Abstract
The involvement of the basal ganglia in motor control is well documented, particularly in its association with the neurological disorders, Parkinson’ s disease (PD) and Huntington’ s disease (HD). It is the dorsal basal ganglia that is most affected in these diseases. In contrast, the ventral basal ganglia (the ventral striatum [VS] and ventral pallidum [VP]) are associated with mental health problems including schizophrenia and drug abuse and addiction (1–5). Taken as a whole, the basal ganglia, both dorsal and ventral components, are involved in motor, cognitive, and limbic functions. These functions are thought to be contained in separate, segregated corticobasal ganglia circuits (6). However, although severe motoric dysfunctions are associated with the dorsal striatum, and cognitive, emotional, and motivational problems are associated with the VS diseases effecting these striatal regions often have a mixed set of dysfunctions (7–15). For example, often the earliest detectable symptoms in PD patients occur on cognitive tasks requiring attentional set-shifting and tasks requiring organizational skills and use of working memory. Thus, although different basal ganglia regions are involved in various functions, the basal ganglia as a whole operates in concert with cortex in mediating overall behavioral responses. This involves a complex coordination of motivational, cognitive, and motor elements.
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References
Koob, G.F. and Nestler, E.J. (1997) The neurobiology of drug addiction. J. Neuropsychiatry Clin. Neurosci. 9, 482–497.
Singer, H.S., Butler, I.J., Tune, L.E., Seifert, W.E. Jr., and Coyle, J.T. (1982) Dopaminergic dsyfunction in Tourette syndrome. Ann. Neurol. 12, 361–366.
Grace, A.A. (1991) Phasic versus tonic dopmaine release and the modulation of dopamine system responsivity: a hypothesis for the etiology of schizophrenia. Neuroscience 41, 1–24.
Swerdlow, N.R. and Koob, G.F. (1987) Dopamine, schizophrenia, mania, and depression: toward a unified hypothesis of cortico-striato-pallido-thalamic function. Behav. Brain Res. 10, 197–245.
Cooper, J.A., Sagar, H.J., Doherty, S.M., Jordan, N., Tidswell, P., and Sullivan, E.V. (1992) Different effects of dopaminergic and anticholinergic therapies on cognitive and motor function in Parkinson’s disease. A follow-up study of untreated patients. Brain 115, 1701–1725.
Alexander, G.E. and Crutcher, M.D. (1990) Functional architecture of basal ganglia circuits: neural substrates of parallel processing. Trends Neurosci. 13, 266–271.
Cooper, JA., Sagar, H.J., Jordan, N., Harvey, N.S., and Sullivan, E.V. (1991) Cognitive impairment in early, untreated Parkinson’s disease and its relationship to motor disability. Brain 114, 2095–2122.
Owen, A.M., Iddon, J.L., Hodges, J.R., Summers, B.A., and Robbins, T.W. (1997) Spatial and non-spatial working memory at different stages of Parkinson’s disease. Neuropsychologia 35, 519–532.
Taylor, A.E., Saint-Cyr, JA., Lang, A.E., and Kenny, F.T. (1986) Parkinson’s disease and depression: a critical re-evaluation. Brain 109, 279–292.
Taylor, A.E., Saint-Cyr, J.A., and Lang, A.E. (1990) Memory and learning in early Parkinson’s disease: evidence for a “frontal lobe syndrome.” Brain Cogn. 13, 211–232.
Folstein, S.E., Folstein, M.F., and McHugh, P.R. (1979) Psychiatric syndromes in Huntington’s disease, in Advances in Neurology (Chase, TN., ed.), Raven Press, New York, pp. 281–280.
J, B. (1991) Cognitive impairments in Huntington’s disease: insights into the neuropsychology of the striatum, in Handbook of Neuropsychology (Boller, F. and Grafman, J., ed.), Elsevier, Amsterdam, pp. 241–264.
Kalivas, P.W., Churchill, L., and Klitenick, M.A. (1993) The circuitry mediating the translation of motivational stimuli into adaptive motor responses, in Limbic Motor Circuits and Neuropsychiatry (Kalivas, P.W. and Barnes, C.D., eds.), CRC Press, Boca Raton, pp. 237–275.
Mogenson, G.J., Wu, M., and Jones, D.L. (1980) Locomotor activity elicited by injections of picrotoxin into the ventral tegmental area is attenuated by injections of GABA into the globus pallidus. Brain Res. 191, 569–571.
Mogenson, G.J. and Nielsen, M.A. (1983) Evidence that an accumbens to subpallidal GAGAergic projection contributes to locomotor activity. Brain Res. Bull. 11, 309–314.
Heimer, L. and Wilson, R.D. (1975) The subcortical projections of the allocortex: similarities in the neural associations of the hippocampus, the piriform cortex, and the neocortex, in Golgi Centennial Symposium: Perspectives in Neurobiology (Santini, M., ed.), Raven Press, New York, pp. 177–193.
Alexander, G.E., DeLong, M.R., and Strick, P.L. (1986) Parallel organization of functionally segregated circuits linking basal ganglia and cortex. Annu. Rev. Neurosci. 9, 357–381.
Alexander, G.E., Crutcher, M.D., and DeLong, M.R. (1990) Basal ganglia-thalamocortical circuits: parallel substrates for motor, oculomotor, “prefrontal” and “limbic” functions. Prog. Brain Res. 85, 119–110.
Middleton, F.A. and Strick, P.L. (1997) New concepts about the organization of basal ganglia output. Adv. Neurol. 74, 57–68.
Nauta, W.J.H., Smith, G.P., Faull, R.L.M., and Domesick, V.B. (1978) Efferent connections and nigral afferents of the nucleus accumbens septi in the rat. Neuroscience 3, 385–401.
Percheron, G., Yelnik, J., and Francois, C. (1984) The primate striato-pallido-nigral system: an integrative system for cortical information, in The Basal Ganglia: Structure and Function (McKenzie, J.S., Kemm, R.E., and Wilcock, L.N., eds.), Plenum Press, London, pp. 87–105.
Haber, S.N., Fudge, J.L., and McFarland, N. (2000) Striatonigrostriatal pathways in primates form an ascending spiral from the shell to the dorsolateral striatum. J. Neurosci. 20, 2369–2382.
Mogenson, G.J., Jones, D.L., and Yim, C.Y. (1980) From motivation to action: functional interface between the limbic system and the motor system. Prog. Neurobiol. 14, 69–97.
Haber, S.N. and McFarland, N.R. (2001) The place of the thalamus in frontal cortical-basal ganglia circuits. Neuroscientist, in press…
Dum, R.P. and Strick, P.L. (1993) Cingulate motor areas, in Neurobiology of Cingulate Cortex and Limbic Thalamus: A Comprehensive Treatise (Vogt, B.A. and Gabriel, M., eds.), Birkhauser, Boston, pp. 415–441….
Kurata, K. (1993) Premotor cortex of monkeys: set- and movement-related activity reflecting amplitude and direction of wrist movements. J. Neurophysiol. 69, 187–200.
Matsuzaka, Y., Aizawa, H., and Tanji, J. (1992) A motor area rostral to the supplementary motor area (presupplementary motor area) in the monkey: neuronal activity during a learned motor task. J. Neurophysiol. 68, 653–662.
Passingham, R.E. (1995) The Frontal Lobes and Voluntary Action. Oxford Psychology Series, vol. 21, Oxford University Press, Oxford.
Levy, R. and Goldman-Rakic, P.S. (1999) Association of storage and processing functions in the dorsolateral prefrontal cortex of the nonhuman primate. J. Neurosci. 19, 5149–5158.
Cummings, J.L. (1995) Anatomic and behavioral aspects of frontal-subcortical circuits. [review]. Ann. NY Acad Sci. 769, 1–13.
Filley, C.M. (1995) Frontal lobe syndromes, in Neurobehavioral Anatomy, 1st ed. University Press of Colorado, Niwot, pp. 149–162.
Schall, J.D. (1997) Visuomotor areas of the frontal lobe, in Cerebral Cortex, Vol. 12, Extrastriate Cortex in Primates, 1st ed. (Rockland, K.S., Kaas, J.H., and Peters, A., eds.), Plenum Press, New York, pp. 527–638.
Cummings, J.L. (1993) Frontal-subcortical circuits and human behavior [review]. Arch. Neurol. 50, 873–880.
Eslinger, P.J. and Damasio, A.R. (1985) Severe disturbance of higher cognition after bilateral frontal lobe ablation: patient EVR. Neurology 35, 1731–1741.
Fuster, J.M. (1989) Lesion studies, in The Prefrontal Cortex Anatomy, Physiology, and Neuropsychology of the Frontal Lobe, 2nd ed., Raven Press, New York, pp. 51–82.
Rolls, E.T., Burton, M.J., and Mora, F. (1980) Neurophysiological analysis of brain-stimulation reward in the monkey. Brain Res. 194, 339–357.
Carmichael, S.T. and Price, J.L. (1996) Limbic connections of the orbital and medial prefrontal cortex in macaque monkeys. J. Comp. Neurol. 363, 615–641.
Butter, C.M. (1969) Perseveration in extinction and in discrimination reversal tasks following selective fronal ablations in macaca mulatta. Physiol. Behav. 4, 163–171.
Fuster, J.M. (1989) The Prefrontal Cortex, Raven, New York.
Künzle, H. (1975) Bilateral projections from precentral motor cortex to the putamen and other parts of the basal ganglia. An autoradiographic study in Macaca fascicularis. Brain Res. 88, 195–209.
Künzle, H. (1978) An autoradiographic analysis of the efferent connections from premotor and adjacent prefrontal regions (areas 6 and 9) in macaca fascicularis. Brain Behav. Evol. 15, 185–234.
Künzle, H. (1978) An autoradiographic analysis of the efferent connections from premotor and adjacent prefrontal regions (areas 6 and 9) in Macaca fascicularis. Brain Behav. Evol. 15. 185–234.
McFarland, N.R. and Haber, S.N. (2000) Convergent inputs from thalamic motor nuclei and frontal cortical areas to the dorsal striatum in the primate. J. Neurosci. 20, 3798–3813.
Selemon, L.D. and Goldman-Rakic, P.S. (1988) Common cortical and subcortical targets of the dorsolateral prefronal and posterior parietal cortices in the Rhesus monkey: evidence for a distributed neural network subserving spatially guided behavior. J. Neurosci. 8, 4049–4068.
Kunishio, K. and Haber, S.N. (1994) Primate cingulostriatal projection: limbic striatal versus sensorimotor striatal input. J. Comp. Neurol. 350, 337–356.
Chikama, M., McFarland, N., Amaral, D.G., and Haber, S.N. (1997) Insular cortical projections to functional regions of the striatum correlate with cortical cytoarchitectonic organization in the primate. J. Neurosci. 17, 9686–9705.
Haber, S.N., Kunishio, K., Mizobuchi, M., and Lynd-Balta, E. (1995) The orbital and medial prefrontal circuit through the primate basal ganglia. J. Neurosci. 15, 4851–4867.
Wilson, C.J. and Phelan, K.D. (1982) Dual topographic representation of neostriatum in the globus pallidus of rats. Brain Res. 243, 354–359.
Shink, E., Sidibé, M., and Smith, Y. (1997) Efferent connections of the internal globus pallidus in the squirrel monkey: II. Topography and synaptic organization of pallidal efferents to the pedunclulopontine nucleus. J. Comp. Neurol. 382, 348–363.
Shammah-Lagnado, S.J., Alheid, G.F., and Heimer, L. (1996) Efferent connections of the caudal part of the globus pallidus in the rat. J. Comp. Neurol. 376, 489–507.
Kim, R., Nakano, K., Jayaraman, A., and Carpenter, M.B. (1975) Projections of the globus pallidus and adjacent structures: an autoradiographic study in the monkey. J. Comp. Neurol. 169, 263–290.
Inase, M. and Tanji, J. (1994) Projections from the globus pallidus to the thalamic areas projecting to the dorsal area 6 of the macaque monkey: a multiple tracing study. Neurosci. Lett. 180, 135–137.
Haber, S.N., Groenewegen, H.J., Grove, E.A., and Nauta, W.J.H. (1985) Efferent connections of the ventral pallidum. Evidence of a dual striatopallidofugal pathway. J. Comp. Neurol. 235, 322–335.
Maurice, N., Deniau, J.M., Menetrey, A., Glowinski, J., and Thierry, A.M. (1997) Position of the ventral pallidum in the rat prefrontal cortex-basal ganglia circuit. Neuroscience 80, 523–534.
Maurice, N., Deniau, J.M., Menetrey, A., Glowinski, J., and Thierry, A.M. (1998) Prefrontal cortex-basal ganglia circuits in the rat: involvement of ventral pallidum and subthalamic nucleus. Synapse 29, 363–370.
Parent, A. and De Bellefeuille, L. (1982) Organization of efferent projections from the internal segment of the globus pallidus in the primate as revealed by fluorescence retrograde labeling method. Brain Res. 245, 201–213.
Vogt, B.A., Pandya, D.N., and Rosene, D.L. (1987) Cingulate cortex of the Rhesus monkey: I. Cytoarchitecture and thalamic afferents. J. Comp. Neurol. 262, 256–270.
Schell, G.R. and Strick, P.L. (1984) The origin of thalamic inputs to the arcuate premotor and supplementary motor areas. J. Neurosci. 4, 539–560.
Wiesendanger, R. and Wiesendanger, M. (1985) The thalamic connections with medial area 6 (supplementary motor cortex) in the monkey (macaca fascicularis). Exp. Brain Res. 59, 91–104.
Matelli, M., Luppino, G., Fogassi, L., and Rizzolatti, G. (1989) Thalamic input to inferior area 6 and area 4 in the macaque monkey. J. Comp. Neurol. 280, 468–488.
Holsapple, J.W., Preston, J.B., and Strick, P.L. (1991) The origin of thalamic inputs to the “hand” representation in the primary motor cortex. J. Neurosci. 11, 2644–2654.
Kurata, K. (1994) Site of origin of projections from the thalamus to dorsal versus ventral aspects of the premotor cortex of monkeys. Neurosci. Res. 21, 71–76.
Matelli, M. and Luppino, G. (1996) Thalamic input to mesial and superior area 6 in the Macaque monkey. J. Comp. Neurol. 372, 59–87.
Nakano, K., Tokushige, A., Kohno, M., Hasegawa, Y., Kayahara, T., and Sasaki, K. (1992) An autoradiographic study of cortical projections from motor thalamic nuclei in the macaque monkey. Neurosci. Res. 13, 119–137.
Goldman-Rakic, P.S. and Porrino, L.J. (1985) The primate mediodorsal (MD) nucleus and its projection to the frontal lobe. J. Comp. Neurol. 242, 535–560.
Garver, D.L. and Sladek, J.R. (1875) Monoamine distribution in primate brain. I. Catecholamine-containing perikarya in the brain stem of macaca speciosa. J. Comp. Neurol. 159, 289–304.
Schofield, S.P.M. and Everitt, B.J. (1981) The organization of catecholamine-containing neurons in the brain of the rhesus monkey (macaca mulatta). J. Anat. 132, 391–418.
Pearson, J., Goldstein, M., Markey, K., and Brandeis, L. (1983) Human brainstem catecholamine neuronal anatomy as indicated by immunocytochemistry with antibodies to tyrosine hydroxylase. Neuroscience 8, 3–32.
Tanaka, C. (1982) Histochemical mapping of catecholaminergic neurons and their ascending fiber pathways in the rhesus monkey brain. Brain Res. Bull. 9, 255–270.
Olszewski, J. and Baxter, D. (1954) Cytoarchitecture of the Human Brain Stem, S. Karger, Basil.
Lynd-Balta, E. and Haber, S.N. (1994) The organization of midbrain projections to the striatum in the primate: sensorimotor-related striatum versus ventral striatum. Neuroscience 59, 625–640.
Poirier, L.J., Giguere, M., and Marchand, R. (1983) Comparative morphology of the substantia nigra and ventral tegmental area in the monkey, cat and rat. Brain Res. Bull. 11, 371–397.
Lavoie, B. and Parent, A. (1991) Dopaminergic neurons expressing calbindin in normal and parkinsonian monkeys. Neuroreport 2, 601–604.
McRitchie, D.A. and Halliday, G.M. (1995) Calbindin D28K-containing neurons are restricted to the medial substantia nigra in humans. Neuroscience 65, 87–91.
Haber, S.N., Ryoo, H., Cox, C., and Lu, W. (1995) 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. 362, 400–410.
Ciliax, B.J., Heilman, C., Demchyschyn, L.L., et al. (1995) The dopamine transporter: immunochemical characterization and localization in brain. J. Neurosci. 15, 1714–1723.
Freed, C., Revay, R., Vaughan, RA., et al. (1995) Dopamine transporter immunoreactivity in rat brain..1. Comp. Neurol. 359, 340–349.
Pifl, C., Schingnitz, G., and Hornykiewicz, O. (1991) Effect of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine on the regional distribution of brain monoamines in the rhesus monkey. Neuroscience 44, No. 3,591–605.
Schneider, J.S., Yuwiler, A., and Markham, C.H. (1987) Selective loss of subpopulations of ventral mesencephalic dopaminergic neurons in the monkey following exposure to MPTP. Brain Res. 411, 144–150.
Parent, A. and Lavoie, B. (1993) The heterogeneity of the mesostriatal dopaminergic system as revealed in normal and Parkinsonian monkeys. Adv. Neurol. 60, 25–20.
Deniau, J.M., Menetrey, A., and Charpier, S. (1996) The lamellar organization of the rat substantia nigra pars reticulata: segretated patterns of striatal afferents and relationship to the topography of corticostriatal projections. Neuroscience 73, 761–781.
Szabo, J. (1967) The efferent projections of the putamen in the monkey. Exp. Neurol. 19, 463–416.
Szabo, J. (1970) Projections from the body of the caudate nucleus in the rhesus monkey. Exp. Neurol. 27, 1–15.
Selemon, L.D. and Goldman-Rakic, P.S. (1990) Topographic intermingling of striatonigral and striatopallidal neurons in the rhesus monkey. J. Comp. Neurol. 297, 359–376…
Lynd-Balta, E. and Haber, S.N. (1994) Primate striatonigral projections: a comparison ot the sensorimotor-related striatum and the ventral striatum. J. Comp. Neurol. 343, 1–17.
Szabo, J. (1980) Organization of the ascending striatal afferents in monkeys..1. Comp. Neurol. 189, 307–321.
Parent, A. and Hazrati, L.-N. (1994) Multiple striatal representation in primate substantia nigra. J. Comp. Neurol. 344, 305–320.
Carpenter, M.B. and Peter, P. (1971) Nigrostriatal and nigrothalamic fibers in the rhesus monkey. J. Comp. Neurol. 144, 93–116.
Parent, A., Mackey, A., and De Bellefeuille, L. (1983) The subcortical afferents to caudate nucleus and putamen in primate: a fluorescence retrograde double labeling study. Neuroscience 10, 1137–1150.
Magee, J.C. and Johnston, D. (1997) A synaptically controlled, associative signal for Hebbian plasticity in hippocampal neurons [see comments]. Science 275, 209–213.
Spruston, N., Jaffe, D.B., and Johnston, D. (1994) Dendritic attenuation of synaptic potentials and currents: the role of passive membrane properties. Trends Neurosci. 17, 161–166.
Schultz, W. (1992) Activity of dopamine neurons in the behaving primate. Semin. Neurosci. 4, 129–138.
Schultz, W., Apicella, P., and Ljungberg, T. (1993) Responses of monkey dopamine neurons to reward and conditioned stimuli during successive steps of learning a delayed response task. J. Neurosci. 13, 900–913.
Wilson, C., Nomikos, G.G., Collu, M., and Fibiger, H.C. (1995) Dopaminergic correlates of motivated behavior: importance of drive. J. Neurosci. 15, 5169–5178. • •
Richardson, N.R. and Gratton, A. (1996) Behavior-relevant changes in nucleus accumbens dopamine transmission elicited by food reinforcement: an electrochemical study in rat. J. Neurosci. 16, 8160–8169.
Smith, I.D. and Grace, A.A. (1992) Role of subthalamic nucleus in the regulation of nigral dopamine neuron activity. Synapse 12, 287–303.
Grace, A.A. and Bunney, B.S. (1995) Electrophysiological properties of midbrain dopamine neurons, in Psychopharmacology: The Fourth Generation of Progress (Bloom, F.E. and Kupfer, D.J., eds.), Raven Press, New York, pp. 163–177.
Francois, C., Percheron, G., Yelnik, J., and Heyner, S. (1979) Demonstration of the existence of small local circuit neurons in the Golgi-stained primate substantia nigra. Brain Res. 172, 160–164.
Johnson, S.W. and North, R.A. (1992) Two types of neurone in the rat ventral tegmental area and their synaptic inputs. J. Physiol. 450, 455–468.
Cepeda, C. and Levine, M.S. (1998) Dopamine and N-methyl-D-aspartate receptor interactions in the neostriatum. Dev. Neurosci. 20, 1–18.
Mogenson, G.J., Brudzynski, S.M., Wu, M., Yang, C.R., and Yim, C.C.Y. (1993) From motiviation to action: a review of dopaminergic regulation of limbic-nucleus accumbens-pedunculopontine nucleus circuitries involved in limbic-motor integration, in Limbic Motor Circuits and Neuropsychiatry (Kalivas, P.W. and Barnes, C.D., eds.), CRC Press, Boca Raton, pp. 193–236.
Groenewegen, H.J., Wright, C.I., and Beijer, A.V.J. (1996) The nucleus accumbens: gateway for limbic structures to reach the motor system? in Progress in Brain Research (Holstege, G., Bandler, R., and Saper, C.P., eds.), Amsterdam, Elsevier Science, pp. 485–511.
Schultz, W., Dayan, P., and Montague, P.R. (1997) A neural substrate of prediction and reward [review]. Science 275, 1593–1599.
Ljungberg, T., Apicella, P., and Schultz, W. (1992) Responses of monkey dopamine neurons during learning of behavioral reactions. J. Neurophysiol. 67, 145–163.
Parent, A. and Hazrati, L.N. (1995) Functional anatomy of the basal ganglia. I. The cortico-basal ganglia-thalamocortical loop. Brain Res. Brain Res. Rev. 20, 91–127.
Sherman, S.M. and Guillery, R.W. (1996) Functional organization of thalamocortical relays. J. Neurophysiol. 76, 1367–1395.
Pare, D., Curro’Dossi, R., and Steriade, M. (1990) Neuronal basis of the parkinsonian resting tremor: a hypothesis and its implications for treatment. Neuroscience 35, 217–226.
Jones, E.G. (1998) The thalamus of primates, in The Primate Nervous System, Part II, Vol. 14 (Bloom, F. E., Björklund, A., and Hökfelt, T., eds.), Elsevier Science, Amsterdam, pp. 1–298.
Contreras, D. and Steriade, M. (1997) Synchronization of low-frequency rhythms in corticothalamic networks. Neuroscience 76, 11–24.
Steriade, M. (1999) Coherent oscillations and short-term plasticity in corticothalamic networks. Trends Neurosci. 22, 337–345.
Destexhe, A., Contreras, D., and Steriade, M. (1998) Mechanisms underlying the synchronizing action of corticothalamic feedback through inhibition of thalamic relay cells. J. Neurophysiol. 79, 999–1016.
Bal, T., Debay, D., and Destexhe, A. (2000) Cortical feedback controls the frequency and synchrony of oscillation in the visual thalamus. J. Neurosci. 20, 7478–7488.
Catsman-Berrevoets, C.E. and Kuypers, H.G. (1978) Differential laminar distribution of corticothalamic neurons projecting to the VL and the center median. An HRP study in the cynomolgus monkey. Brain Res. 154, 359–365.
Deschenes, M., Veinante, P., and Zhang, Z.W. (1998) The organization of corticothalamic projections: reciprocity versus parity. Brain Res. Brain Res. Rev. 28, 286–308.
Murphy, P.C. and Sillito, A.M. (1996) Functional morphology of the feedback pathway from area 17 of the cat visual cortex to the lateral geniculate nucleus. J. Neurosci. 16. 1180–1192.
Hoogland, P.V., Welker, E., and Van der Loos, H. (1987) Organization of the projections from barrel cortex to thalamus in mice studied with Phaseolus vulgaris-leucoagglutinin and HRP. Exp. Brain Res. 68, 73–87.
Darian-Smith, C., Tan, A., and Edwards, S. (1999) Comparing thalamocortical and corticothalamic microstructure and spatial reciprocity in the macaque ventral posterolateral nucleus (VPLc) and medial pulvinar. J. Comp. Neurol. 410, 211–234.
Jones, E.G. and Wise, S.P. (1977) Size, laminar and columnar distribution of efferent cells in the sensory-motor cortex of monkeys. J. Comp. Neurol. 175, 391–438.
Giguere, M. and Goldman-Rakic, P.S. (1988) Mediodorsal nucleus: area 1 laminar and tangential distribution of afferents and efferents in the frontal lobe of rhesus monkeys. J. Comp. Neurol. 277, 195–213.
Arikuni, T. and Kubota, K. (1986) The organization of prefrontocaudate projections and their laminar origin in the macaque monkey: a retrograde study using HRP-gel. J. Comp. Neurol. 244, 492–510.
Chmielowska, J. and Pons, T.P. (1995) Patterns of thalamocortical degeneration after ablation of somatosensory cortex in monkeys. J. Comp. Neurol. 360, 377–392.
Destexhe, A., Contreras, D., and Steriade, M. (1999) Cortically-induced coherence of a thalamic-generated oscillation. Neuroscience 92, 427–443.
Ray, J.P. and Price, J.L. (1993) The organization of projections from the mediodorsal nucleus of the thalamus to orbital and medial prefrontal cortex in Macaque monkeys. J. Comp. Neurol. 337, 1–31.
Russchen, F.T., Amaral, D.G., and Price, J.L. (1987) The afferent input to the magnocellular division of the mediodorsal thalamic nucleus in the monkey, Macaca fascicularis. J. Comp. Neurol. 256, 175–210.
Nakajima, S. (1984) Serotonergic mediation of habenular self-stimulation in the rat. Pharmacol. Biochem. Behav. 20, 859–862.
McFarland, N.R. and Haber, S.N. (2002) Thalamic relay nuclei of the basal ganglia form both reciprocal and nonreciprocal cortical connections linking multiple frontal cortical areas. J. Neurosci. 22, 8117–8132.
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Haber, S.N. (2003). Integrating Cognition and Motivation into the Basal Ganglia Pathways of Action. In: Bédard, MA., Agid, Y., Chouinard, S., Fahn, S., Korczyn, A.D., Lespérance, P. (eds) Mental and Behavioral Dysfunction in Movement Disorders. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-326-2_3
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