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Basal ganglia circuit loops, dopamine and motivation: A review and enquiry
Open accessAbstract
Dopamine neurons located in the midbrain play a role in motivation that regulates approach behavior (approach motivation). In addition, activation and inactivation of dopamine neurons regulate mood and induce reward and aversion, respectively. Accumulating evidence suggests that such motivational role of dopamine neurons is not limited to those located in the ventral tegmental area, but also in the substantia nigra. The present paper reviews previous rodent work concerning dopamine's role in approach motivation and the connectivity of dopamine neurons, and proposes two working models: One concerns the relationship between extracellular dopamine concentration and approach motivation. High, moderate and low concentrations of extracellular dopamine induce euphoric, seeking and aversive states, respectively. The other concerns circuit loops involving the cerebral cortex, basal ganglia, thalamus, epithalamus, and midbrain through which dopaminergic activity alters approach motivation. These models should help to generate hypothesis-driven research and provide insights for understanding altered states associated with drugs of abuse and affective disorders.
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“Intriguingly, the caudate nucleus receives projections from midbrain DA and is part of the nigrostriatal DA system, which, like the mesolimbic DA system, plays a role in reward and motivation (Ikemoto et al., 2015).”
From Convergence of oxytocin and dopamine signalling in neuronal circuits: Insights into the neurobiology of social interactions across species (2024) · cites this paper as Ikemoto et al., 2015
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A neural substrate of prediction and reward
Schultz, W., Dayan, P., & Montague, P. R. (1997) · Science · doi:10.1126/science.275.5306.1593 · Cited by 9,388 · cited 2×
“While phasic activity of DA neurons and thereby phasic DA release has been implicated in reinforcement learning [93–96], both phasic and tonic DA activity appear to be involved in motivational state.”
Parallel organization of functionally segregated circuits linking basal ganglia and cortex
Alexander, G. E., DeLong, M. R., & Strick, P. L. (1986) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.09.030186.002041 · Cited by 8,527
LeDoux, J. E. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.155 · Cited by 8,444 · cited 2×
“First of all, functional anatomical data suggest that the medial part of the DStr is more important than the lateral DStr in affective functions, because the medial, but not lateral, DStr receives inputs from the prefrontal cortex and amygdala, which are strongly implicated in affective functions [32,90–92].”
The functional anatomy of basal ganglia disorders
Albin, R. L., Young, A. B., & Penney, J. B. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90074-x · Cited by 5,353
Di Chiara, G., & Imperato, A. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.14.5274 · Cited by 4,733 · cited 2×
“Thus, administration of these drugs markedly increases extracellular DA concentrations in the striatum, especially the VStr [45].”
Predictive reward signal of dopamine neurons
Schultz, W. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.1.1 · Cited by 4,564
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 · cited 3×
“, the VStr nd DStr [2,84–86,144], which also receives topographicallyrganized inputs from the entire cerebral cortex (Fig.”
The reward circuit: linking primate anatomy and human imaging
Haber, S. N., & Knutson, B. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.129 · Cited by 3,718
Contributions of anterior cingulate cortex to behaviour
Devinsky, O., Morrell, M. J., & Vogt, B. A. (1995) · Brain · doi:10.1093/brain/118.1.279 · Cited by 3,377
Bardo, M. T., & Hammer, R. P. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90226-e · Cited by 3,229
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- Smith, 1998, Microcircuitry of the direct and indirect pathways of the basal ganglia, Neuroscience, 86, 353
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Items 101–200 of 225
Hu, S., Xu, C.-S., Wang, Y., Dong, T., Wu, H.-L., Wang, A.-Q., Li, C.-F., & Qiu, B. (2021) · Brain Imaging and Behavior · doi:10.1007/s11682-021-00485-w · Cited by 10
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Booher, W. C., Martínez, G. J. R., & Ehringer, M. A. (2020) · Genes Brain & Behavior · doi:10.1111/gbb.12632 · Cited by 10
“Dopamine signaling is widely used as a “marker” for measuring feelings of reward.(27) One approach to measuring mes-”
MethodSalinas-Velarde, I. D., Bernal‐Morales, B., Pacheco, P., Sánchez-Aparicio, P., Pascual-Mathey, L. I., & Venebra-Muñoz, A. (2021) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2021.10.001 · Cited by 10
de Lima, B. F. C., Ramos, D. C., Barbiero, J. K., Pulido, L. N., Redgrave, P., Robinson, D. L., Gómez‐A, A., & Cunha, C. D. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.02.052 · Cited by 10
“A similar finding was reported previously by Schwarting and Huston (1996) and is likely due to impairment in approach behavior (Ikemoto et al., 2015) rather than to reduction in hedonic ‘‘liking” (Berridge and Kringelbach, 2015).”
ResultNucleus accumbens pathways control cell-specific gene expression in the medial prefrontal cortex
Hikida, T., Yao, S., Macpherson, T., Fukakusa, A., Morita, M., Kimura, H., Hirai, K., Ando, T., Toyoshiba, H., & Sawa, A. (2020) · Scientific Reports · doi:10.1038/s41598-020-58711-2 · Cited by 10
Xu, H., Das, S., Sturgill, M. G., Hodgkinson, C. A., Yuan, Q., Goldman, D. A., & Grasing, K. (2017) · Psychopharmacology · doi:10.1007/s00213-017-4640-7 · Cited by 10
“The neurotransmitter dopamine plays a key role as a mediator of drug reward (Ikemoto et al. 2015).”
BackgroundZhang, T., Nishitani, N., Niitani, K., Nishida, R., Futami, Y., Deyama, S., & Kaneda, K. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.113981 · Cited by 9
Milanesi, L. H., Rossato, D. R., da Rosa, J. L. O., D’avila, L. F., Metz, V. G., Rampelotto, C. R., Pereira, V. G., Schaffazick, S. R., da Silva, C. D. B., & Bürger, M. E. (2023) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-023-02420-w · Cited by 9
“At molecular level, addiction development and drug reinstatement modify different brain areas, evoking neuroadaptive and neurochemical mechanisms to dysregulate the reward system (Ikemoto et al. 2015).”
BackgroundKanarik, M., & Harro, J. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.08.049 · Cited by 9
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Acevedo, B. P., Poulin, M. J., Geher, G., Grafton, S. T., & Brown, L. L. (2019) · Brain and Behavior · doi:10.1002/brb3.1289 · Cited by 11
Nazari-Serenjeh, F., Jamali, S., Rezaee, L., Zarrabian, S., & Haghparast, A. (2020) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000546 · Cited by 9
“Development of addiction impresses different brain areas and changes different neuroadaptive and neurochemical mechanisms to dysregulate the reward system (Ikemoto et al., 2015).”
BackgroundDysfunction of the Lenticular Nucleus Is Associated with Dystonia in Wilson’s Disease
Yang, Y., Wei, T., Yang, W., Hu, S., Jiang, H., Dong, W., Hao, W., Yang, Y., Qian, N., & Ding, Y. (2022) · Brain Sciences · doi:10.3390/brainsci13010007 · Cited by 9
“The MCC, part of the cingulate cortex, projects into the striatum and is involved in decision-making, emotion and motivation [6,42].”
BackgroundPsychosocial Modulators of Motor Learning in Parkinson’s Disease
Zemánková, P., Lungu, O., & Bareš, M. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00074 · Cited by 10
“…from the environment (Hultsch et al., 1999; Vance et al., 2010), it is conceivable that practicing or learning motor sequences in a rich and stimulating context may increase the effectiveness of non-pharmacological interventions aimed to preserve or restore motor function in Parkinson’s.”
BackgroundSilkstone, M., & Brudzyński, S. M. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.01.044 · Cited by 11
Overwalle, F. V., Heleven, E., Haihambo, N. P., Li, M., Ma, Q., Pu, M., Baeken, C., Deroost, N., & Baetens, K. (2024) · Human Brain Mapping · doi:10.1002/hbm.70098 · Cited by 9
Zaher, A., Leonards, J., Reif, A., & Grimm, O. (2025) · Scientific Reports · doi:10.1038/s41598-025-96780-3 · Cited by 8
“…patterns between the NAc, the DMN and the SN, potentially reflects the differential involvement of direct and indirect basal ganglia pathways 65,66 , which might explain how dopamine modulation affects these large-scale networks in ADHD further underlying neurobiological processes of our FC…”
Burks, S. M., Bowyer, J. F., Walters, J. L., & Talpos, J. C. (2020) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2020.106890 · Cited by 8
Chan, Y. E., Chen, M., Bai, Y., Li, C., Chen, T., & Su, T. (2021) · Journal of Affective Disorders · doi:10.1016/j.jad.2021.01.056 · Cited by 8
Demin, D. B., & Poskotinova, L. V. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph19052759 · Cited by 8
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Kislov, A., Шестакова, А. Н., Ushakov, V., Martinez‐Saito, M., Beliaeva, V., Savelo, O., Vasilchuk, A., & Klucharev, V. A. (2023) · PLoS ONE · doi:10.1371/journal.pone.0286648 · Cited by 8
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BackgroundSamancı, B., Tan, S. K. H., Michielse, S., Kuijf, M. L., & Temel, Y. (2024) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2024.102392 · Cited by 10
c‐Fos marking of identified midbrain neurons coactive after nicotine administration in‐vivo
Baur, K., Hach, A., Bernardi, R. E., Spanagel, R., Bading, H., & Bengtson, C. P. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24471 · Cited by 9
Balcıoğlu, Y. H., Doğan, M., Kaya, İ. İ., et al. (2020) · Journal of Forensic Sciences · doi:10.1111/1556-4029.14477 · Cited by 7
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BackgroundBayesian predictive coding hypothesis: Brain as observer’s key role in insight
Dutta, A. (2024) · Medical Hypotheses · doi:10.1016/j.mehy.2024.111546 · Cited by 9
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Bronner, G., & Gurevich, T. (2022) · Cambridge University Press eBooks · doi:10.1017/9781009039291.015 · Cited by 6
Zhang, D., Chen, J., Chen, X., et al. (2023) · Journal of Electroanalytical Chemistry · doi:10.1016/j.jelechem.2023.117752 · Cited by 6
Rizkita, A. D., Dewi, S. A., Fakih, T. M., & Lee, C. (2024) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2024.2305315 · Cited by 8
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Zhou, F.-M., Li, L., Yue, J., & Dani, J. A. (2016) · Frontiers in Biology · doi:10.1007/s11515-016-1429-8 · Cited by 6
“, 2014), habit learning and formation (Graybiel and Grafton, 2015), and emotional and motivational regulation (Haber and Knutson, 2010; Sesack and Grace, 2010; Lobo et al., 2013, Révy et al., 2014; Francis et al., 2015; Ikemoto et al., 2015).”
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Grillo, L. (2018) · Schizophrenia Research and Treatment · doi:10.1155/2018/5917475 · Cited by 4
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BackgroundShibuya, T., Nakane, T., Takano, A., Yamauchi, J., & Morimoto, T. (2020) · Phytomedicine Plus · doi:10.1016/j.phyplu.2020.100007 · Cited by 6
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Pamplona, G. S. P., Zweerings, J., Lor, C. S., deErney, L., Roecher, E., Taebi, A., Hellrung, L., Amano, K., Scheinost, D., Krause, F., et al. (2025) · Human Brain Mapping · doi:10.1002/hbm.70279 · Cited by 10
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Wang, L., Wei, L., Jin, L. H., Li, Y., Wei, Y., He, W., Shi, L. M., Sun, Q., Li, W., Li, Q., et al. (2022) · American Journal of Neuroradiology · doi:10.3174/ajnr.a7707 · Cited by 5
“The DA reward circuit consists of 3 pathways: the nigrostriatal pathway, along which the substantia nigra (SN) sends a dopaminergic projection to the dorsal striatum; the mesolimbic pathway, where the ventral tegmental area (VTA) sends a similar type of dopaminergic projection to the nucleus accumbens (NAc); and the m…”
BackgroundResultMedina, A. C., Kabani, A. A., Reyes-Vasquez, C., & Dafny, N. (2022) · Journal of Neural Transmission · doi:10.1007/s00702-022-02526-0 · Cited by 5
Morelli, N., & Hoch, M. C. (2020) · Perceptual and Motor Skills · doi:10.1177/0031512520930868 · Cited by 6
“Multiple theories and computational models have attempted to explain how neural circuits within the central nervous system (CNS) acquire highly skilled and contextually specific motor movements (Caligiore et al., 2017; D’Angelo et al., 2016; Galea et al., 2015; Ikemoto et al., 2015; Packard & Knowlton, 2002).”
BackgroundVentral striatum links motivational and motor networks during operant-conditioned movement in rats
Hori, Y., Ihara, N., Sugai, C., Ogura, J., Honda, M., Kato, K., Isomura, Y., & Hanakawa, T. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.10.018 · Cited by 5
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Kamada, T., & Hata, T. (2020) · Learning & Memory · doi:10.1101/lm.052266.120 · Cited by 5
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Spark, D. L., Ma, S., Nowell, C. J., Langmead, C. J., Stewart, G. D., & Nithianantharajah, J. (2023) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2023.05.003 · Cited by 4
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BackgroundRodriguez‐Sabate, C., Moráles, I., Puertas‐Avendaño, R., & Rodrı́guez, M. (2019) · Brain Communications · doi:10.1093/braincomms/fcz044 · Cited by 4
Mulvihill, K. G., & Brudzyński, S. M. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146505 · Cited by 4
Rilling, J. K., Lee, M., Zhou, C., Jung, E., Arrant, E. J., Wu, S., Cooper, J. A., Davenport-Nicholson, A., & Treadway, M. T. (2025) · Journal of Neuroendocrinology · doi:10.1111/jne.70127 · Cited by 3
“17 In human males, although multiple studies have reported changes in regional cortical volume across the transition to fatherhood, 18 – 21 only one study has longitudinally examined changes in brain function.”
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Zhao, Q., Milecki, L., Kuceyeski, A. F., Grosenick, L., Brumback, T., Adolf Pfefferbaum, A., Sullivan, E. V., & Pohl, K. M. (2025) · JAMA Network Open · doi:10.1001/jamanetworkopen.2025.31378 · Cited by 6
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Laurentino, S. G., & Sougey, É. B. (2020) · Open Journal of Psychiatry · doi:10.4236/ojpsych.2020.104015 · Cited by 3
“Once GPi is inhibited, it won’t send inhibitory GABAergic projections to mediodorsal thalamus, which, in turn, becomes disinhibited and increases excitatory predictions back to the DLPC closing the disinhibitory looping [18] [19] [23] [31] [35] [39] [58] [59].”
BackgroundGpr88 Deletion Impacts Motivational Control Without Overt Disruptions to Striatal Dopamine
Spark, D. L., Vermeulen, M. H., Gonzalez, R. D. L. F., Hatzipantelis, C. J., Rueda, P., Sepehrizadeh, T., de Veer, M., la Cour, C. M., Fornito, A., Langiu, M., et al. (2022) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2022.10.008 · Cited by 3
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BackgroundLuο, X., Lin, X., Ide, J. S., Luo, X., Zhang, Y., Xu, J., Wang, L., Chen, Y. S., Cheng, W., Zheng, J., et al. (2023) · Child and Adolescent Psychiatry and Mental Health · doi:10.1186/s13034-022-00536-0 · Cited by 3
“The limbic loops involve projections to the limbic subregions of the BG (nucleus accumbens and ventral pallidum) from the ventral ACC, hippocampus, and insula [51], and play a central role in reward learning, emotion, attention and saliency processing.”
BackgroundA significant, functional and replicable risk KTN1 variant block for schizophrenia
Mao, Q., Lin, X., Yin, Q., Liu, P., Zhang, Y., Qu, S., Xu, J., Cheng, W., Luo, X., Kang, L., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-27448-z · Cited by 3
Sub-second and multi-second dopamine dynamics underlie variability in human time perception
Sadibolova, R., DiMarco, E. K., Jiang, A., Maas, B., Tatter, S. B., Laxton, A. W., Kishida, K. T., & Terhune, D. B. (2026) · Brain · doi:10.1093/brain/awag336 · Cited by 5
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Cai, Z.-J. (2021) · OALib · doi:10.4236/oalib.1107603 · Cited by 3
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Vasconcellos, L. F., Tiel, C., Sudo, F. K., et al. (2016) · Dementia & Neuropsychologia · doi:10.1590/s1980-5764-2016dn1004019 · Cited by 3
“1,8 This is consistent with the preserved orientation and adequate performance on the calculation task (depicted in Table).”
BackgroundBelliveau, S., Kang, W., Bovaird, S., Hamadjida, A., Bédard, D., Dancause, N., Stroh, T., & Huot, P. (2020) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2020.101881 · Cited by 3
Chen, Y., Hu, Y., Talishinsky, A., Potter, C. T., Ramsey, L. A., Kesner, A. J., Don, R. F., Junn, S., Tan, A., Pierce, A. F., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.19.104026 · Cited by 3
Lewis, A. F., Bohnenkamp, R., Myers, M., den Ouden, D., Fritz, S. L., & Stewart, J. C. (2024) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2024.107930 · Cited by 4
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Hu, S., Wei, T., Li, C., Wang, X., Nguchu, B. A., Wang, Y., Dong, T., Yang, Y., Ding, Y., Qiu, B., et al. (2024) · NeuroImage Clinical · doi:10.1016/j.nicl.2024.103618 · Cited by 2
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BackgroundBiphasic Model of Addiction: Neurobehavioral Adaptations
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“Centred in the basal ganglia, the system facilitates learning about reinforcing stimuli and experiences [ 25].”
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Sayegh, F. J. P., & Bonnavion, P. (2025) · npj Biological Timing and Sleep · doi:10.1038/s44323-025-00059-9 · Cited by 2
“While positive reinforcement involves learning the relationship between environmental cues and outcomes, reward also encompasses the arousal and motivational drive that enhance attentional engagement with salient stimuli 18,19 .”
Treviranus, G. R. S. (2017) · Universal Journal of Psychology · doi:10.13189/ujp.2017.050203 · Cited by 1
“Classically triadic instead is the influential associative, sensori-motor, and limbic tripartite division [59], albeit some”
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Jha, S., & Tiwari, M. (2023) · Indian Journal of Psychological Medicine · doi:10.1177/02537176231201559 · Cited by 2
Fadhilah, M. R., Andriyanti, E., & Putera, A. R. (2023) · International Journal of Education and Digital Learning (IJEDL) · doi:10.47353/ijedl.v1i5.30 · Cited by 3
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BackgroundTreviranus, G. R. S. (2017) · Universal Journal of Psychology · doi:10.13189/ujp.2017.050202 · Cited by 2
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Asl, A. R., Issazadegan, A., Amirani, M. C., & Bagherzadeh, J. (2018) · The Neuroscience Journal of Shefaye Khatam · doi:10.29252/shefa.6.2.1 · Cited by 2
Negrelli, B., Pochapski, J. A., Villas-Boas, C. A., Jessen, L. F., Teixeira, M. A. L., & Cunha, C. D. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.112858 · Cited by 2
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Whelan, M. T., Vasilaki, E., & Prescott, T. J. (2019) · Lecture notes in computer science · doi:10.1007/978-3-030-24741-6_24 · Cited by 2
Anokhin, P. K., Razumkina, E. V., & Shamakina, I. Y. (2019) · Neurochemical Journal · doi:10.1134/s1819712419010033 · Cited by 2
Wei, C., Zhang, F., Chen, L., Ma, X., Zhang, N., & Hao, J. (2018) · Journal of Neurology · doi:10.1007/s00415-018-8745-7 · Cited by 2
RetractedJoint Attention, Learning and Social-Cognitive Development
Mundy, P. C. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.23601-8 · Cited by 2
Elfouly, M. A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.08.647898 · Cited by 2
Dafny, N., Claussen, C. M., Frazier, E., & Liu, Y. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25115938 · Cited by 1
Du, C., Wang, J., Tan, H., Han, N., Li, X., Sun, B., Zhang, G., & Chang, M. (2024) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2024.111122 · Cited by 1
Alexis, E.-A. C., Janeth, M.-Z., Daniel, R.-M. J., Garcı́a-Ramı́rez, M., & Chuc-Meza, E. (2025) · Brain Research · doi:10.1016/j.brainres.2025.149495 · Cited by 1
Pragmatic representations of self- and others’ action in the monkey putamen
Rotunno, C., Reni, M., Ferroni, C. G., Ismaiel, E., Ballestrazzi, G., Borra, E., Maranesi, M., & Bonini, L. (2026) · Nature Communications · doi:10.1038/s41467-026-68403-6 · Cited by 1
Prasad, S., Deelchand, D. K., Kumar, M., Yadav, R., Pal, P. K., & Saini, J. S. (2026) · npj Parkinson s Disease · doi:10.1038/s41531-026-01405-9 · Cited by 1
“Non-dopaminergic systems interact with GABAergic and dopaminergic pathways to create a complex excitatory-inhibitory balance that is likely to form the basis for the diverse symptom pro fi le observed in PD 18 .”
Pittenger, S. T. (2016) · Lincoln (University of Nebraska) · Cited by 1
IN PURSUIT OF A FUNCTIONAL PERSONALITY MODEL
Roxby, J., Chaundhry, N., Nolan, J., Fletcher, T. R., & Omelchenko-Comer, N. (2017) · Proceedings of the West Virginia Academy of Science · doi:10.55632/pwvas.v89i2.143 · Cited by 1
Mood Disorders in Parkinson’s Disease
Tsai, P., & Gopalakrishna, G. (2022) · Cambridge University Press eBooks · doi:10.1017/9781009039291.010 · Cited by 1
Pu, J., Wang, J., Yao, C., Kuai, C., Pan, M., & Xue, S. (2025) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2025.05.021 · Cited by 2
Category Learning as a Cognitive Foundation of Language Evolution
Zhang, E. Q., Shi, E. R., & Pleyer, M. (2025) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.70007 · Cited by 2
Reward Network Activations of Win Versus Loss in a Monetary Gambling Task
Kamarajan, C., Ardekani, B. A., Pandey, A. K., Pandey, G., Kinreich, S., Kuang, W., Meyers, J. L., & Porjesz, B. (2025) · Behavioral Sciences · doi:10.3390/bs15080994 · Cited by 1
Boron‐Doped Nano‐Crystalline Coated Carbon Fibers for Phasic Dopamine Sensing
Higham, S. J., Cabrera, J. M. R., Kwak, Y., et al. (2025) · Advanced Healthcare Materials · doi:10.1002/adhm.202503945 · Cited by 1
Deneysel Hayvan Çalışmalarında Robot Kullanımı
Nas, O., & Ünal, G. (2021) · Nesne Psikoloji Dergisi · doi:10.7816/nesne-09-19-14 · Cited by 1
Beckes, L., Medina-DeVilliers, S., Gunderson, E. W., & Coan, J. A. (2022) · Psychophysiology · doi:10.1111/psyp.14076 · Cited by 1
Winkelmeier, L., Filosa, C., Scheller, M. F., Hartig, R., Sack, M., Becker, R., Wolf, D., Reinwald, J., Gerchen, M. F., Sartorius, A., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.22.432268 · Cited by 1
“In line with anatomical input gradients from sensory and reward regions (Ikemoto et al., 2015), posterior parts of the Tu correlated with the reward component of the PE at US.”
BackgroundLayer-dependent activity in the human superior colliculus during working memoryPreprint
Chen, D., Kragel, P. A., Wager, T. D., Wald, L. L., Bianciardi, M., Satpute, A. B., Quigley, K. S., Barrett, L. F., Katsumi, Y., & Theriault, J. E. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.06.518975 · Cited by 2
“These regions have also been found to be functionally important for vision-related processing, visceromotor regulation, and working memory (e.g., Aston-Jones et al., 1996; Davern, 2014; Grieve et al., 2000; Ikemoto et al., 2015; Kragel et al., 2019; Öngür & Price, 2000; Sherman & Koch, 1986; Sotres-Bayón et al., 2001).”
BackgroundCategorical Learning and the Cognitive Foundations of Language Evolution and DevelopmentPreprint
Zhang, E. Q., Shi, E. R., & Pleyer, M. (2023) · doi:10.31234/osf.io/nkzrp · Cited by 1
Hovik, K. T. (2016) · NORA - Norwegian Open Research Archives
Executive Control and Emerging Behavior in Youth With Tourette’s Syndrome
Hovik, K. T. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803676-1.00014-3 · Cited by 1
Klüver–Bucy Syndrome Induced by Bilateral Basal Ganglion Lesion
Huang, Y. J., & Liu, H. C. (2017) · Neuropsychiatry · doi:10.4172/neuropsychiatry.1000282
Efficacy of Rhythmic Acquisition on Gait Performance Among Individuals with Parkinson’s Disease
Kogutek, D. (2018) · Scholarship@Western (Western University)
Role of Tissue Plasminogen Activator in Central Nervous System Physiology and Pathology
Stevenson, T. K. (2018) · Deep Blue (University of Michigan)
Treviranus, G. R. S. (2018) · PubMed
Intimacy, parkinson’s disease and dementia in the time of the coronavirus
Gila, B., Gurevich, T., & Korczyn, A. D. (2020) · Archive of Gerontology and Geriatrics Research · doi:10.17352/aggr.000022
“Decreased dopamine activity induces dysphoria and decreased motivation for sexual response [4].”
Rehabilitative Movement Approaches and Dance Interventions in Parkinson’s Disease
Fontanesi, C. (2020) · CUNY Academic Works (City University of New York)
Schwerz, J. P. (2020) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.47.2020.tde-08022021-150207
Călinescu, P.-M. (2021) · Bulletin of Integrative Psychiatry · doi:10.36219/bpi.2021.1.02
Wang, L., Wei, L., Jin, L. H., Li, Y., Wei, Y., He, W., Shi, L., Sun, Q., Li, W., Li, Q., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-842940/v1
Exploring the in vivo subthreshold membrane activity of phasic firing in midbrain dopamine neurons
Otomo, K. (2021) · Publication Server of Goethe University Frankfurt am Main (Goethe University Frankfurt) · doi:10.21248/gups.61388
Gpr88 deletion impacts motivational control independently of striatal dopamine functionPreprint
Spark, D. L., Vermeulen, M. H., Rueda, P., Gonzalez, R. D. L. F., Sepehrizadeh, T., de Veer, M., la Cour, C. M., Fornito, A., Langiu, M., Stewart, G. D., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.19.492565
“These pathways are embedded in broader cortico-striatal-thalamo-cortical loops that regulate a range of behaviours, including motivation (24,25).”
BackgroundAlhassen, W., Alhassen, S., Chen, J., Monfared, R. V., & Alachkar, A. (2022) · Research Square · doi:10.21203/rs.3.rs-1804396/v1
Grillo, L. (2022) · Scandinavian Journal of Child and Adolescent Psychiatry and Psychology · doi:10.2478/sjcapp-2022-0011
“The dopamine released in the nucleus accumbens is the basis for producing pleasure (44, 45), so that stress can cause anhedonia by reducing”
BackgroundFerreira, J. V., Chaves, G. A., Batista, M. A., Correia, L. C., de Souza, L. R., da Costa, D. C., Barcelos, M. P., da Silva, C. H. T. D. P., Taft, C. A., & Hage-Melim, L. I. D. S. (2022) · Engineering materials · doi:10.1007/978-3-031-07622-0_16
Metadata
- Authors
- Ikemoto, S., Yang, C., & Tan, A.
- Affiliations
- National Institutes of Health (US)
- Corresponding author
- Ikemoto, Satoshi
- Venue
- Behavioural Brain Research
- Publisher
- Elsevier BV
- Published
- 2015-09
- Volume
- 290
- Pages
- 17-31
- ISSN
- 0166-4328 (ISSN-L)
- PMC
- PMC4447603
- OpenAlex
- W2081845928
- Semantic Scholar
- bb06782b6fb20361735cf21f960fea754adbcf67
- Cited by
- 226
- References
- 255
- Citations by year
- 2026: 12 · 2025: 16 · 2024: 14 · 2023: 15 · 2022: 21 · 2021: 25 · 2020: 29 · 2019: 22 · 2018: 22 · 2017: 21 · 2016: 26 · 2015: 3
- FWCI
- 2.85
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Behavioural Brain Research (publishedVersion, cc-by)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute on Drug Abuse (ZIADA000575, ZIADA000439, ZIADA000550)
- 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 › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- dopamine, approach motivation, substantia nigra, ventral tegmental area, reward, aversion, thalamus, epithalamus, drugs of abuse, mood disorders
- MeSH terms
- Animals, Basal Ganglia, Motivation, Nerve Net, Reward, Dopaminergic Neurons
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