Corticostriatal circuitry

Dialogues in Clinical Neuroscience

Volumn 18, Issue 1, 2016, Pages 7-21

  Haber, Suzanne N ^a  

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

Author keywords

Basal ganglia; Cognition; Dopamine; Dorsal striatum; Functional integration; Motor control; Prefrontal cortex; Reward; Ventral striatum

Indexed keywords

BRAIN CORTEX; CAUDATE NUCLEUS; COGNITION; MOTIVATION; MOTOR CONTROL; MOTOR PERFORMANCE; PUTAMEN; REWARD; VENTRAL STRIATUM; ANIMAL; CORPUS STRIATUM; HUMAN; NERVE CELL NETWORK; NERVE TRACT; PHYSIOLOGY;

ANIMALS; CEREBRAL CORTEX; COGNITION; CORPUS STRIATUM; HUMANS; NERVE NET; NEURAL PATHWAYS; REWARD;

EID: 84964573553     PISSN: 12948322     EISSN: None     Source Type: Journal    
DOI: 10.1007/978-1-4614-6434-1_135-1     Document Type: Article

References (123)

1. Wise RA. Addictive drugs and brain stimulation reward. Ann Rev Neurosci. 1996;19:319-340
2. Schultz W. Dopamine neurons and their role in reward mechanisms. Curr Opin Neurobiol. 1997;7(2):191-197
3. Robbins TW., Everitt BJ. Motivation and reward. In: Squire LR, Roberts JL, Spitzer NC, Zigmond MJ, McConnell SK, Bloom FE, eds. Fundamental Neuroscience. 2nd ed. San Diego, CA: Academic Press; 1999:1245-1259
4. Koob GF. Drug reward and addiction. In: Fundamental Neuroscience. New York, NY: Academic Press; 1999:1261-1279
5. Kalivas PW., Churchill L., Klitenick MA. The circuitry mediating the translation of motivational stimuli into adaptive motor responses. In: Kalivas PW, Barnes CD, eds. Limbic Motor Circuits and Neuropsychiatry. Boca Raton, FL: CRC Press, Inc; 1993:237-275
6. Nestler EJ., Hope BT., Widnell KL. Drug addiction: a model for the molecular basis of neural plasticity. Neuron. 1993;11(6):995-1006
7. Jog MS., Kubota Y., Connolly CI., Hillegaart V., Graybiel AM. Building neural representations of habits. Science. 1999;286(26):1745-1749
8. Bergman H., Feingold A., Nini A., et al Physiological aspects of information processing in the basal ganglia of normal and parkinsonian primates. Trends Neurosci. 1998;21(1):32-38
9. Cohen MX., Frank MJ. Neurocomputational models of basal ganglia function in learning, memory and choice. Behav Brain Res. 2009;199(1):141-156
10. Alexander GE., Crutcher MD. Functional architecture of basal ganglia circuits: neural substrates of parallel processing. Trends Neurosci. 1990;13(7):266-271
11. Percheron G., Filion M. Parallel processing in the basal ganglia: up to a point. Trends Neurosci. 1991;14(2):55-59
12. Haber SN., Fudge JL., McFarland NR. Striatonigrostriatal pathways in primates form an ascending spiral from the shell to the dorso lateral striatum. J Neurosci. 2000;20(6):2369-2382
13. Haber SN., Kim KS., Mailly P., Calzavara R. Reward-related cortical inputs define a large striatal region in primates that interface with associative cortical connections, providing a substrate for incentive-based learning. J Neurosci. 2006;26(32):8368-8376
14. Averbeck BB., Lehman J., Jacobson M., Haber SN. Estimates of projection overlap and zones of convergence within frontal-striatal circuits. J Neurosci. 2014;34(29):9497-9505
15. Haber SN., McFarland NR. The concept of the ventral striatum in nonhuman primates. Ann NY Acad Sci. 1999;877:33-48
16. Heimer L., Alheid GF., Zahm DS. Basal forebrain organization: an anatomical framework for motor aspects of drive and motivation. In: Kalivas PW, Barnes CD, eds. Limbic Motor Circuits and Neuropsychiatry. Boca Raton, FL: CRC Press, Inc; 1993:1-43
17. Parent A. Comparative Neurobiology of the Basal Ganglia. New York, NY: John Wiley and Sons; 1986
18. Selemon LD., Goldman-Rakic PS. Longitudinal topography and interdigitation of corticostriatal projections in the rhesus monkey. J Neurosci. 1985;5(3):776-794
19. McFarland NR., Haber SN. The thalamostriatal projection and its relation to corticostriatal and cortiocthalamic inputs. Soc Neurosci Abst. 1996;22:412
20. 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. 1990;293(2):282-298
21. Lynd-Balta E., Haber SN. Primate striatonigral projections: a comparison of the sensorimotor-related striatum and the ventral striatum. J Comp Neurol. 1994;345(4):562-578
22. Smith Y., Shink E., Sidibe M. Neuronal circuitry and synaptic connectivity of the basal ganglia. Neurosurg Clin N Am. 1998;9(2):203-222
23. Parent A., Hazrati LN. Functional anatomy of the basal ganglia. I. The cortico-basal ganglia-thalamo-cortical loop. Brain Res Brain Res Rev. 1995;20(1):91-127
24. Haber SN., Lynd-Balta E., Mitchell SJ. The organization of the descending ventral pallidal projections in the monkey. J Comp Neurol. 1993;329(1):111-128
25. Lyons D., Friedman DP., Nader MA., Porrino LJ. Cocaine alters cerebral metabolism within the ventral striatum and limbic cortex of monkeys. J Neurosci. 1996;16(3):1230-1238
26. Haynes WL., Haber SN. The organization of prefrontal-subthalamic inputs in primates provides an anatomical substrate for both functional specificity and integration: implications for basal ganglia models and deep brain stimulation. J Neurosci. 2013;33(11):4804-4814
27. DiFiglia M., Carey J. Large neurons in the primate neostriatum examined with the combined Golgi-electron microscopic method. J Comp Neurol. 1986;244(1):36-52
28. Graveland GA., DiFiglia M. The frequency and distribution of medium-sized neurons with indented nuclei in the primate and rodent neostriatum. Brain Res. 1985;327(1-2):307-311
29. Preston RJ., Bishop GA., Kitai ST. Medium spiny neuron projection from the rat striatum: an intracellular horseradish peroxidase study. Brain Res. 1980;183(2):253-263
30. Szabo J. The course and distribution of efferents from the tail of the caudate nucleus in the monkey. Exp Neurol. 1972;37(3):562-572
31. Chang HT. Single neostriatal efferent axons in the globus pallidus: a light and electron microscopic study. Science. 1981;213(4510):915-918
32. Smith Y., Bevan MD., Shink E., Bolam JP. Microcircuitry of the direct and indirect pathways of the basal ganglia. Neuroscience. 1998;86(2):353-387
33. Bolam JP., Ingham CA., Izzo PN., et al Substance P-containing terminals in synaptic contact with cholinergic neurons in the neostriatum and basal forebrain: a double immunocytochemical study in the rat. Brain Res. 1986;397(2):279-289
34. Pickel VM., Chan J. Spiny neurons lacking choline acetyltransferase immunoreactivity are major targets of cholinergic and catecholaminergic terminals in rat striatum. J Neurosci Res. 1990;25(3):263-280
35. Rav-Acha M., Sagiv N., Segev I., Bergman H., Yarom Y. Dynamic and spatial features of the inhibitory pallidal GABAergic synapses. Neuroscience. 2005;135(3):791-802
36. Haber S., Elde R. Correlation between Met-enkephalin and substance P immunoreactivity in the primate globus pallidus. Neuroscience. 1981;6(7):1291-1297
37. Reiner A., Medina L., Haber SN. The distribution of dynorphinergic terminals in striatal target regions in comparison to the distribution of substance P-containing and enkephalinergic terminals in monkeys and humans. Neuroscience. 1999;88(3):775-793
38. Somogyi P., Bolam JP., Smith AD. Monosynaptic cortical input and local axon collaterals of identified striatonigral neurons. A light and electron microscopic study using the Golgi-peroxidase transport-degeneration procedure. J Comp Neurol. 1981;195(4):567-584
39. Sadikot AF., Parent A., Smith Y., Bolam JP. Efferent connections of the centromedian and parafascicular thalamic nuclei in the squirrel monkey: a light and electron microscopic study of the thalamostriatal projection in relation to striatal heterogeneity. J Comp Neurol. 1992;320(2):228-242
40. Sidibé M., Smith Y. Differential synaptic innervation of striatofugal neurones projecting to the internal or external segments of the globus pallidus by thalamic afferents in the squirrel monkey. J Comp Neurol. 1996;365(3):445-465
41. Smith Y., Raju DV., Pare JF., Sidibé M. The thalamostriatal system: a highly specific network of the basal ganglia circuitry. Trends Neurosci. 2004;27(9):520-527
42. Ding J., Peterson JD., Surmeier DJ. Corticostriatal and thalamostriatal synapses have distinctive properties. J Neurosci. 2008;28(25):6483-6492
43. Moss J., Bolam JP. A dopaminergic axon lattice in the striatum and its relationship with cortical and thalamic terminals. J Neurosci. 2008;28(44):11221-11230
44. Kimura M., Kato M., Shimazaki H., Watanabe K., Matsumoto N. Neural information transferred from the putamen to the globus pallidus during learned movement in the monkey. J Neurophysiol. 1996;76(6):3771-3786
45. Kimura M. Behaviorally contingent property of movement-related activity of the primate putamen. J Neurophysiol. 1990;63(6):1277-1296
46. Crutcher MD., DeLong MR. Single cell studies of the primate putamen II. Relations to direction of movement and pattern of muscular activity. Exp Brain Res. 1984;53(2):244-258
47. Freund TF., Powell JF., Smith AD. Tyrosine hydroxylase-immunoreactive boutons in synaptic contact with identified striatonigral neurons, with particular reference to dendritic spines. Neuroscience. 1984;13(4):1189-1215
48. Kung L., Force M., Chute DJ., Roberts RC. Immunocytochemical localization of tyrosine hydroxylase in the human striatum: a postmortem ultrastructural study. J Comp Neurol. 1998;390(1):52-62
49. Smith Y., Bennett BD., Bolam JP., Parent A., Sadikot AF. Synaptic relationships between dopaminergic afferents and cortical or thalamic input in the sensorimotor territory of the striatum in monkey. J Comp Neurol. 1994;344(1):1-19
50. DiFiglia M. Synaptic organization of cholinergic neurons in the monkey neostriatum. J Comp Neurol. 1987;255(2):245-258
51. Yung KK., Smith AD., Levey AI., Bolam JP. Synaptic connections between spiny neurons of the direct and indirect pathways in the neostriatum of the rat: evident from dopamine receptro and neuropeptide immostaining. Eur Journal Neurosci. 1996;8(5):861-869
52. Goldman-Rakic PS. Cytoarchitectonic heterogeneity of the primate neostriatum: subdivision into island and matrix cellular compartments. J Comp Neurol. 1982;205(4):398-413
53. Goldman PS., Nauta WL. An intricately patterned prefronto-caudate projection in the rhesus monkey. J Comp Neurol. 1977;72(3):369-386
54. Graybiel AM. Neurotransmitters and neuromodulators in the basal ganglia. Trends Neurosci. 1990;13(7):244-254
55. Meyer G., Gonzalez-Hernandez T., Carrillo-Padilla F., Ferres-Torres R. Aggregations of granule cells in the basal forebrain (islands of Calleja): Golgi and cytoarchitectonic study in different mammals, including man. J Comp Neurol. 1989;284(3):405-428
56. Heimer L., De Olmos JS., Alheid GF., et al The human basal forebrain. Part II. In: Bloom FE, Bjorkland A, Hokfelt T, eds. Handbook of Chemical Neuroanatomy. Amsterdam, The Netherlands: Elsevier; 1999:57-226
57. Mai JK., Stephens PH., Hopf A., Cuello AC. Substance P in the human brain. Neuroscience. 1986;17(3):709-739
58. Heimer L. Basal forebrain in the context of schizophrenia. Brain Res Brain Res Rev. 2000;31(2-3):205-235
59. Bernier PJ., Parent A. Bcl-2 protein as a marker of neuronal immaturity in postnatal primate brain. J Neurosci. 1998;18(7):2486-2497
60. Fudge JL., Kunishio K., Walsh P., Richard C., Haber SN. Amygdaloid projections to ventromedial striatal subterritories in the primate. Neuroscience. 2002;110(2):257-275
61. Zaborszky L., Alheid GF., Beinfeld MC., Eiden LE., Heimer L., Palkovits M. Cholecystokinin innervation of the ventral striatum: a morphological and radioimmunological study. Neuroscience. 1985;14(2):427-453
62. Brog JS., Salyapongse A., Deutch AY., Zahm DS. The patterns of afferent innervation of the core and shell in the "accumbens" part of the rat ventral striatum: immunohistochemical detection of retrogradely transported fluoro-gold. J Comp Neurol. 1993;338(2):255-278
63. Heimer L., Zahm DS., Churchill L., Kalivas PW., Wohltmann C. Specificity in the projection patterns of accumbal core and shell in the rat. Neuroscience. 1991;41(1):89-125
64. Meredith GE., Pattiselanno A., Groenewegen HJ., Haber SN. Shell and core in monkey and human nucleus accumbens identified with antibodies to calbindin-D28k. J Comp Neurol. 1996;365(4):628-639
65. Russchen FT., Bakst I., Amaral DG., Price JL. The amygdalostriatal projections in the monkey. An anterograde tracing study. Brain Res. 1985;329(1-2):241-257
66. Haber SN., Ryoo H., Cox C., Lu W. Subsets of midbrain dopaminergic neurons in monkeys are distinguished by different levels of mRNA for the dopamine transporter: comparison with the mRNA for the D2 receptor, tyrosine hydroxylase and calbindin immunoreactivity. J Comp Neurol. 1995;362(3):400-410
67. Yeterian EH., Van Hoesen GW. Cortico-striate projections in the rhesus monkey: the organization of certain cortico-caudate connections. Brain Res. 1978;139(1):43-63
68. Flaherty AW., Graybiel AM. Two input systems for body representations in the primate striatal matrix: experimental evidence in the squirrel monkey. J Neurosci. 1993;13(3):1120-1137
69. Goldman-Rakic PS., Selemon LD. Topography of corticostriatal projections in nonhuman primates and implications for functional panellation of the neostriatum. In: Jones EG, Peters A, eds. Cerebral Cortex. Vol 5. New York, NY: Plenum Publishing Corporation; 1986:447-466
70. McFarland NR., Haber SN. Convergent inputs from thalamic motor nuclei and frontal cortical areas to the dorsal striatum in the primate. J Neurosci. 2000;20(10):3798-3813
71. Kunzle H. Bilateral projections from precentral motor cortex to the putamen and other parts of the basal ganglia. An autoradiographic study in Macaca fascicularis. Brain Res. 1975;88(2):195-209
72. Flaherty AW., Graybiel AM. Input-output organization of the sensorimotor striatum in the squirrel monkey. J Neurosci. 1994;14(2):599-610
73. Kimura M. The role of primate putamen neurons in the association of sensory stimulus with movement. Neurosci Res. 1986;3(5):436-443
74. Yin HH., Mulcare SP., Hilario MR., et al Dynamic reorganization of striatal circuits during the acquisition and consolidation of a skill. Nat Neurosci. 2009;12(3):333-341
75. Boecker H., Dagher A., Ceballos-Baumann AO., et al Role of the human rostral supplementary motor area and the basal ganglia in motor sequence control: investigations with H2 15O PET. J Neurophysiol. 1998;79(2):1070-1080
76. Kermadi I., Joseph JP. Activity in the caudate nucleus of monkey during spatial sequencing. J Neurophysiol. 1995;74(3):911-933
77. Chen LL., Wise SP. Supplementary eye field contrasted with the frontal eye field during acquisition of conditional oculomotor associations. J Neurophysiol. 1995;73(3):1122-1134
78. Kunishio K., Haber SN. Primate cingulostriatal projection: limbic striatal versus sensorimotor striatal input. J Comp Neurol. 1994;350(3):337-356
79. Hikosaka O., Rand MK., Miyachi S., Miyashita K. Learning of sequential movements in the monkey: process of learning and retention of memory. J Neurophysiol. 1995;74(4):1652-1661
80. Haber SN., Kunishio K., Mizobuchi M., Lynd-Balta E. The orbital and medial prefrontal circuit through the primate basal ganglia. J Neurosci. 1995;15(7 pt 1):4851-4867
81. Chikama M., McFarland NR., Amaral DG., Haber SN. Insular cortical projections to functional regions of the striatum correlate with cortical cytoarchitectonic organization in the primate. J Neurosci. 1997;17(24):9686-9705
82. Pandya DN., Van Hoesen GW., Mesulam MM. Efferent connections of the cingulate gyrus in the rhesus monkey. Exp Brain Res. 1981;42(3-4):319-330
83. Fudge JL., Haber SN. Defining the caudal ventral striatum in primates: cellular and histochemical features. J Neurosci. 2002;22(23):10078-10082
84. Bouret S., Richmond BJ. Ventromedial and orbital prefrontal neurons differentially encode internally and externally driven motivational values in monkeys. J Neurosci. 2010;30(25):8591-8601
85. Behrens TE., Hunt LT., Woolrich MW., Rushworth MF. Associative learning of social value. Nature. 2008;456(7219):245-249
86. Padoa-Schioppa C., Assad JA. Neurons in the orbitofrontal cortex encode economic value. Nature. 2006;441(7090):223-226
87. Wallis JD., Miller EK. Neuronal activity in primate dorsolateral and orbital prefrontal cortex during performance of a reward preference task. Eur J Neurosci. 2003;18(7):2069-2081
88. Fellows LK., Farah MJ. Ventromedial frontal cortex mediates affective shifting in humans: evidence from a reversal learning paradigm. Brain. 2003;126(pt 8):1830-1837
89. Izquierdo A., Suda RK., Murray EA. Bilateral orbital prefrontal cortex lesions in rhesus monkeys disrupt choices guided by both reward value and reward contingency. J Neurosci. 2004;24(34):7540-7548
90. Rudebeck PH., Behrens TE., Kennerley SW., et al Frontal cortex subregions play distinct roles in choices between actions and stimuli. J Neurosci. 2008;28(51):13775-13785
91. Camille N., Tsuchida A., Fellows LK. Double dissociation of stimulusvalue and action-value learning in humans with orbitofrontal or anterior cingulate cortex damage. J Neurosci. 2011;31(42):15048-15052
92. Alexander WH., Brown JW. Medial prefrontal cortex as an action-outcome predictor. Nat Neurosci. 2011;14(10):1338-1344
93. 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. 2007;26(7):2005-2024
94. Goldman-Rakic PS., Funahashi S., Bruce CJ. Neocortical memory circuits. Cold Spring Harb Symp Quant Biol. 1990;55:1025-1038
95. Goldman-Rakic PS. Circuitry of the frontal association cortex and its relevance to dementia. Arch Gerontol Geriatr. 1987;6(3):299-309
96. Arikuni T., Kubota K. The organization of prefrontocaudate projections and their laminar origin in the macaque monkey-a retrograde study using HRP-gel. J Comp Neurol. 1986;244(4):492-510
97. Hikosaka O., Sakamoto M., Usui S. Functional properties of monkey caudate neurons. III. Activities related to expectation of target and reward. J Neurophysiol. 1989;61(4):814-832
98. Elliott R., Dolan RJ. Differential neural responses during performance of matching and nonmatching to sample tasks at two delay intervals. J Neurosci. 1999;19(12):5066-5073
99. Partiot A., Verin M., Pillon B., Teixeira-Ferreira C., Agid Y., Dubois B. Delayed response tasks in basal ganglia lesions in man: further evidence for a striato-frontal cooperation in behavioural adaptation. Neuropsychologia. 1996;34(7):709-721
100. Van Hoesen GW., Yeterian EH., Lavizzo-Mourey R. Widespread corticostriate projections from temporal cortex of the rhesus monkey. J Comp Neurol. 1981;199(2):205-219
101. Yeterian EH., Pandya DN. Corticostriatal connections of the superior temporal region in rhesus monkeys. J Comp Neurol. 1998;399(3):384-402
102. Friedman DP., Aggleton JP., Saunders RC. Comparison of hippocampal, amygdala, and perirhinal projections to the nucleus accumbens: combined anterograde and retrograde tracing study in the macaque brain. J Comp Neurol. 2002;450(4):345-365
103. Ramanathan S., Hanley JJ., Deniau JM., Bolam JP. Synaptic convergence of motor and somatosensory cortical afferents onto GABAergic interneurons in the rat striatum. J Neurosci. 2002;22:8158-8169
104. Mallet N., Le Moine C., Charpier S., Gonon F. Feedforward inhibition of projection neurons by fast-spiking GABA interneurons in the rat striatum in vivo. J Neurosci. 2005;25(15):3857-3869
105. Takada M., Tokuno H., Nambu A., Inase M. Corticostriatal input zones from the supplementary motor area overlap those from the contra-rather than ipsilateral primary motor cortex. Brain Res. 1998;791(12):335-340
106. Wilson CJ. The basal ganglia. In: Shepherd GM, ed. Synaptic Organization of the Brain. 5th ed. New York, NY: Oxford University Press; 2004:361-413
107. Draganski B., Kherif F., Kloppel S., et al Evidence for segregated and integrative connectivity patterns in the human basal ganglia. J Neurosci. 2008;28(28):7143-7152
108. Buckner RL., Andrews-Hanna JR., Schacter DL. The brain's default network: anatomy, function, and relevance to disease. Ann N Y Acad Sci. 2008;1124:1-38
109. Power JD., Schlaggar BL., Lessov-Schlaggar CN., Petersen SE. Evidence for hubs in human functional brain networks. Neuron. 2013;79(4):798-813
110. Wise RA., Rompre PP. Brain dopamine and reward. Ann Rev Psychol. 1989;40:191-225
111. Fibiger HC., Phillips AG. Reward, motivation, cognition: psychobiology of mesotelencephalic dopamine systems. In: Mountcastle VB, Bloom F, Geiger SR, eds. Handbook of Physiology. Section I: the Nervous System. Vol 4. Bethesda, MD: American Physiological Society; 1986:647-674
112. Schultz W. Predictive reward signal of dopamine neurons. J Neurophysiol. 1998;80(1):1-27
113. Koob GF., Volkow ND. Neurocircuitry of addiction. Neuropsychopharmacology. 2010;35(1):217-238
114. Nestler EJ., Malenka RC. The addicted brain. Sci Am. 2004;290(3):78-85
115. Lavoie B., Parent A. Dopaminergic neurons expressing calbindin in normal and parkinsonian monkeys. Neuroreport. 1991;2(10):601-604
116. McRitchie DA., Halliday GM. Calbindin D28k-containing neurons are restricted to the medial substantia nigra in humans. Neuroscience. 1995;65(1):87-91
117. Lynd-Balta E., Haber SN. The organization of midbrain projections to the striatum in the primate: sensor imotor-re late d striatum versus ventral striatum. Neuroscience. 1994;59(3):625-640
118. Parent A., Hazrati LN. Multiple striatal representation in primate substantia nigra. J Comp Neurol. 1994;344(2):305-320
119. Bevan MD., Clarke NP., Bolam JP. Synaptic integration of functionally diverse pallidal information in the entopeduncular nucleus and subthalamic nucleus in the rat. J Neurosci. 1997;17(1):308-324
120. Somogyi P., Bolam JP., Totterdell S., Smith AD. Monosynaptic input from the nucleus accumbens-ventral striatum region to retrograde ly labelled nigrostriatal neurones. Brain Res. 1981;217(2):245-263
121. Nauta WJ., Smith GP., Faull RLM., Domesick VB. Efferent connections and nigral afferents of the nucleus accumbens septi in the rat. Neuroscience. 1978;3(4-5):385-401
122. McFarland NR., Haber SN. Thalamic relay nuclei of the basal ganglia form both reciprocal and nonreciprocal cortical connections, linking multiple frontal cortical areas. J Neurosci. 2002;22(18):8117-8132
123. Bar-Gad I., Havazelet-Heimer G., Goldberg JA., Ruppin E., Bergman H. Reinforcement-driven dimensionality reduction-a model for information processing in the basal ganglia. J Basic Clin Physiol Pharmacol. 2000;11(4):305-320