Cortico-basal ganglia circuits - Parallel closed loops and convergent/divergent connections

Brain and Nerve

Volumn 61, Issue 4, 2009, Pages 351-359

  Miyachi, Shigehiro ^a  

^a KYOTO UNIVERSITY   (Japan)

Author keywords

Globus pallisus; Neuronal tracing; Rabies virus; Striatum; Substantia nigra; Transsynaptic tracers

Indexed keywords

ARTICLE; BASAL GANGLION; BRAIN CORTEX; CORPUS STRIATUM; FRONTAL CORTEX; GLOBUS PALLIDUS; LIMBIC CORTEX; MOTOR CONTROL; MOTOR CORTEX; SUBSTANTIA NIGRA; THALAMUS NUCLEUS;

ANIMALS; BASAL GANGLIA; CEREBRAL CORTEX; COGNITION; CORPUS STRIATUM; GLOBUS PALLIDUS; HUMANS; MOTOR ACTIVITY; NEURAL PATHWAYS; NEURONS; RABIES VIRUS; SUBSTANTIA NIGRA; SYNAPTIC TRANSMISSION;

EID: 64849089612     PISSN: 18816096     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (34)

1. Keefe K, Gerfen C: D1-D2 dopamine receptor synergy in striatum: effects of intrastriatal infusions of dopamine agonists and antagonists on immediate early gene expression. Neuroscience 66: 903-913, 1995
2. Calabresi P, Maj R, Mercuri NB, Bernardi G: Coactivation of Dl and D2 dopamine receptors is required for long-term synaptic depression in the striatum. Neurosci Lett 142: 95-99, 1992
3. Wickens JR, Begg AJ, Arbuthnott GW: Dopamine reverses the depression of rat corticostriatal synapses which normally follows high-frequency stimulation of cortex in vitro. Neuroscience 70: 1-5, 1996
4. Nambu A, Tokuno H, Takada M: Functional significance of the cortico-subthalamo-pallidal 'hyperdirect' pathway. Neurosci Res 43: 111-117, 2002
5. Takada M, Tokuno H, Nambu A, Inase M: Corticostriatal projections from the somatic motor areas of the frontal cortex in the macaque monkey: segregation versus overlap of input zones from the primary motor cortex, the supplementary motor area, and the premotor cortex. Exp Brain Res 120: 114-128, 1998
6. Alexander GE, DeLong MR: Microstimulation of the primate neostriatum. II. Somatotopic organization of striatal microexcitable zones and their relation to neuronal response properties. J Neurophysiol 53:1417-1430, 1985
7. Tokuno H, Inase M, Nambu A, Akazawa T, Miyachi S, et al: Corticostriatal projections from distal and proximal forelimb representations of the monkey primary motor cortex. Neurosci Lett 269: 33-36, 1999
8. Inase M, Tokuno H, Nambu A, Akazawa T, Takada M: Corticostriatal and corticosubthalamic input zones from the presupplementary motor area in the macaque monkey: comparison with the input zones from the supplementary motor area. Brain Res 833: 191-201, 1999
9. Flaherty AW, Graybiel AM: Two input systems for body representations in the primate striatal matrix: experimental evidence in the squirrel monkey. J Neurosci 13: 1120-1137, 1993
10. Selemon LD, Goldman-Rakic PS: Longitudinal topography and interdigitation of corticostriatal projections in the rhesus monkey. J Neurosci 5: 776-794, 1985
11. Cavada C, Goldman-Rakic PS: Topographic segregation of corticostriatal projections from posterior parietal subdivisions in the macaque monkey. Neuroscience 42: 683-696, 1991
12. Yeterian EH, Pandya DN: Striatal connections of the parietal association cortices in rhesus monkeys. J Comp Neurol 332: 175-197, 1993
13. Yeterian EH, Pandya DN: Corticostriatal connections of the superior temporal region in rhesus monkeys. J Comp Neurol 399: 384-402, 1998
14. Cheng K, Saleem KS, Tanaka K: Organization of corticostriatal and corticoamygdalar projections arising from the anterior inferotemporal area TE of the macaque monkey: a Phaseolus vulgaris leucoagglutinin study. J Neurosci 17: 7902-7925, 1997
15. Calzavara R, Mailly P, Haber SN: Relationship between the corticostriatal terminals from areas 9 and 46, and those from area 8A, dorsal and rostral premotor cortex and area 24c: an anatomical substrate for cognition to action. Eur J Neurosci 26: 2005- 2024, 2007
16. Miyachi S, Hasegawa YT, Gerfen CR: Coincident stimulation of convergent cortical inputs enhances immediate early gene induction in the striatum. Neuroscience 134: 1013-1022, 2005
17. Guzowski JF, Lyford GL, Stevenson GD, Houston FP, McGaugh JL, et al: Inhibition of activity-dependent arc protein expression in the rat hippocampus impairs the maintenance of long-term potentiation and the consolidation of long-term memory. J Neurosci 20: 3993-4001, 2000
18. Bramham CR, Worley PF, Moore MJ, Guzowski JF: The immediate early gene arc/arg3.1: regulation, mechanisms, and function. J Neurosci 28:11760-11767, 2008
19. Parent A, Bouchard C, Smith Y: The striatopallidal and striatonigral projections: two distinct fiber systems in primate. Brain Res 303: 385-390, 1984
20. Selemon LD, Goldman-Rakic PS: Topographic intermingling of striatonigral and striatopallidal neurons in the rhesus monkey. J Comp Neurol 297: 359-376, 1990
21. Hazrati LN, Parent A: The striatopallidal projection displays a high degree of anatomical specificity in the primate. Brain Res 592: 213-227, 1992
22. Parent A, Hazrati LN: Multiple striatal representation in primate substantia nigra. J Comp Neurol 344: 305-320, 1994
23. Kaneda K, Nambu A, Tokuno H, Takada M: Differential processing patterns of motor information via striatopallidal and striatonigral projections. J Neuro- physiol 88: 1420-1432, 2002
24. Parent A, De Bellefeuille L: Organization of efferent projections from the internal segment of globus pallidus in primate as revealed by fluorescence retrograde labeling method. Brain Res 245: 201-213, 1982
25. Parent A, Mackey A, Smith Y, Boucher R: The output organization of the substantia nigra in primate as revealed by a retrograde double labeling method. Brain Res Bull 10: 529-537, 1983
26. Sidibe M, Bevan MD, Bolam JP, Smith Y: Efferent connections of the internal globus pallidus in the squirrel monkey: I. Topography and synaptic organization of the pallidothalamic projection. J Comp Neurol 382: 323-347, 1997
27. Yelnik J, Percheron G, Francois C: A Golgi analysis of the primate globus pallidus. II. Quantitative morphology and spatial orientation of dendritic arborizations. J Comp Neurol 227: 200-213, 1984
28. Hoover JE, Strick PL: Multiple output channels in the basal ganglia. Science 259: 819-821, 1993
29. Hoover JE, Strick PL: The organization of cerebellar and basal ganglia outputs to primary motor cortex as revealed by retrograde transneuronal transport of herpes simplex virus type 1. J Neurosci 19: 1446-1463, 1999
30. Miyachi S, Lu X, Imanishi M, Sawada K, Nambu A, et al: Somatotopically arranged inputs from putamen and subthalamic nucleus to primary motor cortex. Neurosci Res 56: 300-308, 2006
31. Haber SN, Lynd E, Klein C, Groenewegen HJ: Topographic Organization of the ventral striatal efferent projections in the rhesus monkey: an anterograde tracing study. J Comp Neurol 293: 282-298, 1990
32. Russchen FT, Amaral DG, Price JL: The afferent connections of the substantia innominata in the monkey, Macaca fascicularis. J Comp Neurol 242: 1-27, 1985
33. Gerfen C: The neostriatal mosaic: multiple levels of compartmental organization. Trends Neurosci 15: 133-139, 1992
34. Haber SN: The primate basal ganglia: parallel and integrative networks. J Chem Neuroanat 26: 317-330, 2003