From motivation to action: Functional interface between the limbic system and the motor system

EVIDENCE FOR THE EXISTENCE OF MONOAMINE-CONTAINING NEURONS IN THE CENTRAL NERVOUS SYSTEM. I. DEMONSTRATION OF MONOAMINES IN THE CELL BODIES OF BRAIN STEM NEURONS.

Dahlstroem, A., & Fuxé, K. (1964) · PubMed · Cited by 5,133

The co-ordination and regulation of movements

Bernshteĭn, N. A. (1969) · Brain Research · doi:10.1016/0006-8993(69)90278-9 · Cited by 5,087

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

Posterior parietal association cortex of the monkey: command functions for operations within extrapersonal space

Mountcastle, V. B., Lynch, J. C., Georgopoulos, A., Sakata, H., & Acuna, C. (1975) · Journal of Neurophysiology · doi:10.1152/jn.1975.38.4.871 · Cited by 2,061

Integrative activity of the brain

Konorski, J. (1967) · University of Chicago Press eBooks · Cited by 2,043

Amphetamine and apomorphine responses in the rat following 6-OHDA lesions of the nucleus accumbens septi and corpus striatum

Kelly, P. H., Seviour, P. W., & Iversen, S. D. (1975) · Brain Research · doi:10.1016/0006-8993(75)90233-4 · Cited by 1,740

Flexion‐reflex of the limb, crossed extension‐reflex, and reflex stepping and standing

Sherrington, C. (1910) · The Journal of Physiology · doi:10.1113/jphysiol.1910.sp001362 · Cited by 1,336

Adipsia and Aphagia after 6‐Hydroxydopamine Induced Degeneration of the Nigro‐striatal Dopamine System

Ungerstedt, U. (1971) · Acta Physiologica Scandinavica · doi:10.1111/j.1365-201x.1971.tb11001.x · Cited by 1,294

Cerebrocerebellar communication systems.

Allen, G. I., & Tsukahara, N. (1974) · Physiological Reviews · doi:10.1152/physrev.1974.54.4.957 · Cited by 1,084

Neurophysiology of locomotor automatism

Shik, M. L., & Orlovsky, G. N. (1976) · Physiological Reviews · doi:10.1152/physrev.1976.56.3.465 · Cited by 1,071

Motivation and movement: the effect of monetary incentive on performance speed

Mir, P., Trender‐Gerhard, I., Edwards, M. J., Schneider, S. A., Bhatia, K. P., & Jahanshahi, M. (2011) · Experimental Brain Research · doi:10.1007/s00221-011-2583-5 · Cited by 67

Effects of social sustainability signaling on neural valuation signals and taste-experience of food products

Enax, L., Krapp, V., Piehl, A., & Weber, B. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00247 · Cited by 70

Neuropsychopharmacology of drug seeking: Insights from studies with second-order schedules of drug reinforcement

Ciano, P. D., & Everitt, B. J. (2005) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2005.09.024 · Cited by 64

Electrophysiological Properties of Cholinergic and Noncholinergic Neurons in the Ventral Pallidal Region of the Nucleus Basalis in Rat Brain Slices

Bengtson, C. P., & Osborne, P. B. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.5.2649 · Cited by 63

Cerebroventricular dilation in spontaneously hypertensive rats (SHRs) is not attenuated by reduction of blood pressure

Ritter, S., Dinh, T. T., Stone, S., & Ross, N. (1988) · Brain Research · doi:10.1016/0006-8993(88)91574-0 · Cited by 62

Nucleus Accumbens Deep Brain Stimulation Results in Insula and Prefrontal Activation: A Large Animal fMRI Study

Knight, E. J., Min, H.-K. P., Hwang, S.-C., Marsh, M. P., Paek, S. B., Kim, I., Felmlee, J. P., Abulseoud, O. A., Bennet, K. E., Frye, M. A., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056640 · Cited by 66

Increased volume of the nucleus accumbens in schizophrenia

Lauer, M., Senitz, D., & Beckmann, H. (2001) · Journal of Neural Transmission · doi:10.1007/s007020170042 · Cited by 63

A scale-free systems theory of motivation and addiction

Chambers, R. A., Bickel, W. K., & Potenza, M. N. (2007) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2007.04.005 · Cited by 63

From Physical Aggression to Verbal Behavior: Language Evolution and Self-Domestication Feedback Loop

Progovac, L., & Benítez‐Burraco, A. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.02807 · Cited by 59

Effects of selective NMDA and non-NMDA blockade in the nucleus accumbens on the plus-maze test

MARTINEZ, G., ROPERO, C., FUNES, A., FLORES, E., BLOTTA, C., Landa, A. I., & Gargiulo, P. Á. (2002) · Physiology & Behavior · doi:10.1016/s0031-9384(02)00704-7 · Cited by 62

Understanding the Placebo Effect: Contributions from Neuroimaging

Lidstone, S. C., & Stoessl, A. J. (2007) · Molecular Imaging and Biology · doi:10.1007/s11307-007-0098-z · Cited by 61

Memory-dependent c-Fos expression in the nucleus accumbens and extended amygdala following the expression of a conditioned taste aversive in the rat

Yasoshima, Y., Scott, T. R., & Yamamoto, T. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.03.019 · Cited by 58

Timing-dependent limbic-motor synaptic integration in the nucleus accumbens

Goto, Y., & O’Donnell, P. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.202303199 · Cited by 62

Two types of motivation revealed by ibotenic acid nucleus accumbens lesions: Dissociation of food carrying and hoarding and the role of primary and incentive motivation

Whishaw, I. Q., & Kornelsen, R. A. (1993) · Behavioural Brain Research · doi:10.1016/0166-4328(93)90123-8 · Cited by 62

Effects of ventral striatal 6-OHDA lesions or amphetamine sensitization on ethanol consumption in the rat

Fahlke, C., Hansen, S., Engel, J. A., & Hȧrd, E. (1994) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(94)90020-5 · Cited by 62

Neuroscience and Human Motivation

Reeve, J., & Lee, W. (2012) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780195399820.013.0021 · Cited by 62

Love-related changes in the brain: a resting-state functional magnetic resonance imaging study

Song, H., Zou, Z., Kou, J., Liu, Y., Yang, L., Zilverstand, A., Uquillas, F. D., & Zhang, X. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00071 · Cited by 64

The role of δ‐opioid receptors in learning and memory underlying the development of addiction

Klenowski, P. M., Morgan, M., & Bartlett, S. E. (2014) · British Journal of Pharmacology · doi:10.1111/bph.12618 · Cited by 60

Stimulation of P2 receptors in the ventral tegmental area enhances dopaminergic mechanisms in vivo

Krügel, U., Kittner, H., Franke, H., & Illés, P. (2001) · Neuropharmacology · doi:10.1016/s0028-3908(01)00033-8 · Cited by 61

Complementary Roles for Ventral Pallidum Cell Types and Their Projections in Relapse

Prasad, A. A., Xie, C., Chaichim, C., Nguyen, J. H. G., McClusky, H. E., Killcross, S., Power, J., & McNally, G. P. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.0262-19.2019 · Cited by 61

Mu‐opioid receptor cellular function in the nucleus accumbens is essential for hedonically driven eating

Ward, H. G., Nicklous, D. M., Aloyo, V. J., & Simansky, K. J. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04674.x · Cited by 61

Electrophysiological responses of neurons of the ventral tegmental area to electrical stimulation of amygdala and lateral septum

Maeda, H., & Mogenson, G. J. (1981) · Neuroscience · doi:10.1016/0306-4522(81)90130-5 · Cited by 61

Biphasic effects of intra‐accumbens histamine administration on spontaneous motor activity in the rat; a role for central histamine receptors

Bristow, L. J., & Bennett, G. W. (1988) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1988.tb11767.x · Cited by 61

The role of the lateral hypothalamus and orexin in ingestive behavior: a model for the translation of past experience and sensed deficits into motivated behaviors

Hurley, S. W., & Johnson, A. K. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00216 · Cited by 61

Nucleus Accumbens and Posterior Amygdala Mediate Cue-Triggered Alcohol Seeking and Suppress Behavior During the Omission of Alcohol-Predictive Cues

Millan, E. Z., Reese, R. M., Grossman, C. D., Chaudhri, N., & Janak, P. H. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.102 · Cited by 60

Reinforcement learning models of the dopamine system and their behavioral implications

Daw, N. D., & Touretzky, D. S. (2003) · Cited by 62

The Influence of Self-Generated Emotions on Physical Performance: An Investigation of Happiness, Anger, Anxiety, and Sadness

Rathschlag, M., & Memmert, D. (2013) · Journal of Sport and Exercise Psychology · doi:10.1123/jsep.35.2.197 · Cited by 67

Synaptic Plasticity in the Nucleus Accumbens: Lessons Learned from Experience

Turner, B. D., Kashima, D. T., Manz, K. M., Grueter, C. A., & Grueter, B. A. (2017) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.7b00420 · Cited by 62

Microinfusion of corticotropin-releasing factor into the nucleus accumbens shell results in increased behavioral arousal and oral motor activity

Holahan, M. R., Kalin, N. H., & Kelley, A. E. (1997) · Psychopharmacology · doi:10.1007/s002130050228 · Cited by 60

Different behavioral functions of dopamine in the nucleus accumbens and ventrolateral striatum: a microdialysis and behavioral investigation

Cousins, M. S., Trevitt, J. T., Atherton, A., & Salamone, J. D. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00617-4 · Cited by 60

Effects of excitotoxic lesions of the rat ventral striatum on the perception of reward cost

Bowman, E. M., & Brown, V. J. (1998) · Experimental Brain Research · doi:10.1007/s002210050588 · Cited by 60

Fornix, medial prefrontal cortex, nucleus accumbens, and mediodorsal thalamic nucleus: Roles in a fear-based context discrimination task

Antoniadis, E. A., & McDonald, R. J. (2005) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.08.011 · Cited by 59

Dopaminergic agonists administered into the nucleus accumbens: Effects on extracellular glutamate and on locomotor activity

Dalia, A., Uretsky, N. J., & Wallace, L. J. (1998) · Brain Research · doi:10.1016/s0006-8993(97)01518-7 · Cited by 60

The effect of cholinergic stimulation in the nucleus accumbens on locomotor behavior

Austin, M. C., & Kalivas, P. W. (1988) · Brain Research · doi:10.1016/0006-8993(88)91400-x · Cited by 60

Persistent increase in dopamine release following activation of metabotropic glutamate receptors in the rat nucleus accumbens

Ohno, M., & Watanabe, S. (1995) · Neuroscience Letters · doi:10.1016/0304-3940(95)12091-h · Cited by 60

A selective role for dopamine in the nucleus accumbens of the rat in random foraging but not delayed spatial win-shift-based foraging

Floresco, S. B., Seamans, J. K., & Phillips, A. G. (1996) · Behavioural Brain Research · doi:10.1016/0166-4328(96)00031-9 · Cited by 56

Ventral pallidal regulation of motivated behaviors and reinforcement

Soares‐Cunha, C., & Heinsbroek, J. A. (2023) · Frontiers in Neural Circuits · doi:10.3389/fncir.2023.1086053 · Cited by 63

Memory reactivation and consolidation during sleep: from cellular mechanisms to human performance

Pennartz, C. M. A., Uylings, H. B. M., Barnes, C. A., & McNaughton, B. L. (2002) · Progress in brain research · doi:10.1016/s0079-6123(02)38076-2 · Cited by 59

Distribution of fos-like immunoreactivity in the rat brain following intravenous lipopolysaccharide administration

Elmquist, J. K., Scammell, T. E., Jacobson, C. D., & Saper, C. B. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960715)371:1 · Cited by 335

Glucose utilization rates regulate intake levels of artificial sweeteners

Téllez, L. A., Ren, X., Han, W., Medina, S., Ferreira, J. G. P., Yeckel, C. W., & de Araújo, I. E. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2013.263103 · Cited by 57

Differential roles of ventral pallidum subregions during cocaine self‐administration behaviors

Root, D. H., Ma, S., Barker, D. J., Megehee, L., Striano, B. M., Ralston, C. M., Fabbricatore, A. T., & West, M. O. (2012) · The Journal of Comparative Neurology · doi:10.1002/cne.23191 · Cited by 57

Regional Differences in the Coupling between Resting Cerebral Blood Flow and Metabolism may Indicate Action Preparedness as a Default State

Gur, R. C., Ragland, J. D., Reivich, M., Greenberg, J. H., Alavi, A. A., & Gur, R. E. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn087 · Cited by 60

Engaging Environments Enhance Motor Skill Learning in a Computer Gaming Task

Lohse, K. R., Boyd, L. A., & Hodges, N. J. (2015) · Journal of Motor Behavior · doi:10.1080/00222895.2015.1068158 · Cited by 62

Safety out of control: dopamine and defence

Lloyd, K., & Dayan, P. (2016) · Behavioral and Brain Functions · doi:10.1186/s12993-016-0099-7 · Cited by 64

Microinjections of flupenthixol into the caudate-putamen but not the nucleus accumbens, amygdala or frontal cortex of rats produce intra-session declines in food-rewarded operant responding

Beninger, R. J., & Ranaldi, R. (1993) · Behavioural Brain Research · doi:10.1016/0166-4328(93)90116-8 · Cited by 59

Different patterns of local brain energy metabolism associated with high and low doses of methylphenidate relevance to its action in hyperactive children

Porrino, L. J., & Lucignani, G. (1987) · Biological Psychiatry · doi:10.1016/0006-3223(87)90223-x · Cited by 59

The Interface Between Dopamine Neurons and the Amygdala: Implications for Schizophrenia

Haber, S. N., & Fudge, J. L. (1997) · Schizophrenia Bulletin · doi:10.1093/schbul/23.3.471 · Cited by 60

Dynorphin‐immunoreactive terminals in the rat nucleus accumbens: Cellular sites for modulation of target neurons and interactions with catecholamine afferents

Bockstaele, E. J. V., Sesack, S. R., & Pickel, V. M. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903410102 · Cited by 59

Motor Cortex Excitability Reflects the Subjective Value of Reward and Mediates Its Effects on Incentive-Motivated Performance

Galaro, J. K., Celnik, P. A., & Chib, V. S. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1254-18.2018 · Cited by 59

Enhanced acquisition of discriminative approach following intra-amygdala d-amphetamine

Hitchcott, P., Harmer, C., & Phillips, G. (1997) · Psychopharmacology · doi:10.1007/s002130050341 · Cited by 66

Presynaptic dopamine D4 receptor localization in the rat nucleus accumbens shell

Svingos, A. L., Periasamy, S., & Pickel, V. M. (2000) · Synapse · doi:10.1002/(sici)1098-2396(20000601)36:3 · Cited by 58

In vivo stimulated dopamine release in the nucleus accumbens: modulation by the prefrontal cortex

Thompson, T. L., & Moss, R. L. (1995) · Brain Research · doi:10.1016/0006-8993(95)00429-t · Cited by 58

When a good taste turns bad: Neural mechanisms underlying the emergence of negative affect and associated natural reward devaluation by cocaine

Carelli, R. M., & West, E. A. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.04.025 · Cited by 60

Physiology of the normal and dopamine-depleted basal ganglia: Insights into levodopa pharmacotherapy

Grace, A. A. (2008) · Movement Disorders · doi:10.1002/mds.22020 · Cited by 57

Toward sophisticated basal ganglia neuromodulation: Review on basal ganglia deep brain stimulation

Cunha, C. D., Boschen, S. L., Gómez‐A, A., Ross, E. K., Gibson, W. S. J., Min, H.-K. P., Lee, K. H., & Blaha, C. D. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.02.003 · Cited by 61

The Biopsychology of Maternal Behavior in Nonhuman Mammals

Kristal, M. B. (2009) · ILAR Journal · doi:10.1093/ilar.50.1.51 · Cited by 57

Functional organization of the circuits connecting the cerebral cortex and the basal ganglia: implications for the role of the basal ganglia in epilepsy

Slaght, S., Paz, J. T., Mahon, S., Maurice, N., Charpier, S., & Deniau, J. (2002) · Epileptic Disorders · doi:10.1684/j.1950-6945.2002.tb00542.x · Cited by 57

Nucleus accumbens dopamine receptors in the consolidation of spatial memory

Mele, A., Avena, M. J., Roullet, P., Leonibus, E. D., Mandillo, S., Sargolini, F., Coccurello, R., & Oliverio, A. (2004) · Behavioural Pharmacology · doi:10.1097/00008877-200409000-00017 · Cited by 57

In VivoElectrochemical Studies of Dopamine Clearance in Subregions of Rat Nucleus Accumbens: Differential Properties of the Core and Shell

David, D., Zahniser, N. R., Hoffer, B. J., & Gerhardt, G. A. (1998) · Experimental Neurology · doi:10.1006/exnr.1998.6898 · Cited by 57

Dopaminergic involvement in locomotion elicited from the ventral pallidum/substantia innominata

Austin, M. C., & Kalivas, P. W. (1991) · Brain Research · doi:10.1016/0006-8993(91)91005-l · Cited by 57

Effects of peripheral stimulation on the activity of neurons in the ventral tegmental area, substantia nigra and midbrain reticular formation of rats

Maeda, H., & Mogenson, G. J. (1982) · Brain Research Bulletin · doi:10.1016/0361-9230(82)90021-1 · Cited by 57

Microinfusion of the Metabotropic Glutamate Receptor Agonist 1S, 3R–1‐Aminocyclopentane‐1, 3‐dicarboxylic Acid Into the Nucleus Accumbens Induces Dopamine‐dependent Locomotor Activation in the Rat

Attarian, S., & Amalric, M. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01430.x · Cited by 57

Origins of multisynaptic projections from the basal ganglia to the forelimb region of the ventral premotor cortex in macaque monkeys

Ishida, H., Inoue, K., Takada, M., & Hoshi, E. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13127 · Cited by 56

Considerations for general anaesthesia in Parkinson’s disease

Roberts, D. P., & Lewis, S. J. G. (2017) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2017.10.062 · Cited by 56

Cannabinoid, melanocortin and opioid receptor expression on DRD1 and DRD2 subpopulations in rat striatum

Ophuis, R. J. A. O., Boender, A. J., van Rozen, A. J., & Adan, R. A. H. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00014 · Cited by 54

Grand challenge for movement science and sport psychology: embracing the social-cognitive–affective–motor nature of motor behavior

Lewthwaite, R. (2010) · Frontiers in Psychology · doi:10.3389/fpsyg.2010.00042 · Cited by 56

Motivational Processes Underlying Substance Abuse Disorder

Meyer, P., King, C. P., & Ferrario, C. R. (2015) · Current topics in behavioral neurosciences · doi:10.1007/7854_2015_391 · Cited by 59

Activation of specific central dopamine pathways: Locomotion and footshock

Speciale, S. G., Miller, J. D., McMillen, B. A., & German, D. C. (1986) · Brain Research Bulletin · doi:10.1016/0361-9230(86)90009-2 · Cited by 56

The neural control of feeding in primates

Rolls, E. T. (1993) · Elsevier eBooks · doi:10.1016/b978-0-08-041988-6.50013-4 · Cited by 55

Effect of Lorcaserin Alone and in Combination with Phentermine on Food Cravings After 12‐Week Treatment: A Randomized Substudy

Rebello, C. J., Nikonova, E. V., Zhou, S., Aronne, L. J., Fujioka, K., Garvey, W. T., Smith, S. R., Coulter, A. A., & Greenway, F. L. (2018) · Obesity · doi:10.1002/oby.22094 · Cited by 55

Effects of typical and atypical antipsychotic drugs on maternal behavior in postpartum female rats

Li, M., Davidson, P., Budin, R., Kapur, S., & Fleming, A. S. (2003) · Schizophrenia Research · doi:10.1016/j.schres.2003.09.013 · Cited by 55

Treatment Issues Pertaining to Pathological Gamblers with a Comorbid Disorder

Winters, K. C., & Kushner, M. G. (2003) · Journal of Gambling Studies · doi:10.1023/a:1024203403982 · Cited by 55

Paraventricular hypothalamic and amygdalar CRF neurons synapse in the external globus pallidus

Hunt, A. J., Dasgupta, R., Rajamanickam, S., Jiang, Z., Beierlein, M., Chan, C. S., & Justice, N. J. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1652-y · Cited by 55

The effects of electrolytic lesion to the shell subterritory of the nucleus accumbens on delayed non-matching-to-sample and four-arm baited eight-arm radial-maze tasks.

Gal, G., Joel, D., Gusak, O., Feldon, J., & Weiner, I. (1997) · Behavioral Neuroscience · doi:10.1037//0735-7044.111.1.92 · Cited by 59

Effect of local infusion of glutamate analogues into the nucleus accumbens of rats: an electrochemical and behavioural study

Svensson, L., Zhang, J., Johannessen, K., & Engel, J. A. (1994) · Brain Research · doi:10.1016/0006-8993(94)90021-3 · Cited by 55

Functions of the dopaminergic innervation of the nucleus accumbens.

Gray, J. A., Kumari, V., Lawrence, N., & Young, A. M. J. (1999) · Psychobiology · doi:10.3758/bf03332116 · Cited by 52

Selective filtering of excitatory inputs to nucleus accumbens by dopamine and serotonin

Christoffel, D. J., Walsh, J. J., Hoerbelt, P., Heifets, B. D., Llorach, P., Lopez, R. C., Ramakrishnan, C., Deisseroth, K., & Malenka, R. C. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2106648118 · Cited by 54

The medial preoptic area is necessary for motivated choice of pup- over cocaine-associated environments by early postpartum rats

Pereira, M., & Morrell, J. I. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.02.015 · Cited by 54

Hemispheric differences in the mesostriatal dopaminergic system

Molochnikov, I., & Cohen, D. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00110 · Cited by 53

Extinction of drug seeking: Neural circuits and approaches to augmentation

McNally, G. P. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.06.007 · Cited by 56

Conjunctive Processing of Locomotor Signals by the Ventral Tegmental Area Neuronal Population

Wang, D. V., & Tsien, J. Z. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016528 · Cited by 52

Nucleus accumbens shell, but not core, tracks motivational value of salt

Loriaux, A. L., Roitman, J. D., & Roitman, M. F. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00153.2011 · Cited by 54

Effectiveness of the Virtual Reality System Toyra on Upper Limb Function in People with Tetraplegia: A Pilot Randomized Clinical Trial

Dimbwadyo-Terrer, I., Gil-Agudo, A. M., Segura‐Fragoso, A., Reyes-Guzmán, A. D. L., Trincado-Alonso, F., Piazza, S., & López, B. P. (2016) · BioMed Research International · doi:10.1155/2016/6397828 · Cited by 58

Drug addiction: An affective-cognitive disorder in need of a cure

Fattore, L., & Diana, M. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.04.006 · Cited by 58

Adolescent Mice Are Resilient to Alcohol Withdrawal-Induced Anxiety and Changes in Indices of Glutamate Function within the Nucleus Accumbens

Lee, K. M., Coelho, M. A., McGregor, H. A., Solton, N. R., Cohen, M., & Szumlinski, K. K. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00265 · Cited by 53

Ventral pallidum is essential for cocaine relapse after voluntary abstinence in rats

Farrell, M. R., Ruiz, C. M., Castillo, E., Faget, L. C., Khanbijian, C., Liu, S., Schoch, H., Rojas, G. R., Huerta, M. Y., Hnasko, T. S., et al. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0507-4 · Cited by 57

N -Methyl- D -aspartate receptors in the nucleus accumbens⋅are involved in detection of spatial novelty in mice

Usiello, A., Sargolini, F., Roullet, P., Ammassari‐Teule, M., Passino, E., Oliverio, A., & Mele, A. (1998) · Psychopharmacology · doi:10.1007/s002130050607 · Cited by 54

Differences Between Accumbens Core and Shell Neurons Exhibiting Phasic Firing Patterns Related to Drug-Seeking Behavior During a Discriminative-Stimulus Task

Ghitza, U. E., Fabbricatore, A. T., Prokopenko, V. F., & West, M. O. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00268.2004 · Cited by 54

Chronic morphine induces long-lasting changes in acetylcholine release in rat nucleus accumbens core and shell: an in vivo microdialysis study

Šustková-Fišerová, M., Consolo, S., & Kršiak, M. (1999) · Psychopharmacology · doi:10.1007/s002130050866 · Cited by 54

Asymmetric dopamine and serotonin metabolism in nigrostriatal and limbic structures of the trained circling rat

Yamamoto, B. K., & Freed, C. R. (1984) · Brain Research · doi:10.1016/0006-8993(84)90547-x · Cited by 55

Don't leave the “psych” out of neuropsychology

Gray, J. A., & Baruch, I. (1987) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00047579 · Cited by 54

Distinct regions of the striatum underlying effort, movement initiation and effort discounting

Suzuki, S., Lawlor, V. M., Cooper, J. A., Arulpragasam, A. R., & Treadway, M. T. (2020) · Nature Human Behaviour · doi:10.1038/s41562-020-00972-y · Cited by 66

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