Physiology and Pharmacology of Striatal Neurons

The functional anatomy of basal ganglia disorders

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Primate models of movement disorders of basal ganglia origin

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NEURAL MECHANISMS OF ADDICTION: The Role of Reward-Related Learning and Memory

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The role of the basal ganglia in habit formation

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Functional anatomy of the basal ganglia. I. The cortico-basal ganglia-thalamo-cortical loop

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A gene expression atlas of the central nervous system based on bacterial artificial chromosomes

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The molecular logic of endocannabinoid signalling

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Habits, Rituals, and the Evaluative Brain

Graybiel, A. M. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.112851 · Cited by 1,697

Multiple dopamine functions at different time courses

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The organization of the projection from the cerebral cortex to the striatum in the rat

McGeorge, A. J., & Faull, R. L. M. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90128-0 · Cited by 1,360

The Basal Ganglia and Adaptive Motor Control

Graybiel, A. M., Aosaki, T., Flaherty, A. W., & Kimura, M. (1994) · Science · doi:10.1126/science.8091209 · Cited by 1,324

D1 and D2 dopamine-receptor modulation of striatal glutamatergic signaling in striatal medium spiny neurons

Surmeier, D. J., Ding, J., Day, M., Wang, Z., & Shen, W. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.008 · Cited by 1,203

Striatal interneurones: chemical, physiological and morphological characterization

Kawaguchi, Y., Wilson, C. J., Augood, S. J., & Emson, P. C. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)98374-8 · Cited by 1,197

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

Brog, J. S., Salyapongse, A., Deutch, A. Y., & Zahm, D. S. (1993) · Journal of Comparative Neurology · doi:10.1002/cne.903380209 · Cited by 1,102

The basal ganglia

Graybiel, A. M. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00593-5 · Cited by 1,051

Behavioral dopamine signals.

Schultz, W. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.007 · Cited by 1,028

The neostriatal mosaic: multiple levels of compartmental organization in the basal ganglia

Gerfen, C. R. (1992) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.15.030192.001441 · Cited by 1,004

Discussion

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Synaptic organisation of the basal ganglia

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Dopaminergic modulation of neuronal excitability in the striatum and nucleus accumbens

Nicola, S. M., Surmeier, D. J., & Malenka, R. C. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.185 · Cited by 931

Tyrosine hydroxylase-immunoreactive boutons in synaptic contact with identified striatonigral neurons, with particular reference to dendritic spines

Freund, T. F., Powell, J. F., & Smith, A. D. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90294-x · Cited by 875

Inhibitory control of neostriatal projection neurons by GABAergic interneurons

Koós, T. Z., & Tepper, J. M. (1999) · Nature Neuroscience · doi:10.1038/8138 · Cited by 863

The neostriatal mosaic: compartmentalization of corticostriatal input and striatonigral output systems

Gerfen, C. R. (1984) · Nature · doi:10.1038/311461a0 · Cited by 842

Differential loss of striatal projection neurons in Huntington disease.

Reiner, A., Albin, R. L., Anderson, K. D., D'Amato, C. J., Penney, J. B., & Young, A. B. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.15.5733 · Cited by 839

Physiological, morphological, and histochemical characterization of three classes of interneurons in rat neostriatum

Kawaguchi, Y. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-11-04908.1993 · Cited by 814

The origins of two-state spontaneous membrane potential fluctuations of neostriatal spiny neurons

Wilson, C. J., & Kawaguchi, Y. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-07-02397.1996 · Cited by 798

Histochemically distinct compartments in the striatum of human, monkeys, and cat demonstrated by acetylthiocholinesterase staining

Graybiel, A. M., & Ragsdale, C. W. (1978) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.75.11.5723 · Cited by 784

Dopamine activation of endogenous cannabinoid signaling in dorsal striatum

Giuffrida, A., Parsons, L. H., Kerr, T. M., de Fonseca, F. R., Navarro, M. A., & Piomelli, D. (1999) · Nature Neuroscience · doi:10.1038/7268 · Cited by 782

Coordinated Expression of Dopamine Receptors in Neostriatal Medium Spiny Neurons

Surmeier, D. J., Song, W., & Yan, Z. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-20-06579.1996 · Cited by 762

Selective Sparing of a Class of Striatal Neurons in Huntington's Disease

Ferrante, R. J., Kowall, N. W., Beal, M. F., Richardson, E. P., Bird, E. D., & Martin, J. B. (1985) · Science · doi:10.1126/science.2931802 · Cited by 757

Selective elimination of glutamatergic synapses on striatopallidal neurons in Parkinson disease models

Day, M., Wang, Z., Ding, J., An, X., Ingham, C. A., Shering, A. F., Wokosin, D., Ilijic, E., Sun, Z., Sampson, A. R., et al. (2006) · Nature Neuroscience · doi:10.1038/nn1632 · Cited by 745

Endocannabinoid-mediated rescue of striatal LTD and motor deficits in Parkinson's disease models

Kreitzer, A. C., & Malenka, R. C. (2007) · Nature · doi:10.1038/nature05506 · Cited by 735

Bilateral projections from precentral motor cortex to the putamen and other parts of the basal ganglia. An autoradiographic study inMacaca fascicularis

Künzle, H. (1975) · Brain Research · doi:10.1016/0006-8993(75)90384-4 · Cited by 714

The structure of the caudate nucleus of the cat: light and electron microscopy

Kemp, J. M., & Powell, T. P. S. (1971) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1971.0102 · Cited by 672

Distribution of striatonigral and striatopallidal peptidergic neurons in both patch and matrix compartments: an in situ hybridization histochemistry and fluorescent retrograde tracing study

Gerfen, C. R., & Scott Young, W. (1988) · Brain Research · doi:10.1016/0006-8993(88)91217-6 · Cited by 658

The neostriatal mosaic: compartmental distribution of calcium-binding protein and parvalbumin in the basal ganglia of the rat and monkey.

Gerfen, C. R., Baimbridge, K. G., & Miller, J. J. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.24.8780 · Cited by 645

Ventral Tegmental Area Neurons in Learned Appetitive Behavior and Positive Reinforcement

Fields, H. L., Hjelmstad, G. O., Margolis, E. B., & Nicola, S. M. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094341 · Cited by 632

Localization of D1 and D2 dopamine receptors in brain with subtype-specific antibodies.

Levey, A. I., Hersch, S. M., Rye, D. B., Sunahara, R. K., Niznik, H. B., Kitt, C. A., Price, D. L., Maggio, R., Brann, M. R., & Ciliax, B. J. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.19.8861 · Cited by 625

Responses of tonically active neurons in the primate's striatum undergo systematic changes during behavioral sensorimotor conditioning

Aosaki, T., Tsubokawa, H., Ishida, A., Watanabe, K., Graybiel, A. M., & Kimura, M. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-06-03969.1994 · Cited by 600

Coincident but Distinct Messages of Midbrain Dopamine and Striatal Tonically Active Neurons

Morris, G., Arkadir, D., Nevet, A., Vaadia, E., & Bergman, H. (2004) · Neuron · doi:10.1016/j.neuron.2004.06.012 · Cited by 574

The neostriatal mosaic. I. compartmental organization of projections from the striatum to the substantia nigra in the rat

Gerfen, C. R. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902360404 · Cited by 563

Modulation of calcium currents by a D1 dopaminergic protein kinase/phosphatase cascade in rat neostriatal neurons

Surmeier, D. J., Bargas, J., Hemmings, H. C., Nairn, A. C., & Greengard, P. (1995) · Neuron · doi:10.1016/0896-6273(95)90294-5 · Cited by 548

Mosaic distribution of opiate receptors, parafascicular projections and acetylcholinesterase in rat striatum

Herkenham, M. A., & Pert, C. B. (1981) · Nature · doi:10.1038/291415a0 · Cited by 544

Immunocytochemical localization of D1 and D2 dopamine receptors in the basal ganglia of the rat: Light and electron microscopy

Yung, K. K. L., Bolam, J. P., Smith, A. D., Hersch, S. M., Ciliax, B. J., & Levey, A. I. (1995) · Neuroscience · doi:10.1016/0306-4522(94)00536-e · Cited by 543

Striatal Restricted Adenosine A2 Receptor (RDC8) Is Expressed by Enkephalin but Not by Substance P Neurons: An In Situ Hybridization Histochemistry Study

Schiffmann, S. N., Jacobs, O. E., & Vanderhaeghen, J. (1991) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1991.tb08257.x · Cited by 530

Functional diversity and specificity of neostriatal interneurons

Tepper, J. M., & Bolam, J. P. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.10.003 · Cited by 526

Firing patterns and synaptic potentials of identified giant aspiny interneurons in the rat neostriatum

Wilson, C. J., Chang, H., & Kitai, S. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-02-00508.1990 · Cited by 520

Neuronal localization of cannabinoid receptors in the basal ganglia of the rat

Herkenham, M. A., Lynn, A. B., de Costa, B. R., & Richfield, E. K. (1991) · Brain Research · doi:10.1016/0006-8993(91)90970-7 · Cited by 515

Dopaminergic Control of Corticostriatal Long-Term Synaptic Depression in Medium Spiny Neurons Is Mediated by Cholinergic Interneurons

Wang, Z., Li, K., Day, M., Ronesi, J. A., Yin, H. H., Ding, J., Tkatch, T., Lovinger, D. M., & Surmeier, D. J. (2006) · Neuron · doi:10.1016/j.neuron.2006.04.010 · Cited by 513

An intricately patterned prefronto‐caudate projection in the rhesus monkey

Goldman, P. S., & Nauta, W. J. H. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901710305 · Cited by 509

Oscillatory Entrainment of Striatal Neurons in Freely Moving Rats

Berke, J. D., Okatan, M., Skurski, J., & Eichenbaum, H. (2004) · Neuron · doi:10.1016/j.neuron.2004.08.035 · Cited by 507

D1Receptor Activation Enhances Evoked Discharge in Neostriatal Medium Spiny Neurons by Modulating an L-Type Ca2+Conductance

Hernández‐López, S., Bargas, J., Surmeier, D. J., Reyes, A., & Galarraga, E. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-09-03334.1997 · Cited by 495

Regional, cellular, and subcellular variations in the distribution of D1 and D5 dopamine receptors in primate brain

Bergson, C. M., Mrzljak, L., Smiley, J., Pappy, M., Levenson, R. G., & Goldman-Rakic, P. S. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-12-07821.1995 · Cited by 488

An integrative neuroanatomical perspective on some subcortical substrates of adaptive responding with emphasis on the nucleus accumbens

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Characterization of cholinergic neurons in the rat neostriatum. A combination of choline acetyltransferase immunocytochemistry, Golgi-impregnation and electron microscopy

Bolam, J. P., Wainer, B. H., & Smith, A. D. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90165-9 · Cited by 485

Expression of muscarinic acetylcholine and dopamine receptor mRNAs in rat basal ganglia.

Weiner, D. M., Levey, A. I., & Brann, M. R. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.18.7050 · Cited by 481

Cholinergic interneuron characteristics and nicotinic properties in the striatum

Zhou, F., Wilson, C. J., & Dani, J. A. (2002) · Journal of Neurobiology · doi:10.1002/neu.10150 · Cited by 465

Acetylcholine-mediated modulation of striatal function

Calabresi, P., Centonze, D., Gubellini, P., Pisani, A., & Bernardi, G. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(99)01501-5 · Cited by 452

Input from the frontal cortex and the parafascicular nucleus to cholinergic interneurons in the dorsal striatum of the rat

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Neurons in the Thalamic CM-Pf Complex Supply Striatal Neurons With Information About Behaviorally Significant Sensory Events

Matsumoto, N., Minamimoto, T., Graybiel, A. M., & Kimura, M. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.2.960 · Cited by 451

The pathophysiological basis of dystonias

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Anatomical and affinity state comparisons between dopamine D1 and D2 receptors in the rat central nervous system

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D2Dopamine Receptors in Striatal Medium Spiny Neurons Reduce L-Type Ca2+Currents and Excitability via a Novel PLCβ1–IP3–Calcineurin-Signaling Cascade

Hernández-López, S., Tkatch, T., Perez-Garci, E., Galarraga, E., Bargas, J., Hamm, H., & Surmeier, D. J. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-24-08987.2000 · Cited by 443

GABAergic microcircuits in the neostriatum

Tepper, J. M., Koós, T. Z., & Wilson, C. J. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.08.007 · Cited by 436

Dopamine receptor subtypes colocalize in rat striatonigral neurons.

Surmeier, D. J., Eberwine, J. H., Wilson, C. J., Cao, Y., Stefani, A., & Kitai, S. T. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.21.10178 · Cited by 433

Parvalbumin-immunoreactive neurons in the rat neostriatum: a light and electron microscopic study

Kita, H., Kosaka, T., & Heizmann, C. W. (1990) · Brain Research · doi:10.1016/0006-8993(90)90002-s · Cited by 431

The organization of the basal ganglia-thalamocortical circuits: Open interconnected rather than closed segregated

Joel, D., & Weiner, I. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90536-3 · Cited by 430

Effect of the nigrostriatal dopamine system on acquired neural responses in the striatum of behaving monkeys

Aosaki, T., Graybiel, A. M., & Kimura, M. (1994) · Science · doi:10.1126/science.8023166 · Cited by 427

NADPH‐diaphorase: A selective histochemical marker for striatal neurons containing both somatostatin‐ and avian pancreatic polypeptide (APP)‐like immunoreactivities

Vincent, S. R., Johansson, O., Hökfelt, T. G. M., Skirboll, L. R., Elde, R. P., Terenius, L. Y., KIMMEL, J. R., & Goldstein, M. (1983) · The Journal of Comparative Neurology · doi:10.1002/cne.902170303 · Cited by 424

Neostriatal projections from individual cortical fields conform to histochemically distinct striatal compartments in the rat

Donoghue, J. P., & Herkenham, M. A. (1986) · Brain Research · doi:10.1016/0006-8993(86)91658-6 · Cited by 418

Cortical Inputs and GABA Interneurons Imbalance Projection Neurons in the Striatum of Parkinsonian Rats

Mallet, N. P., Ballion, B., Moine, C. L., & Gonon, F. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4439-05.2006 · Cited by 413

Heterogeneity of striatal and limbic dopamine innervation: Highly fluorescent islands in developing and adult rats

Olson, L., Seiger, Å., & Fuxé, K. (1972) · Brain Research · doi:10.1016/0006-8993(72)90385-x · Cited by 405

Distribution of m1-m4 muscarinic receptor proteins in the rat striatum: light and electron microscopic immunocytochemistry using subtype- specific antibodies

Hersch, S. M., Gutekunst, C., Rees, H., Heilman, C. J., & Levey, A. I. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-05-03351.1994 · Cited by 404

Immunocytochemical localization of choline acetyltransferase within the rat neostriatum: A correlated light and electron microscopic study of cholinergic neurons and synapses

Phelps, P. E., Houser, C. R., & Vaughn, J. E. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902380305 · Cited by 394

Temporal and spatial characteristics of tonically active neurons of the primate's striatum

Aosaki, T., Kimura, M., & Graybiel, A. M. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.73.3.1234 · Cited by 385

The nucleus accumbens as part of a basal ganglia action selection circuit

Nicola, S. M. (2006) · Psychopharmacology · doi:10.1007/s00213-006-0510-4 · Cited by 383

Feedforward Inhibition of Projection Neurons by Fast-Spiking GABA Interneurons in the Rat StriatumIn Vivo

Mallet, N. P., Moine, C. L., Charpier, S., & Gonon, F. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.5027-04.2005 · Cited by 380

DAncing past the DAT at a DA synapse

Cragg, S. J., & Rice, M. E. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.03.011 · Cited by 373

Selective Innervation of Neostriatal Interneurons by a Subclass of Neuron in the Globus Pallidus of the Rat

Bevan, M. D., Booth, P. A. C., Eaton, S. A., & Bolam, J. P. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-22-09438.1998 · Cited by 373

Spontaneous firing patterns of identified spiny neurons in the rat neostriatum.

Wilson, C., & Groves, P. (1981) · Brain Research · doi:10.1016/0006-8993(81)90211-0 · Cited by 369

Chapter 18 The generation of natural firing patterns in neostriatal neurons

Wilson, C. J. (1993) · Progress in brain research · doi:10.1016/s0079-6123(08)61352-7 · Cited by 359

Dopamine Modulation of State-Dependent Endocannabinoid Release and Long-Term Depression in the Striatum

Kreitzer, A. C., & Malenka, R. C. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2959-05.2005 · Cited by 358

Potassium currents responsible for inward and outward rectification in rat neostriatal spiny projection neurons

Nisenbaum, E., & Wilson, C. J. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-06-04449.1995 · Cited by 348

State-Dependent Calcium Signaling in Dendritic Spines of Striatal Medium Spiny Neurons

Carter, A. G., & Sabatini, B. L. (2004) · Neuron · doi:10.1016/j.neuron.2004.10.013 · Cited by 347

Membrane potential synchrony of simultaneously recorded striatal spiny neurons in vivo

Stern, E. A., Jaeger, D., & Wilson, C. J. (1998) · Nature · doi:10.1038/28848 · Cited by 340

Behavioural assessment of mice lacking D1A dopamine receptors

Smith, D., Striplin, C. D., Geller, A. M., Mailman, R. B., Drago, J., Lawler, C. P., & Gallagher, M. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00608-8 · Cited by 334

Intrinsic Membrane Properties Underlying Spontaneous Tonic Firing in Neostriatal Cholinergic Interneurons

Bennett, B. D., Callaway, J. C., & Wilson, C. J. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-22-08493.2000 · Cited by 332

Phenotypical characterization of the rat striatal neurons expressing muscarinic receptor genes

Bernard, V., Normand, E., & Bloch, B. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-09-03591.1992 · Cited by 327

Synaptic relationships between dopaminergic afferents and cortical or thalamic input in the sensorimotor territory of the striatum in monkey

Smith, Y., Bennett, B. D., Bolam, J. P., Parent, A., & Sadikot, A. F. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903440102 · Cited by 312

The termination of fibres from the cerebral cortex and thalamus upon dendritic spines in the caudate nucleus: a study with the Golgi method

Kemp, J. M., & Powell, T. P. S. (1971) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1971.0105 · Cited by 306

Dual Cholinergic Control of Fast-Spiking Interneurons in the Neostriatum

Koós, T. Z., & Tepper, J. M. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-02-00529.2002 · Cited by 302

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

Sadikot, A. F., Parent, A., Smith, Y., & Bolam, J. P. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903200207 · Cited by 294

Cholinergic modulation of Kir2 channels selectively elevates dendritic excitability in striatopallidal neurons

Shen, W., Tian, X., Day, M., Ulrich, S., Tkatch, T., Nathanson, N. M., & Surmeier, D. J. (2007) · Nature Neuroscience · doi:10.1038/nn1972 · Cited by 291

Parvalbumin‐containing gabaergic interneurons in the rat neostriatum

Cowan, R. L., Wilson, C. J., Emson, P. C., & Heizmann, C. W. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903020202 · Cited by 290

Space, time and dopamine

Arbuthnott, G. W., & Wickens, J. R. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.12.003 · Cited by 287

Connectivity and Convergence of Single Corticostriatal Axons

Kincaid, A. E., Zheng, T., & Wilson, C. J. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-12-04722.1998 · Cited by 277

D 2 Dopamine Receptors Reduce N-Type Ca 2+ Currents in Rat Neostriatal Cholinergic Interneurons Through a Membrane-Delimited, Protein-Kinase-C-Insensitive Pathway

Yan, Z., Song, W., & Surmeier, D. J. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.77.2.1003 · Cited by 273

Subdivisions of the dopamine-containing A8-A9-A10 complex identified by their differential mesostriatal innervation of striosomes and extrastriosomal matrix

Jiménez-Castellanos, J., & Graybiel, A. M. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90285-5 · Cited by 272

Substance P-Containing terminals in synaptic contact with cholinergic neurons in the neostriatum and basal forebrain: a double immunocytochemical study in the rat

Bolam, J. P., Ingham, C. A., Izzo, P. N., Levey, A. I., Rye, D. B., Smith, A. D., & Wainer, B. H. (1986) · Brain Research · doi:10.1016/0006-8993(86)90629-3 · Cited by 271

Synaptic input and output of parvalbumin-immunoreactive neurons in the neostriatum of the rat

Bennett, B. D., & Bolam, J. P. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90471-5 · Cited by 262

Distinct Roles of D1and D5Dopamine Receptors in Motor Activity and Striatal Synaptic Plasticity

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