The DOI matches its Crossref record; 56 of the 56 references it cites were found in a registry or an index.
Controls of Tonic and Phasic Dopamine Transmission in the Dorsal and Ventral Striatum
Open accessAbstract
Dopamine (DA) release varies within subregions and local environments of the striatum, suggesting that controls intrinsic and extrinsic to the DA fibers and terminals regulate release. While applying fast-scan cyclic voltammetry and using tonic and phasic stimulus trains, we investigated the regulation of DA release in the dorsolateral to ventral striatum. The ratio of phasic-to-tonic-evoked DA signals varied with the average ongoing firing frequency, and the ratio was generally higher in the nucleus accumbens (NAc) compared with the dorsolateral striatum. At the normal average firing frequency, burst stimulation produces a larger increase in the DA response in the NAc than the dorsolateral striatum. This finding was comparable whether the DA measurements were made using in vitro brain slices or were recorded in vivo from freely moving rodents. Blockade of the dopamine transporters and dopamine D(2) receptors particularly enhanced the tonic DA signals. Conversely, blockade of nicotinic acetylcholine receptors (nAChRs) containing the beta(2) subunit (beta(2)(*)) predominantly suppressed tonic DA signals. The suppression of tonic DA release increased the contrast between phasic and tonic DA signals, and that made the frequency-dependent DA dynamics between the dorsolateral striatum and NAc more similar. The results indicate that intrinsic differences in the DA fibers that innervate specific regions of the striatum combine with (at least) DA transporters, DA receptors, and nAChRs to regulate the frequency dependence of DA release. A combination of mechanisms provides specific local control of DA release that underlies pathway-specific information associated with motor and reward-related functions.
Overview
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
Cites
Statistics
Verification
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?
In the citing paper
“The present study and others indicate that blockade of β2* nAChRs caused less inhibition of phasic DA signals than tonic signals (12).”
From Withdrawal from Chronic Nicotine Exposure Alters Dopamine Signaling Dynamics in the Nucleus Accumbens (2012) · cites this paper as [12]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
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
Grace, A. A. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90196-u · Cited by 1,831
Multiple dopamine functions at different time courses
Schultz, W. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135722 · Cited by 1,415
Floresco, S. B., West, A. R., Ash, B., Moore, H., & Grace, A. A. (2003) · Nature Neuroscience · doi:10.1038/nn1103 · Cited by 1,106
Effects of nicotine on the nucleus accumbens and similarity to those of addictive drugs.
Pontieri, F. E., Tanda, G., Orzi, F., & Chiara, G. D. (1996) · Nature · doi:10.1038/382255a0 · Cited by 1,073
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
Unique properties of mesoprefrontal neurons within a dual mesocorticolimbic dopamine system
Lammel, S., Hetzel, A., Häckel, O., Jones, I., Liss, B., & Roeper, J. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.022 · Cited by 976
Dopamine and drug addiction: the nucleus accumbens shell connection
Di Chiara, G., Bassareo, V., Fenu, S., De Luca, M. A., Spina, L., Cadoni, C., Acquas, E., Carboni, E., Valentini, V., & Lecca, D. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.06.032 · Cited by 935
The control of firing pattern in nigral dopamine neurons: single spike firing
Grace, A., & Bunney, B. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-11-02866.1984 · Cited by 862
Gonon, F. G. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90307-7 · Cited by 676
Cited by
Sorted by citations
Dopamine in motivational control: rewarding, aversive, and alerting
Bromberg-Martin, E. S., Matsumoto, M., & Hikosaka, O. (2010) · Neuron · doi:10.1016/j.neuron.2010.11.022 · Cited by 2,396
Understanding dopamine and reinforcement learning: the dopamine reward prediction error hypothesis
Glimcher, P. W. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1014269108 · Cited by 955
Reward, addiction, withdrawal to nicotine
De Biasi, M., & Dani, J. A. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113734 · Cited by 366
Dopamine neurons share common response function for reward prediction error
Eshel, N., Tian, J., Bukwich, M., & Uchida, N. (2016) · Nature Neuroscience · doi:10.1038/nn.4239 · Cited by 321
Sufficiency of Mesolimbic Dopamine Neuron Stimulation for the Progression to Addiction
Pascoli, V., Terrier, J. E., Hiver, A., & Lüscher, C. (2015) · Neuron · doi:10.1016/j.neuron.2015.10.017 · Cited by 317
Dopamine modulates novelty seeking behavior during decision making.
Costa, V. D., Tran, V. L., Turchi, J., & Averbeck, B. B. (2014) · Behavioral Neuroscience · doi:10.1037/a0037128 · Cited by 263
“DAT inhibition with GBR-12909 is known to increase tonic dopamine levels in the striatum by slowing reuptake (Zhang et al., 2009).”
BackgroundWilluhn, I., Burgeno, L. M., Everitt, B. J., & Phillips, P. E. M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1213460109 · Cited by 241
Dual Control of Dopamine Synthesis and Release by Presynaptic and Postsynaptic Dopamine D2 Receptors
Anzalone, A., Lizardi-Ortiz, J. E., Ramos, M., Mei, C. D., Hopf, F. W., Iaccarino, C., Halbout, B., Jacobsen, J. P. R., Kinoshita, C., Welter, M., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0918-12.2012 · Cited by 198
α6β2* and α4β2* Nicotinic Acetylcholine Receptors As Drug Targets for Parkinson’s Disease
Quik, M., & Wonnacott, S. (2011) · Pharmacological Reviews · doi:10.1124/pr.110.003269 · Cited by 201
Endocannabinoid modulation of dopamine neurotransmission
Covey, D. P., Mateo, Y., Sulzer, D., Cheer, J. F., & Lovinger, D. M. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.04.033 · Cited by 197
Brown, H. D., McCutcheon, J. E., Cone, J. J., Ragozzino, M. E., & Roitman, M. F. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07914.x · Cited by 179
Gonzales, K. K., & Smith, Y. (2015) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12762 · Cited by 175
Dopaminergic Modulation of Cortical Plasticity in Alzheimer’s Disease Patients
Koch, G., Lorenzo, F. D., Bonnı̀, S., Giacobbe, V., Bozzali, M., Caltagirone, C., & Martorana, A. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.119 · Cited by 157
Dopamine and addiction: what have we learned from 40 years of research
Solinas, M., Belujon, P., Fernagut, P., Jaber, M., & Thiriet, N. (2018) · Journal of Neural Transmission · doi:10.1007/s00702-018-1957-2 · Cited by 163
Zhang, L., Dong, Y., Doyon, W. M., & Dani, J. A. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.07.024 · Cited by 135
Xiao, C., Zhou, C., Jiang, J., & Cui, Y. (2019) · Acta Pharmacologica Sinica · doi:10.1038/s41401-019-0299-4 · Cited by 124
Dopaminergic Reward Signals Selectively Decrease fMRI Activity in Primate Visual Cortex
Arsenault, J. T., Nelissen, K., Jarraya, B., & Vanduffel, W. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.008 · Cited by 122
Caligiore, D., Mannella, F., Arbib, M. A., & Baldassarre, G. (2017) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005395 · Cited by 115
Nucleus Accumbens Cholinergic Interneurons Oppose Cue-Motivated Behavior
Collins, A. L., Aitken, T. J., Huang, I.-W., Shieh, C., Greenfield, V. Y., Monbouquette, H. G., Ostlund, S. B., & Wassum, K. M. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.02.014 · Cited by 110
Dopaminergic and cholinergic learning mechanisms in nicotine addiction
Subramaniyan, M., & Dani, J. A. (2015) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12871 · Cited by 110
Delays Conferred by Escalating Costs Modulate Dopamine Release to Rewards But Not Their Predictors
Wanat, M. J., Kuhnen, C. M., & Phillips, P. E. M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2691-10.2010 · Cited by 100
Nucleus Accumbens Acetylcholine Receptors Modulate Dopamine and Motivation
Collins, A. L., Aitken, T. J., Greenfield, V. Y., Ostlund, S. B., & Wassum, K. M. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.81 · Cited by 97
Heterogeneity in striatal dopamine circuits: Form and function in dynamic reward seeking
Collins, A. L., & Saunders, B. T. (2020) · Journal of Neuroscience Research · doi:10.1002/jnr.24587 · Cited by 93
Martorana, A., Lorenzo, F. D., Esposito, Z., Giudice, T. L., Bernardi, G., Caltagirone, C., & Koch, G. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.07.015 · Cited by 95
Ostlund, S. B., Wassum, K. M., Murphy, N. P., Balleine, B. W., & Maidment, N. T. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4759-10.2011 · Cited by 94
Dopamine and opioid systems interact within the nucleus accumbens to maintain monogamous pair bonds
Resendez, S. L., Keyes, P. C., Day, J. J., Hambro, C., Austin, C. J., Maina, F. K., Eidson, L. N., Porter-Stransky, K. A., Nevárez, N., McLean, J. W., et al. (2016) · eLife · doi:10.7554/elife.15325 · Cited by 88
Nicotinic Receptors in Addiction Pathways
Leslie, F. M., Mojica, C., & Reynaga, D. D. (2012) · Molecular Pharmacology · doi:10.1124/mol.112.083659 · Cited by 92
Chuhma, N., Choi, W., Mingote, S., & Rayport, S. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.08.057 · Cited by 85
Brimblecombe, K. R., Threlfell, S., Dautan, D., Kosillo, P., Mena‐Segovia, J., & Cragg, S. J. (2018) · eNeuro · doi:10.1523/eneuro.0397-17.2018 · Cited by 84
Motor learning and metaplasticity in striatal neurons: relevance for Parkinson’s disease
Giordano, N., Iemolo, A., Mancini, M., Cacace, F., Risi, M. D., Latagliata, E. C., Ghiglieri, V., Bellenchi, G. C., Puglisi‐Allegra, S., Calabresi, P., et al. (2017) · Brain · doi:10.1093/brain/awx351 · Cited by 78
GABA B modulation of dopamine release in the nucleus accumbens core
Pitman, K. A., Puil, E., & Borgland, S. L. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12733 · Cited by 81
Doyon, W. M., Thomas, A. M., Ostroumov, A., Dong, Y., & Dani, J. A. (2013) · Biochemical Pharmacology · doi:10.1016/j.bcp.2013.07.007 · Cited by 78
Stability of fMRI striatal response to alcohol cues: A hierarchical linear modeling approach
Schacht, J. P., Anton, R. F., Randall, P. K., Li, X., Henderson, S., & Myrick, H. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.02.004 · Cited by 79
Neural systems analysis of decision making during goal-directed navigation
Penner, M. R., & Mizumori, S. J. Y. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.08.010 · Cited by 80
Regional Heterogeneity of D2-Receptor Signaling in the Dorsal Striatum and Nucleus Accumbens
Marcott, P. F., Gong, S., Donthamsetti, P., Grinnell, S. G., Nelson, M., Newman, A. H., Birnbaumer, L., Martemyanov, K. A., Javitch, J. A., & Ford, C. (2018) · Neuron · doi:10.1016/j.neuron.2018.03.038 · Cited by 77
Condon, M. D., Platt, N. J., Zhang, Y.-F., Roberts, B. M., Clements, M. A., Vietti‐Michelina, S., Tseu, M.-Y., Brimblecombe, K. R., Threlfell, S., Mann, E. O., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-12264-9 · Cited by 72
Feduccia, A. A., Simms, J. A., Mill, D., Yi, H. Y., & Bartlett, S. E. (2014) · British Journal of Pharmacology · doi:10.1111/bph.12690 · Cited by 70
Nair, A. G., Gutierrez‐Arenas, O., Eriksson, O., Vincent, P., & Kotaleski, J. H. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0730-15.2015 · Cited by 69
Salinas, A. G., Davis, M. I., Lovinger, D. M., & Mateo, Y. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.03.049 · Cited by 68
Development and Characterization of a Voltammetric Carbon-Fiber Microelectrode pH Sensor
Makos, M. A., Omiatek, D. M., Ewing, A. G., & Heien, M. L. (2010) · Langmuir · doi:10.1021/la100134r · Cited by 69
Ferris, M. J., Calipari, E. S., Yorgason, J. T., & Jones, S. R. (2013) · ACS Chemical Neuroscience · doi:10.1021/cn400026v · Cited by 74
Melchior, J. R., Ferris, M. J., Stuber, G. D., Riddle, D. R., & Jones, S. R. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13177 · Cited by 70
Biphasic Mechanisms of Amphetamine Action at the Dopamine Terminal
Siciliano, C. A., Calipari, E. S., Ferris, M. J., & Jones, S. R. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4050-13.2014 · Cited by 67
Age-related changes in dopamine signaling in Nurr1 deficient mice as a model of Parkinson's disease
Zhang, L., Le, W., Xie, W., & Dani, J. A. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.03.022 · Cited by 68
Nicotinic receptors regulate the dynamic range of dopamine release in vivo
Koranda, J. L., Cone, J. J., McGehee, D. S., Roitman, M. F., Beeler, J. A., & Zhuang, X. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00269.2013 · Cited by 68
L-DOPA reduces model-free control of behavior by attenuating the transfer of value to action
Kroemer, N. B., Lee, Y., Pooseh, S., Eppinger, B., Goschke, T., & Smolka, M. N. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.10.075 · Cited by 62
Perez, X. A., Bordia, T., McIntosh, J. M., & Quik, M. (2010) · Molecular Pharmacology · doi:10.1124/mol.110.067561 · Cited by 58
Salinas, A. G., Mateo, Y., Carlson, V. C. C., Stinnett, G. S., Luo, G., Seasholtz, A. F., Grant, K. A., & Lovinger, D. M. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-020-00938-8 · Cited by 55
Role of trace amine-associated receptor 1 in nicotine’s behavioral and neurochemical effects
Liu, J., Seaman, R. W., Siemian, J. N., Bhimani, R. V., Johnson, B., Zhang, Y., Zhu, Q., Hoener, M. C., Park, J., Dietz, D., et al. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0017-9 · Cited by 50
Enhanced heroin self-administration and distinct dopamine adaptations in female rats
George, B. E., Barth, S. H., Kuiper, L. B., Holleran, K. M., Lacy, R. T., Raab‐Graham, K. F., & Jones, S. R. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01035-0 · Cited by 52
Lischinsky, J. E., Sokolowski, K., Li, P., Esumi, S., Kamal, Y., Goodrich, M., Oboti, L., Hammond, T. R., Krishnamoorthy, M., Feldman, D., et al. (2017) · eLife · doi:10.7554/elife.21012 · Cited by 48
Harmine augments electrically evoked dopamine efflux in the nucleus accumbens shell
Brierley, D., & Davidson, C. (2013) · Journal of Psychopharmacology · doi:10.1177/0269881112463125 · Cited by 44
Dreyer, J. K., & Hounsgaard, J. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00502.2012 · Cited by 47
Gilles de la Tourette syndrome is associated with hypermethylation of the dopamine D2 receptor gene
Müller‐Vahl, K., Loeber, G., Kotsiari, A., Müller-Engling, L., & Frieling, H. (2016) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2016.11.004 · Cited by 44
Singer, B. F., Guptaroy, B., Austin, C. J., Wohl, I., Lovic, V., Seiler, J. L., Vaughan, R. A., Gnegy, M. E., Robinson, T. E., & Aragona, B. J. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13134 · Cited by 43
Neurochemical and behavioral effects elicited by bupropion and diethylpropion in rats
Santamarı́a, A., & Arias, H. R. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.03.023 · Cited by 42
Geerts, H. (2010) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s12460 · Cited by 40
Cell type-specific synaptic encoding of ethanol exposure in the nucleus accumbens shell
Jeanes, Z. M., Buske, T. R., & Morrisett, R. A. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.06.063 · Cited by 40
Lv, X., Dickerson, J. W., Rook, J. M., Lindsley, C. W., Conn, P. J., & Xiang, Z. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.03.017 · Cited by 40
Acute in vivo nicotine administration enhances synchrony among dopamine neurons
Li, W., Doyon, W. M., & Dani, J. A. (2011) · Biochemical Pharmacology · doi:10.1016/j.bcp.2011.06.006 · Cited by 42
Cocaine inhibition of nicotinic acetylcholine receptors influences dopamine release
Acevedo-Rodriguez, A., Zhang, L., Zhou, F., Gong, S., Gu, H. H., Biasi, M. D., Zhou, F.-M., & Dani, J. A. (2014) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2014.00019 · Cited by 37
Bérubé‐Carrière, N., Guay, G., Fortin, G. M., Kullander, K., Olson, L., Wallén‐Mackenzie, Å., Trudeau, L., & Descarries, L. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.07992.x · Cited by 37
Trihexyphenidyl rescues the deficit in dopamine neurotransmission in a mouse model of DYT1 dystonia
Downs, A. M., Fan, X., Donsante, C., Jinnah, H. A., & Hess, E. J. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.01.012 · Cited by 36
Tobacco smoking and dopaminergic function in humans: a meta-analysis of molecular imaging studies
Ashok, A. H., Mizuno, Y., & Howes, O. D. (2019) · Psychopharmacology · doi:10.1007/s00213-019-05196-1 · Cited by 36
Nair, A. G., Bhalla, U. S., & Kotaleski, J. H. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005080 · Cited by 35
Dopamine Triggers CTCF-Dependent Morphological and Genomic Remodeling of Astrocytes
Galloway, A. L., Adeluyi, A., O’Donovan, B., Fisher, M. L., Rao, C. N., Critchfield, P., Sajish, M., Turner, J. R., & Ortinski, P. I. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.3349-17.2018 · Cited by 35
Pharmacological approaches for Alzheimer’s disease: neurotransmitter as drug targets
Prakash, A. K., Kalra, J., Mani, V., Ramasamy, K., & Majeed, A. B. A. (2014) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.2015.988709 · Cited by 35
Movassaghi, C. S., Perrotta, K. A., Yang, H., Iyer, R. K., Cheng, X., Dagher, M., Alcañiz-Fillol, M., & Andrews, A. M. (2021) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-021-03665-1 · Cited by 35
Frequency-Dependent Effects of Ethanol on Dopamine Release in the Nucleus Accumbens
Yorgason, J. T., Ferris, M. J., Steffensen, S. C., & Jones, S. R. (2013) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.12287 · Cited by 35
Mesolimbic Dopamine and Habenulo-Interpeduncular Pathways in Nicotine Withdrawal
Dani, J. A., & De Biasi, M. (2013) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a012138 · Cited by 34
Self-citationDopamine Release Dynamics in the Tuberoinfundibular Dopamine System
Stagkourakis, S., Dunevall, J., Taleat, Z., Ewing, A. G., & Broberger, C. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2339-18.2019 · Cited by 36
Neural control of dopamine neurotransmission: implications for reinforcement learning
Aggarwal, M., Hyland, B. I., & Wickens, J. R. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08055.x · Cited by 32
Bordia, T., Zhang, D., Perez, X. A., & Quik, M. (2016) · Experimental Neurology · doi:10.1016/j.expneurol.2016.09.009 · Cited by 32
Fox, M. E., & Wightman, R. M. (2016) · Pharmacological Reviews · doi:10.1124/pr.116.012948 · Cited by 32
Yu, Y., Dhavan, R., Chevalier, M. W., Yudowski, G. A., & von Zastrow, M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.6282-09.2010 · Cited by 32
Lutas, A., Fernando, K., Zhang, S. X., Sambangi, A., & Andermann, M. L. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110297 · Cited by 30
Castagnola, E., Robbins, E. M., Wu, B., Pwint, M. Y., Garg, R., Cohen‐Karni, T., & Cui, X. T. (2022) · Biosensors · doi:10.3390/bios12070540 · Cited by 29
Striosome Circuitry Stimulation Inhibits Striatal Dopamine Release and Locomotion
Okunomiya, T., Watanabe, D., Banno, H., Kondo, T., Imamura, K., Takahashi, R., & Inoue, H. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.0457-24.2024 · Cited by 28
Perez, X. A., Khroyan, T. V., McIntosh, J. M., & Quik, M. (2014) · Pharmacology Research & Perspectives · doi:10.1002/prp2.105 · Cited by 30
Regional and sex differences in spontaneous striatal dopamine transmission
Brundage, J., Mason, C. P., Wadsworth, H. A., Finuf, C., Nelson, J. J., Ronström, P. J. W., Jones, S. R., Siciliano, C. A., Steffensen, S. C., & Yorgason, J. T. (2021) · Journal of Neurochemistry · doi:10.1111/jnc.15473 · Cited by 32
The “highs and lows” of the human brain on dopaminergics: Evidence from neuropharmacology
Martins, D., Mehta, M. A., & Prata, D. P. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.06.003 · Cited by 32
Chen, Y.-H., Huang, E. Y., Kuo, T., Ma, H.-I., Hoffer, B. J., Tsui, P.-F., Tsai, J.-J., Chou, Y., & Chiang, Y. H. (2014) · Cell Transplantation · doi:10.3727/096368914x683584 · Cited by 28
Melchior, J. R., & Jones, S. R. (2017) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2017.09.007 · Cited by 30
Adelodun, S. T., Ishola, O. A., Abijo, A. Z., Olatunji, S., Owolabi, J., Olanrewaju, J. A., & Adekomi, D. A. (2021) · Phytomedicine Plus · doi:10.1016/j.phyplu.2021.100104 · Cited by 30
Driscoll, N., Antonini, M., Cannon, T. M., Maretich, P., Olaitan, G. O., Van, V. D. P., Nagao, K., Sahasrabudhe, A., Paniagua, E. V., Frey, E. J., et al. (2024) · Advanced Materials · doi:10.1002/adma.202408154 · Cited by 29
Perez, X. A., McIntosh, J. M., & Quik, M. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12442 · Cited by 28
Cholinergic control of striatal neurons to modulate L‐dopa‐induced dyskinesias
Bordia, T., & Perez, X. A. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14048 · Cited by 26
Beloate, L. N., & Coolen, L. M. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.10.024 · Cited by 26
The striatal cholinergic system in l-dopa-induced dyskinesias
Perez, X. A., Bordia, T., & Quik, M. (2018) · Journal of Neural Transmission · doi:10.1007/s00702-018-1845-9 · Cited by 25
Remote effects on the striatal dopamine system after fluid percussion injury
Huang, E. Y., Tsai, T.-H., Kuo, T., Tsai, J.-J., Tsui, P.-F., Chou, Y., Ma, H.-I., Chiang, Y. H., & Chen, Y.-H. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.03.033 · Cited by 23
Pitx3 deficiency produces decreased dopamine signaling and induces motor deficits in Pitx3(−/−) mice
Le, W., Zhang, L., Xie, W., Li, S., & Dani, J. A. (2015) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2015.08.012 · Cited by 25
Sgobio, C., Kupferschmidt, D. A., Cui, G., Sun, L., Li, Z., Cai, H., & Lovinger, D. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0111749 · Cited by 22
Regionally distinct phasic dopamine release patterns in the striatum during reversal learning
Klanker, M., Fellinger, L., Feenstra, M. G. P., Willuhn, I., & Denys, D. A. J. P. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.05.011 · Cited by 21
Varaschin, R. K., Osterstock, G., Ducrot, C., Leino, S., Bourque, M.-J., Prado, M. A. M., Prado, V. F., Salminen, O., Nuutinen), S. R. (., & Trudeau, L. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.01.027 · Cited by 24
Arencibia‐Albite, F., Vázquez, R., Velásquez-Martínez, M. C., & Jiménez‐Rivera, C. A. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00818.2011 · Cited by 22
Reward-Induced Phasic Dopamine Release in the Monkey Ventral Striatum and Putamen
Yoshimi, K., Kumada, S., Weitemier, A. Z., Jo, T., & Inoue, M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0130443 · Cited by 21
Fennell, A. M., Pitts, E. G., Sexton, L. L., & Ferris, M. J. (2020) · Scientific Reports · doi:10.1038/s41598-019-56884-z · Cited by 24
Estrogen modulates reward prediction errors and reinforcement learning
Golden, C. E. M., Martin, A. C., Kaur, D., Mah, A., Levy, D. H., Yamaguchi, T., Lasek, A. W., Lin, D., Aoki, C. J., & Constantinople, C. M. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-02104-z · Cited by 26
Ferris, M. J., Milenkovic, M., Liu, S., Mielnik, C. A., Beerepoot, P., John, C. E., España, R. A., Sotnikova, T. D., Gainetdinov, R. R., Borgland, S. L., et al. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12594 · Cited by 19
Liu, Y., Montgomery, S. E., Juarez, B., Morel, C., Zhang, S., Kong, Y., Calipari, E. S., Nestler, E. J., Zhang, L., & Han, M. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.108176 · Cited by 21
Metadata
- Authors
- Zhang, L., Doyon, W. M., Clark, J. J., Phillips, P. E. M., & Dani, J. A.
- Affiliations
- Baylor College of Medicine (US)
- Venue
- Molecular Pharmacology
- Publisher
- Elsevier BV
- Published
- 2009-08
- Volume
- 76
- Issue
- 2
- Pages
- 396-404
- ISSN
- 0026-895X (ISSN-L)
- PMC
- PMC2713129
- OpenAlex
- W2133709709
- Cited by
- 161
- References
- 56
- Citations by year
- 2026: 5 · 2025: 4 · 2024: 7 · 2023: 4 · 2022: 12 · 2021: 6 · 2020: 8 · 2019: 8 · 2018: 11 · 2017: 9 · 2016: 13 · 2015: 12 · 2014: 16 · 2013: 12 · 2012: 13
- FWCI
- 4.70
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Molecular Pharmacology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Diana Helis Henry Medical Research Foundation
- National Institutes of Health (NS021229)
- National Institute on Drug Abuse (F32DA024540, R01DA009411, DA009411)
- National Institute of Neurological Disorders and Stroke (NS021229, R01NS021229)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
- Keywords
- dopamine release, phasic dopamine release, dorsal striatum, ventral striatum, nucleus accumbens, dorsolateral striatum, burst stimulation, firing rate, dopamine transporter, dopamine D2 receptor, nicotinic acetylcholine receptors, beta2 subunit, striatal subregions
- MeSH terms
- Action Potentials, Animals, Basal Ganglia, Corpus Striatum, Dopamine, Electric Stimulation, Mice, Inbred C57BL, Microelectrodes, Nucleus Accumbens, Receptors, Nicotinic, Reference Standards, Tungsten, Receptors, Dopamine D2, Mice, Knockout, Dopamine Antagonists, Area Under Curve, Mice
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