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Striatal Contributions to Reward and Decision Making: Making Sense of Regional Variations in a Reiterated Processing Matrix
Abstract
The striatum is the major input nucleus of the basal ganglia. It is thought to play a key role in learning on the basis of positive reinforcement and in action selection. One view of the striatum conceives it as comprising a reiterated matrix of processing units that perform common operations in different striatal regions, namely synaptic plasticity according to a three-factor rule, and lateral inhibition. These operations are required for reinforcement learning and selection of previously reinforced actions. Analysis of the behavioral effects of circumscribed lesions of the striatum, however, suggests regional specialization of learning and decision-making operations. We consider how a basic processing unit may be modified by regional variations in neurochemical parameters, for example, by the gradient in density of dopamine terminals from dorsal to ventral striatum. These variations suggest subtle differences between dorsolateral and ventromedial striatal regions in the temporal properties of dopamine signaling, which are superimposed on regional differences in connectivity. We propose that these variations make sense in relation to the temporal structure of activity in striatal inputs from different regions, and the requirements of different learning operations. Dorsolateral striatal (DLS) regions may be subject to brief, precisely timed pulses of dopamine, whereas ventromedial striatal regions integrate dopamine signals over a longer time course. These differences may be important for understanding regional variations in the contribution to reinforcement of habits, versus incentive processes that are sensitive to the value of expected rewards.
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“Of particular interest, dopamine appears to play a diminishing role in behavioral expression over the course of extended training [38, 42].”
From Cortical and basal ganglia contributions to habit learning and automaticity (2010) · cites this paper as [38]
Citations
Cites
Parallel organization of functionally segregated circuits linking basal ganglia and cortex
Alexander, G. E., DeLong, M. R., & Strick, P. L. (1986) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.09.030186.002041 · Cited by 8,527
The neural basis of drug craving: An incentive-sensitization theory of addiction
Robinson, T. (1993) · Brain Research Reviews · doi:10.1016/0165-0173(93)90013-p · Cited by 7,346
Dahlstroem, A., & Fuxé, K. (1964) · PubMed · Cited by 5,133
What is the role of dopamine in reward: hedonic impact, reward learning, or incentive salience?
Berridge, K. C., & Robinson, T. E. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(98)00019-8 · Cited by 4,127
Stereotaxic mapping of the monoamine pathways in the rat brain
Ungerstedt, U. (1971) · Acta Physiologica Scandinavica · doi:10.1111/j.1365-201x.1971.tb10998.x · Cited by 3,819
The role of the basal ganglia in habit formation
Yin, H. H., & Knowlton, B. J. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1919 · Cited by 2,402
From motivation to action: Functional interface between the limbic system and the motor system
MOGENSON, G., JONES, D., & YIM, C. (1980) · Progress in Neurobiology · doi:10.1016/0301-0082(80)90018-0 · Cited by 2,331
Emotion and motivation: the role of the amygdala, ventral striatum, and prefrontal cortex
Cardinal, R. N., Parkinson, J. A., Hall, J., & Everitt, B. J. (2002) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(02)00007-6 · Cited by 2,129
Discrete coding of reward probability and uncertainty by dopamine neurons
Fiorillo, C. D., Tobler, P. N., & Schultz, W. (2003) · Science · doi:10.1126/science.1077349 · Cited by 2,085
Integrative activity of the brain
Konorski, J. (1967) · University of Chicago Press eBooks · Cited by 2,043
Learning and Memory Functions of the Basal Ganglia
Packard, M. G., & Knowlton, B. J. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142937 · Cited by 1,717
Haber, S. N., Fudge, J. L., & McFarland, N. R. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-06-02369.2000 · Cited by 1,610
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
Schultz, W., Apicella, P., & Ljungberg, T. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-03-00900.1993 · Cited by 1,291
Adaptive Coding of Reward Value by Dopamine Neurons
Tobler, P. N., Fiorillo, C. D., & Schultz, W. (2005) · Science · doi:10.1126/science.1105370 · Cited by 1,276
Yin, H. H., Knowlton, B. J., & Balleine, B. W. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03095.x · Cited by 1,226
Putting a spin on the dorsal-ventral divide of the striatum
Voorn, P., Vanderschuren, L. J. M. J., Groenewegen, H. J., Robbins, T. W., & Pennartz, C. M. A. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.06.006 · Cited by 1,188
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 role of the dorsomedial striatum in instrumental conditioning
Yin, H. H., Ostlund, S. B., Knowlton, B. J., & Balleine, B. W. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04218.x · Cited by 1,099
Dopamine responses comply with basic assumptions of formal learning theory
Waelti, P., Dickinson, A., & Schultz, W. (2001) · Nature · doi:10.1038/35083500 · Cited by 1,018
Responses of monkey dopamine neurons during learning of behavioral reactions
Ljungberg, T., Apicella, P., & Schultz, W. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.67.1.145 · Cited by 987
Synaptic organisation of the basal ganglia
Bolam, J. P., Hanley, J. J., Booth, P. A. C., & Bevan, M. D. (2000) · Journal of Anatomy · doi:10.1046/j.1469-7580.2000.19640527.x · Cited by 946
Kelley, A. E. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2003.11.015 · Cited by 942
Representation of Action-Specific Reward Values in the Striatum
Samejima, K., Ueda, Y., Doya, K., & Kimura, M. (2005) · Science · doi:10.1126/science.1115270 · Cited by 939
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
Impulsive choice induced in rats by lesions of the nucleus accumbens core
Cardinal, R. N., Pennicott, D. R., Lakmali, C., Sugathapala, Robbins, T. W., & Everitt, B. J. (2001) · Science · doi:10.1126/science.1060818 · Cited by 923
A cellular mechanism of reward-related learning
Reynolds, J. N. J., Hyland, B. I., & Wickens, J. R. (2001) · Nature · doi:10.1038/35092560 · Cited by 879
Self-citationGerfen, C. R. (1984) · Nature · doi:10.1038/311461a0 · Cited by 842
Preferential activation of midbrain dopamine neurons by appetitive rather than aversive stimuli
Mirenowicz, J., & Schultz, W. (1996) · Nature · doi:10.1038/379449a0 · Cited by 829
Sesack, S. R., & Pickel, V. M. (1992) · Journal of Comparative Neurology · doi:10.1002/cne.903200202 · Cited by 820
Gerfen, C. R., Herkenham, M. A., & Thibault, J. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-12-03915.1987 · Cited by 804
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
Graybiel, A. M., & Ragsdale, C. W. (1978) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.75.11.5723 · Cited by 784
A motivational view of learning, performance, and behavior modification.
Bindra, D. (1974) · Psychological Review · doi:10.1037/h0036330 · Cited by 594
Modulation of Caudate Activity by Action Contingency
Tricomi, E. M., Delgado, M. R., & Fiez, J. A. (2004) · Neuron · doi:10.1016/s0896-6273(03)00848-1 · Cited by 592
Dopamine: a potential substrate for synaptic plasticity and memory mechanisms
Jay, T. M. (2003) · Progress in Neurobiology · doi:10.1016/s0301-0082(03)00085-6 · Cited by 579
Corbit, L. H., Muir, J. L., & Balleine, B. W. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-09-03251.2001 · Cited by 564
Behavioral effects of selective ablation of the caudate nucleus.
Divac, I., Rosvold, H. E., & Szwarcbart, M. K. (1967) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0024348 · Cited by 562
Parkinson, J. A., Olmstead, M. C., Burns, L. H., Robbins, T. W., & Everitt, B. J. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-06-02401.1999 · Cited by 555
Importance of unpredictability for reward responses in primate dopamine neurons
Mirenowicz, J., & Schultz, W. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.72.2.1024 · Cited by 544
Herkenham, M. A., & Pert, C. B. (1981) · Nature · doi:10.1038/291415a0 · Cited by 544
YIN, H., KNOWLTON, B., & BALLEINE, B. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.07.012 · Cited by 532
Dopamine-dependent plasticity of corticostriatal synapses
Reynolds, J. N. J., & Wickens, J. R. (2002) · Neural Networks · doi:10.1016/s0893-6080(02)00045-x · Cited by 528
Self-citationMargolis, E. B., Lock, H., Hjelmstad, G. O., & Fields, H. L. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.117069 · Cited by 527
Nauta, H. J. W., Pritz, M. B., & Lasek, R. J. (1974) · Brain Research · doi:10.1016/0006-8993(74)90274-1 · Cited by 519
Firing modes of midbrain dopamine cells in the freely moving rat
Hyland, B. I., Reynolds, J. N. J., HAY, J. G., Perk, C. G., & Miller, R. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00267-1 · Cited by 487
Self-citationThe Neostriatal Mosaic: Striatal Patch-Matrix Organization Is Related to Cortical Lamination
Gerfen, C. R. (1989) · Science · doi:10.1126/science.2799392 · Cited by 456
Somogyi, P., Bolam, J. P., & Smith, A. D. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.901950403 · Cited by 455
Yin, H. H., Knowlton, B. J., & Balleine, B. W. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04219.x · Cited by 447
Sesack, S. R., & Pickel, V. M. (1990) · Brain Research · doi:10.1016/0006-8993(90)91146-8 · Cited by 439
Pan, W.-X., Schmidt, R., Wickens, J. R., & Hyland, B. I. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1478-05.2005 · Cited by 429
Self-citationGarris, P. A., & Wightman, R. M. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-01-00442.1994 · Cited by 419
Lesion to the nigrostriatal dopamine system disrupts stimulus-response habit formation
Faure, A., Haberland, U., Condé, F., & Massioui, N. E. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3894-04.2005 · Cited by 402
Kerr, J. N. D., & Wickens, J. R. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.1.117 · Cited by 395
Self-citationInvolvement of the dorsal striatum in cue-controlled cocaine seeking
Vanderschuren, L. J. M. J., Di Ciano, P., & Everitt, B. J. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.0925-05.2005 · Cited by 393
Responses of midbrain dopamine neurons to behavioral trigger stimuli in the monkey
Schultz, W. (1986) · Journal of Neurophysiology · doi:10.1152/jn.1986.56.5.1439 · Cited by 390
Relations between Pavlovian-instrumental transfer and reinforcer devaluation
Holland, P. C. (2004) · Journal of Experimental Psychology: Animal Behavior Processes · doi:10.1037/0097-7403.30.2.104 · Cited by 388
Functional–anatomical implications of the nucleus accumbens core and shell subterritories
ZAHM, D. S. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09264.x · Cited by 384
Influence of Reward Expectation on Behavior-Related Neuronal Activity in Primate Striatum
Hollerman, J. R., Tremblay, L., & Schultz, W. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.2.947 · Cited by 380
Postconditioning devaluation of a reinforcer affects instrumental responding.
Colwill, R. M., & Rescorla, R. A. (1985) · Journal of Experimental Psychology Animal Behavior Processes · doi:10.1037/0097-7403.11.1.120 · Cited by 375
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
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
The effect of the instrumental training contingency on susceptibility to reinforcer devaluation
Dickinson, A., Nicholas, D. J., & Adams, C. D. (1983) · The Quarterly Journal of Experimental Psychology Section B · doi:10.1080/14640748308400912 · Cited by 338
Dissociation of Pavlovian and instrumental incentive learning under dopamine antagonists.
Dickinson, A., Smith, J. W., & Mirenowicz, J. (2000) · Behavioral Neuroscience · doi:10.1037//0735-7044.114.3.468 · Cited by 322
Taylor, J. R., & Robbins, T. W. (1986) · Psychopharmacology · doi:10.1007/bf00179197 · Cited by 317
A New Anatomical Framework for Neuropsychiatric Disorders and Drug Abuse
Heimer, L. (2003) · American Journal of Psychiatry · doi:10.1176/appi.ajp.160.10.1726 · Cited by 314
Parkinson, J. A., Willoughby, P. J., Robbins, T. W., & Everitt, B. J. (2000) · Behavioral Neuroscience · doi:10.1037/0735-7044.114.1.42 · Cited by 314
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
Inhibitory Interactions Between Spiny Projection Neurons in the Rat Striatum
Tunstall, M. J., Oorschot, D. E., Kean, A., & Wickens, J. R. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.88.3.1263 · Cited by 311
Self-citationParkinson, J. A., Willoughby, P. J., Robbins, T. W., & Everitt, B. J. (2000) · Behavioral Neuroscience · doi:10.1037//0735-7044.114.1.42 · Cited by 309
Comparison of IPSCs Evoked by Spiny and Fast-Spiking Neurons in the Neostriatum
Koós, T. Z., Tepper, J. M., & Wilson, C. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2163-04.2004 · Cited by 309
Coding of Predicted Reward Omission by Dopamine Neurons in a Conditioned Inhibition Paradigm
Tobler, P. N., Dickinson, A., & Schultz, W. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-32-10402.2003 · Cited by 300
Correlated Coding of Motivation and Outcome of Decision by Dopamine Neurons
Satoh, T., Nakai, S., Sato, T., & Kimura, M. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-30-09913.2003 · Cited by 298
Kelley, A. E., Smith‐Roe, S. L., & Holahan, M. R. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.22.12174 · Cited by 293
Motivational control after extended instrumental training
Dickinson, A., Balleine, B. W., Watt, A. A., González, F., & Boakes, R. A. (1995) · Animal Learning & Behavior · doi:10.3758/bf03199935 · Cited by 286
Neural mechanisms of reward-related motor learning
Wickens, J. R., Reynolds, J. N., & Hyland, B. I. (2003) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2003.10.013 · Cited by 284
Self-citationCorrespondence between the Dopamine islands and striosomes of the mammalian striatum
Graybiel, A. M. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90293-8 · Cited by 282
Models of information processing in the basal ganglia
Alexander, G. E. (1996) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0921-884x(96)89703-7 · Cited by 281
Jiménez-Castellanos, J., & Graybiel, A. M. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90285-5 · Cited by 272
Miller, J. D., Farber, J., Gatz, P., Roffwarg, H. P., & German, D. C. (1983) · Brain Research · doi:10.1016/0006-8993(83)91101-0 · Cited by 269
Totterdell, S., & Smith, A. D. (1989) · PubMed · Cited by 266
Floresco, S., Blaha, C. D., Yang, C. R., & Phillips, A. G. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-08-02851.2001 · Cited by 242
Nirenberg, M. J., Chan, J., Pohorille, A., Vaughan, R. A., Uhl, G. R., Kuhar, M. J., & Pickel, V. M. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-18-06899.1997 · Cited by 242
Contributions of Striatal Subregions to Place and Response Learning
Yin, H. H., & Knowlton, B. J. (2004) · Learning & Memory · doi:10.1101/lm.81004 · Cited by 238
Surround inhibition among projection neurons is weak or nonexistent in the rat neostriatum
Jaeger, D., Kita, H., & Wilson, C. J. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.72.5.2555 · Cited by 232
Meredith, G. E., Agolia, R., Arts, M. P. M., Groenewegen, H. J., & Zahm, D. S. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90389-j · Cited by 231
Facilitation of instrumental behavior by a Pavlovian appetitive conditioned stimulus.
Lovibond, P. F. (1983) · Journal of Experimental Psychology Animal Behavior Processes · doi:10.1037/0097-7403.9.3.225 · Cited by 225
Changes in behavior-related neuronal activity in the striatum during learning
Schultz, W. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00122-x · Cited by 225
The Synaptic Framework for Chemical Signaling in Nucleus Accumbens
Meredith, G. E. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09266.x · Cited by 215
Partridge, J. G., Tang, K., & Lovinger, D. M. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.3.1422 · Cited by 215
Quantification of the dopamine innervation in adult rat neostriatum
Doucet, G., Descarries, L., & Garcia, S. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90272-1 · Cited by 214
Pan, W. X., & Hyland, B. I. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0277-05.2005 · Cited by 209
Self-citationMosaic architecture of the somatic sensory-recipient sector of the cat's striatum
Malach, R., & Graybiel, A. M. (1986) · Journal of Neuroscience · doi:10.1523/jneurosci.06-12-03436.1986 · Cited by 194
Fast synaptic transmission between striatal spiny projection neurons
Czubayko, U., & Plenz, D. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.242428599 · Cited by 194
The cytoarchitecture of the interfascicular nucleus and ventral tegmental area of tsai in the rat
Phillipson, O. T. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901870106 · Cited by 193
Synaptic Plasticity in an In Vitro Slice Preparation of the Rat Nucleus Accumbens
Pennartz, C. M. A., Ameerun, R. F., Groenewegen, H. J., & Lopes, F. H. D. S. (1993) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1993.tb00475.x · Cited by 178
Basal forebrain in the context of schizophrenia
Heimer, L. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00039-9 · Cited by 176
Golgi centennial symposium: Perspectives in neurobiology
Eidelberg, E. (1976) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(76)90169-3 · Cited by 173
Physiological and morphological properties of accumbens core and shell neurons recorded in vitro
O’Donnell, P., & Grace, A. A. (1993) · Synapse · doi:10.1002/syn.890130206 · Cited by 170
Sokolowski, J. D., & Salamone, J. D. (1998) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(97)00544-3 · Cited by 166
Johnson, L. R., Aylward, R. L. M., Hussain, Z., & Totterdell, S. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90408-1 · Cited by 162
Striatal dopamine in motor activation and reward-mediated learning: steps towards a unifying model
Wickens, J. R. (1990) · Journal of Neural Transmission · doi:10.1007/bf01245020 · Cited by 145
Self-citationEffects of ibotenic acid lesions of the Nucleus Accumbens on instrumental action
Balleine, B. W., & Killcross, S. (1994) · Behavioural Brain Research · doi:10.1016/0166-4328(94)90104-x · Cited by 142
Projection neurons of the nucleus accumbens: an intracellular labeling study
Chang, H. T., & Kitai, S. T. (1985) · Brain Research · doi:10.1016/0006-8993(85)90894-7 · Cited by 138
Electrical and chemical transmission between striatal GABAergic output neurones in rat brain slices
Venance, L., Glowinski, J., & Giaume, C. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.065672 · Cited by 134
Taverna, S., van Dongen, Y. C., Groenewegen, H. J., & Pennartz, C. M. A. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00892.2003 · Cited by 130
Responses of monkey midbrain dopamine neurons during delayed alternation performance
Ljungberg, T., Apicella, P., & Schultz, W. (1991) · Brain Research · doi:10.1016/0006-8993(91)90816-e · Cited by 128
Yung, K. K. L., Smith, A. D., Levey, A. I., & Bolam, J. P. (1996) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1996.tb01573.x · Cited by 128
Reward-Dependent Spatial Selectivity of Anticipatory Activity in Monkey Caudate Neurons
Takikawa, Y., Kawagoe, R., & Hikosaka, O. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00288.2001 · Cited by 124
Effects of cytotoxic nucleus accumbens lesions on instrumental conditioning in rats
de Borchgrave, R., Rawlins, J. N. P., Dickinson, A., & Balleine, B. W. (2002) · Experimental Brain Research · doi:10.1007/s00221-002-1031-y · Cited by 123
Ragsdale, C. W., & Graybiel, A. M. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.16.6196 · Cited by 117
Corbit, L. H., & Balleine, B. W. (2003) · Journal of Experimental Psychology Animal Behavior Processes · doi:10.1037/0097-7403.29.2.99 · Cited by 112
Uptake of Dopamine Released by Impulse Flow in the Rat Mesolimbic and Striatal Systems In Vivo
Suaud‐Chagny, M., Dugast, C., Chergui, K., Msghina, M., & Gonon, F. (1995) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1995.65062603.x · Cited by 103
Rhythmic delta-frequency activities in the nucleus accumbens of anesthetized and freely moving rats
Leung, L.-W. S., & Yim, C. Y. (1993) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y93-049 · Cited by 96
Wright, A. K., Norrie, L., Ingham, C. A., Hutton, E. A. M., & Arbuthnott, G. W. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00186-9 · Cited by 93
Self-citationChemical anatomy of the human ventral striatum and adjacent basal forebrain structures
Prensa, L., Richard, S., & Parent, A. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10627 · Cited by 90
Wickens, J. R., Arbuthnott, G. W., & Shindou, T. (2007) · Progress in brain research · doi:10.1016/s0079-6123(06)60018-6 · Cited by 58
Self-citationThe pattern of innervation of the corpus striatum by the substantia nigra
Wright, A. K., & Arbuthnott, G. W. (1981) · Neuroscience · doi:10.1016/0306-4522(81)90044-0 · Cited by 50
Self-citationRegional differences in the expression of corticostriatal synaptic plasticity
Smith, R. B., Musleh, W., Akopian, G. K., Buckwalter, J. G., & Walsh, J. P. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00260-3 · Cited by 44
Neurotransmitter Interactions in the Basal Ganglia
Trugman, J. M. (1988) · Archives of Neurology · doi:10.1001/archneur.1988.00520260015003 · Cited by 39
Ahn, S., & Phillips, A. G. (2006) · Psychopharmacology · doi:10.1007/s00213-006-0526-9 · Cited by 39
Chesselet, M., Gonzales, C., & Levitt, P. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90008-c · Cited by 35
Canales, J. J., & Iversen, S. D. (1998) · European Journal of Pharmacology · doi:10.1016/s0014-2999(98)00752-3 · Cited by 22
Neuropsychology of reinforcement processes in the rat
Cardinal, R. N. (2001) · PubMed · doi:10.17863/cam.16462 · Cited by 5
Research works printed but not linked: 5
- Brockhaus H., 1942, Zur feineren Anatomie des Septum und des Striatum, J. Psychol. Neurol. (Leipzig), 51, 1
- 10.1038/311461a0 · DOI
- Lindvall O., 1974, The organisation of the ascending catecholamine neuron systems in the rat brain: as revealed by the glyoxylic acid flourescence method, Acta Physiol. Scand. Suppl., 412, 1
- 10.1111/j.1365-201X.1971.tb10998.x · DOI · Paper page
- Garris P.A., 1995, Neuromethods, 179
Cited by
Sorted by citations
Bardo, M. T., & Hammer, R. P. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90226-e · Cited by 3,229
The Vertebrate mesolimbic reward system and social behavior network: A comparative synthesis
O'Connell, L. A., & Hofmann, H. A. (2011) · Journal of Comparative Neurology · doi:10.1002/cne.22735 · Cited by 986
Dynamic reorganization of striatal circuits during the acquisition and consolidation of a skill
Yin, H. H., Mulcare, S. P., Hilário, M. R. F., Clouse, E., Holloway, T., Davis, M. I., Hansson, A. C., Lovinger, D. M., & Costa, R. M. (2009) · Nature Neuroscience · doi:10.1038/nn.2261 · Cited by 818
Evolution of a Vertebrate Social Decision-Making Network
O’Connell, L. A., & Hofmann, H. A. (2012) · Science · doi:10.1126/science.1218889 · Cited by 608
Tripp, G., & Wickens, J. R. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.07.026 · Cited by 492
Self-citation
Metadata
- Authors
- WICKENS, J. R., BUDD, C. S., HYLAND, B. I., & ARBUTHNOTT, G. W.
- Affiliations
- Okinawa Institute of Science and Technology Graduate University (JP)
- University of Otago (NZ)
- Corresponding author
- WICKENS, JEFFERY R.
- Venue
- Annals of the New York Academy of Sciences
- Publisher
- Wiley
- Published
- 2007-05
- Volume
- 1104
- Issue
- 1
- Pages
- 192-212
- ISSN
- 0077-8923 (ISSN-L)
- 1749-6632
- OpenAlex
- W2001576766
- Cited by
- 165
- References
- 124
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 6 · 2023: 3 · 2022: 4 · 2021: 5 · 2020: 1 · 2019: 9 · 2018: 9 · 2017: 5 · 2016: 9 · 2015: 9 · 2014: 15 · 2013: 9 · 2012: 13
- FWCI
- 1.27
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annals of the New York Academy of Sciences (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- striatum, reward, decision-making, reinforcement learning, action selection, dopamine signaling, dorsolateral striatum, ventromedial striatum, basal ganglia, synaptic plasticity, lateral inhibition, regional specialization, habit formation, striatal connectivity
- MeSH terms
- Animals, Basal Ganglia, Behavior, Corpus Striatum, Decision Making, Dopamine, Humans, Learning, Models, Anatomic, Models, Neurological, Neural Pathways, Nucleus Accumbens, Reinforcement, Psychology, Reward, Time Factors
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