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
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–161 of 161
Cell-intrinsic effects of TorsinA(ΔE) disrupt dopamine release in a mouse model of TOR1A dystonia
Downs, A. M., Fan, X., Kadakia, R. F., Donsante, Y., Jinnah, H. A., & Hess, E. J. (2021) · Neurobiology of Disease · doi:10.1016/j.nbd.2021.105369 · Cited by 17
Downs, A. M., Donsante, Y., Jinnah, H. A., & Hess, E. J. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105699 · Cited by 18
Presynaptic Dopamine Dynamics in Striatal Brain Slices with Fast-scan Cyclic Voltammetry
Maina, F. K., Khalid, M., Apawu, A. K., & Mathews, T. A. (2012) · Journal of Visualized Experiments · doi:10.3791/3464 · Cited by 19
Yildirim, B. O., & Derksen, J. J. L. (2015) · Psychiatry Research · doi:10.1016/j.psychres.2015.07.005 · Cited by 20
Shp‐2 knockdown prevents l ‐dopa‐induced dyskinesia in a rat model of Parkinson's disease
Fiorentini, C., Savoia, P., Savoldi, D., Bono, F., Busi, C., Barbon, A., & Missale, C. (2016) · Movement Disorders · doi:10.1002/mds.26581 · Cited by 17
Pina, M. M., & Cunningham, C. L. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.06.063 · Cited by 16
Altered Accumbal Dopamine Terminal Dynamics Following Chronic Heroin Self-Administration
George, B. E., Dawes, M. H., Peck, E. G., & Jones, S. R. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158106 · Cited by 17
Sgobio, C., Sun, L., Ding, J., Herms, J. W., Lovinger, D. M., & Cai, H. (2019) · Scientific Reports · doi:10.1038/s41598-019-41091-7 · Cited by 16
Azocar, V. H., Sepúlveda, G., Ruiz, C., Aguilera, C., Andrés, M. E., & Fuentealba, J. A. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14612 · Cited by 16
Wigestrand, M. B., Mineur, Y., Heath, C. J., Fonnum, F., Picciotto, M. R., & Walaas, S. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07415.x · Cited by 18
Siwakoti, U., Jones, S. A., Kumbhare, D., Cui, X. T., & Castagnola, E. (2025) · Biosensors · doi:10.3390/bios15020100 · Cited by 16
Nunes, E. J., & Addy, N. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109336 · Cited by 13
Cockburn, J., & Holroyd, C. B. (2010) · Brain Research · doi:10.1016/j.brainres.2010.09.065 · Cited by 16
A role for α4(non-α6)* nicotinic acetylcholine receptors in motor behavior
Soll, L. G., Grady, S. R., Salminen, O., Marks, M. J., & Tapper, A. R. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.05.001 · Cited by 15
Trace amine-associated receptor 1 and drug abuse
Wu, R., Liu, J., & Li, J. (2022) · Advances in pharmacology · doi:10.1016/bs.apha.2021.10.005 · Cited by 12
Goutier, W., Lowry, J. P., McCreary, A. C., & O'Connor, J. J. (2016) · Neurochemical Research · doi:10.1007/s11064-015-1786-8 · Cited by 13
The relationships among aberrant salience, reward motivation, and reward sensitivity
Neumann, S. R., & Linscott, R. J. (2018) · International Journal of Methods in Psychiatric Research · doi:10.1002/mpr.1615 · Cited by 17
Region-specific effects of acute haloperidol in the human midbrain, striatum and cortex
Wächtler, C. O., Chakroun, K., Clos, M., Bayer, J., Hennies, N., Beaulieu, J., & Sommer, T. (2020) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2020.04.008 · Cited by 11
Koranda, J. L., Krok, A. C., Xu, J., Contractor, A., McGehee, D. S., Beeler, J. A., & Zhuang, X. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2754-15.2016 · Cited by 13
A Critical Review of Repurposing Apomorphine for Smoking Cessation
Morales‐Rosado, J. A., Cousin, M. A., Ebbert, J. O., & Klee, E. W. (2015) · Assay and Drug Development Technologies · doi:10.1089/adt.2015.680 · Cited by 11
Spiking and Membrane Properties of Rat Olfactory Bulb Dopamine Neurons
Korshunov, K. S., Blakemore, L. J., Bertram, R., & Trombley, P. Q. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00060 · Cited by 11
Reward System Dysfunction and the Motoric-Cognitive Risk Syndrome in Older Persons
Lauretani, F., Testa, C., Salvi, M., Zucchini, I., Lorenzi, B., Tagliaferri, S., Cattabiani, C., & Maggio, M. G. (2022) · Biomedicines · doi:10.3390/biomedicines10040808 · Cited by 10
Everett, A. C., Graul, B., Ronström, J. W., Robinson, J. K., Watts, D. B., España, R. A., Siciliano, C. A., & Yorgason, J. T. (2022) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.2c00033 · Cited by 11
Robinson, J. D., Howard, C. D., Pastuzyn, E. D., Byers, D. L., Keefe, K. A., & Garris, P. A. (2014) · Neurotoxicity Research · doi:10.1007/s12640-014-9459-y · Cited by 11
Wu, C.-T., Magaña, D. G., Roshgadol, J., Tian, L., & Ryan, K. K. (2024) · Appetite · doi:10.1016/j.appet.2024.107673 · Cited by 11
Katz, B. M., Walton, L. R., Houston, K. M., Cerri, D. H., & Shih, Y. I. (2022) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x221142533 · Cited by 10
Comparison of dopamine release and uptake parameters across sex, species and striatal subregions
Kuiper, L. B., Dawes, M. H., West, A. M., DiMarco, E. K., Galante, E. V., Kishida, K. T., & Jones, S. R. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16495 · Cited by 10
Regional Variation in Striatal Dopamine Spillover and Release Plasticity
Walters, S. H., Shu, Z., Michael, A. C., & Levitan, E. S. (2020) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.9b00577 · Cited by 9
Davis, S. E., Ferris, M. J., Ananthan, S., Augelli‐Szafran, C. E., & Zhu, J. (2022) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.122.001291 · Cited by 9
Srivastav, S., Cui, X., Varela, R. B., Kesby, J. P., & Eyles, D. W. (2023) · Schizophrenia · doi:10.1038/s41537-023-00397-2 · Cited by 8
Rooney, K. E., & Wallace, L. J. (2015) · Synapse · doi:10.1002/syn.21845 · Cited by 8
Evolution of in vivo dopamine monitoring techniques
Yocky, A. G., & Covey, D. P. (2020) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2020.173078 · Cited by 8
Estrogenic control of reward prediction errors and reinforcement learningPreprint
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. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.09.570945 · Cited by 5
Regulation of Dopamine Release by Tonic Activity Patterns in the Striatal Brain Slice
Boumhaouad, S., Makowicz, E. A., Choi, S., Bouhaddou, N., Balla, J., Taghzouti, K., Sulzer, D., & Mosharov, E. V. (2025) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.4c00323 · Cited by 4
Fast Scan Cyclic Voltammetry to Assess Dopamine Function: From Circuits to Behavior
Clark, P. J., & España, R. A. (2022) · Neuromethods · doi:10.1007/978-1-0716-2799-0_11 · Cited by 3
Obesity: An Addiction? Imaging of Neurotransmitter Systems in Obesity
van de Giessen, E., McIlwrick, S., Veltman, D. J., van den Brink, W., & Booij, J. (2020) · Springer eBooks · doi:10.1007/978-3-030-57231-0_26 · Cited by 3
Alamsyah, R. M., Satari, M. H., Pintauli, S., & Iskandar, S. (2023) · Pharmacia · doi:10.3897/pharmacia.70.e111049 · Cited by 2
Chase, T. N., Al‐Sabbagh, A., Koga, M., & Clarence‐Smith, K. (2024) · Clinical Pharmacology in Drug Development · doi:10.1002/cpdd.1360 · Cited by 2
Trutti, A. C., Sjoerds, Z., & Hommel, B. (2019) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-019-00717-z · Cited by 2
Obesity an Addiction? Imaging of Neurotransmitter Systems in Obesity
van de Giessen, E., McIlwrick, S., Veltman, D. J., van den Brink, W., & Booij, J. (2014) · Springer eBooks · doi:10.1007/978-3-642-40384-2_27 · Cited by 1
Consolidación de la Memoria y Sustrato Nervioso del Refuerzo
Redolar-Ripoll, E. (2012) · Revista Argentina de Ciencias del Comportamiento ( RACC ) · doi:10.32348/1852.4206.v4.n2.5174 · Cited by 1
Role of alpha-synuclein in the regulation of dopamine neurotransmission in the striatum
Chadchankar, H. (2013) · UEF eRepo (University of Eastern Finland) · Cited by 1
Heroin Self-Administration Induces Altered Dopamine Terminal Dynamics in the Nucleus AccumbensPreprint
George, B. E., Dawes, M. H., Peck, E. G., & Jones, S. R. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.02.478890 · Cited by 1
Wu, C.-T., Magaña, D. G., Roshgadol, J., Tian, L., & Ryan, K. K. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.21.600074 · Cited by 1
Soll, L. G. (2013) · eScholarship@UMassChan · doi:10.13028/m2ng64
Dopamine Modulation of Choice Behavior Following Unexpected Reward Omission
Porter‐Stransky, K. A. (2014) · Deep Blue (University of Michigan)
Avances y Desafíos en Neuropsicología
Godoy, J. C. (2012) · Redalyc (Universidad Autónoma del Estado de México) · doi:10.30882/1852.4206.v4.n2.5168
Boschen, S. L. (2015) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
Mesocorticolimbic adaptations in synaptic plasticity underlie the development of alcohol dependence
Jeanes, Z. M. (2012) · Texas ScholarWorks (Texas Digital Library)
Measurement of Spine Density in Mouse Models of Hypodopaminergia
Bermejo, M. K. (2013) · TSpace (University of Toronto)
Arulkadacham, L. (2017) · Figshare
Frank, M. J. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.7340957.7601055
Anisetty, N., & Manchanda, R. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.24.630270
Computational modeling of midbrain dopamine neurons
Canavier, C. C., Knowlton, C., Liss, B., Khaliq, Z., & Roeper, J. (2025) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-443-29867-7.00001-3
Xu, X.-F., & Dong, G.-H. (2026) · Progress in Neuro-psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2026.111689
Lousada, E. L. R. D. S. (2023) · theses.fr (ABES) · doi:10.70675/23797e5dz9c89z49a2zafdaz58cbefdf74fa
Damdoum, M., Kar, S., & Kavdia, M. (2026) · Cognitive Neurodynamics · doi:10.1007/s11571-026-10486-4
Changes in Junb Expression in the Rat Striatum during the Early Postnatal Period
Dneprovskaya, V. B., Drozd, U. S., Bulygina, V. V., Kalinina, T. S., & Lanshakov, D. A. (2026) · Neurochemical Journal · doi:10.1134/s1819712426700170
Altered striatal dopamine regulation in Adgrl3 knockout mice
Perry, N. A., Torres-Herraez, A., Boumhaouad, S., Makowicz, E. A., Lowes, D. C., Jin, M., Denny, C. A., Sulzer, D., Mosharov, E. V., Kellendonk, C., et al. (2026) · Neuropsychopharmacology · doi:10.1038/s41386-026-02474-3
Levy, C. C., Carlson, V. C. C., Grant, K. A., & Salinas, A. G. (2026) · Neuropsychopharmacology · doi:10.1038/s41386-026-02473-4
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