneurons by a subclass of neuron in the globus pallidus of the rat. J Neurosci 1998; 18:9438–9452.
60. Hedreen JC, DeLong MR. Organization of striatopallidal, striatonigral, nigrostriatal projections in the macaque. J Comp Neurol 1991; 304:569–595.
61. Haber SN, Fudge JL, McFarland NR. Striatonigrostriatal pathways in primates form an ascending spiral from the shell to the dorsolateral striatum. J Neurosci 2000; 20:2369–2382.
62. Kita H. Responses of globus pallidus neurons to cortical stimulation: intracellular study in the rat. Brain Res 1992; 589:84–90.
63. Maurice N, Deniau J, Glowinski J, Thierry A. Relationships between the prefrontal cortex and the basal ganglia in the rat: physiology of the cortico-nigral circuits. J Neurosci 1999; 19:4674–4681.
64. Nambu A, Tokuno H, Hamada I, Kita H, Imanishi M, Akazawa T, Ikeuchi Y, Hasegawa N. Excitatory cortical inputs to pallidal neurons via the subthalamic nucleus in the monkey. J Neurophysiol 2000; 84:289–300.
65. Parent A, Hazrati L-N. Anatomical aspects of information processing in primate basal ganglia. Trends Neurosci 1993; 16:111–116.
66. Mink JW, Thach WT. Basal ganglia intrinsic circuits and their role in behavior. Curr Opin Neurobiol 1993; 3:950–957.
67. Thach WT, Mink JW, Goodkin HP, Keating JG. Combining versus gating motor programs: differential roles for cerebellum and basal ganglia. In: Mano N, Hamada I, DeLong MR, eds. Role of the Cerebellum and Basal Ganglia in Voluntary Movement. Amsterdam: Elsevier Science Publishers, 1993:235–245.
68. Mink JW, Thach WT. Basal ganglia motor control. III. Pallidal ablation: normal reaction time, muscle cocontraction, slow movement. J Neurophysiol 1991; 65:330–351.
69. Hikosaka O, Wurtz RH. Modification of saccadic eye movements by GABA related substances. II. Effects of muscimol in monkey substantia nigra pars reticulata. J Neurophysiol 1985; 53:292–308.
70. Ferry A, Lu X-C, Price JL. Effects of excitotoxic lesions in the ventral striatopallidal– thalamocortical pathway on odor reversal learning: inability to extinguish an incorrect response. Exp Brain Res 2000; 131:320–335.
71. Perlmutter JS, Tempel LW, Black KJ, Parkinson MPTP induces dystonia D, Todd RD. and parkinsonism. Clues to the pathophysiology of dystonia. Neurology 1997; 49:1432–1438.
72. Carpenter MB, Carpenter CS. Analysis of somatotopic relations of the corpus Luysi in man and monkey. J Comp Neurol 1951; 95:349–370.
73. Alexander GE, DeLong MR. Microstimulation of the primate striatum. II. Somatotopic organization of striatal microexcitable zones and their relation to neuronal response properties. J Neurophysiol 1985; 53:1417–1430.
74. Peterson B, Leckman J. The temporal dynamics of tics in Gilles de la Tourette syndrome. Biol Psychiatry 1998; 44:1337–1348.
75. Singer HS. Neurobiological issues in Tourette syndrome. Brain Dev 1994; 16:353–364.
76. Kalsner S, Westfall TC. Presynaptic receptors and the question of autoregulation of neurotransmitter release. Ann NY Acad Sci 1990; 604:652–655.
77. Nicola S, Surmeier J, Malenka R. Dopaminergic modulation of neuronal excitability in the striatum and nucleus accumbens. Annu Rev Neurosci 2000; 23:185–215.
78. Wilson CJ, Kawaguchi Y. The origins of two-state spontaneous membrane potential fluctuations of neostriatal spiny neurons. J Neurosci 1996; 16:2397– 2410.
79. Groves PM, Garcia-Munoz M, Linder JC, Manley MS, Martine ME, Young SJ. Elements of the intrinsic organization and information processing in the neostriatum. In: Houk JC, Davis JL, Beiser DG, eds. Models of Information Processing in the Basal Ganglia. Cambridge, MA: MIT Press, 1995:51–96.
80. Wickens J, Kotter R. Cellular models of reinforcement. In: Houk JC, Davis JL, Beiser DG, eds. Models of Information Processing in the Basal Ganglia. Cambridge, MA: MIT Press, 1995:187–214.
81. Centonze D, Gubellini P, Picconi B, Calabresi P, Giacomini P, Bernardi G. Unilateral dopamine denervation blocks corticostriatal LTP. J Neurophysiol 1999; 82:3575–3579.
82. Jog M, Kubota Y, Connolly C, Hillegaart V, Graybiel A. Building neural representations of habits. Science 1999; 286:1745–1749.
83. Knowlton B, Mangels J, Squire L. A neostriatal habit learning system in humans. Science 1996; 273:1399–1402.
84. Aosaki T, Kimura M, Graybiel AM. Temporal and spatial characteristics of tonically active neurons of the primate’s striatum. J Neurophysiol 1995; 73:1234– 1252.
85. Schultz W, Romo R, Ljungberg T, Mirenowicz J, Hollerman JR, Dickinson A. Reward-related signals carried by dopamine neurons. In: Houk JC, Davis JL, Beiser DG, eds. Models of Information Processing in the Basal Ganglia. Cambridge, MA: MIT Press, 1995:233–249.
86. Tremblay L, Hollerman J, Schultz W. Modifications of reward expectationrelated neuronal activity during learning in primate striatum. J Neurophysiol 1998; 80:964–977.
87. Matsumoto N, Hanakawa T, Maki S, Graybiel AM, Kimura M. Role of nigrostriatal dopamine system in learning to perform sequential motor tasks in a predictive manner. J Neurophysiol 1999; 82:978–998.
88. Gilbert D, Sethuraman G, Sine L, Peters S, Sallee F. Tourette’s syndrome improvement with pergolide in a randomized, double-blind, crossover trial. Neurology 2000; 54:1310–1315.