The DOI matches its Crossref record; 28 of the 28 references it cites were found in a registry or an index.
Phasic Firing in Dopaminergic Neurons Is Sufficient for Behavioral Conditioning
Open accessAbstract
Rewarding Bursts of Dopamine: Dopaminergic neurons are thought to be involved in the cognitive and hedonic underpinnings of motivated behaviors. However, it is still unclear whether dopaminergic neuron activation is sufficient to elicit reward-related behavior and which type of neuronal activity pattern serves this purpose. Tsai et al. (p. 1080; published online 23 April) directly compared tonic versus phasic firing of dopaminergic cells in the ventral tegmental area, and the effects on both behavior and dopamine release. Using a transgenic system and virus injection in mice, they targeted the dopaminergic cells with rhodopsin. Light stimulation was then used to drive dopaminergic cells either with a tonic low level of pulses or bursts of high-frequency pulses, with the number of pulses being equal across conditions. Only the high-frequency phasic firing induced a conditioned place preference and dopamine release.
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
“There is an increase in DA release (measured in awake, behaving animals by microdialysis or by fastscanning cyclic voltammetry) in the NAc in response to unexpected food rewards or stimuli that predict food rewards [72,308-310].”
From Reward circuitry dysfunction in psychiatric and neurodevelopmental disorders and genetic syndromes: animal models and clinical findings (2012) · cites this paper as [72]
In the citing paper
“This evidence was recently further investigated in an animal study using optogenetics, which showed that activation of the VTA leads to dopamine release in the NAc (Tsai et al., 2009; for a review, see Lenz and Lobo, 2013).”
From Circuit Mechanisms of Reward, Anhedonia, and Depression (2019) · cites this paper as Tsai et al., 2009
In the citing paper
“However, since optogenetic activation of VTA DA neurons increases social interaction (Gunaydin et al., 2014) and supports positive reinforcement (Tsai et al., 2009, Witten et al., 2011), they are thought to play a causal role in social reward.”
From Dorsal raphe dopamine neurons represent the experience of social isolation (2016) · cites this paper as Tsai et al., 2009
In the citing paper
“The light activated channelrhodopsin (ChR2) (19, 20) has been used in other neural systems to activate specific cell populations and produce learning (21–23).”
From Optical activation of lateral amygdala pyramidal cells instructs associative fear learning (2010) · cites this paper as [21]
In the citing paper
“conversely, simulating burst firing using channelrhodopsin is sufficient to induce behavioral conditioning [42].”
From A neoHebbian framework for episodic memory; role of dopamine-dependent late LTP (2011) · cites this paper as [42]
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
The neural basis of drug craving: An incentive-sensitization theory of addiction
Robinson, T. (1993) · Brain Research Reviews · doi:10.1016/0165-0173(93)90013-p · Cited by 7,346
Millisecond-timescale, genetically targeted optical control of neural activity
Boyden, E. S., Zhang, F., Bamberg, E., Nagel, G., & Deisseroth, K. A. (2005) · Nature Neuroscience · doi:10.1038/nn1525 · Cited by 5,015
Self-citationNeural systems of reinforcement for drug addiction: from actions to habits to compulsion
Everitt, B. J., & Robbins, T. W. (2005) · Nature Neuroscience · doi:10.1038/nn1579 · Cited by 3,785
Dopamine, learning and motivation.
Wise, R. A. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1406 · Cited by 3,379
Channelrhodopsin-2, a directly light-gated cation-selective membrane channel
Nagel, G., Szellas, T., Huhn, W., Kateriya, S., Adeishvili, N., Berthold, P. R., Ollig, D., Hegemann, P., & Bamberg, E. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1936192100 · Cited by 2,730
Drug abuse: hedonic homeostatic dysregulation
Koob, G. F., & Moal, M. L. (1997) · Science · doi:10.1126/science.278.5335.52 · Cited by 2,535
The mesolimbic dopamine reward circuit in depression
Nestler, E. J., & Carlezon, W. A. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.09.018 · Cited by 2,059
Dopamine neuron systems in the brain: An update
Björklund, A., & Dunnett, S. B. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.006 · Cited by 1,777
Multimodal fast optical interrogation of neural circuitry
Zhang, F., Wang, L., Brauner, M., Liewald, J. F., Kay, K., Watzke, N., Wood, P. G., Bamberg, E., Nagel, G., GOTTSCHALK, A. R., et al. (2007) · Nature · doi:10.1038/nature05744 · Cited by 1,766
Self-citationHabits, Rituals, and the Evaluative Brain
Graybiel, A. M. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.112851 · Cited by 1,697
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 1,000
Anatomy and Function of Ventral Tegmental Area Glutamate Neurons
Cai, J., & Tong, Q. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.867053 · Cited by 101
Multiple memory systems as substrates for multiple decision systems
Doll, B. B., Shohamy, D., & Daw, N. D. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.04.014 · Cited by 101
Zhang, T. A., Placzek, A. N., & Dani, J. A. (2010) · Neuropharmacology · doi:10.1016/j.neuropharm.2010.06.004 · Cited by 100
An Intrinsic Neuronal Oscillator Underlies Dopaminergic Neuron Bursting
Deister, C. A., Teagarden, M. A., Wilson, C. J., & Paladini, C. A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4053-09.2009 · Cited by 100
Functional Connectome Analysis of Dopamine Neuron Glutamatergic Connections in Forebrain Regions
Mingote, S., Chuhma, N., Kusnoor, S. V., Field, B. C., Deutch, A. Y., & Rayport, S. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1674-15.2015 · Cited by 100
Han, X., Jing, M.-Y., Zhao, T.-Y., Wu, N., Song, R., & Li, J. (2017) · Metabolic Brain Disease · doi:10.1007/s11011-017-0023-3 · Cited by 99
Progress in understanding mood disorders: optogenetic dissection of neural circuits
Lammel, S., Tye, K. M., & Warden, M. R. (2014) · Genes, Brain and Behavior · doi:10.1111/gbb.12049 · Cited by 98
Yamashita, A., Hamada, A., Suhara, Y., Kawabe, R., Yanase, M., Kuzumaki, N., Narita, M., Matsui, R., Okano, H., & Narita, M. (2014) · Synapse · doi:10.1002/syn.21733 · Cited by 98
Dopamine tunes prefrontal outputs to orchestrate aversive processing
Weele, C. M. V., Siciliano, C. A., & Tye, K. M. (2018) · Brain Research · doi:10.1016/j.brainres.2018.11.044 · Cited by 98
Selective optogenetic stimulation of cholinergic axons in neocortex
Kalmbach, A., Hedrick, T. P., & Waters, J. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00870.2011 · Cited by 98
Wang, Y., Lin, X., Chen, X., Chen, X., Xu, Z. C., Zhang, W., Liao, Q., Duan, X., Wang, X., Liu, M., et al. (2017) · Biomaterials · doi:10.1016/j.biomaterials.2017.07.017 · Cited by 97
The Dopamine Prediction Error: Contributions to Associative Models of Reward Learning
Nasser, H. M., Calu, D. J., Schoenbaum, G. M., & Sharpe, M. J. (2017) · Frontiers in Psychology · doi:10.3389/fpsyg.2017.00244 · Cited by 97
Lu, Y., Li, Y., Pan, J., Wei, P., Liu, N., Wu, B., Cheng, J., Lu, C., & Wang, L. (2011) · Biomaterials · doi:10.1016/j.biomaterials.2011.09.083 · Cited by 97
Electronic and Ionic Materials for Neurointerfaces
Ferro, M. D., & Melosh, N. A. (2017) · Advanced Functional Materials · doi:10.1002/adfm.201704335 · Cited by 96
Kollins, S. H., & Adcock, R. A. (2014) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2014.02.002 · Cited by 95
Gruber, J., Hanßen, R., Qubad, M., Bouzouina, A., Schack, V., Sochor, H., Schiweck, C., Aichholzer, M., Matura, S., Slattery, D. A., et al. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105179 · Cited by 96
Optogenetic control of striatal dopamine release in rats
Bass, C. E., Grinevich, V. P., Vance, Z. B., Sullivan, R. P., Bonin, K., & Budygin, E. A. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06850.x · Cited by 95
Optogenetic insights into striatal function and behavior
Lenz, J. D., & Lobo, M. K. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.04.018 · Cited by 95
Consolidating the Circuit Model for Addiction
Lüscher, C., & Janak, P. H. (2021) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-092920-123905 · Cited by 94
Chuhma, N., Mingote, S., Kalmbach, A., Yetnikoff, L., & Rayport, S. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.07.002 · Cited by 93
Recent advances in understanding the role of phasic dopamine activity
Schultz, W. (2019) · F1000Research · doi:10.12688/f1000research.19793.1 · Cited by 94
Chen, M., Zhao, Y., Yang, H., Luan, W., Song, J., Cui, D., Dong, Y. W., Lai, B., Ma, L., & Zheng, P. (2015) · eLife · doi:10.7554/elife.09275 · Cited by 92
The role of learning-related dopamine signals in addiction vulnerability
Huys, Q. J. M., Tobler, P. N., Hasler, G., & Flagel, S. B. (2014) · Progress in brain research · doi:10.1016/b978-0-444-63425-2.00003-9 · Cited by 92
Locus Coeruleus and Dopamine-Dependent Memory Consolidation
Yamasaki, M., & Takeuchi, T. (2017) · Neural Plasticity · doi:10.1155/2017/8602690 · Cited by 91
Elucidation of G-protein and β-arrestin functional selectivity at the dopamine D2 receptor
Peterson, S. M., Pack, T. F., Wilkins, A. D., Urs, N. M., Urban, D. J., Bass, C. E., Lichtarge, O., & Caron, M. G. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1502742112 · Cited by 91
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
Illicit dopamine transients: reconciling actions of abused drugs
Covey, D. P., Roitman, M. F., & Garris, P. A. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.02.002 · Cited by 90
Optogenetics and Psychiatry: Applications, Challenges, and Opportunities
Deisseroth, K. A. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.12.021 · Cited by 91
Self-citationObsessive-compulsive disorder: Insights from animal models
Szechtman, H., Ahmari, S. E., Beninger, R. J., Eilam, D., Harvey, B. H., Edemann-Callesen, H., & Winter, C. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.04.019 · Cited by 90
A photoswitchable GPCR-based opsin for presynaptic inhibition
Copits, B. A., Gowrishankar, R., O’Neill, P., Li, J.-N., Girven, K. S., Yoo, J. J., Meshik, X., Parker, K. E., Spangler, S. M., Elerding, A. J., et al. (2021) · Neuron · doi:10.1016/j.neuron.2021.04.026 · Cited by 90
Amygdala Kisspeptin Neurons: Putative Mediators of Olfactory Control of the Gonadotropic Axis
Pineda, R., Plaisier, F., Millar, R. P., & Ludwig, M. (2016) · Neuroendocrinology · doi:10.1159/000445895 · Cited by 90
Mesolimbic Dopamine Transients in Motivated Behaviors: Focus on Maternal Behavior
Robinson, D. L., Zitzman, D. L., & Williams, S. K. (2011) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2011.00023 · Cited by 89
Pang, X.-Y., Liu, L., Ngolab, J., Zhao-Shea, R., McIntosh, J. M., Gardner, P. D., & Tapper, A. R. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.03.039 · Cited by 89
Phasic dopamine signals: from subjective reward value to formal economic utility
Schultz, W., Carelli, R. M., & Wightman, R. M. (2015) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2015.09.006 · Cited by 88
The role of serotonergic, adrenergic and dopaminergic receptors in antidepressant-like effect
Pytka, K., Podkowa, K., Rapacz, A., Podkowa, A., Żmudzka, E., Olczyk, A., Sapa, J., & Filipek, B. (2015) · Pharmacological Reports · doi:10.1016/j.pharep.2015.08.007 · Cited by 88
Franklin, N. T., & Frank, M. J. (2015) · eLife · doi:10.7554/elife.12029 · Cited by 88
Optogenetic tools for mammalian systems
Müller, K., & Weber, W. (2013) · Molecular BioSystems · doi:10.1039/c3mb25590e · Cited by 87
Immune and Neuroprotective Effects of Physical Activity on the Brain in Depression
Phillips, C., & Fahimi, A. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00498 · Cited by 89
DeGroot, S. R., Zhao-Shea, R., Chung, L., Klenowski, P. M., Sun, F., Molas, S., Gardner, P. D., Li, Y., & Tapper, A. R. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.06.018 · Cited by 87
From cudgel to scalpel: toward precise neural control with optogenetics
Peron, S., & Svoboda, K. (2010) · Nature Methods · doi:10.1038/nmeth.f.325 · Cited by 87
Functional wiring of hypocretin and LC-NE neurons: implications for arousal
Carter, M. E., de Lecea, L., & Adamantidis, A. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00043 · Cited by 86
Self-citationDopamine transients do not act as model-free prediction errors during associative learning
Sharpe, M. J., Batchelor, H. M., Mueller, L. E., Chang, C. Y., Maes, E. J. P., Niv, Y., & Schoenbaum, G. M. (2020) · Nature Communications · doi:10.1038/s41467-019-13953-1 · Cited by 87
Hedonic eating is controlled by dopamine neurons that oppose GLP-1R satiety
Zhu, Z., Gong, R., Rodriguez, V., Quach, K. T., Chen, X., & Sternson, S. M. (2025) · Science · doi:10.1126/science.adt0773 · Cited by 85
Gu, Z., Lamb, P. W., & Yakel, J. L. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2129-12.2012 · Cited by 86
Anhedonia in schizophrenia: Deficits in both motivation and hedonic capacity
Wang, J., Huang, J., Yang, X., Lui, S. S. Y., Cheung, E. F. C., & Chan, R. C. K. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2015.06.019 · Cited by 86
Aversion hot spots in the dopamine system
Verharen, J. P. H., Zhu, Y., & Lammel, S. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.02.002 · Cited by 85
Interpreting the role of the striatum during multiple phases of motor learning
Cataldi, S., Stanley, A. T., Miniaci, M. C., & Sulzer, D. (2021) · FEBS Journal · doi:10.1111/febs.15908 · Cited by 85
The nucleus accumbens in reward and aversion processing: insights and implications
Xu, Y., Lin, Y., Yu, M., & Zhou, K. (2024) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2024.1420028 · Cited by 86
Chuhma, N., Choi, W., Mingote, S., & Rayport, S. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.08.057 · Cited by 85
van den Oever, M. C., Rotaru, D. C., Heinsbroek, J. A., Gouwenberg, Y., Deisseroth, K. A., Stuber, G. D., Mansvelder, H. D., & Smit, A. B. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2412-13.2013 · Cited by 85
Self-citationOptogenetic Blockade of Dopamine Transients Prevents Learning Induced by Changes in Reward Features
Chang, C. Y., Gardner, M., di Tillio, M. G., & Schoenbaum, G. M. (2017) · Current Biology · doi:10.1016/j.cub.2017.09.049 · Cited by 85
Rein, M. L., & Deussing, J. M. (2011) · Molecular Genetics and Genomics · doi:10.1007/s00438-011-0663-7 · Cited by 84
Oxytocin functions as a spatiotemporal filter for excitatory synaptic inputs to VTA dopamine neurons
Xiao, L., Priest, M. F., & Kozorovitskiy, Y. (2018) · eLife · doi:10.7554/elife.33892 · Cited by 83
“These DA increases have been directly assayed using fast-scan cyclic voltammetry (Tsai et al., 2009) and are well-matched by recent optical imaging studies that demonstrate unpredicted reward-associated calcium transients in the axons of VTA DA neurons expressing genetically encoded calcium sensors…”
BackgroundPauli, W. M., Larsen, T., Collette, S., Tyszka, J. M., Seymour, B., & O’Doherty, J. P. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2277-15.2015 · Cited by 83
Remote control of neural function by X-ray-induced scintillation
Matsubara, T., Takayuki, Y., Kawaguchi, N., Nakano, T., Yoshimoto, J., Sezaki, M., Takizawa, H., Tsunoda, S. P., Horigane, S., Ueda, S., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-24717-1 · Cited by 83
Astrocytes in Memory Function: Pioneering Findings and Future Directions
Adamsky, A., & Goshen, I. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.05.033 · Cited by 83
Jay, M., De Faveri, F., & McDearmid, J. R. (2015) · Current Biology · doi:10.1016/j.cub.2014.12.033 · Cited by 82
Laricchiuta, D., & Petrosini, L. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00238 · Cited by 82
Regrowth of Serotonin Axons in the Adult Mouse Brain Following Injury
Jin, Y., Dougherty, S., Wood, K. M., Sun, L. T., Cudmore, R. H., Abdalla, A., Kannan, G., Pletnikov, M. V., Hashemi, P., & Linden, D. J. (2016) · Neuron · doi:10.1016/j.neuron.2016.07.024 · Cited by 82
Inhibitory inputs tune the light response properties of dopaminergic amacrine cells in mouse retina
Newkirk, G., Hoon, M., Wong, R., & Detwiler, P. B. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00118.2013 · Cited by 82
From Experienced Utility to Decision Utility
Berridge, K. C., & O’Doherty, J. P. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-416008-8.00018-8 · Cited by 82
Stress transforms lateral habenula reward responses into punishment signals
Shabel, S. J., Wang, C., Monk, B., Aronson, S., & Malinow, R. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1903334116 · Cited by 82
Dougalis, A. G., Matthews, G. A. C., Bishop, M. W., Brischoux, F., Kobayashi, K., & Ungless, M. A. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08255.x · Cited by 81
Dopamine and fear memory formation in the human amygdala
Frick, A., Björkstrand, J., Lubberink, M., Eriksson, A., Fredrikson, M., & Åhs, F. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01400-x · Cited by 81
Phasic dopamine release in the medial prefrontal cortex enhances stimulus discrimination
Popescu, A. T., Zhou, M., & Poo, M. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1606098113 · Cited by 80
Drug-Evoked Synaptic Plasticity Causing Addictive Behavior
Lüscher, C. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3406-13.2013 · Cited by 81
Optical developments for optogenetics
Papagiakoumou, E. I. (2013) · Biology of the Cell · doi:10.1111/boc.201200087 · Cited by 80
Xiao, Q., Zhou, X., Wei, P., Xie, L., Han, Y., Wu, B., Wang, J., Cai, A., Xu, F., Lu, Y., et al. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0816-3 · Cited by 80
Dopaminergic Dynamics Contributing to Social BehaviorPreprint
Gunaydin, L. A., & Deisseroth, K. A. (2014) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2014.79.024711 · Cited by 80
Self-citationWu, G., Zhang, N., Matarasso, A. K., Heck, I., Li, H., Lu, W., Phaup, J. G., Schneider, M. J., Wu, Y., Weng, Z., et al. (2022) · Nano Letters · doi:10.1021/acs.nanolett.2c00289 · Cited by 79
Jafari, M. R., Deng, L., Kitov, P. I., Ng, S., Matochko, W. L., Tjhung, K. F., Zeberoff, A. F., Elias, A. L., Klassen, J. S., & Derda, R. (2013) · ACS Chemical Biology · doi:10.1021/cb4006722 · Cited by 79
Neurotransmission systems in Parkinson’s disease
Moghaddam, H. S., Zare-Shahabadi, A., Rahmani, F., & Rezaei, N. (2017) · Reviews in the Neurosciences · doi:10.1515/revneuro-2016-0068 · Cited by 78
A circuit-based mechanism underlying familiarity signaling and the preference for novelty
Molas, S., Zhao-Shea, R., Liu, L., DeGroot, S. R., Gardner, P. D., & Tapper, A. R. (2017) · Nature Neuroscience · doi:10.1038/nn.4607 · Cited by 78
Optogenetic manipulation of neural circuitry in vivo
Kravitz, A. V., & Kreitzer, A. C. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.02.010 · Cited by 76
Physiological state gates acquisition and expression of mesolimbic reward prediction signals
Cone, J. J., Fortin, S. M., McHenry, J. A., Stuber, G. D., McCutcheon, J. E., & Roitman, M. F. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1519643113 · Cited by 77
Self-citationNeural substrates of the impaired effort expenditure decision making in schizophrenia.
Huang, J., Yang, X., Lan, Y., Cui-ying, Z., Liu, X.-Q., Wang, Y., Cheung, E. F. C., Xie, G., & Chan, R. C. K. (2016) · Neuropsychology · doi:10.1037/neu0000284 · Cited by 76
Midbrain circuits of novelty processing
Tapper, A. R., & Molas, S. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107323 · Cited by 74
Neuroanatomy of the spleen: Mapping the relationship between sympathetic neurons and lymphocytes
Murray, K. M., Godinez, D. R., Brust‐Mascher, I., Miller, E. N., Gareau, M. G., & Reardon, C. (2017) · PLoS ONE · doi:10.1371/journal.pone.0182416 · Cited by 75
Mikhailova, M. A., Bass, C. E., Grinevich, V. P., Chappell, A. M., Deal, A. L., Bonin, K., Weiner, J. L., Gainetdinov, R. R., & Budygin, E. A. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.07.006 · Cited by 74
Evidence for a neural law of effect
Athalye, V. R., Santos, F. J., Carmena, J. M., & Costa, R. M. (2018) · Science · doi:10.1126/science.aao6058 · Cited by 75
Pantazis, C. B., Gonzalez, L. A., Tunstall, B. J., Carmack, S. A., Koob, G. F., & Vendruscolo, L. F. (2021) · Science Advances · doi:10.1126/sciadv.abf0364 · Cited by 74
Ko, D., & Wanat, M. J. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1279-15.2016 · Cited by 74
Place field assembly distribution encodes preferred locations
Mamad, O., Stumpp, L., McNamara, H. M., Ramakrishnan, C., Deisseroth, K., Reilly, R. B., & Tsanov, M. (2017) · PLoS Biology · doi:10.1371/journal.pbio.2002365 · Cited by 73
Self-citationSchiller, M., Azulay‐Debby, H., Boshnak, N., Elyahu, Y., Korin, B., Ben-Shaanan, T. L., Koren, T., Krot, M., Hakim, F., & Rolls, A. (2021) · Immunity · doi:10.1016/j.immuni.2021.04.007 · Cited by 73
Prefrontal/accumbal catecholamine system processes high motivational salience
Puglisi‐Allegra, S., & Ventura, R. (2012) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2012.00031 · Cited by 71
Smittenaar, P., Chase, H. W., Aarts, E., Nusselein, B., Bloem, B. R., & Cools, R. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08043.x · Cited by 73
Pristerà, A., Lin, W., Kaufmann, A.-K., Brimblecombe, K. R., Threlfell, S., Dodson, P. D., Magill, P. J., Fernandes, C., Cragg, S. J., & Ang, S. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1503911112 · Cited by 73
van Zessen, R., Plasse, G., & Adan, R. A. H. (2012) · Proceedings of The Nutrition Society · doi:10.1017/s0029665112000614 · Cited by 72
Optogenetic strategies to investigate neural circuitry engaged by stress
Sparta, D. R., Jennings, J. H., Ung, R. L., & Stuber, G. D. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.05.007 · Cited by 72
Self-citationCuttoli, R. D.-D., Mondoloni, S., Marti, F., Lemoine, D., Nguyen, C., Naudé, J., d’Izarny-Gargas, T., Pons, S., Maskos, U., Trauner, D. H., et al. (2018) · eLife · doi:10.7554/elife.37487 · Cited by 73
Yoest, K. E., Cummings, J., & Becker, J. B. (2018) · British Journal of Pharmacology · doi:10.1111/bph.14531 · Cited by 73
Stress relief as a natural resilience mechanism against depression-like behaviors
Dong, Y., Li, Y., Xiang, X., Xiao, Z.-C., Hu, J., Li, Y., Li, H., & Hu, H. (2023) · Neuron · doi:10.1016/j.neuron.2023.09.004 · Cited by 73
Distinct µ-opioid ensembles trigger positive and negative fentanyl reinforcement
Chaudun, F., Python, L., Liu, Y., Hiver, A., Cand, J., Kieffer, B. L., Valjent, E., & Lüscher, C. (2024) · Nature · doi:10.1038/s41586-024-07440-x · Cited by 71
Pandit, R., Omrani, A., Luijendijk, M. C. M., de Vrind, V. A. J., van Rozen, A. J., Ophuis, R. J. A. O., Garner, K. M., Kalló, I., Ghanem, A., Liposits, Z., et al. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.19 · Cited by 71
Multiple Dopamine Systems: Weal and Woe of DopaminePreprint
Watabe‐Uchida, M., & Uchida, N. (2018) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2018.83.037648 · Cited by 71
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
Self-citationMedial septum regulates the hippocampal spatial representation
Mamad, O., McNamara, H. M., Reilly, R. B., & Tsanov, M. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00166 · Cited by 70
Role of the Primate Ventral Tegmental Area in Reinforcement and Motivation
Arsenault, J. T., Rima, S., Stemmann, H., & Vanduffel, W. (2014) · Current Biology · doi:10.1016/j.cub.2014.04.044 · Cited by 70
Cholinergic modulation of dopamine pathways through nicotinic acetylcholine receptors
de Kloet, S. F., Mansvelder, H. D., & De Vries, T. J. (2015) · Biochemical Pharmacology · doi:10.1016/j.bcp.2015.07.014 · Cited by 69
Seidemann, R., Duek, O. A., Jia, R., Levy, I., & Harpaz‐Rotem, I. (2021) · Chronic Stress · doi:10.1177/2470547021996006 · Cited by 69
Metadata
- Authors
- Tsai, H.-C., Zhang, F., Adamantidis, A., Stuber, G. D., Bonci, A., de Lecea, L., & Deisseroth, K.
- Affiliations
- Stanford University (US)
- University of California, San Francisco (US)
- Department of Psychiatry and Behavioral Sciences, W083 Clark Center, 318 Campus Drive West, Stanford University, Stanford, CA 94305, USA.
- Corresponding author
- Tsai, Hsing-Chen
- Zhang, Feng
- Deisseroth, Karl
- ORCID
- Venue
- Science
- Published
- 2009-05-22
- Volume
- 324
- Issue
- 5930
- Pages
- 1080-1084
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC5262197
- OpenAlex
- W1980737345
- Cited by
- 1,266
- References
- 28
- Citations by year
- 2026: 31 · 2025: 53 · 2024: 63 · 2023: 51 · 2022: 68 · 2021: 58 · 2020: 74 · 2019: 68 · 2018: 74 · 2017: 92 · 2016: 90 · 2015: 99 · 2014: 105 · 2013: 87 · 2012: 82
- FWCI
- 34.69
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Bern Open Repository and Information System (University of Bern) (submittedVersion)
- Funders
- National Institute of Mental Health (R01MH087592)
- National Institute on Drug Abuse (R01DA021880)
- National Institute of Neurological Disorders and Stroke (K99NS065009)
- 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 › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Keywords
- phasic firing, dopaminergic neurons, ventral tegmental area, behavioral conditioning, optogenetic stimulation, natural reward, drugs of abuse
- MeSH terms
- Channelrhodopsins, Action Potentials, Animals, Behavior, Animal, Conditioning, Psychological, Dopamine, Electrodes, Implanted, Genetic Vectors, Light, Mice, Transgenic, Neurons, Reward, Transduction, Genetic, Ventral Tegmental Area, Patch-Clamp Techniques, 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