Locus coeruleus and dopaminergic consolidation of everyday memory
Open accessAbstract
The retention of episodic-like memory is enhanced, in humans and animals, when something novel happens shortly before or after encoding. Using an everyday memory task in mice, we sought the neurons mediating this dopamine-dependent novelty effect, previously thought to originate exclusively from the tyrosine-hydroxylase-expressing (TH+) neurons in the ventral tegmental area. Here we report that neuronal firing in the locus coeruleus is especially sensitive to environmental novelty, locus coeruleus TH+ neurons project more profusely than ventral tegmental area TH+ neurons to the hippocampus, optogenetic activation of locus coeruleus TH+ neurons mimics the novelty effect, and this novelty-associated memory enhancement is unaffected by ventral tegmental area inactivation. Surprisingly, two effects of locus coeruleus TH+ photoactivation are sensitive to hippocampal D 1/D 5 receptor blockade and resistant to adrenoceptor blockade: memory enhancement and long-lasting potentiation of synaptic transmission in CA1 ex vivo. Thus, locus coeruleus TH+ neurons can mediate post-encoding memory enhancement in a manner consistent with possible co-release of dopamine in the hippocampus.
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
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?
Stimulation of locus coeruleus neurons enhances hippocampus-dependent memory.
“Notably, stimulation of locus coeruleus neurons, presumably releasing noradrenaline or dopamine, enhances hippocampus-dependent memory [105–108].”
From Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutons (2024) · cites this paper as [105]
Memory consolidation induced by contextual novelty was modulated by DA release from the locus coeruleus rather than the ventral tegmental area, dependent on hippocampal DA D1/5-R but not adrenergic-R.
“Memory consolidation induced by contextual novelty was modulated by the DA release from the locus coeruleus, rather than ventral tegmental area, which is dependent on the hippocampal DA D1/5-R, but not adrenergic-R”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Takeuchi et al., 2016
DAergic projections to the dorsal hippocampus originate primarily from the locus coeruleus rather than the ventral tegmental area.
“the DAergic projections to the dorsal hippocampus, which originate primarily from the locus coeruleus, rather than ventral tegmental area”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Takeuchi et al., 2016
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans.
Squire, L. R. (1992) · Psychological Review · doi:10.1037/0033-295x.99.2.195 · Cited by 5,376 · see citing works
Memory: A Contribution to Experimental Psychology
Ebbinghaus, H. (2013) · Annals of Neurosciences · doi:10.5214/ans.0972.7531.200408 · Cited by 2,827 · see citing works
Simple memory: a theory for archicortex
Marr, D. (1971) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1971.0078 · Cited by 2,771 · see citing works
The hippocampal-VTA loop: controlling the entry of information into long-term memory
Lisman, J. E., & Grace, A. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.002 · Cited by 1,983 · see citing works
Aston-Jones, G., & Bloom, F. (1981) · The Journal of Neuroscience · doi:10.1523/jneurosci.01-08-00876.1981 · Cited by 1,960 · see citing works
The locus coeruleus and noradrenergic modulation of cognition
Sara, S. J. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2573 · Cited by 1,848 · see citing works
Synaptic tagging and long-term potentiation
Frey, U., & Morris, R. G. M. (1997) · Nature · doi:10.1038/385533a0 · Cited by 1,736 · see citing works
Brown, R., & Kulik, J. (1977) · Cognition · doi:10.1016/0010-0277(77)90018-x · Cited by 1,373 · see citing works
Neuron-type-specific signals for reward and punishment in the ventral tegmental area
Cohen, J. Y., Haesler, S., Vong, L., Lowell, B. B., & Uchida, N. (2012) · Nature · doi:10.1038/nature10754 · Cited by 1,318 · see citing works
Memory; a contribution to experimental psychology,
Ebbinghaus, H., Bussenius, C. E., & Ruger, H. A. (n.d.) · University of Michigan Library Repository · Cited by 1,284 · see citing works
Phasic Firing in Dopaminergic Neurons Is Sufficient for Behavioral Conditioning
Tsai, H.-C., Zhang, F., Adamantidis, A., Stuber, G. D., Bonci, A., de Lecea, L., & Deisseroth, K. (2009) · Science · doi:10.1126/science.1168878 · Cited by 1,266 · see citing works
Self-citationEnvironment-specific expression of the immediate-early gene Arc in hippocampal neuronal ensembles
Guzowski, J. F., McNaughton, B. L., Barnes, C. A., & Worley, P. F. (1999) · Nature Neuroscience · doi:10.1038/16046 · Cited by 1,035 · see citing works
The Psychology and Neuroscience of Forgetting
Wixted, J. T. (2004) · Annual Review of Psychology · doi:10.1146/annurev.psych.55.090902.141555 · Cited by 999 · see citing works
Grace, A. A., & Bunney, B. S. (1983) · Neuroscience · doi:10.1016/0306-4522(83)90135-5 · Cited by 937 · see citing works
The molecular biology of memory: cAMP, PKA, CRE, CREB-1, CREB-2, and CPEB
Kandel, E. R. (2012) · Molecular Brain · doi:10.1186/1756-6606-5-14 · Cited by 904 · see citing works
A causal link between prediction errors, dopamine neurons and learning
Steinberg, E. E., Keiflin, R., Boivin, J. R., Witten, I. B., Deisseroth, K. A., & Janak, P. H. (2013) · Nature Neuroscience · doi:10.1038/nn.3413 · Cited by 879 · see citing works
Self-citationThe neuropsychological basis of addictive behaviour
Everitt, B. J., Dickinson, A., & Robbins, T. W. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00088-1 · Cited by 808 · see citing works
Making memories last: the synaptic tagging and capture hypothesis
Redondo, R. L., & Morris, R. G. M. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn2963 · Cited by 792 · see citing works
Self-citationViral-genetic tracing of the input-output organization of a central noradrenaline circuit
Schwarz, L. A., Miyamichi, K., Gao, X. J., Beier, K. T., Weissbourd, B., DeLoach, K. E., Ren, J., Ibanes, S., Malenka, R. C., Kremer, E. J., et al. (2015) · Nature · doi:10.1038/nature14600 · Cited by 744 · see citing works
The synaptic plasticity and memory hypothesis: encoding, storage and persistence
Takeuchi, T., Duszkiewicz, A. J., & Morris, R. (2013) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0288 · Cited by 665 · see citing works
Self-citationSynaptic tagging: implications for late maintenance of hippocampal long-term potentiation
Frey, U., & Morris, R. G. M. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01189-2 · Cited by 615 · see citing works
Self-citationDopaminergic neurons inhibit striatal output through non-canonical release of GABA
Tritsch, N. X., Ding, J. B., & Sabatini, B. L. (2012) · Nature · doi:10.1038/nature11466 · Cited by 576 · see citing works
Dopamine-dependent facilitation of LTP induction in hippocampal CA1 by exposure to spatial novelty
Li, S., Cullen, W. K., Anwyl, R., & Rowan, M. J. (2003) · Nature Neuroscience · doi:10.1038/nn1049 · Cited by 568 · see citing works
Huang, Y.-Y., & Kandel, E. R. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.7.2446 · Cited by 544 · see citing works
Hippocampal CA3 NMDA Receptors Are Crucial for Memory Acquisition of One-Time Experience
Nakazawa, K., Sun, L. D., Quirk, M. C., Rondi‐Reig, L., Wilson, M. A., & Tonegawa, S. (2003) · Neuron · doi:10.1016/s0896-6273(03)00165-x · Cited by 506 · see citing works
Dopaminergic neurons promote hippocampal reactivation and spatial memory persistence
McNamara, C. G., Tejero-Cantero, Á., Trouche, S., Campo-Urriza, N., & Dupret, D. (2014) · Nature Neuroscience · doi:10.1038/nn.3843 · Cited by 486 · see citing works
Morris, R. G. M. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04888.x · Cited by 398 · see citing works
Self-citationModeling the Spatiotemporal Dynamics of Light and Heat Propagation for In Vivo Optogenetics
Stujenske, J. M., Spellman, T., & Gordon, J. A. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.06.036 · Cited by 390 · see citing works
Optetrode: a multichannel readout for optogenetic control in freely moving mice
Anikeeva, P., Andalman, A. S., Witten, I. B., Warden, M. R., Goshen, I., Grosenick, L., Gunaydin, L. A., Frank, L. M., & Deisseroth, K. A. (2011) · Nature Neuroscience · doi:10.1038/nn.2992 · Cited by 381 · see citing works
Self-citationUchigashima, M., Narushima, M., Fukaya, M., Katona, I., Kano, M., & Watanabe, M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0448-07.2007 · Cited by 375 · see citing works
Self-citationMoncada, D., & Viola, H. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1083-07.2007 · Cited by 370 · see citing works
Biophysical constraints of optogenetic inhibition at presynaptic terminals
Mahn, M., Prigge, M., Ron, S., Levy, R., & Yizhar, O. (2016) · Nature Neuroscience · doi:10.1038/nn.4266 · Cited by 361 · see citing works
Lemon, N., & Manahan‐Vaughan, D. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1454-06.2006 · Cited by 345 · see citing works
Emotional learning selectively and retroactively strengthens memories for related events
Dunsmoor, J. E., Murty, V. P., Davachi, L., & Phelps, E. A. (2015) · Nature · doi:10.1038/nature14106 · Cited by 332 · see citing works
Frey, U., Matthies, H., Reymann, K. G., & Matthies, H. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90732-9 · Cited by 314 · see citing works
Response to Novelty and its Rapid Habituation in Locus Coeruleus Neurons of the Freely Exploring Rat
Vankov, A., Hervé‐Minvielle, A., & Sara, S. J. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb01108.x · Cited by 309 · see citing works
Synaptic tagging during memory allocation
Rogerson, T., Cai, D. J., Frank, A. C., Sano, Y., Shobe, J. L., López‐Aranda, M. F., & Silva, A. J. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3667 · Cited by 305 · see citing works
Gasbarri, A., Verney, C., Innocenzi, R., Campana, E., & Pacitti, C. (1994) · Brain Research · doi:10.1016/0006-8993(94)90512-6 · Cited by 302 · see citing works
Wang, S.-H., Redondo, R. L., & Morris, R. G. M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1008638107 · Cited by 251 · see citing works
Self-citationDopamine Neurons Mediate a Fast Excitatory Signal via Their Glutamatergic Synapses
Chuhma, N., Zhang, H., Masson, J., Zhuang, X., Sulzer, D. L., Hen, R., & Rayport, S. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4317-03.2004 · Cited by 228 · see citing works
Locus coeruleus neurons: cessation of activity during cataplexy
Wu, M.-F., Gulyani, S., Yau, E., Mignot, E. J.-M., Phan, B., & Siegel, J. M. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00600-9 · Cited by 220 · see citing works
Post-learning hippocampal dynamics promote preferential retention of rewarding events
Gruber, M. J., Ritchey, M., Wang, S.-F., Doss, M. K., & Ranganath, C. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.017 · Cited by 212 · see citing works
Transgenic expression of Cre recombinase from the tyrosine hydroxylase locus
Lindeberg, J., Usoskin, D., Bengtsson, H., Gustafsson, A., Kylberg, A., Söderström, S., & Ebendal, T. (2004) · genesis · doi:10.1002/gene.20065 · Cited by 211 · see citing works
Yamasaki, M., Matsui, M., & Watanabe, M. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5719-09.2010 · Cited by 203 · see citing works
Self-citationEschenko, O., Magri, C., Panzeri, S., & Sara, S. J. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr121 · Cited by 194 · see citing works
Hansen, N., & Manahan‐Vaughan, D. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs362 · Cited by 185 · see citing works
Midbrain dopamine neurons bidirectionally regulate CA3-CA1 synaptic drive
Rosen, Z. B., Cheung, S., & Siegelbaum, S. A. (2015) · Nature Neuroscience · doi:10.1038/nn.4152 · Cited by 183 · see citing works
CNS Dopamine Transmission Mediated by Noradrenergic Innervation
Smith, C. C., & Greene, R. W. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6486-11.2012 · Cited by 178 · see citing works
Self-citationBcl-x Is Required for Proper Development of the Mouse Substantia Nigra
Savitt, J. M., Jang, S. S., Mu, W., Dawson, V. L., & Dawson, T. M. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0760-05.2005 · Cited by 173 · see citing works
Communication in Neural Circuits: Tools, Opportunities, and Challenges
Lerner, T. N., Ye, L., & Deisseroth, K. (2016) · Cell · doi:10.1016/j.cell.2016.02.027 · Cited by 159 · see citing works
Self-citationOn the Origin of Cortical Dopamine: Is it a Co-Transmitter in Noradrenergic Neurons?
Devoto, P., & Flore, G. (2006) · Current Neuropharmacology · doi:10.2174/157015906776359559 · Cited by 137 · see citing works
Harley, C. W. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)63818-2 · Cited by 126 · see citing works
Clonidine modulates dopamine cell firing in rat ventral tegmental area
Grenhoff, J., & Svensson, T. H. (1989) · European Journal of Pharmacology · doi:10.1016/0014-2999(89)90765-6 · Cited by 125 · see citing works
Cytochemical and cytological properties of perineuronal oligodendrocytes in the mouse cortex
Takasaki, C., Yamasaki, M., Uchigashima, M., Konno, K., Yanagawa, Y., & Watanabe, M. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07377.x · Cited by 106 · see citing works
Self-citationChapter 15 Reward-related activity in the monkey striatum and substantia nigra
Schultz, W., Apicella, P., Ljungberg, T., Romo, R., & Scarnati, E. (1993) · Progress in brain research · doi:10.1016/s0079-6123(08)61349-7 · Cited by 99 · see citing works
Lemon, N., & Manahan‐Vaughan, D. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr297 · Cited by 72 · see citing works
Pharmacological Dissociation of Novelty Responses in the Human Brain
Bunzeck, N., Guitart‐Masip, M., Dolan, R. J., & Düzel, E. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs420 · Cited by 61 · see citing works
Otmakhova, N. A., Düzel, E., Deutch, A. Y., & Lisman, J. E. (2012) · Springer eBooks · doi:10.1007/978-3-642-32375-1_10 · Cited by 57 · see citing works
Flagged first, then by citations
Research works printed but not linked: 2
- [6]Dudai Y Morris RGM Brain, Perception and Memory: Advances in Cognitive Neuroscience Bolhuis JJ 147 162 Oxford Univ. Press 2000
- [53]Franklin KBJ Paxinos G The Mouse Brain in Stereotaxic Coordinates 3rd Academic Press San Diego 2007
Cited by
Sorted by citations
Ventral tegmental area: cellular heterogeneity, connectivity and behaviour
Morales, M., & Margolis, E. B. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.165 · Cited by 1,108 · see citing works
Discovering Event Structure in Continuous Narrative Perception and Memory
Baldassano, C., Chen, J., Zadbood, A., Pillow, J. W., Hasson, U., & Norman, K. A. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.041 · Cited by 952 · see citing works
Locus coeruleus: a new look at the blue spot
Poe, G. R., Foote, S., Eschenko, O., Johansen, J. P., Bouret, S., Aston-Jones, G., Harley, C. W., Manahan-Vaughan, D., Weinshenker, D., Valentino, R., et al. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-020-0360-9 · Cited by 720 · see citing works
Nobili, A., Latagliata, E. C., Viscomi, M. T., Cavallucci, V., Cutuli, D., Giacovazzo, G., Krashia, P., Rizzo, F. R., Marino, R., Federici, M., et al. (2017) · Nature Communications · doi:10.1038/ncomms14727 · Cited by 514 · see citing works
The Role of Hippocampal Replay in Memory and Planning
Ólafsdóttir, H. F., Bush, D., & Barry, C. (2018) · Current Biology · doi:10.1016/j.cub.2017.10.073 · Cited by 413 · see citing works
Memory-enhancing properties of sleep depend on the oscillatory amplitude of norepinephrine
Kjaerby, C., Andersen, M., Hauglund, N., Untiet, V., Dall, C., Sigurdsson, B., Ding, F., Feng, J., Li, Y., Weikop, P., et al. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01102-9 · Cited by 306 · see citing works
Turi, G. F., Li, W.-K., Chavlis, S., Pandi, I., O’Hare, J., Priestley, J. B., Grosmark, A. D., Liao, Z., Ladow, M., Zhang, J. F., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.01.009 · Cited by 218 · see citing works
Kaufman, A. M., Geiller, T., & Losonczy, A. (2020) · Neuron · doi:10.1016/j.neuron.2019.12.029 · Cited by 193 · see citing works
Forgetting as a form of adaptive engram cell plasticity
Ryan, T. J., & Frankland, P. W. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00548-3 · Cited by 182 · see citing works
Bariselli, S., Hörnberg, H., Prévost-Solié, C., Musardo, S., Hatstatt-Burklé, L., Scheiffele, P., & Bellone, C. (2018) · Nature Communications · doi:10.1038/s41467-018-05382-3 · Cited by 171 · see citing works
Chao, O. Y., de Souza Silva, M. A., Yang, Y.-M., & Huston, J. P. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.007 · Cited by 158 · see citing works
Neuropeptide and small transmitter coexistence: Fundamental studies and relevance to mental illness
Hökfelt, T., Barde, S., Xu, Z.-Q. D., Kuteeva, E., Rüegg, J., Le Maitre, E., Risling, M., Kehr, J., Ihnatko, R., Theodorsson, E., et al. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00106 · Cited by 139 · see citing works
Diversity of oxytocin neurones: Beyond magno‐ and parvocellular cell types?
Althammer, F., & Grinevich, V. (2018) · Journal of Neuroendocrinology · doi:10.1111/jne.12549 · Cited by 138 · see citing works
Hippocampal reactivation extends for several hours following novel experience
Giri, B., Miyawaki, H., Mizuseki, K., Cheng, S., & Diba, K. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.1950-18.2018 · Cited by 99 · see citing works
Ruggiero, R. N., Rossignoli, M. T., Marques, D. B., de Sousa, B. M., Romcy-Pereira, R. N., Lopes-Aguiar, C., & Leite, J. P. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.732360 · Cited by 111 · see citing works
Respiratory modulation of cognitive performance during the retrieval process
Nakamura, N. H., Fukunaga, M., & Oku, Y. (2018) · PLOS ONE · doi:10.1371/journal.pone.0204021 · Cited by 88 · see citing works
Locus Coeruleus and Dopamine-Dependent Memory Consolidation
Yamasaki, M., & Takeuchi, T. (2017) · Neural Plasticity · doi:10.1155/2017/8602690 · Cited by 91 · see citing works
Self-citationLa Barbera, L., Vedele, F., Nobili, A., Krashia, P., Spoleti, E., Latagliata, E. C., Cutuli, D., Cauzzi, E., Marino, R., Viscomi, M. T., et al. (2021) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2021.102031 · Cited by 98 · see citing works
Cordella, A., Krashia, P., Nobili, A., Pignataro, A., La Barbera, L., Viscomi, M. T., Valzania, A., Keller, F., Ammassari-Teule, M., Mercuri, N. B., et al. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.05.006 · Cited by 82 · see citing works
Tian, J., Guo, L., Sui, S., Driskill, C., Phensy, A., Wang, Q., Gauba, E., Zigman, J. M., Swerdlow, R. H., Kroener, S., et al. (2019) · Science Translational Medicine · doi:10.1126/scitranslmed.aav6278 · Cited by 72 · see citing works
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 · see citing works
Hippocampal release of dopamine and norepinephrine encodes novel contextual information
Moreno‐Castilla, P., Pérez‐Ortega, R., Violante‐Soria, V., Balderas, I., & Bermúdez‐Rattoni, F. (2017) · Hippocampus · doi:10.1002/hipo.22711 · Cited by 67 · see citing works
Naïve to expert: Considering the role of previous knowledge in memory
Alonso, A., van der Meij, J., Tse, D., & Genzel, L. (2020) · Brain and Neuroscience Advances · doi:10.1177/2398212820948686 · Cited by 46 · see citing works
Iaccarino, L., Sala, A., Caminiti, S. P., Presotto, L., Perani, D., & Initiative, F. T. A. D. N. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-190954 · Cited by 40 · see citing works
Memory corticalization triggered by REM sleep: mechanisms of cellular and systems consolidation
Almeida-Filho, D. G., Queiroz, C. M., & Ribeiro, S. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2886-9 · Cited by 38 · see citing works
Kim, O., Okamoto, Y., Kaufmann, W. A., Brose, N., Shigemoto, R., & Jonas, P. (2024) · PLOS Biology · doi:10.1371/journal.pbio.3002879 · Cited by 15 · see citing works
“Notably, stimulation of locus coeruleus neurons, presumably releasing noradrenaline or dopamine, enhances hippocampus-dependent memory [105–108].”
Zhang, Y., Wang, Z., Ju, J., Liao, J., & Zhou, Q. (2021) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.200151 · Cited by 14 · see citing works
The Functions of Dopamine in Operant Conditioned Reflexes
Maiorov, V. I. (2019) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-019-00815-y · Cited by 10 · see citing works
- Authors
- Takeuchi, T., Duszkiewicz, A. J., Sonneborn, A., Spooner, P. A., Yamasaki, M., Watanabe, M., Smith, C. C., Fernández, G., Deisseroth, K., Greene, R. W., & Morris, R. G. M.
- Affiliations
- University of Edinburgh (GB)
- The University of Texas Southwestern Medical Center (US)
- Hokkaido University (JP)
- Radboud University Nijmegen (NL)
- Stanford University (US)
- University of Tsukuba (JP)
- Instituto de Neurociencias (ES)
- Corresponding author
- Greene, Robert W.
- Morris, Richard G. M.
- ORCID
- Venue
- Nature
- Published
- 2016-09
- Volume
- 537
- Issue
- 7620
- Pages
- 357-362
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC5161591
- OpenAlex
- W2508644210
- Cited by
- 827
- References
- 58
- Citations by year
- 2026: 82 · 2025: 91 · 2024: 121 · 2023: 98 · 2022: 73 · 2021: 81 · 2020: 79 · 2019: 63 · 2018: 87 · 2017: 47 · 2016: 4 · 2014: 1
- FWCI
- 42.64
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Edinburgh Research Explorer (University of Edinburgh) (submittedVersion, other-oa)
- RePEc: Research Papers in Economics (submittedVersion)
- DIGITAL.CSIC (Spanish National Research Council (CSIC)) (submittedVersion)
- Research Explorer (The University of Manchester) (submittedVersion)
- Radboud Repository (Radboud University) (submittedVersion)
- Funders
- U.S. Department of Veterans Affairs
- European Commission (600725)
- University of Tsukuba
- National Institutes of Health
- Medical Research Council (MC_UU_12024/3)
- National Institute of Mental Health (R01MH080297)
- National Institute on Drug Abuse (T32DA007290)
- FP7 Ideas: European Research Council (268800)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Keywords
- locus coeruleus, everyday memory, episodic-like memory, novelty effect, tyrosine hydroxylase neurons, ventral tegmental area, hippocampus, dopamine D1/D5 receptors, synaptic potentiation, CA1, optogenetic stimulation, flashbulb memory
- MeSH terms
- Memory Consolidation, Animals, Dopamine, Locus Coeruleus, Male, Mice, Inbred C57BL, Synaptic Transmission, Neurons, Receptors, Adrenergic, Receptors, Dopamine D1, Ventral Tegmental Area, Receptors, Dopamine D5, Mice, CA1 Region, Hippocampal, Optogenetics, In Vitro Techniques
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