Emerging, reemerging, and forgotten brain areas of the reward circuit: Notes from the 2010 Motivational Neural Networks conference

McGinty, Vincent B.; Hayden, Benjamin Y.; Heilbronner, Sarah R.; Dumont, Eric C.; Graves, Steven M.; Mirrione, Martine M.; du Hoffmann, Johann; Sartor, Gregory C.; España, Rodrigo A.; Millan, E. Zayra; DiFeliceantonio, Alexandra G.; Marchant, Nathan J.; Napier, T. Celeste; Root, David H.; Borgland, Stephanie L.; Treadway, Michael T.; Floresco, Stan B.; McGinty, Jacqueline F.; Haber, Suzanne

doi:10.1016/j.bbr.2011.07.036

Cited by 36Neurotransmitter Receptor Influence on BehaviorNeural and Behavioral Psychology StudiesMemory and Neural Mechanisms

Emerging, reemerging, and forgotten brain areas of the reward circuit: Notes from the 2010 Motivational Neural Networks conference

Open access

McGinty, Vincent B., Hayden, Benjamin Y., Heilbronner, Sarah R., Dumont, Eric C., Graves, Steven M., Mirrione, Martine M., du Hoffmann, Johann, Sartor, Gregory C. +11 more·2011·Behavioural Brain Research

DOI 10.1016/j.bbr.2011.07.036PMC PMC3445023

Open this paper in CoChat — free account

Abstract

On April 24-27, 2010, the Motivational Neuronal Networks meeting took place in Wrightsville Beach, North Carolina. The conference was devoted to "Emerging, re-emerging, and forgotten brain areas" of the reward circuit. A central feature of the conference was four scholarly discussions of cutting-edge topics related to the conference's theme. These discussions form the basis of the present review, which summarizes areas of consensus and controversy, and serves as a roadmap for the next several years of research.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1016/j.bbr.2011.07.036

Cites

165 of 165 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Multiple brain regions not addressed in the review contribute to reward processing, including the subthalamic nucleus, ventral pallidum, subiculum, lateral habenula, and extended amygdala.
“Additionally, there are multiple brain regions not addressed in this review that contribute to reward processing, including the subthalamic nucleus and ventral pallidum, the subiculum, the lateral habenula, and the extended amygdala [736,737].”
From Reward circuitry dysfunction in psychiatric and neurodevelopmental disorders and genetic syndromes: animal models and clinical findings (2012) · cites this paper as [736]

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works
The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat
O'Keefe, J., & Dostrovsky, J. (1971) · Brain Research · doi:10.1016/0006-8993(71)90358-1 · Cited by 6,151 · see citing works
The Psychology of Learning and Motivation: Advances in Research and Theory
(2010) · The Psychology of learning and motivation/The psychology of learning and motivation · doi:10.1016/c2009-0-62209-1 · Cited by 6,035 · see citing works
The rat nervous system
Paxinos, G. (1985) · Cited by 3,715 · see citing works
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 · see citing works
Which elements are excited in electrical stimulation of mammalian central nervous system: A review
Ranck, J. B. (1975) · Brain Research · doi:10.1016/0006-8993(75)90364-9 · Cited by 2,024 · see citing works
Head-direction cells recorded from the postsubiculum in freely moving rats. I. Description and quantitative analysis
Taube, J., Muller, R., & Ranck, J. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-02-00420.1990 · Cited by 1,809 · see citing works
Optical Deconstruction of Parkinsonian Neural Circuitry
Gradinaru, V., Mogri, M., Thompson, K. R., Henderson, J. M., & Deisseroth, K. A. (2009) · Science · doi:10.1126/science.1167093 · Cited by 1,536 · see citing works
Anatomical analysis of afferent projections to the medial prefrontal cortex in the rat
Hoover, W. B., & Vertes, R. P. (2007) · Brain Structure and Function · doi:10.1007/s00429-007-0150-4 · Cited by 1,365 · see citing works
A role for lateral hypothalamic orexin neurons in reward seeking
Harris, G. C., Wimmer, M., & Aston-Jones, G. (2005) · Nature · doi:10.1038/nature04071 · Cited by 1,311 · see citing works
Cortical pathways to the mammalian amygdala
McDonald, A. J. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00003-3 · Cited by 1,303 · see citing works
Lateral habenula as a source of negative reward signals in dopamine neurons
Matsumoto, M., & Hikosaka, O. (2007) · Nature · doi:10.1038/nature05860 · Cited by 1,292 · see citing works
New perspectives in basal forebrain organization of special relevance for neuropsychiatric disorders: The striatopallidal, amygdaloid, and corticopetal components of substantia innominata
Alheid, G. F., & Heimer, L. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90217-5 · Cited by 1,217 · see citing works
Afferent modulation of dopamine neuron firing differentially regulates tonic and phasic dopamine transmission
Floresco, S. B., West, A. R., Ash, B., Moore, H., & Grace, A. A. (2003) · Nature Neuroscience · doi:10.1038/nn1103 · Cited by 1,106 · see citing works
Self-citation
Dopamine neurons report an error in the temporal prediction of reward during learning
Hollerman, J. R., & Schultz, W. (1998) · Nature Neuroscience · doi:10.1038/1124 · Cited by 1,103 · see citing works
The anatomy of memory: an interactive overview of the parahippocampal–hippocampal network
van Strien, N. M., Cappaert, N. L. M., & Witter, M. P. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2614 · Cited by 1,041 · see citing works
Regulation of firing of dopaminergic neurons and control of goal-directed behaviors
Grace, A. A., Floresco, S. B., Goto, Y., & Lodge, D. J. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.003 · Cited by 1,034 · see citing works
Self-citation
Cortico-Basal Ganglia Reward Network: Microcircuitry
Sesack, S. R., & Grace, A. A. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.93 · Cited by 985 · see citing works
Subthalamic nucleus stimulation in severe obsessive-compulsive disorder
Mallet, L., Polosan, M., Jaafari, N., Baup, N., Welter, M.-L., Fontaine, D., Montcel, S. T. D., Yelnik, J., Chéreau, I., Arbus, C., et al. (2008) · New England Journal of Medicine · doi:10.1056/nejmoa0708514 · Cited by 965 · see citing works
Intracellular Features Predicted by Extracellular Recordings in the Hippocampus In Vivo
Henze, D. A., Borhegyi, Z., Csicsvari, J., Mamiya, A., Harris, K. D., & Buzsáki, G. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.1.390 · Cited by 942 · see citing works
The circuitry mediating cocaine-induced reinstatement of drug-seeking behavior
McFarland, K., & Kalivas, P. W. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-21-08655.2001 · Cited by 905 · see citing works
Head-direction cells recorded from the postsubiculum in freely moving rats. II. Effects of environmental manipulations
Taube, J. S., Muller, R., & Ranck, J. B. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-02-00436.1990 · Cited by 887 · see citing works
Efferent connections of the habenular nuclei in the rat
Herkenham, M. A., & Nauta, W. J. H. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901870103 · Cited by 855 · see citing works
Role of the bed nucleus of the stria terminalis versus the amygdala in fear, stress, and anxiety
Walker, D. L., Toufexis, D. J., & Davis, M. (2003) · European Journal of Pharmacology · doi:10.1016/s0014-2999(03)01282-2 · Cited by 838 · see citing works
Afferent connections of the habenular nuclei in the rat. A horseradish peroxidase study, with a note on the fiber‐of‐passage problem
Herkenham, M. A., & Nauta, W. J. H. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901730107 · Cited by 798 · see citing works
Synaptic interactions among excitatory afferents to nucleus accumbens neurons: hippocampal gating of prefrontal cortical input
O’Donnell, P., & Grace, A. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-05-03622.1995 · Cited by 760 · see citing works
Topography of projections from amygdala to bed nuclei of the stria terminalis
Dong, H.-W., Petrovich, G. D., & Swanson, L. W. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00079-0 · Cited by 714 · see citing works
The rostromedial tegmental nucleus (RMTg), a GABAergic afferent to midbrain dopamine neurons, encodes aversive stimuli and inhibits motor responses.
Jhou, T. C., Fields, H. L., Baxter, M. G., Saper, C. B., & Holland, P. C. (2009) · Neuron · doi:10.1016/j.neuron.2009.02.001 · Cited by 696 · see citing works
Double Dissociation between the Involvement of the Bed Nucleus of the Stria Terminalis and the Central Nucleus of the Amygdala in Startle Increases Produced by Conditioned versus Unconditioned Fear
Walker, D. L., & Davis, M. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-23-09375.1997 · Cited by 627 · see citing works
Brain circuitry and the reinstatement of cocaine-seeking behavior
Kalivas, P., & McFarland, K. (2003) · Psychopharmacology · doi:10.1007/s00213-003-1393-2 · Cited by 613 · see citing works
Remission of major depression under deep brain stimulation of the lateral habenula in a therapy-refractory patient
Sartorius, A., Kiening, K. L., Kirsch, P., von Gall, C. C., Haberkorn, U., Unterberg, A. W., Henn, F. A., & Meyer-Lindenberg, A. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.08.027 · Cited by 611 · see citing works
Decision-making and addiction (part II): myopia for the future or hypersensitivity to reward?
Bechara, A., Dolan, S., & Hindes, A. (2002) · Neuropsychologia · doi:10.1016/s0028-3932(02)00016-7 · Cited by 580 · see citing works
Glutamatergic Afferents from the Hippocampus to the Nucleus Accumbens Regulate Activity of Ventral Tegmental Area Dopamine Neurons
Floresco, S., Todd, C. L., & Grace, A. A. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-13-04915.2001 · Cited by 556 · see citing works
Self-citation
Ventral pallidum roles in reward and motivation
Smith, K. S., Tindell, A. J., Aldridge, J. W., & Berridge, K. C. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.09.038 · Cited by 548 · see citing works
Glutamate Transmission in the Nucleus Accumbens Mediates Relapse in Cocaine Addiction
Cornish, J. L., & Kalivas, P. W. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-15-j0006.2000 · Cited by 546 · see citing works
High-Frequency Stimulation Produces a Transient Blockade of Voltage-Gated Currents in Subthalamic Neurons
Beurrier, C., Bioulac, B. H., Audin, J., & Hammond, C. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.4.1351 · Cited by 532 · see citing works
Basic organization of projections from the oval and fusiform nuclei of the bed nuclei of the stria terminalis in adult rat brain
Dong, H., Petrovich, G. D., Watts, A. G., & Swanson, L. W. (2001) · Journal of Comparative Neurology · doi:10.1002/cne.1079 · Cited by 521 · see citing works
The Role of the Dorsomedial Prefrontal Cortex, Basolateral Amygdala, and Dorsal Hippocampus in Contextual Reinstatement of Cocaine Seeking in Rats
Fuchs, R. A., Evans, K. A., Ledford, C. C., Parker, M. P., Case, J. M., Mehta, R. H., & See, R. E. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300579 · Cited by 517 · see citing works
The mesopontine rostromedial tegmental nucleus: A structure targeted by the lateral habenula that projects to the ventral tegmental area of tsai and substantia nigra compacta
Jhou, T. C., Geisler, S., Marinelli, M., Degarmo, B. A., & Zahm, D. S. (2009) · Journal of Comparative Neurology · doi:10.1002/cne.21891 · Cited by 503 · see citing works
Glutamatergic Afferents of the Ventral Tegmental Area in the Rat
Geisler, S., Derst, C., Veh, R. W., & Zahm, D. S. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0012-07.2007 · Cited by 486 · see citing works
Hypothalamic Arousal Regions Are Activated during Modafinil-Induced Wakefulness
Scammell, T. E., Estabrooke, I. V., McCarthy, M. T., Chemelli, R. M., Yanagisawa, M., Miller, M. S., & Saper, C. B. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-22-08620.2000 · Cited by 484 · see citing works
Aberrant Hippocampal Activity Underlies the Dopamine Dysregulation in an Animal Model of Schizophrenia
Lodge, D., & Grace, A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2847-07.2007 · Cited by 475 · see citing works
Noradrenaline in the ventral forebrain is critical for opiate withdrawal-induced aversion
Delfs, J. M., Zhu, Y., Druhan, J. P., & Aston-Jones, G. (2000) · Nature · doi:10.1038/35000212 · Cited by 462 · see citing works
Habenula: crossroad between the basal ganglia and the limbic system
Hikosaka, O., Sesack, S. R., Lecourtier, L., & Shepard, P. D. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.3463-08.2008 · Cited by 432 · see citing works
Stimulation of subterritories of the subthalamic nucleus reveals its role in the integration of the emotional and motor aspects of behavior
Mallet, L., Schüpbach, M. W. M., N’Diaye, K., Rémy, P., Bardinet, É., Czernecki, V., Welter, M., Pélissolo, A., Ruberg, M., Agid, Y., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610849104 · Cited by 428 · see citing works
Two transpallidal pathways originating in the rat nucleus accumbens
Zahm, D. S., & Heimer, L. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903020302 · Cited by 406 · see citing works
Storage, recall, and novelty detection of sequences by the hippocampus: Elaborating on the SOCRATIC model to account for normal and aberrant effects of dopamine
Lisman, J. E., & Otmakhova, N. A. (2001) · Hippocampus · doi:10.1002/hipo.1071 · Cited by 402 · see citing works
The Ventral Pallidum and Hedonic Reward: Neurochemical Maps of Sucrose “Liking” and Food Intake
Smith, K. S., & Berridge, K. C. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1902-05.2005 · Cited by 391 · see citing works
Chapter 21 Chapter Comparison of spatial and temporal characteristics of neuronal activity in sequential stages of hippocampal processing
Barnes, C. A., McNaughton, B. L., Mizumori, S. J. Y., Leonard, B. W., & Lin, L.-H. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)61257-1 · Cited by 371 · see citing works
Studies on the cellular architecture of the bed nuclei of the stria terminalis in the rat: I. cytoarchitecture
Ju, G., & Swanson, L. W. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902800409 · Cited by 359 · see citing works
Direct and Indirect Activation of Cortical Neurons by Electrical Microstimulation
Tehovnik, E. J., Tolias, A. S., Sultan, F. R., Slocum, W. M., & Logothetis, N. K. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00126.2006 · Cited by 355 · see citing works
A Role for the Bed Nucleus of the Stria Terminalis, But Not the Amygdala, in the Effects of Corticotropin-Releasing Factor on Stress-Induced Reinstatement of Cocaine Seeking
Erb, S. M., & Stewart, J. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-20-j0006.1999 · Cited by 347 · see citing works
Afferents to the GABAergic tail of the ventral tegmental area in the rat
Kaufling, J., Veinante, P., Pawlowski, S. A., Freund‐Mercier, M., & Barrot, M. (2009) · Journal of Comparative Neurology · doi:10.1002/cne.21983 · Cited by 347 · see citing works
Organization of axonal projections from the anterolateral area of the bed nuclei of the stria terminalis
Dong, H., & Swanson, L. W. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10949 · Cited by 347 · see citing works
The globus pallidus sends reward-related signals to the lateral habenula
Hong, S., & Hikosaka, O. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.035 · Cited by 346 · see citing works
Selective participation of the bed nucleus of the stria terminalis and CRF in sustained anxiety-like versus phasic fear-like responses
Walker, D. L., Miles, L. A., & Davis, M. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2009.06.022 · Cited by 331 · see citing works
The Society for Neuroscience 1995 annual meeting.
Hu, R. J. (1996) · PubMed · Cited by 313 · see citing works
Occasion Setting in Pavlovian Conditioning
Holland, P. (1992) · The Psychology of learning and motivation/The psychology of learning and motivation · doi:10.1016/s0079-7421(08)60488-0 · Cited by 312 · see citing works
Cortical afferents to the extended amygdala
McDONALD, A. J., SHAMMAH‐LAGNADO, S. J., SHI, C., & DAVIS, M. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09275.x · Cited by 306 · see citing works
Origin of the dopaminergic innervation of the central extended amygdala and accumbens shell: A combined retrograde tracing and immunohistochemical study in the rat
Hasue, R. H., & Shammah‐Lagnado, S. J. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10420 · Cited by 306 · see citing works
GABAA receptor antagonism in the extended amygdala decreases ethanol self-administration in rats
Hyytiä, P., & Koob, G. F. (1995) · European Journal of Pharmacology · doi:10.1016/0014-2999(95)00314-b · Cited by 302 · see citing works
The subthalamic nucleus and the external pallidum: two tightly interconnected structures that control the output of the basal ganglia in the monkey
Shink, É., Bevan, M. D., Bolam, J. P., & Smith, Y. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00022-x · Cited by 296 · see citing works
Projections from bed nuclei of the stria terminalis, posterior division: Implications for cerebral hemisphere regulation of defensive and reproductive behaviors
Dong, H., & Swanson, L. W. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20002 · Cited by 294 · see citing works
Topographic organization of the ventral striatal efferent projections in the rhesus monkey: An anterograde tracing study
Haber, S. N., Lynd‐Balta, E., Klein, C. M., & Groenewegen, H. J. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902930210 · Cited by 291 · see citing works
Self-citation
Effects of the dopamine D-1 antagonist SCH 23390 microinjected into the accumbens, amygdala or striatum on cocaine self-administration in the rat
Caine, S. B., Heinrichs, S. C., Coffin, V. L., & Koob, G. F. (1995) · Brain Research · doi:10.1016/0006-8993(95)00598-k · Cited by 286 · see citing works
The subiculum: what it does, what it might do, and what neuroanatomy has yet to tell us
O'Mara, S. (2005) · Journal of Anatomy · doi:10.1111/j.1469-7580.2005.00446.x · Cited by 285 · see citing works
Connections of the subthalamic nucleus with ventral striatopallidal parts of the basal ganglia in the rat
Groenewegen, H. J., & Berendse, H. W. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902940408 · Cited by 279 · see citing works
Temporary Inactivation of the Bed Nucleus of the Stria Terminalis But Not of the Amygdala Blocks Freezing Induced by Trimethylthiazoline, a Component of Fox Feces
Fendt, M., Endres, T., & Apfelbach, R. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-01-00023.2003 · Cited by 278 · see citing works
Connections of the subthalamic nucleus in the monkey
Carpenter, M. B., Carleton, S. C., Keller, J. T., & Conte, P. (1981) · Brain Research · doi:10.1016/0006-8993(81)91113-6 · Cited by 274 · see citing works
Bilateral Lesions of the Subthalamic Nucleus Induce Multiple Deficits in an Attentional Task in Rats
Baunez, C., & Robbins, T. W. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01376.x · Cited by 269 · see citing works
A Discrete GABAergic Relay Mediates Medial Prefrontal Cortical Inhibition of the Neuroendocrine Stress Response
Radley, J. J., Gosselink, K. L., & Sawchenko, P. E. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5924-08.2009 · Cited by 268 · see citing works
Visual and oculomotor functions of monkey subthalamic nucleus
Matsumura, M., Kojima, J., Gardiner, T. W., & Hikosaka, O. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.67.6.1615 · Cited by 265 · see citing works
Latent inhibition of conditioned dopamine release in rat nucleus accumbens
Young, A. M. J., Joseph, M. H., & Gray, J. A. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90378-s · Cited by 261 · see citing works
Reciprocal connections between the entorhinal cortex and hippocampal fields CA1 and the subiculum are in register with the projections from CA1 to the subiculum
Naber, P. A., da Silva, F. H. L., & Witter, M. P. (2001) · Hippocampus · doi:10.1002/hipo.1028 · Cited by 258 · see citing works
Lateral habenula projections to dopamine and GABA neurons in the rat ventral tegmental area
Omelchenko, N., Bell, R., & Sesack, S. R. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06924.x · Cited by 253 · see citing works
Modulation of Hippocampal and Amygdalar-Evoked Activity of Nucleus Accumbens Neurons by Dopamine: Cellular Mechanisms of Input Selection
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 · see citing works
Self-citation
Deep brain stimulation of the subthalamic nucleus for Parkinson's disease: methodologic aspects and clinical criteria.
Benabid, A., Krack, P., Benazzouz, A., Limousin, P. D., Koudsié, A., & Pollak, P. (2000) · PubMed · Cited by 239 · see citing works
Role of the ventral subiculum in stress integration
Herman, J. P., & Mueller, N. K. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.05.035 · Cited by 235 · see citing works
Role of the extended amygdala in short-duration versus sustained fear: a tribute to Dr. Lennart Heimer
Walker, D. L., & Davis, M. (2008) · Brain Structure and Function · doi:10.1007/s00429-008-0183-3 · Cited by 231 · see citing works
The subthalamic nucleus exerts opposite control on cocaine and 'natural' rewards
Baunez, C., Dias, C., Cador, M., & Amalric, M. (2005) · Nature Neuroscience · doi:10.1038/nn1429 · Cited by 223 · see citing works
Where does damage lead to enhanced food aversion: the ventral pallidum/substantia innominata or lateral hypothalamus?
Cromwell, H. C., & Berridge, K. C. (1993) · Brain Research · doi:10.1016/0006-8993(93)90053-p · Cited by 220 · see citing works
Dopaminergic antagonism within the nucleus accumbens or the amygdala produces differential effects on intravenous cocaine self-administration under fixed and progressive ratio schedules of reinforcement
McGregor, A., & Roberts, D. C. S. (1993) · Brain Research · doi:10.1016/0006-8993(93)90084-z · Cited by 215 · see citing works
Organization of efferent projections from the internal segment of globus pallidus in primate as revealed by flourescence retrograde labeling method
Parent, A., & Bellefeuille, L. D. (1982) · Brain Research · doi:10.1016/0006-8993(82)90802-2 · Cited by 211 · see citing works
Reducing the desire for cocaine with subthalamic nucleus deep brain stimulation
Rouaud, T., Lardeux, S., Panayotis, N., Paleressompoulle, D., Cador, M., & Baunez, C. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908189107 · Cited by 200 · see citing works
Studies on the cellular architecture of the bed nuclei of the stria terminalis in the rat: II. chemoarchitecture
Ju, G., Swanson, L. W., & Simerly, R. B. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902800410 · Cited by 197 · see citing works
Evidence for the coexistence of glutamate decar☐ylase and Met-enkephalin immunoreactivities in axon terminals of rat ventral pallidum
Zahm, D. S., Záborszky, L., Alones, V., & Heimer, L. (1985) · Brain Research · doi:10.1016/0006-8993(85)90331-2 · Cited by 196 · see citing works
Cue-Evoked Firing of Nucleus Accumbens Neurons Encodes Motivational Significance During a Discriminative Stimulus Task
Nicola, S. M., Yun, I. A., Wakabayashi, K. T., & Fields, H. L. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00657.2003 · Cited by 196 · see citing works
The Response of Subthalamic Nucleus Neurons to Dopamine Receptor Stimulation in a Rodent Model of Parkinson’s Disease
Kreiss, D. S., Mastropietro, C. W., Rawji, S. S., & Walters, J. R. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-17-06807.1997 · Cited by 194 · see citing works
The organization of the efferent projections and striatal afferents of the entopeduncular nucleus and adjacent areas in the rat
van der Kooy, D., & Carter, D. (1981) · Brain Research · doi:10.1016/0006-8993(81)90064-0 · Cited by 190 · see citing works
The organization of the descending ventral pallidal projections in the monkey
Haber, S., Lynd-Balta, E., & Mitchell, S. (1993) · The Journal of comparative neurology · doi:10.1002/cne.903290108 · Cited by 184 · see citing works
Self-citation
A Pallidus-Habenula-Dopamine Pathway Signals Inferred Stimulus Values
Bromberg-Martin, E. S., Matsumoto, M., Hong, S., & Hikosaka, O. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00158.2010 · Cited by 182 · see citing works
Individual nucleus accumbens-projection neurons receive both basolateral amygdala and ventral subicular afferents in rats
French, S. J., & Totterdell, S. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00150-7 · Cited by 180 · see citing works
ΔFosB accumulates in a GABAergic cell population in the posterior tail of the ventral tegmental area after psychostimulant treatment
Perrotti, L. I., Bolaños, C. A., Choi, K., Russo, S. J., Edwards, S., Ulery, P. G., Wallace, D. L., Self, D. W., Nestler, E. J., & Barrot, M. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04110.x · Cited by 178 · see citing works
Aversive stimuli alter ventral tegmental area dopamine neuron activity via a common action in the ventral hippocampus
Valenti, O., Lodge, D. J., & Grace, A. A. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.5310-10.2011 · Cited by 173 · see citing works
Localization of nicotinic receptor subunit mRNAs in monkey brain by in situ hybridization
Quik, M., Polonskaya, Y., Gillespie, A. J., Jakowec, M. W., Lloyd, G. K., & Langston, J. W. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20000911)425:1 · Cited by 172 · see citing works
Hippocampus, amygdala, and stress: interacting systems that affect susceptibility to addiction
Belujon, P., & Grace, A. A. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05896.x · Cited by 171 · see citing works
Medial prefrontal cortex control of the paraventricular hypothalamic nucleus response to psychological stress: Possible role of the bed nucleus of the stria terminalis
Spencer, S. J., Buller, K. M., & Day, T. A. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20376 · Cited by 171 · see citing works
Projections from the rhomboid nucleus of the bed nuclei of the stria terminalis: Implications for cerebral hemisphere regulation of ingestive behaviors
Dong, H., & Swanson, L. W. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10758 · Cited by 168 · see citing works
Evidence for a dopaminergic innervation of the subthalamic nucleus in the rat
Hassani, O.-K., François, C., Yelnik, J., & Féger, J. (1997) · Brain Research · doi:10.1016/s0006-8993(96)01167-5 · Cited by 166 · see citing works
Subthalamic neurons in primates: A quantitative and comparative analysis
Yelnik, J., & Percheron, G. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90030-7 · Cited by 165 · see citing works
The efferent projections of the rat lateral habenular nucleus revealed by the PHA-L anterograde tracing method
Araki, M., McGeer, P. L., & Kimura, H. (1988) · Brain Research · doi:10.1016/0006-8993(88)91410-2 · Cited by 163 · see citing works
Amygdala and Extended Amygdala of the Rat: A Cytoarchitectonical, Fibroarchitectonical, and Chemoarchitectonical Survey
de Olmos, J. S., Beltramino, C. A., & Alheid, G. F. (2004) · Elsevier eBooks · doi:10.1016/b978-012547638-6/50020-1 · Cited by 160 · see citing works
Interconnections and organization of pallidal and subthalamic nucleus neurons in the monkey
Carpenter, M. B., Batton, R. R., Carleton, S. C., & Keller, J. T. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.901970404 · Cited by 158 · see citing works
Glutamate Receptor-Dependent Modulation of Dopamine Efflux in the Nucleus Accumbens by Basolateral, But Not Central, Nucleus of the Amygdala in Rats
Howland, J. G., Taepavarapruk, P., & Phillips, A. G. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-03-01137.2002 · Cited by 155 · see citing works
Selective inactivation of the ventral hippocampus attenuates cue-induced and cocaine-primed reinstatement of drug-seeking in rats
Rogers, J. L., & See, R. E. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.01.003 · Cited by 153 · see citing works
Body weight gain rate in patients with Parkinson's disease and deep brain stimulation
Barichella, M., Marczewska, A. M., Mariani, C. B., Landi, A., Vairo, A., & Pezzoli, G. (2003) · Movement Disorders · doi:10.1002/mds.10543 · Cited by 147 · see citing works
Distribution of dopaminergic fibers in the central division of the extended amygdala of the rat
Freedman, L. J., & Cassell, M. D. (1994) · Brain Research · doi:10.1016/0006-8993(94)91545-8 · Cited by 145 · see citing works
Lidocaine Inactivation of Ventral Subiculum Attenuates Cocaine-Seeking Behavior in Rats
Sun, W.-L., & Rebec, G. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-32-10258.2003 · Cited by 138 · see citing works
Effects of STN lesions on simple vs choice reaction time tasks in the rat: preserved motor readiness, but impaired response selection
Baunez, C., Humby, T., Eagle, D. M., Ryan, L. J., Dunnett, S. B., & Robbins, T. W. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01521.x · Cited by 137 · see citing works
Neuronal activity in the striatum and pallidum of primates related to the execution of externally cued reaching movements
Jaeger, D., Gilman, S., & Aldridge, J. W. (1995) · Brain Research · doi:10.1016/0006-8993(95)00780-t · Cited by 134 · see citing works
Monoamine innervation of bed nucleus of stria terminalis: An electron microscopic investigation
Phelix, C. F., Liposits, Z., & Paull, W. K. (1992) · Brain Research Bulletin · doi:10.1016/0361-9230(92)90218-m · Cited by 133 · see citing works
Dissociations in dopamine release in medial prefrontal cortex and ventral striatum during the acquisition and extinction of classical aversive conditioning in the rat
Wilkinson, L. S., Humby, T., Killcross, S., Torres, E. M., Everitt, B. J., & Robbins, T. W. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00119.x · Cited by 132 · see citing works
The dopamine D-1 receptor antagonist SCH 23390 injected into the dorsolateral bed nucleus of the stria terminalis decreased cocaine reinforcement in the rat
Epping-Jordan, M. P., Markou, A., & Koob, G. F. (1998) · Brain Research · doi:10.1016/s0006-8993(97)01190-6 · Cited by 131 · see citing works
Subthalamic nucleus lesions increase impulsive action and decrease impulsive choice − mediation by enhanced incentive motivation?
Uslaner, J. M., & Robinson, T. E. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05117.x · Cited by 131 · see citing works
The pallidosubthalamic projection: An anatomical substrate for nonmotor functions of the subthalamic nucleus in primates
Karachi, C., Yelnik, J., Tandé, D., Tremblay, L., Hirsch, É. C., & François, C. (2004) · Movement Disorders · doi:10.1002/mds.20302 · Cited by 130 · see citing works
THE ROLE OF THE SUBTHALAMIC NUCLEUS IN EXPERIMENTAL CHOREA
Mitchell, I., Jackson, A., Sambrook, M. A., & Crossman, A. R. (1989) · Brain · doi:10.1093/brain/112.6.1533 · Cited by 128 · see citing works
The evolving theory of basal forebrain functional—anatomical ‘macrosystems’
Zahm, D. S. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2005.06.003 · Cited by 128 · see citing works
Ventral Pallidal Representation of Pavlovian Cues and Reward: Population and Rate Codes
Tindell, A. J., Berridge, K. C., & Aldridge, J. W. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1437-03.2004 · Cited by 128 · see citing works
Differential Expression of Intrinsic Membrane Currents in Defined Cell Types of the Anterolateral Bed Nucleus of the Stria Terminalis
Hammack, S. E., Mania, I., & Rainnie, D. G. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00382.2007 · Cited by 128 · see citing works
Organization of projections from the juxtacapsular nucleus of the BST: a PHAL study in the rat
Dong, H.-W., Petrovich, G. D., & Swanson, L. W. (2000) · Brain Research · doi:10.1016/s0006-8993(99)02246-5 · Cited by 125 · see citing works
Intracellular labelling of rat subthalamic neurones with horseradish peroxidase: Computer analysis of dendrites and characterization of axon arborization
Hammond, C., & Yelnik, J. (1983) · Neuroscience · doi:10.1016/0306-4522(83)90009-x · Cited by 124 · see citing works
Differential but Complementary Mnemonic Functions of the Hippocampus and Subiculum
Deadwyler, S. A., & Hampson, R. E. (2004) · Neuron · doi:10.1016/s0896-6273(04)00195-3 · Cited by 123 · see citing works
Networks of the Hippocampal Memory System of the Rat: The Pivotal Role of the Subiculum a
Naber, P. A., Witter, M. P., & da Silva, F. H. L. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06739.x · Cited by 122 · see citing works
Hyperlocomotion and increased dopamine efflux in the rat nucleus accumbens evoked by electrical stimulation of the ventral subiculum: role of ionotropic glutamate and dopamine D 1 receptors
Taepavarapruk, P., Floresco, S., & Phillips, A. G. (2000) · Psychopharmacology · doi:10.1007/s002130000376 · Cited by 121 · see citing works
Self-citation
Functional Disconnection of the Medial Prefrontal Cortex and Subthalamic Nucleus in Attentional Performance: Evidence for Corticosubthalamic Interaction
Chudasama, Y., Baunez, C., & Robbins, T. W. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-13-05477.2003 · Cited by 114 · see citing works
Opioid Modulation of Ventral Pallidal Inputs
Napier, T. C., & Mitrovic, I. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09268.x · Cited by 106 · see citing works
Self-citation
Striatal Versus Hippocampal Representations During Win-Stay Maze Performance
Berke, J. D., Breck, J. T., & Eichenbaum, H. (2009) · Journal of Neurophysiology · doi:10.1152/jn.91106.2008 · Cited by 105 · see citing works
6-Hydroxydopamine lesion of ventral pallidum blocks acquisition of place preference conditioning to cocaine
Gong, W., Neill, D. B., & Justice, J. B. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00059-0 · Cited by 100 · see citing works
D1 dopamine receptor regulates alcohol‐motivated behaviors in the bed nucleus of the stria terminalis in alcohol‐preferring (P) rats
Eiler, W. J. A., Seyoum, R., Foster, K. L., Mailey, C., & June, H. L. (2003) · Synapse · doi:10.1002/syn.10181 · Cited by 98 · see citing works
Dopamine System Dysregulation by the Ventral Subiculum as the Common Pathophysiological Basis for Schizophrenia Psychosis, Psychostimulant Abuse, and Stress
Grace, A. A. (2010) · Neurotoxicity Research · doi:10.1007/s12640-010-9154-6 · Cited by 96 · see citing works
Beyond the Reward Pathway: Coding Reward Magnitude and Error in the Rat Subthalamic Nucleus
Lardeux, S., Pernaud, R., Paleressompoulle, D., & Baunez, C. (2009) · Journal of Neurophysiology · doi:10.1152/jn.91009.2008 · Cited by 93 · see citing works
Reward modulates neuronal activity in the hippocampus of the rat
Hölscher, C., Jacob, W., & Mallot, H. A. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00422-9 · Cited by 90 · see citing works
Topographic commissural and descending projections of the habenula in the rat
Kim, U. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.21951 · Cited by 85 · see citing works
Prominent Activation of Brainstem and Pallidal Afferents of the Ventral Tegmental Area by Cocaine
Geisler, S., Marinelli, M., DeGarmo, B., Becker, M. L., Freiman, A. J., Beales, M., Meredith, G. E., & Zahm, D. S. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301650 · Cited by 84 · see citing works
Reward-related neuronal activity in the subthalamic nucleus of the monkey
Darbaky, Y., Baunez, C., Arecchi, P., Legallet, E., & Apicella, P. (2005) · Neuroreport · doi:10.1097/00001756-200508010-00022 · Cited by 84 · see citing works
Orexin neurons in the hypothalamus mediate cardiorespiratory responses induced by disinhibition of the amygdala and bed nucleus of the stria terminalis
Zhang, W., Zhang, N., Sakurai, T., & Kuwaki, T. (2009) · Brain Research · doi:10.1016/j.brainres.2009.01.022 · Cited by 79 · see citing works
Excitatory effect of iontophoretically applied dopamine on identified neurons of the rat subthalamic nucleus
Mintz, I. M., Hammond, C., & Féger, J. (1986) · Brain Research · doi:10.1016/0006-8993(86)90971-6 · Cited by 78 · see citing works
Ventral pallidum self-stimulation: a moveable electrode mapping study
Panagis, G., Miliaressis, E., Anagnostakis, Y., & Spyraki, C. (1995) · Behavioural Brain Research · doi:10.1016/0166-4328(94)00169-g · Cited by 75 · see citing works
The Effects of Activation or Inhibition of the Subthalamic Nucleus on the Metabolic and Electrophysiological Activities Within the Pallidal Complex and Substantia Nigra in the Rat
Féger, J., & Robledo, P. (1991) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1991.tb00030.x · Cited by 72 · see citing works
Effects of dorsal and ventral hippocampal NMDA stimulation on nucleus accumbens core and shell dopamine release
Peleg‐Raibstein, D., & Feldon, J. (2006) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.06.002 · Cited by 67 · see citing works
Differential dopaminergic innervation of the two pallidal segments in the squirrel monkey (Saimiri sciureus)
Parent, A., & Smith, Y. (1987) · Brain Research · doi:10.1016/0006-8993(87)90896-1 · Cited by 66 · see citing works
Dopamine in the rat ventral pallidum/substantia innominata: Biochemical and electrophysiological studies
Napier, T. C., & Potter, P. E. (1989) · Neuropharmacology · doi:10.1016/0028-3908(89)90163-9 · Cited by 64 · see citing works
Self-citation
Regulation of Limbic Information Outflow by the Subthalamic Nucleus: Excitatory Amino Acid Projections to the Ventral Pallidum
Turner, M. S., Lavı́n, A., Grace, A. A., & Napier, T. C. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-08-02820.2001 · Cited by 63 · see citing works
Self-citation
Involvement of the lateral orbitofrontal cortex in drug context‐induced reinstatement of cocaine‐seeking behavior in rats
Lasseter, H. C., Ramirez, D. R., Xie, X., & Fuchs, R. A. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06906.x · Cited by 61 · see citing works
Subicular place cells generate the same “map” for different environments: Comparison with hippocampal cells
Sharp, P. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.05.034 · Cited by 61 · see citing works
Differential projections from subfields in the lateral preoptic area to the lateral habenular complex of the rat
Kowski, A. B., Geisler, S., Krauss, M. I., & Veh, R. W. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21610 · Cited by 58 · see citing works
Dysfunction of the subthalamic nucleus induces behavioral and movement disorders in monkeys
Karachi, C., Grabli, D., Baup, N., Mounayar, S., Tandé, D., François, C., & Hirsch, É. C. (2009) · Movement Disorders · doi:10.1002/mds.22547 · Cited by 52 · see citing works
Common Firing Patterns of Hippocampal Cells in a Differential Reinforcement of Low Rates of Response Schedule
Young, B., & McNaughton, N. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-18-07043.2000 · Cited by 50 · see citing works
Basolateral amygdala efferents to the ventral subiculum preferentially innervate pyramidal cell dendritic spines
French, S. J., Hailstone, J. C., & Totterdell, S. (2003) · Brain Research · doi:10.1016/s0006-8993(03)03017-8 · Cited by 50 · see citing works
The role of the subthalamic nucleus in ‘compulsive’ behavior in rats
Winter, C., Flash, S., Klavir, O., Klein, J., Sohr, R., & Joel, D. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06148.x · Cited by 46 · see citing works
The encoding of cocaine vs. natural rewards in the striatum of nonhuman primates: categories with different activations
Opriș, I. C., Hampson, R. E., & Deadwyler, S. A. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.06.002 · Cited by 44 · see citing works
Hippocampal regulation of contextual cue-induced reinstatement of cocaine-seeking behavior
Atkins, A. L., Mashhoon, Y., & Kantak, K. M. (2008) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2008.04.007 · Cited by 44 · see citing works
Electrolytic lesions of the habenula attenuate brain stimulation reward
Morissette, M.-C., & Boye, S. M. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.08.021 · Cited by 43 · see citing works
Rapid phasic activity of ventral pallidal neurons during cocaine self‐administration
Root, D. H., Fabbricatore, A. T., Ma, S., Barker, D. J., & West, M. O. (2010) · Synapse · doi:10.1002/syn.20792 · Cited by 40 · see citing works
Self-citation
Neurons of the Bed Nucleus of the Stria Terminalis (BNST): Electrophysiological Properties and Their Response to Serotonin
Rainnie, D. G. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09304.x · Cited by 40 · see citing works
Dorsal diencephalic self-stimulation: A movable electrode mapping study.
Vachon, M. P., & Miliaressis, E. (1992) · Behavioral Neuroscience · doi:10.1037//0735-7044.106.6.981 · Cited by 35 · see citing works
Dopamine-somatostatin interactions in the rat striatum: An in vivo microdialysis study
Thermos, K., Radke, J. M., Kastellakis, A., Anagnostakis, Y., & Spyraki, C. (1996) · Synapse · doi:10.1002/(sici)1098-2396(199603)22:3 · Cited by 35 · see citing works
Self-citation
Intra-ventral pallidal glutamate antagonists block expression of morphine-induced place preference.
Dallimore, J. E., Mickiewicz, A. L., & Napier, T. C. (2006) · Behavioral Neuroscience · doi:10.1037/0735-7044.120.5.1103 · Cited by 33 · see citing works
Self-citation
Axon terminals containing tyrosine hydroxylase- and dopamine-β-hydroxylase immunoreactivity form synapses with galanin immunoreactive neurons in the lateral division of the bed nucleus of the stria terminalis in the rat
Kozicz, T. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02770-6 · Cited by 33 · see citing works
Effects of GPi and STN inactivation on physiological, motor, cognitive and motivational processes in animal models of Parkinson’s disease
Baunez, C., & Gubellini, P. (2010) · Progress in brain research · doi:10.1016/s0079-6123(10)83012-2 · Cited by 30 · see citing works
Quantification of morphological differences in boutons from different afferent populations to the nucleus accumbens
French, S. J., & Totterdell, S. (2004) · Brain Research · doi:10.1016/j.brainres.2004.02.018 · Cited by 28 · see citing works
Dorsal diencephalic self-stimulation: A movable electrode mapping study.
Vachon, M. P., & Miliaressis, E. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.6.981 · Cited by 28 · see citing works
Dissociating ventral and dorsal subicular dopamine D₁ receptor involvement in instrumental learning, spontaneous motor behavior, and motivation.
Andrzejewski, M. E., Spencer, R. C., & Kelley, A. E. (2006) · Behavioral Neuroscience · doi:10.1037/0735-7044.120.3.542 · Cited by 24 · see citing works
Fos expression following activation of the ventral pallidum in normal rats and in a model of Parkinson’s Disease: implications for limbic system and basal ganglia interactions
Turner, M. S., Gray, T. S., Mickiewicz, A. L., & Napier, T. C. (2008) · Brain Structure and Function · doi:10.1007/s00429-008-0190-4 · Cited by 13 · see citing works
Self-citation
Lidocaine inactivation of the ventral pallidum affects responding for brain stimulation reward more than it affects the stimulation's reward value
Waraczynski, M. A., & DEMCO, C. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.06.040 · Cited by 12 · see citing works

Flagged first, then by citations

Research works printed but not linked: 1

[28]Baunez C Gubellini P Effects of GPi and STN inactivation on physiological, motor, cognitive and motivational processes in animal models of Parkinson's disease Prog Brain Res 183 235 58 20696323

Sorted by citations

Reward circuitry dysfunction in psychiatric and neurodevelopmental disorders and genetic syndromes: animal models and clinical findings
Dichter, G. S., Damiano, C. A., & Allen, J. A. (2012) · Journal of Neurodevelopmental Disorders · doi:10.1186/1866-1955-4-19 · Cited by 299 · see citing works
Subsecond Dopamine Release in the Nucleus Accumbens Predicts Conditioned Punishment and Its Successful Avoidance
Oleson, E. B., Gentry, R. N., Chioma, V. C., & Cheer, J. F. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.3087-12.2012 · Cited by 272 · see citing works
Enriched Encoding: Reward Motivation Organizes Cortical Networks for Hippocampal Detection of Unexpected Events
Murty, V. P., & Adcock, R. A. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht063 · Cited by 159 · see citing works
Brain’s Reward Circuits Mediate Itch Relief. A Functional MRI Study of Active Scratching
Papoiu, A. D. P., Nattkemper, L. A., Sanders, K. M., Kraft, R., Chan, Y.-H., Coghill, R. C., & Yosipovitch, G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0082389 · Cited by 131 · see citing works
Neural substrates underlying effort, time, and risk-based decision making in motivated behavior
Bailey, M. R., Simpson, E. H., & Balsam, P. D. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.07.015 · Cited by 119 · see citing works
Repeated exposure with short-term behavioral stress resolves pre-existing stress-induced depressive-like behavior in mice
Lee, E.-H., Park, J.-Y., Kwon, H.-J., & Han, P.-L. (2021) · Nature Communications · doi:10.1038/s41467-021-26968-4 · Cited by 82 · see citing works
Abnormalities of brain neural circuits related to obesity: A Diffusion Tensor Imaging study
Papageorgiou, I., Astrakas, L. G., Xydis, V. G., Alexiou, G. Α., Bargiotas, P., Tzarouchi, L. C., Zikou, A. K., Kiortsis, D. N., & Argyropoulou, M. I. (2016) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2016.11.018 · Cited by 73 · see citing works
Arbitration of Approach-Avoidance Conflict by Ventral Hippocampus
Bryant, K. G., & Barker, J. M. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.615337 · Cited by 72 · see citing works
Pervasive competition between threat and reward in the brain
Choi, J. M., Padmala, S., Spechler, P. A., & Pessoa, L. (2013) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nst053 · Cited by 62 · see citing works
What about me…? The PVT: a role for the paraventricular thalamus (PVT) in drug-seeking behavior
James, M. H., & Dayas, C. V. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00018 · Cited by 60 · see citing works
On the role of subsecond dopamine release in conditioned avoidance
Oleson, E. B., & Cheer, J. F. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00096 · Cited by 43 · see citing works
Paranoid thinking, suspicion, and risk for aggression: A neurodevelopmental perspective
Tone, E. B., & Davis, J. S. (2012) · Development and Psychopathology · doi:10.1017/s0954579412000521 · Cited by 42 · see citing works
Neuromodulation for substance addiction in human subjects: A review
Bari, A., DiCesare, J. A. T., Babayan, D., Runcie, M., Sparks, H. D., & Wilson, B. R. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.09.013 · Cited by 41 · see citing works
The Misnomer of Attention-Deficit Hyperactivity Disorder
Wasserman, T. H., & Wasserman, L. D. (2015) · Applied Neuropsychology Child · doi:10.1080/21622965.2015.1005487 · Cited by 26 · see citing works
Insights for Developing Pharmacological Treatments for Psychostimulant Relapse Targeting Hypothalamic Peptide Systems
James, M. H., Yeoh, J. W., Graham, B. A., & Dayas, C. V. (2012) · Journal of Addiction Research & Therapy · doi:10.4172/2155-6105.s4-008 · Cited by 22 · see citing works
The motivational role of affect in an ecological model
Gabriel, R. H. (2021) · Theory & Psychology · doi:10.1177/0959354321992869 · Cited by 10 · see citing works
Comparative Analysis of the Axonal Collateralization Patterns of Basal Ganglia Output Nuclei in the Rat
Mengual, E., Prensa, L., Tripathi, A., Cebrián, C., & Mongia, S. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-801393-9.00003-7 · Cited by 5 · see citing works
Emerging Roles for Glial Pathology in Addiction
Reissner, K. J., & Kalivas, P. W. (2014) · Springer eBooks · doi:10.1007/978-1-4939-0974-2_17 · Cited by 4 · see citing works
Arborization patterns of amygdalopetal axons from the rat ventral pallidum
Mongia, S., Tripathi, A., & Mengual, E. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1184-2 · Cited by 3 · see citing works
Correction: Brain’s Reward Circuits Mediate Itch Relief. A Functional MRI Study of Active Scratching
Papoiu, A. D. P., Nattkemper, L. A., Sanders, K. M., Kraft, R., Chan, Y.-H., Coghill, R. C., & Yosipovitch, G. (2014) · PLoS ONE · doi:10.1371/annotation/c58aebe3-8f01-4c14-991a-c229e35b8f74 · Cited by 2 · see citing works
Effects of deep brain stimulation on non-motor symptoms in Parkinson’s disease: insights from longitudinal studies using consistent evaluation scales
Xu, H., Yan, Z., Ye, Q., Lu, J., Chen, K., Fang, J., Li, Z., & Jiang, J. (2026) · Journal of Neurology · doi:10.1007/s00415-025-13597-w · Cited by 1 · see citing works
The Role of the Reward Recognition Network in Understanding Motivation
Wasserman, T. H., & Wasserman, L. D. (2020) · Springer eBooks · doi:10.1007/978-3-030-58724-6_4 · Cited by 1 · see citing works
Neurobiology of Learning and Valuation
Heilbronner, S. R. (2012) · DukeSpace (Duke University) · Cited by 1 · see citing works
Self-citation
What about me...? The PVT: a role for the paraventricular thalamus (PVT) in drug-seeking behavior
Sousa, N., Dalla, C., & Rodrigues, A. J. (2013)
Scientific Program Directors and Residency Research Coordinators
Gilron, I., Jaeger, M. T., Allard, R. V., Hare, G., Parlow, J. L., Cummings, M., Asselstine, K., Wang, L., & Phelan, R. (2013)
New Principles of Therapy
Wasserman, T. H., & Wasserman, L. D. (2016) · Springer eBooks · doi:10.1007/978-3-319-30910-1_12
Introduction to Neurocognitive Learning Therapy
Wasserman, T. H., & Wasserman, L. D. (2017) · Springer eBooks · doi:10.1007/978-3-319-60849-5_1
The Role of the Reward Recognition Network in Therapy
Wasserman, T. H., & Wasserman, L. D. (2019) · Springer eBooks · doi:10.1007/978-3-030-26921-0_8
Network Modeling and Therapeutic Techniques
Wasserman, T. H., & Wasserman, L. D. (2019) · Springer eBooks · doi:10.1007/978-3-030-26921-0_5
Addendum
Koziol, L. F. (2014) · SpringerBriefs in neuroscience · doi:10.1007/978-3-319-04477-4_31
Cellular and Molecular Mechanisms of Addiction
Reissner, K. J., & Kalivas, P. W. (2017) · Oxford University Press eBooks · doi:10.1093/med/9780190681425.003.0046
Die Rolle des Belohnungserkennungsnetzwerks beim Verständnis von Motivation
Wasserman, T. H., & Wasserman, L. D. (2024) · Springer eBooks · doi:10.1007/978-3-031-48004-1_4
Attention and the Role of the Reward Recognition Network
Wasserman, T. H., & Wasserman, L. D. (2024) · Springer eBooks · doi:10.1007/978-3-031-78732-4_8
Cellular and Molecular Mechanisms of Substance Use Disorders
Reissner, K. J. (2025) · doi:10.1093/med/9780197640654.003.0048
Cytochrome-C-oxidase expression in the subiculum and anterior thalamic nuclei of rats increases following training in an extrapolation of serial stimulus patterns task
da Silva, D. G., Torres-Cruz, M., Helou, A. Y., & Xavier, G. F. (2025) · Physiology & Behavior · doi:10.1016/j.physbeh.2025.114926
Quantitative and Comparative Analysis of Dream Content in Parkinson's Disease Patients Undergoing Deep Brain Stimulation: A Pilot Study
Joswig, H., Oreizi-Esfahani, S., Medack, S., Träger, U., & Staudt, M. D. (2026) · World Neurosurgery · doi:10.1016/j.wneu.2026.124816

Authors: McGinty, V. B., Hayden, B. Y., Heilbronner, S. R., Dumont, E. C., Graves, S. M., Mirrione, M. M., du Hoffmann, J., Sartor, G. C., España, R. A., Millan, E. Z., DiFeliceantonio, A. G., Marchant, N. J., Napier, T. C., Root, D. H., Borgland, S. L., Treadway, M. T., Floresco, S. B., McGinty, J. F., & Haber, S.
Affiliations: Stanford University (US)
University of Rochester (US)
Duke University (US)
Rush University Medical Center (US)
Cold Spring Harbor Laboratory (US)
Medical University of South Carolina (US)
Wake Forest University Health Sciences (US)
UNSW Sydney (AU)
University of Michigan (US)
Rutgers, The State University of New Jersey (US)
University of British Columbia (CA)
Vanderbilt University (US)
Corresponding author: Haber, Suzanne
ORCID: McGinty, Vincent B.
Hayden, Benjamin Y.
Heilbronner, Sarah R.
Graves, Steven M.
Sartor, Gregory C.
España, Rodrigo A.
Millan, E. Zayra
DiFeliceantonio, Alexandra G.
Marchant, Nathan J.
Napier, T. Celeste
Root, David H.
Borgland, Stephanie L.
Treadway, Michael T.
Floresco, Stan B.
McGinty, Jacqueline F.
Haber, Suzanne
Venue: Behavioural Brain Research
Publisher: Elsevier BV
Published: 2011-11
Volume: 225
Issue: 1
Pages: 348-357
ISSN: 0166-4328 (ISSN-L)
DOI: 10.1016/j.bbr.2011.07.036
PMC: PMC3445023
OpenAlex: W2127006344
Cited by: 36
References: 165
Citations by year: 2026: 2 · 2025: 2 · 2024: 2 · 2021: 2 · 2020: 2 · 2019: 2 · 2018: 1 · 2017: 2 · 2016: 5 · 2015: 1 · 2014: 3 · 2013: 7 · 2012: 5
FWCI: 0.46
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Behavioural Brain Research (publishedVersion)
PubMed (publishedVersion)
Europe PMC (PubMed Central) (acceptedVersion)
PubMed Central (acceptedVersion)
Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
Funders: National Institutes of Health (1r13da030034-01)
National Institute on Drug Abuse (1 R13 DA030034-01, R13 DA030034)
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: reward systems, brain reward system, motivation, incentive salience
MeSH terms: Animals, Brain, Brain Mapping, Humans, Motivation, Reward

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Emerging, reemerging, and forgotten brain areas of the reward circuit: Notes from the 2010 Motivational Neural Networks conference

Abstract

Integrity signals

Claims the paper makes

Claims other papers make about this one

Self-check

Cites

Cited by

Related

Record

About these checks