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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

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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

Show all 115 references

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Items 901–1,000 of 1,014

Dopamine Transmission in the Schizophrenic Brain
Laruelle, M. A. (2003) · Wiley eBooks · doi:10.1002/9780470987353.ch20 · Cited by 53
NMDA and dopamine interactions in the nucleus accumbens modulate cortical acetylcholine release
Zmarowski, A., Sarter, M., & Bruno, J. P. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04333.x · Cited by 52
Cocaine abstinence alters nucleus accumbens firing dynamics during goal‐directed behaviors for cocaine and sucrose
Cameron, C. M., & Carelli, R. M. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08024.x · Cited by 54
Amygdalostriatal projections in the neurocircuitry for motivation: a neuroanatomical thread through the career of Ann Kelley
Zorrilla, E. P., & Koob, G. F. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.11.019 · Cited by 59
Food‐reward signalling in the suprachiasmatic clock
Mendoza, J., Clesse, D., Pévet, P., & Challet, É. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06570.x · Cited by 57
Twenty years of dopamine research: Individual differences in the response of accumbal dopamine to environmental and pharmacological challenges
Verheij, M. M. M., & Cools, A. R. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2008.02.084 · Cited by 52
Differentiating the rapid actions of cocaine
Wise, R. A., & Kiyatkin, E. A. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn3043 · Cited by 50
Mechanisms of Reward Circuit Dysfunction in Psychiatric Illness
Pujara, M. S., & Koenigs, M. R. (2013) · The Neuroscientist · doi:10.1177/1073858413499407 · Cited by 51
Behaviors induced or disrupted by complex partial seizures
Leung, L.-W. S., Ma, J., & McLachlan, R. S. (2000) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(00)00035-x · Cited by 52
A Wasp Manipulates Neuronal Activity in the Sub-Esophageal Ganglion to Decrease the Drive for Walking in Its Cockroach Prey
Gal, R., & Libersat, F. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010019 · Cited by 52
Cue‐evoked encoding of movement planning and execution in the rat nucleus accumbens
Taha, S. A., Nicola, S. M., & Fields, H. L. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.140236 · Cited by 52
Infusion of quinpirole and muscimol into the ventral tegmental area inhibits fear-potentiated startle: implications for the role of dopamine in fear expression
Munro, L. J., & Kokkinidis, L. (1997) · Brain Research · doi:10.1016/s0006-8993(96)01225-5 · Cited by 52
A Computational Model of Craving and Obsession
Redish, A. D., & Johnson, A. C. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1390.014 · Cited by 50
Exploration and Its Measurement: A Psychopharmacological Perspective
Kelley, A. E., Cador, M., & Stinus, L. (2003) · Psychopharmacology · doi:10.1385/0-89603-129-2:95 · Cited by 13
An electrophysiological study of inputs to neurons of the ventral tegmental area from the nucleus accumbens and medial preoptic-anterior hypothalamic areas
Maeda, H., & Mogenson, G. J. (1980) · Brain Research · doi:10.1016/0006-8993(80)91122-1 · Cited by 52
Self-citation
Effects of intraaccumbens injections of dopamine agonists and antagonists on sucrose and sucrose-ethanol reinforced responding
Hodge, C. W., Samson, H. H., Tolliver, G. A., & Haraguchi, M. (1994) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(94)90510-x · Cited by 51
Amphetamine regulation of mesolimbic dopamine/cholecystokinin neurotransmission
Hurd, Y. L., Lindefors, N., Brodin, E., Brené, S., Persson, H., Ungerstedt, U., & Ho¨kfelt, T. (1992) · Brain Research · doi:10.1016/0006-8993(92)90264-a · Cited by 52
Dopamine neurons grafted unilaterally to the nucleus accumbens affect drug-induced circling and locomotion
Brundin, P., Strecker, R. E., Londos, E., & Björklund, A. (1987) · Experimental Brain Research · doi:10.1007/bf00247041 · Cited by 52
Closing the Gate in the Limbic Striatum: Prefrontal Suppression of Hippocampal and Thalamic Inputs
Calhoon, G. G., & O’Donnell, P. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.032 · Cited by 50
The projections of the retrorubral field A8 to the hippocampal formation in the rat
Gasbarri, A., Packard, M., Sulli, A., Pacitti, C., Innocenzi, R., & Perciavalle, V. (1996) · Experimental Brain Research · doi:10.1007/bf00227643 · Cited by 51
Real-time assessments of dopamine function during behavior: single-unit recording, iontophoresis, and fast-scan cyclic voltammetry in awake, unrestrained rats
Rebec, G. V. (1998) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.1998.tb03614.x · Cited by 51
Brain Imaging Biomarkers for Chronic Pain
Zhang, Z., Gewandter, J. S., & Geha, P. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2021.734821 · Cited by 60
Error detection in the stop signal task
Chevrier, A., & Schachar, R. J. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.06.056 · Cited by 51
Ramping single unit activity in the medial prefrontal cortex and ventral striatum reflects the onset of waiting but not imminent impulsive actions
Donnelly, N. A., Paulsen, O., Robbins, T. W., & Dalley, J. W. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12895 · Cited by 49
Songbird Ventral Pallidum Sends Diverse Performance Error Signals to Dopaminergic Midbrain
Chen, R., Puzerey, P. A., Roeser, A. C., Riccelli, T. E., Podury, A., Maher, K., Farhang, A., & Goldberg, J. H. (2019) · Neuron · doi:10.1016/j.neuron.2019.04.038 · Cited by 51
A Revised Computational Neuroanatomy for Motor Control
Haar, S., & Donchin, O. (2020) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01602 · Cited by 50
Distinct functions for dopamine and serotonin in locomotor behaviour: Evidence using the 5-HT1 agonist RU 24969 in globus pallidus-lesioned rats
Oberlander, C., Blaquière, B., & Pujol, J. F. (1986) · Neuroscience Letters · doi:10.1016/0304-3940(86)90382-4 · Cited by 51
Dopaminergic Modulation of Appetitive and Aversive Predictive Learning
Iordanova, M. D. (2009) · Reviews in the Neurosciences · doi:10.1515/revneuro.2009.20.5-6.383 · Cited by 50
Orexin-A acts on the paraventricular nucleus of the midline thalamus to inhibit locomotor activity in rats
Li, Y., Li, S., Sui, N., & Kirouac, G. J. (2009) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2009.06.017 · Cited by 54
Limbic-motor integration by neural excitations and inhibitions in the nucleus accumbens
Morrison, S. E., McGinty, V. B., du Hoffmann, J., & Nicola, S. M. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00465.2017 · Cited by 49
The interrelationship of body mass index with gray matter volume and resting-state functional connectivity of the hypothalamus
Le, T. M., Liao, D., Ide, J. S., Zhang, S., Zhornitsky, S., Wang, W., & Li, C.-S. R. (2019) · International Journal of Obesity · doi:10.1038/s41366-019-0496-8 · Cited by 47
The contribution of the amygdala, nucleus accumbens, and prefrontal cortex to emotion and motivated behaviour
Cardinal, R. N., Parkinson, J. A., Hall, J., & Everitt, B. J. (2003) · International Congress Series · doi:10.1016/s0531-5131(03)01013-6 · Cited by 50
Behavioral genetic contributions to the study of addiction-related amphetamine effects
Phillips, T. J., Kamens, H. M., & Wheeler, J. M. (2007) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2007.10.008 · Cited by 51
Dopamine in the nucleus accumbens: cellular actions, drug- and behavior-associated fluctuations, and a possible role in an organism's adaptive activity
Kiyatkin, E. A. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00283-8 · Cited by 49
Dissociable roles of dopamine within the core and medial shell of the nucleus accumbens in memory for objects and place.
Nelson, A. J. D., Thur, K. E., Marsden, C. A., & Cassaday, H. J. (2010) · Behavioral Neuroscience · doi:10.1037/a0021114 · Cited by 50
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
Selective serotonin receptor stimulation of the medial nucleus accumbens causes differential effects on food intake and locomotion.
Pratt, W. E., Blackstone, K., Connolly, M. E., & Skelly, M. J. (2009) · Behavioral Neuroscience · doi:10.1037/a0016882 · Cited by 50
A comparative study of the effects of morphine in the dorsal periaqueductal gray and nucleus accumbens of rats submitted to the elevated plus-maze test
Anseloni, V. C. Z., Coimbra, N. C., Morato, S., & Brandão, M. L. (1999) · Experimental Brain Research · doi:10.1007/s002210050896 · Cited by 51
A Parasitoid Wasp Manipulates the Drive for Walking of Its Cockroach Prey
Gal, R., & Libersat, F. (2008) · Current Biology · doi:10.1016/j.cub.2008.04.076 · Cited by 49
Glutamatergic input from specific sources influences the nucleus accumbens-ventral pallidum information flow
Papp, E., Borhegyi, Z., Tomioka, R., Rockland, K. S., Módy, I., & Freund, T. F. (2011) · Brain Structure and Function · doi:10.1007/s00429-011-0331-z · Cited by 49
Dissociable Roles of the Medial Prefrontal Cortex and Nucleus Accumbens Core in Goal-Directed Actions for Differential Reward Magnitude
Gill, T. M., Castaneda, P. J., & Janak, P. H. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq036 · Cited by 48
1-Methyl-1,2,3,4-Tetrahydroisoquinoline, an Endogenous Amine with Unexpected Mechanism of Action: New Vistas of Therapeutic Application
Antkiewicz‐Michaluk, L., Wąsik, A., & Michaluk, J. (2013) · Neurotoxicity Research · doi:10.1007/s12640-013-9402-7 · Cited by 49
Effects of lesions to the glutamatergic afferents to the nucleus accumbens in the modulation of reactivity to spatial andnon-spatial novelty in mice
Sargolini, F., Roullet, P., Oliverio, A., & Mele, A. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00259-6 · Cited by 49
Nucleus accumbens dichotomically controls social dominance in male mice
Shan, Q., Hu, Y., Chen, S., & Tian, Y. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01220-1 · Cited by 50
The Neural Representation of Goal-Directed Actions and Outcomes in the Ventral Striatum's Olfactory Tubercle
Gadziola, M. A., & Wesson, D. W. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3328-15.2016 · Cited by 52
Do Dopaminergic Impairments Underlie Physical Inactivity in People with Obesity?
Kravitz, A. V., O’Neal, T. J., & Friend, D. M. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00514 · Cited by 48
Multimodal connectivity‐based parcellation reveals a shell‐core dichotomy of the human nucleus accumbens
Xia, X., Fan, L., Chen, C., Eickhoff, S. B., Chen, J., Li, H., & Jiang, T. (2017) · Human Brain Mapping · doi:10.1002/hbm.23636 · Cited by 48
Neural mechanisms of mental fatigue elicited by sustained auditory processing
Moore, T. M., Key, A. P. F., Thelen, A., & Hornsby, B. W. Y. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.10.025 · Cited by 51
Involvement of the nucleus accumbens-ventral pallidal pathway in postictal behavior induced by a hippocampal afterdischarge in rats
Ma, J., Brudzyński, S. M., & Leung, L.-W. S. (1996) · Brain Research · doi:10.1016/s0006-8993(96)00793-7 · Cited by 48
Antagonism at 5-HT2A receptors potentiates the effect of haloperidol in a conditioned avoidance response task in rats
Wadenberg, M.-L. G., Browning, J. L., Young, K. A., & Hicks, P. B. (2001) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(00)00483-4 · Cited by 48
Hysteria following brain injury.
Eames, P. (1992) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.55.11.1046 · Cited by 48
Behavioral activation in rats increases striatal dopamine metabolism measured by dialysis perfusion
Salamone, J. D., Keller, R. W., Zigmond, M. J., & Stricker, E. M. (1989) · Brain Research · doi:10.1016/0006-8993(89)90826-3 · Cited by 48
Excitatory actions of serotonin on GABAergic neurons of the medial septum and diagonal band of broca
Alreja, M. (1996) · Synapse · doi:10.1002/(sici)1098-2396(199601)22:1 · Cited by 67
Parenting Behavior
Lonstein, J. S., Pereira, M., Morrell, J. I., & Marler, C. A. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397175-3.00051-x · Cited by 46
Critical Role of Peripheral Vasoconstriction in Fatal Brain Hyperthermia Induced by MDMA (Ecstasy) under Conditions That Mimic Human Drug Use
Kiyatkin, E. A., Kim, A. H., Wakabayashi, K. T., Baumann, M. H., & Shaham, Y. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0506-14.2014 · Cited by 47
From anticipation to action, the role of dopamine in perceptual decision making: an fMRI-tyrosine depletion study
Nagano‐Saito, A., Cisek, P., Perna, A. S., Shirdel, F. Z., Benkelfat, C., Leyton, M., & Dagher, A. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00592.2011 · Cited by 49
[Decision making and the brain].
Sakagami, M. (2004) · PubMed · Cited by 46
Ventral Pallidum GABA Neurons Mediate Motivation Underlying Risky Choice
Farrell, M. R., Esteban, J. S. D., Faget, L. C., Floresco, S., Hnasko, T. S., & Mahler, S. V. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2039-20.2021 · Cited by 45
Dopamine D1 and D2 antagonists attenuate amphetamine-produced enhancement of responding for conditioned reward in rats
Ranaldi, R., & Beninger, R. J. (1993) · Psychopharmacology · doi:10.1007/bf02244342 · Cited by 47
Effects of repeated amphetamine injections on lateral hypothalamic brain stimulation reward and subsequent locomotion
Wise, R. A., & Munn, E. M. (1993) · Behavioural Brain Research · doi:10.1016/0166-4328(93)90115-7 · Cited by 47
Adolescents let sufficient evidence accumulate before making a decision when large incentives are at stake
Teslovich, T., Mulder, M., Franklin, N. T., Ruberry, E. J., Millner, A., Somerville, L. H., Simen, P., Durston, S., & Casey, B. J. (2014) · Developmental Science · doi:10.1111/desc.12092 · Cited by 45
Long-term, low-level adolescent nicotine exposure produces dose-dependent changes in cocaine sensitivity and reward in adult mice
Kelley, B. M., & Rowan, J. D. (2004) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2004.04.002 · Cited by 59
ΔFosB Enhances the Rewarding Effects of Cocaine While Reducing the Pro-Depressive Effects of the Kappa-Opioid Receptor Agonist U50488
Muschamp, J. W., Nemeth, C. L., Robison, A. J., Nestler, E. J., & Carlezon, W. A. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.08.011 · Cited by 50
Spatiotemporal dissociation of brain activity underlying threat and reward in social anxiety disorder
Richey, J. A., Ghane, M., Valdespino, A., Coffman, M. C., Strege, M. V., White, S. W., & Ollendick, T. H. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw149 · Cited by 52
Endocannabinoids in Body Weight Control
Horn, H., Böhme, B., Dietrich, L., & Koch, M. (2018) · Pharmaceuticals · doi:10.3390/ph11020055 · Cited by 49
Modulation of Feeding and Associated Behaviors by Lateral Hypothalamic Circuits
Qualls‐Creekmore, E., & Münzberg, H. (2018) · Endocrinology · doi:10.1210/en.2018-00449 · Cited by 45
Tics and Emotions
Leisman, G., & Sheldon, D. (2022) · Brain Sciences · doi:10.3390/brainsci12020242 · Cited by 50
Role of dopamine and GABA in the control of motor activity elicited from the rat nucleus accumbens
Wong, L. S., Eshel, G., Dreher, J. K., ONG, J. S. B., & Jackson, D. M. (1991) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(91)90250-6 · Cited by 46
Fluctuations in brain temperature during sexual interaction in male rats: an approach for evaluating neural activity underlying motivated behavior
Kiyatkin, E. A., & Mitchum, R. D. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00222-7 · Cited by 46
Ventral striatal plasticity and spatial memory
Ferretti, V., Roullet, P., Sargolini, F., Rinaldi, A., Perri, V., Fabbro, M. D., Costantini, V. J. A., Annese, V., Scesa, G., Stefano, M. E. D., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911757107 · Cited by 46
Loss of Cocaine Locomotor Response in Pitx3-Deficient Mice Lacking a Nigrostriatal Pathway
Beeler, J. A., Cao, Z. F. H., Kheirbek, M. A., & Zhuang, X. (2008) · Neuropsychopharmacology · doi:10.1038/npp.2008.117 · Cited by 45
Functional differences between macaque prefrontal cortex and caudate nucleus during eye movements with and without reward
Kobayashi, S., Kawagoe, R., Takikawa, Y., Koizumi, M., Sakagami, M., & Hikosaka, O. (2006) · Experimental Brain Research · doi:10.1007/s00221-006-0622-4 · Cited by 47
Severe brain hypothermia as a factor underlying behavioral immobility during cold-water forced swim
Taltavull, J., Chefer, V. I., Shippenberg, T. S., & Kiyatkin, E. A. (2003) · Brain Research · doi:10.1016/s0006-8993(03)02695-7 · Cited by 46
Mammals
Voogd, J., Nieuwenhuys, R., van Dongen, P. A. M., & ten Donkelaar, H. J. (1998) · Springer eBooks · doi:10.1007/978-3-642-18262-4_22 · Cited by 46
The neurosteroid pregnenolone sulphate increases dopamine release and the dopaminergic response to morphine in the rat nucleus accumbens
Barrot, M., Vallée, M., Gingras, M. A., Moal, M. L., Mayo, W., & Piazza, P. V. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00816.x · Cited by 46
Association between cognitive performance and striatal dopamine binding is higher in timing and motor tasks in patients with schizophrenia
Yang, Y. K., Yeh, T. L., Chiu, N.-T., Lee, I. H., Chen, P. S., Lee, L.-C., & Jeffries, K. J. (2004) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2003.07.002 · Cited by 46
Blockade of Enkephalinergic and GABAergic Mediated Locomotion in the Nucleus Accumbens by Muscimol in the Ventral Pallidum
Austin, M. C., & Kalivas, P. W. (1989) · The Japanese Journal of Pharmacology · doi:10.1254/jjp.50.487 · Cited by 46
Anticonvulsant effects of ipsilateral but not contralateral microinjections of the dopamine D2 agonist LY 171555 into the nucleus accumbens of amygdala-kindled rats
Wahnschaffe, U., & ̈scher, W. L. (1991) · Brain Research · doi:10.1016/0006-8993(91)90822-d · Cited by 46
Neurobiological correlates of masculine sexual behavior.
Mas, M. (1995) · Neuroscience and Biobehavioral Reviews · doi:10.1016/0149-7634(94)00059-a · Cited by 45
Activity of a direct VTA to ventral pallidum GABA pathway encodes unconditioned reward value and sustains motivation for reward
Zhou, W.-L., Kim, K., Ali, F., Pittenger, S. T., Calarco, C. A., Mineur, Y. S., Ramakrishnan, C., Deisseroth, K., Kwan, A. C., & Picciotto, M. R. (2022) · Science Advances · doi:10.1126/sciadv.abm5217 · Cited by 45
Cocaine self‐administration disrupts mesolimbic dopamine circuit function and attenuates dopaminergic responsiveness to cocaine
Siciliano, C. A., Ferris, M. J., & Jones, S. R. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12970 · Cited by 50
Opposing roles for striatonigral and striatopallidal neurons in dorsolateral striatum in consolidating new instrumental actions
Smith, A. C. W., Jonkman, S., DiFeliceantonio, A. G., O’Connor, R. M., Ghoshal, S., Romano, M. F., Everitt, B. J., & Kenny, P. J. (2021) · Nature Communications · doi:10.1038/s41467-021-25460-3 · Cited by 46
Dopamine D2 receptors modulate the cholinergic pause and inhibitory learning
Gallo, E. F., Greenwald, J. E., Yeisley, J., Teboul, E., Martyniuk, K. M., Villarin, J. M., Li, Y., Javitch, J. A., Balsam, P. D., & Kellendonk, C. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01364-y · Cited by 48
Behavioral Diversity and Neurochemical Plasticity: Selection of Stress Coping Strategies That Define Social Status
Korzan, W. J., & Summers, C. H. (2007) · Brain Behavior and Evolution · doi:10.1159/000105489 · Cited by 45
Emotional state affects gait initiation in individuals with Parkinson’s disease
Naugle, K. M., Hass, C. J., Bowers, D., & Janelle, C. M. (2011) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-011-0071-9 · Cited by 50
Cocaine's time action profile on regional cerebral blood flow in the rat
Stein, E. A., & Fuller, S. A. (1993) · Brain Research · doi:10.1016/0006-8993(93)90570-d · Cited by 45
L-type calcium channels modulate glutamate-driven bursting activity in the nucleus accumbens in vivo
Cooper, D., & White, F. J. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02868-7 · Cited by 45
Repeated pretreatment with amphetamine sensitizes increases in cortical acetylcholine release
Nelson, C. L., Sarter, M. F., & Bruno, J. P. (2000) · Psychopharmacology · doi:10.1007/s002130000494 · Cited by 45
The Initiation of Movements
Rolls, E. T. (1983) · Experimental brain research. Supplementum · doi:10.1007/978-3-642-68915-4_8 · Cited by 45
Neurotensin in the ventromedial mesencephalon of the rat: Anatomical and functional considerations
Kalivas, P. W. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902260405 · Cited by 45
Approach–withdrawal and the role of the striatum in the temperament of behavioral inhibition.
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Authors: MOGENSON, G., JONES, D., & YIM, C.
Affiliations: Western University (CA)
ORCID: JONES, D
Venue: Progress in Neurobiology
Publisher: Elsevier BV
Published: 1980
Volume: 14
Issue: 2-3
Pages: 69-97
ISSN: 0301-0082 (ISSN-L)
DOI: 10.1016/0301-0082(80)90018-0
OpenAlex: W2035590629
Cited by: 2,331
References: 115
Citations by year: 2026: 24 · 2025: 40 · 2024: 46 · 2023: 59 · 2022: 52 · 2021: 58 · 2020: 63 · 2019: 79 · 2018: 93 · 2017: 56 · 2016: 81 · 2015: 84 · 2014: 86 · 2013: 92 · 2012: 84
FWCI: 5.83
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Progress in Neurobiology (publishedVersion)
PubMed (publishedVersion)
Funders: Medical Research Council Canada
Natural Sciences and Engineering Research Council of Canada
Luonnontieteiden ja Tekniikan Tutkimuksen Toimikunta
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords: nucleus accumbens, ventral tegmental area, globus pallidus, motivation, action initiation, locomotion, feeding behavior, hypothalamus, limbic forebrain
MeSH terms: Animals, Behavior, Behavior, Animal, Brain, Brain Stem, Electrophysiology, Globus Pallidus, Humans, Hypothalamus, Limbic System, Models, Biological, Motivation, Motor Cortex, Movement, Nucleus Accumbens, Tegmentum Mesencephali

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