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Heterogeneous organization of the locus coeruleus projections to prefrontal and motor cortices
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Significance: The locus coeruleus projection system in the brain is thought to exert uniform and synchronous modulatory effects on cells and circuits throughout the CNS by widespread release of its transmitter, norepinephrine. We challenge this notion by demonstrating that neurons in the locus coeruleus maintain segregated connections to brain regions with distinctly different functions. Specifically, cells that communicate with the prefrontal cortex, a region involved in cognition and executive function, are characterized by properties that allow for independent and asynchronous modulation of operations in this area, compared with those that project to the motor cortex and regulate movement generation. These findings have important implications for understanding the role of this system in normal brain physiology and pathologic neuropsychiatric conditions.
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“Indeed, a subset of locus coeruleus neurons project selectively to PFC50, which may accentuate the stress response in this region.”
From Stress weakens prefrontal networks: molecular insults to higher cognition (2015) · cites this paper as [50]
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Cites
Davies, D. L., & Bouldin, D. W. (1979) · IEEE Transactions on Pattern Analysis and Machine Intelligence · doi:10.1109/tpami.1979.4766909 · Cited by 9,145
Stress signalling pathways that impair prefrontal cortex structure and function
Arnsten, A. F. T. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2648 · Cited by 3,299
Berridge, C. W., & Waterhouse, B. D. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(03)00143-7 · Cited by 2,529
Self-citationThe locus coeruleus and noradrenergic modulation of cognition
Sara, S. J. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2573 · Cited by 1,848
Prefrontal executive and cognitive functions in rodents: neural and neurochemical substrates
Dalley, J. W., Cardinal, R. N., & Robbins, T. W. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.09.006 · Cited by 1,329
Input-specific control of reward and aversion in the ventral tegmental area
Lammel, S., Lim, B. K., Ran, C., Huang, K. W., Betley, M. J., Tye, K. M., Deisseroth, K., & Malenka, R. C. (2012) · Nature · doi:10.1038/nature11527 · Cited by 1,300
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
Action potential generation requires a high sodium channel density in the axon initial segment
Kole, M. H. P., Ilschner, S. U., Kampa, B. M., Williams, S. R., Ruben, P. C., & Stuart, G. J. (2008) · Nature Neuroscience · doi:10.1038/nn2040 · Cited by 703
Adaptive gain and the role of the locus coeruleus–norepinephrine system in optimal performance
Aston‐Jones, G., & Cohen, J. D. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20723 · Cited by 671
Adrenergic pharmacology and cognition: Focus on the prefrontal cortex
Ramos, B. P., & Arnsten, A. F. T. (2007) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2006.11.006 · Cited by 641
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Joshi, S., Li, Y., Kalwani, R. M., & Gold, J. I. (2016) · Neuron · doi:10.1016/j.neuron.2015.11.028 · Cited by 1,387
Stress weakens prefrontal networks: molecular insults to higher cognition
Arnsten, A. F. T. (2015) · Nature Neuroscience · doi:10.1038/nn.4087 · Cited by 752
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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
Self-citationMather, M., Clewett, D., Sakaki, M., & Harley, C. W. (2016) · Behavioral and Brain Sciences · doi:10.1017/s0140525x15000667 · Cited by 695
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Schwarz, L. A., & Luo, L. (2015) · Current Biology · doi:10.1016/j.cub.2015.09.039 · Cited by 578
High-throughput mapping of single-neuron projections by sequencing of barcoded RNA
Kebschull, J. M., Garcia da Silva, P., Reid, A. P., Peikon, I. D., Albeanu, D. F., & Zador, A. M. (2016) · Neuron · doi:10.1016/j.neuron.2016.07.036 · Cited by 376
Development of prefrontal cortex
Kolk, S. M., & Rakic, P. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01137-9 · Cited by 378
Arnsten, A. F. T., Raskind, M. A., Taylor, F. B., & Connor, D. F. (2015) · Neurobiology of Stress · doi:10.1016/j.ynstr.2014.10.002 · Cited by 381
Thiele, A., & Bellgrove, M. A. (2018) · Neuron · doi:10.1016/j.neuron.2018.01.008 · Cited by 350
Neuromodulation of brain state and behavior
McCormick, D. A., Nestvogel, D. B., & He, B. J. (2020) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-100219-105424 · Cited by 303
Modular organization of the brainstem noradrenaline system coordinates opposing learning states
Uematsu, A., Tan, B. Z., Ycu, E. A., Cuevas, J. N. S., Koivumaa, J., Junyent, F., Kremer, E. J., Witten, I. B., Deisseroth, K. A., & Johansen, J. P. (2017) · Nature Neuroscience · doi:10.1038/nn.4642 · Cited by 356
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
Locus coeruleus: From global projection system to adaptive regulation of behavior
Aston‐Jones, G., & Waterhouse, B. D. (2016) · Brain Research · doi:10.1016/j.brainres.2016.03.001 · Cited by 268
Self-citationHirschberg, S., Li, Y., Randall, A. D., Kremer, E. J., & Pickering, A. E. (2017) · eLife · doi:10.7554/elife.29808 · Cited by 252
Locus coeruleus norepinephrine activity mediates sensory-evoked awakenings from sleep
Hayat, H., Regev, N., Matosevich, N., Sales, A. C., Paredes-Rodriguez, E., Krom, A. J., Bergman, L., Li, Y., Lavigne, M., Kremer, E. J., et al. (2020) · Science Advances · doi:10.1126/sciadv.aaz4232 · Cited by 268
Chandler, D. J., Jensen, P., McCall, J. G., Pickering, A. E., Schwarz, L. A., & Totah, N. K. B. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1164-19.2019 · Cited by 229
Self-citationThe role of the locus coeruleus in the generation of pathological anxiety
Morris, L. S., McCall, J. G., Charney, D. S., & Murrough, J. W. (2020) · Brain and Neuroscience Advances · doi:10.1177/2398212820930321 · Cited by 244
Noradrenergic Locus Coeruleus pathways in pain modulation
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Ross, J. A., & Bockstaele, E. J. V. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.601519 · Cited by 241
The role of noradrenaline in cognition and cognitive disorders
Holland, N., Robbins, T. W., & Rowe, J. B. (2021) · Brain · doi:10.1093/brain/awab111 · Cited by 216
Noradrenergic Modulation of Cognition in Health and Disease
Borodovitsyna, O., Flamini, M. D., & Chandler, D. J. (2017) · Neural Plasticity · doi:10.1155/2017/6031478 · Cited by 227
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Murley, A. G., & Rowe, J. B. (2017) · Brain · doi:10.1093/brain/awx327 · Cited by 211
Cools, R., & Arnsten, A. F. T. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01100-8 · Cited by 216
Xing, B., Li, Y.-C., & Gao, W.-J. (2016) · Brain Research · doi:10.1016/j.brainres.2016.01.005 · Cited by 196
Self-citationNoradrenergic Modulation of Fear Conditioning and Extinction
Giustino, T. F., & Maren, S. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00043 · Cited by 203
The Locus Coeruleus Is a Complex and Differentiated Neuromodulatory System
Totah, N. K., Neves, R. M., Panzeri, S., Logothetis, N. K., & Eschenko, O. (2018) · Neuron · doi:10.1016/j.neuron.2018.07.037 · Cited by 179
Neuromodulation in circuits of aversive emotional learning
Likhtik, E., & Johansen, J. P. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0503-3 · Cited by 169
Oe, Y., Wang, X., Patriarchi, T., Konno, A., Ozawa, K., Yahagi, K., Hirai, H., Tsuboi, T., Kitaguchi, T., Tian, L., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-14378-x · Cited by 177
The Noradrenergic System in Parkinson’s Disease
Paredes-Rodriguez, E., Vegas‐Suárez, S., Morera‐Herreras, T., Deurwaerdère, P. D., & Miguélez, C. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00435 · Cited by 165
Noradrenergic modulation of rhythmic neural activity shapes selective attention
Dahl, M. J., Mather, M., & Werkle‐Bergner, M. (2021) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2021.10.009 · Cited by 165
Locus Coeruleus in time with the making of memories
Sara, S. J. (2015) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2015.07.004 · Cited by 156
Recent advances in the neurobiology and neuropharmacology of Alzheimer’s disease
Kumar, K., Kumar, A., Keegan, R. M., & Deshmukh, R. R. (2017) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2017.12.053 · Cited by 159
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Jacob, S. N., & Nienborg, H. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00051 · Cited by 147
Sales, A. C., Friston, K. J., Jones, M. W., Pickering, A. E., & Moran, R. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006267 · Cited by 157
Locus Ceruleus Norepinephrine Release: A Central Regulator of CNS Spatio-Temporal Activation?
Atzori, M., Cuevas‐Olguin, R., Esquivel‐Rendon, E., García‐Oscos, F., Salgado‐Delgado, R., Saderi, N., Miranda‐Morales, M., Treviño, M., Pineda, J. C., & Salgado, H. (2016) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2016.00025 · Cited by 156
Locus coeruleus-norepinephrine modulation of sensory processing and perception: A focused review
McBurney-Lin, J., Lu, J., Zuo, Y., & Yang, H. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.06.009 · Cited by 142
Spatiotemporal dynamics of noradrenaline during learned behaviour
Breton‐Provencher, V., Drummond, G. T., Feng, J., Li, Y., & Sur, M. (2022) · Nature · doi:10.1038/s41586-022-04782-2 · Cited by 151
Laminar and Cellular Distribution of Monoamine Receptors in Rat Medial Prefrontal Cortex
Santana, N., & Artigas, F. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00087 · Cited by 135
The Locus Coeruleus in Aging and Alzheimer’s Disease: A Postmortem and Brain Imaging Review
Beardmore, R., Hou, R. H., Darekar, A., Holmes, C., & Boche, D. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-210191 · Cited by 132
Zhang, S., Hu, S., Chao, H. H., & Li, C. R. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv172 · Cited by 119
Volume Transmission in Central Dopamine and Noradrenaline Neurons and Its Astroglial Targets
Fuxé, K., Agnati, L. F., Marcoli, M., & Borroto‐Escuela, D. O. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1574-5 · Cited by 118
Expanding the power of recombinase-based labeling to uncover cellular diversity
Plummer, N. W., Evsyukova, I. Y., Robertson, S. D., de Marchena, J., Tucker, C. J., & Jensen, P. (2015) · Development · doi:10.1242/dev.129981 · Cited by 112
Berridge, C. W., & Spencer, R. C. (2016) · Brain Research · doi:10.1016/j.brainres.2015.11.024 · Cited by 112
Pupil diameter is not an accurate real-time readout of locus coeruleus activity
Megemont, M., McBurney-Lin, J., & Yang, H. (2022) · eLife · doi:10.7554/elife.70510 · Cited by 127
Li, Y., Hickey, L., Perrins, R., Werlen, E., Patel, A. A., Hirschberg, S., Jones, M. W., Salinas, S., Kremer, E. J., & Pickering, A. E. (2016) · Brain Research · doi:10.1016/j.brainres.2016.02.023 · Cited by 97
Waterhouse, B. D., & Navarra, R. L. (2018) · Brain Research · doi:10.1016/j.brainres.2018.08.032 · Cited by 121
Self-citationFernandez, S. P., Cauli, B., Cabezas, C., Muzerelle, A., Poncer, J.-C., & Gaspar, P. (2016) · Brain Structure and Function · doi:10.1007/s00429-015-1142-4 · Cited by 100
The role of norepinephrine in the pathophysiology of schizophrenia
Mäki-Marttunen, V., Andreassen, O. A., & Espeseth, T. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.07.038 · Cited by 100
Persistent Stress-Induced Neuroplastic Changes in the Locus Coeruleus/Norepinephrine System
Borodovitsyna, O., Joshi, N., & Chandler, D. J. (2018) · Neural Plasticity · doi:10.1155/2018/1892570 · Cited by 106
Self-citationUematsu, A., Tan, B. Z., & Johansen, J. P. (2015) · Learning & Memory · doi:10.1101/lm.037283.114 · Cited by 89
Borodovitsyna, O., Flamini, M. D., & Chandler, D. J. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.01.020 · Cited by 93
Self-citationMonoaminergic Modulation of Motor Cortex Function
Vitrac, C., & Benoit‐Marand, M. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00072 · Cited by 94
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Morita, M., Ikeshima‐Kataoka, H., Kreft, M., Vardjan, N., Zorec, R., & Noda, M. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20040941 · Cited by 88
Collins, L. N., Francis, J., Emanuel, B., & McCormick, D. A. (2023) · eLife · doi:10.7554/elife.81826 · Cited by 87
Brainstem Modulation of Large-Scale Intrinsic Cortical Activity Correlations
van den Brink, R. L., Pfeffer, T. A., & Donner, T. H. (2019) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2019.00340 · Cited by 85
Role of the locus coeruleus arousal system in cognitive control
Grueschow, M., Kleim, B., & Ruff, C. C. (2020) · Journal of Neuroendocrinology · doi:10.1111/jne.12890 · Cited by 83
Gompf, H. S., Budygin, E. A., Fuller, P. M., & Bass, C. E. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00152 · Cited by 80
Chandler, D. J. (2015) · Brain Research · doi:10.1016/j.brainres.2015.11.022 · Cited by 87
Self-citationCatecholaminergic Neuromodulation Shapes Intrinsic MRI Functional Connectivity in the Human Brain
van den Brink, R. L., Pfeffer, T. A., Warren, C. M., Murphy, P. R., Tona, K., van der Wee, N. J. A., Giltay, E. J., van Noorden, M. S., Rombouts, S. A. R. B., Donner, T. H., et al. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0744-16.2016 · Cited by 82
Noradrenergic and cholinergic systems take centre stage in neuropsychiatric diseases of ageing
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Prefrontal modulation of anxiety through a lens of noradrenergic signaling
Bouras, N. N., Mack, N. R., & Gao, W. (2023) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2023.1173326 · Cited by 88
Self-citationIntegrating brainstem and cortical functional architectures
Hansen, J. Y., Cauzzo, S., Singh, K., García‐Gomar, M. G., Shine, J. M., Bianciardi, M., & Mišić, B. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01787-0 · Cited by 91
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Luskin, A. T., Li, L., Fu, X., Martin, M. M., Barcomb, K., Girven, K. S., Blackburn, T., Wells, B. A., Thai, S., Li, E. M., et al. (2025) · Nature · doi:10.1038/s41586-025-08952-w · Cited by 68
Briand, M., Gosseries, O., Staumont, B., Laureys, S., & Thibaut, A. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.00933 · Cited by 79
Azizi, S. A. (2020) · The Neuroscientist · doi:10.1177/1073858420974336 · Cited by 81
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Zorec, R., Horvat, A., Vardjan, N., & Verkhratsky, A. (2015) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2015.00056 · Cited by 70
Arousal dependent modulation of thalamo-cortical functional interaction
Stitt, I., Zhou, Z. C., Radtke‐Schuller, S., & Frӧhlich, F. (2018) · Nature Communications · doi:10.1038/s41467-018-04785-6 · Cited by 72
Noradrenergic ensemble-based modulation of cognition over multiple timescales
Totah, N. K. B., Logothetis, N. K., & Eschenko, O. (2018) · Brain Research · doi:10.1016/j.brainres.2018.12.031 · Cited by 75
Gilvesy, A., Husén, E., Maglóczky, Z., Mihály, O. S., Hortobágyi, T., Kanatani, S., Heinsen, H., Renier, N., Hökfelt, T. G. M., Mulder, J., et al. (2022) · Acta Neuropathologica · doi:10.1007/s00401-022-02477-6 · Cited by 77
Yamaguchi, H., Hopf, F. W., Li, S., & de Lecea, L. (2018) · Nature Communications · doi:10.1038/s41467-018-07566-3 · Cited by 71
Borodovitsyna, O., Duffy, B. C., Pickering, A. E., & Chandler, D. J. (2020) · Neurobiology of Stress · doi:10.1016/j.ynstr.2020.100284 · Cited by 61
Self-citationLocus coeruleus MRI contrast is associated with cortical thickness in older adults
Bachman, S. L., Dahl, M. J., Werkle‐Bergner, M., Düzel, S., Forlim, C. G., Lindenberger, U., Kühn, S., & Mather, M. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.12.019 · Cited by 62
Distinct ensembles in the noradrenergic locus coeruleus are associated with diverse cortical states
Noei, S., Zouridis, I. S., Logothetis, N. K., Panzeri, S., & Totah, N. K. B. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2116507119 · Cited by 59
Sadacca, B. F., Wikenheiser, A. M., & Schoenbaum, G. M. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.04.017 · Cited by 59
Dual contributions of noradrenaline to behavioural flexibility and motivation
Jahn, C. I., Gilardeau, S., Varazzani, C., Blain, B., Sallet, J., Walton, M. E., & Bouret, S. (2018) · Psychopharmacology · doi:10.1007/s00213-018-4963-z · Cited by 68
Down but Not Out: The Consequences of Pretangle Tau in the Locus Coeruleus
Chalermpalanupap, T., Weinshenker, D., & Rorabaugh, J. M. (2017) · Neural Plasticity · doi:10.1155/2017/7829507 · Cited by 59
Cellular composition and circuit organization of the locus coeruleus of adult mice
McKinney, A., Hu, M., Hoskins, A., Mohammadyar, A., Naeem, N., Jing, J., Patel, S. S., Sheth, B. R., & Jiang, X. (2023) · eLife · doi:10.7554/elife.80100 · Cited by 58
Regulation of neurological and neuropsychiatric phenotypes by locus coeruleus-derived galanin
Weinshenker, D., & Holmes, P. V. (2015) · Brain Research · doi:10.1016/j.brainres.2015.11.025 · Cited by 63
Ectopic HCN4 expression drives mTOR-dependent epilepsy in mice
Hsieh, L. S., Wen, J. H., Nguyen, L. H., Zhang, L., Getz, S. A., Torres-Reveron, J., Wang, Y., Spencer, D. D., & Bordey, A. (2020) · Science Translational Medicine · doi:10.1126/scitranslmed.abc1492 · Cited by 52
Plummer, N. W., Chandler, D. J., Powell, J. M., Scappini, E., Waterhouse, B. D., & Jensen, P. (2020) · eNeuro · doi:10.1523/eneuro.0010-20.2020 · Cited by 54
Self-citationArnsten, A. F. T., Joyce, M. K. P., & Roberts, A. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.105000 · Cited by 64
Huber, N., Korhonen, S., Hoffmann, D. B., Leskelä, S., Rostalski, H., Remes, A. M., Honkakoski, P., Solje, E., & Haapasalo, A. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01384-8 · Cited by 58
Noradrenergic Hypothesis Linking Neurodegeneration-Based Cognitive Decline and Astroglia
Leanza, G., Gulino, R., & Zorec, R. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00254 · Cited by 54
Fluid intelligence and the locus coeruleus–norepinephrine system
Tsukahara, J. S., & Engle, R. W. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2110630118 · Cited by 56
Pharmacological evidence for the implication of noradrenaline in effort
Borderies, N., Mattioni, J., Bornert, P., Gilardeau, S., & Bouret, S. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000793 · Cited by 49
The expression of established cognitive brain states stabilizes with working memory development
Montez, D. F., Calabro, F. J., & Luna, B. (2017) · eLife · doi:10.7554/elife.25606 · Cited by 52
Two types of locus coeruleus norepinephrine neurons drive reinforcement learningPreprint
Su, Z., & Cohen, J. Y. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.08.519670 · Cited by 52
Köhler, S., Bär, K., & Wagner, G. (2016) · Human Brain Mapping · doi:10.1002/hbm.23173 · Cited by 57
Sigurdardottir, H. L., Kranz, G. S., Rami‐Mark, C., James, G. M., Vanicek, T., Gryglewski, G., Kautzky, A., Hienert, M., Traub‐Weidinger, T., Mitterhauser, M., et al. (2016) · Human Brain Mapping · doi:10.1002/hbm.23071 · Cited by 51
“Another study revealed projections to the PFC and the motor cortex to differ [Chandler et al., 2014].”
BackgroundSlater, C. L., Liu, Y., Weiss, E., Yu, K., & Wang, Q. (2022) · Brain Sciences · doi:10.3390/brainsci12070890 · Cited by 49
Noga, B. R., Turkson, R. P., Xie, S., Taberner, A. M., Pinzón, A., & Hentall, I. D. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00059 · Cited by 50
Janitzky, K. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.00371 · Cited by 56
Gong, L., Shi, M., Wang, J., Xu, R., Yu, S., Liu, D., Ding, X., Zhang, B., Zhang, X., & Xi, C. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.678465 · Cited by 48
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Associative memory cells and their working principle in the brain
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Kelberman, M. A., Keilholz, S. D., & Weinshenker, D. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.583421 · Cited by 46
Metadata
- Authors
- Chandler, D. J., Gao, W.-J., & Waterhouse, B. D.
- Affiliations
- Drexel University (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2014-04-21
- Volume
- 111
- Issue
- 18
- Pages
- 6816-6821
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC4020069
- OpenAlex
- W2109682741
- Cited by
- 341
- References
- 45
- Citations by year
- 2026: 41 · 2025: 35 · 2024: 36 · 2023: 28 · 2022: 31 · 2021: 24 · 2020: 32 · 2019: 26 · 2018: 25 · 2017: 23 · 2016: 16 · 2015: 23 · 2014: 1
- FWCI
- 9.60
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Rowan Digitals Works (Rowan University) (submittedVersion)
- Funders
- National Institute of Mental Health (R01MH085666, R01MH101178)
- 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 › Endocrine and Autonomic Systems › Neuroscience of respiration and sleep
- Keywords
- locus coeruleus, norepinephrine, prefrontal cortex, motor cortex, efferent projections, neuronal heterogeneity, noradrenaline release, noradrenergic neurons, adaptive and maladaptive behavior
- MeSH terms
- Animals, Behavior, Animal, Efferent Pathways, Locus Coeruleus, Male, Motor Cortex, Norepinephrine, RNA, Messenger, Tyrosine 3-Monooxygenase, Receptors, N-Methyl-D-Aspartate, Rats, Sprague-Dawley, Prefrontal Cortex, Receptors, AMPA, alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid, Principal Component Analysis, Vesicular Monoamine Transport Proteins, Rats, Voltage-Gated Sodium Channel beta-3 Subunit
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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.
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