The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.
Viral-genetic tracing of the input-output organization of a central noradrenaline circuit
Open accessAbstract
Deciphering how neural circuits are anatomically organized with regard to input and output is instrumental in understanding how the brain processes information. For example, locus coeruleus noradrenaline (also known as norepinephrine) (LC-NE) neurons receive input from and send output to broad regions of the brain and spinal cord, and regulate diverse functions including arousal, attention, mood and sensory gating. However, it is unclear how LC-NE neurons divide up their brain-wide projection patterns and whether different LC-NE neurons receive differential input. Here we developed a set of viral-genetic tools to quantitatively analyse the input-output relationship of neural circuits, and applied these tools to dissect the LC-NE circuit in mice. Rabies-virus-based input mapping indicated that LC-NE neurons receive convergent synaptic input from many regions previously identified as sending axons to the locus coeruleus, as well as from newly identified presynaptic partners, including cerebellar Purkinje cells. The 'tracing the relationship between input and output' method (or TRIO method) enables trans-synaptic input tracing from specific subsets of neurons based on their projection and cell type. We found that LC-NE neurons projecting to diverse output regions receive mostly similar input. Projection-based viral labelling revealed that LC-NE neurons projecting to one output region also project to all brain regions we examined. Thus, the LC-NE circuit overall integrates information from, and broadcasts to, many brain regions, consistent with its primary role in regulating brain states. At the same time, we uncovered several levels of specificity in certain LC-NE sub-circuits. These tools for mapping output architecture and input-output relationship are applicable to other neuronal circuits and organisms. More broadly, our viral-genetic approaches provide an efficient intersectional means to target neuronal populations based on cell type and projection pattern.
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
“Thus, the input-output architecture of the DR serotonin system differs from that of the locus coeruleus norepinephrine system with more homogeneous input and output (Schwarz et al., 2015), and resembles more closely those of the midbrain dopamine systems (Beier et al., 2015; Lerner et al., 2015), with biased input and segregated output.”
From Anatomically defined and functionally distinct dorsal raphe serotonin sub-systems (2018) · cites this paper as Schwarz et al., 2015
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 robust and high-throughput Cre reporting and characterization system for the whole mouse brain
Madisen, L., Zwingman, T. A., Sunkin, S. M., Oh, S. W., Zariwala, H. A., Gu, H., Ng, L. L., Palmiter, R. D., Hawrylycz, M. J., Jones, A. R., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2467 · Cited by 6,907
Dahlstroem, A., & Fuxé, K. (1964) · PubMed · Cited by 5,133
Aston-Jones, G., & Bloom, F. (1981) · The Journal of Neuroscience · doi:10.1523/jneurosci.01-08-00876.1981 · Cited by 1,960
Swanson, L. W., & Hartman, B. K. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901630406 · Cited by 1,475
Whole-Brain Mapping of Direct Inputs to Midbrain Dopamine Neurons
Watabe‐Uchida, M., Zhu, L., Ogawa, S. K., Vamanrao, A., & Uchida, N. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.017 · Cited by 1,277
Monosynaptic Restriction of Transsynaptic Tracing from Single, Genetically Targeted Neurons
Wickersham, I. R., Lyon, D. C., Barnard, R. J. O., Mori, T., Finke, S., Conzelmann, K., Young, J. A. T., & Callaway, E. M. (2007) · Neuron · doi:10.1016/j.neuron.2007.01.033 · Cited by 1,176
Orienting and reorienting: the locus coeruleus mediates cognition through arousal
Sara, S. J., & Bouret, S. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.011 · Cited by 1,056
Tuning arousal with optogenetic modulation of locus coeruleus neurons
Carter, M. E., Yizhar, O., Chikahisa, S., Nguyen, H., Adamantidis, A., Nishino, S., Deisseroth, K., & de Lecea, L. (2010) · Nature Neuroscience · doi:10.1038/nn.2682 · Cited by 993
Gong, S., Doughty, M., Harbaugh, C. R., Cummins, A., Hatten, M. E., Heintz, N., & Gerfen, C. R. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2707-07.2007 · Cited by 977
Genetic Dissection of Neural Circuits
Luo, L., Callaway, E. M., & Svoboda, K. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.002 · Cited by 771
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–200 of 725
Rabies screen reveals GPe control of cocaine-triggered plasticity
Beier, K. T., Kim, C. K., Hoerbelt, P., Hung, L. W., Heifets, B. D., DeLoach, K. E., Mosca, T. J., Neuner, S., Deisseroth, K. A., Luo, L., et al. (2017) · Nature · doi:10.1038/nature23888 · Cited by 113
Self-citationStreng, M. L., & Krook-Magnuson, E. I. (2020) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2020.106909 · Cited by 113
A thalamic bridge from sensory perception to cognition
Wolff, M., Morceau, S., Folkard, R., Martín-Cortecero, J., & Groh, A. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.11.013 · Cited by 114
A Discrete Dorsal Raphe to Basal Amygdala 5-HT Circuit Calibrates Aversive Memory
Sengupta, A., & Holmes, A. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.029 · Cited by 123
Amygdala-Midbrain Connections Modulate Appetitive and Aversive Learning
Steinberg, E. E., Gore, F., Heifets, B. D., Taylor, M. D., Norville, Z. C., Beier, K. T., Földy, C., Lerner, T. N., Luo, L., Deisseroth, K. A., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.03.016 · Cited by 120
Self-citationCAV-2—why a canine virus is a neurobiologist's best friend
Junyent, F., & Kremer, E. J. (2015) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2015.08.004 · Cited by 120
Self-citationCA1-projecting subiculum neurons facilitate object–place learning
Sun, Y., Jin, S., Lin, X., Chen, L., Qiao, X., Jiang, L., Zhou, P., Johnston, K. G., Golshani, P., Nie, Q. H., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0496-y · Cited by 116
Norepinephrine signals through astrocytes to modulate synapses
Lefton, K. B., Wu, Y., Dai, Y., Okuda, T., Zhang, Y., Yen, A., Rurak, G. M., Walsh, S., Manno, R., Myagmar, B., et al. (2025) · Science · doi:10.1126/science.adq5480 · Cited by 117
Molecular signatures of neural connectivity in the olfactory cortex
Diodato, A., de Brimont, M. R., Yim, Y. S., Dérian, N., Perrin, S., Pouch, J., Klatzmann, D., Garel, S., Choi, G. B., & Fleischmann, A. (2016) · Nature Communications · doi:10.1038/ncomms12238 · Cited by 113
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
Top-down regulation of motivated behaviors via lateral septum sub-circuits
Besnard, A., & Leroy, F. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01599-3 · Cited by 112
Waterhouse, B. D., & Navarra, R. L. (2018) · Brain Research · doi:10.1016/j.brainres.2018.08.032 · Cited by 121
Locus coeruleus-norepinephrine: basic functions and insights into Parkinson’s disease
Bari, B. A., Chokshi, V. B., & Schmidt, K. (2019) · Neural Regeneration Research · doi:10.4103/1673-5374.270297 · Cited by 112
Extraction of Distinct Neuronal Cell Types from within a Genetically Continuous Population
Kim, E. J., Zhang, Z., Huang, L., Ito-Cole, T., Jacobs, M. W., Juavinett, A. L., Senturk, G., Hu, M., Ku, M., Ecker, J. R., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.04.018 · Cited by 103
Detection and manipulation of live antigen-expressing cells using conditionally stable nanobodies
Tang, J. C. Y., Drokhlyansky, E., Etemad, B., Rudolph, S., Guo, B., Wang, S., Ellis, E. G., Li, J. Z., & Cepko, C. L. (2016) · eLife · doi:10.7554/elife.15312 · Cited by 103
Role of GABA in the regulation of the central circadian clock of the suprachiasmatic nucleus
Ono, D., Honma, K., Yanagawa, Y., Yamanaka, A., & Honma, S. (2018) · The Journal of Physiological Sciences · doi:10.1007/s12576-018-0604-x · Cited by 107
A Genetically Defined Compartmentalized Striatal Direct Pathway for Negative Reinforcement
Xiao, X., Deng, H., Furlan, A., Yang, T., Zhang, X., Hwang, G.-R., Tucciarone, J., Wu, P., He, M., Palaniswamy, R., et al. (2020) · Cell · doi:10.1016/j.cell.2020.08.032 · Cited by 101
Watanabe, K., Chiu, H., Pfeiffer, B. D., Wong, A. M., Hoopfer, E. D., Rubin, G. M., & Anderson, D. J. (2017) · Neuron · doi:10.1016/j.neuron.2017.08.017 · Cited by 104
Determinants of seeding and spreading of α-synuclein pathology in the brain
Henrich, M. T., Geibl, F. F., Harini, L., Stegmann, A., Giasson, B. I., Mao, X., Dawson, V. L., Dawson, T. M., Oertel, W. H., & Surmeier, D. J. (2020) · Science Advances · doi:10.1126/sciadv.abc2487 · Cited by 104
Specific and behaviorally consequential astrocyte Gq GPCR signaling attenuation in vivo with iβARK
Nagai, J., Bellafard, A., Qu, Z., Yu, X., Ollivier, M., Gangwani, M. R., Castro, B. D., Coppola, G., Schumacher, S. M., Golshani, P., et al. (2021) · Neuron · doi:10.1016/j.neuron.2021.05.023 · Cited by 108
Approaches and Limitations in the Investigation of Synaptic Transmission and Plasticity
Glasgow, S. D., McPhedrain, R., Madranges, J. F., Kennedy, T. E., & Ruthazer, E. S. (2019) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2019.00020 · Cited by 100
Doppler, C. E. J., Kinnerup, M. B., Brune, C., Farrher, E., Betts, M. J., Fedorova, T. D., Schaldemose, J. L., Knudsen, K., Ismail, R., Seger, A., et al. (2021) · Brain · doi:10.1093/brain/awab236 · Cited by 100
Posterior amygdala regulates sexual and aggressive behaviors in male mice
Yamaguchi, T., Wei, D., Song, S. C., Lim, B. K., Tritsch, N. X., & Lin, D. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0675-x · Cited by 99
The Temporal Association Cortex Plays a Key Role in Auditory-Driven Maternal Plasticity
Tasaka, G., Feigin, L., Maor, I., Groysman, M., DeNardo, L. A., Schiavo, J. K., Froemke, R. C., Luo, L., & Mizrahi, A. (2020) · Neuron · doi:10.1016/j.neuron.2020.05.004 · Cited by 103
Self-citationHippoBellum: Acute Cerebellar Modulation Alters Hippocampal Dynamics and Function
Zeidler, Z., Hoffmann, K., & Krook-Magnuson, E. I. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0763-20.2020 · Cited by 102
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
Self-citationPersistent 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
Palamarchuk, I. S., & Vaillancourt, T. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.719674 · Cited by 105
Neuron-astrocyte coupling in lateral habenula mediates depressive-like behaviors
Xin, Q., Wang, J., Zheng, J., Tan, Y. J., Jia, X., Ni, Z., Xu, Z., Feng, J., Wu, Z., Li, Y., et al. (2025) · Cell · doi:10.1016/j.cell.2025.04.010 · Cited by 96
Npas1 + -Nkx2.1 + Neurons Are an Integral Part of the Cortico-pallido-cortical Loop
Abecassis, Z. A., Berceau, B. L., Win, P. H., García, D., Xenias, H. S., Cui, Q., Pamukcu, A., Cherian, S., Hernández, V. M., Chon, U., et al. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1199-19.2019 · Cited by 97
Rapid Molecular Profiling of Defined Cell Types Using Viral TRAP
Nectow, A. R., Moya, M. V., Ekstrand, M. I., Mousa, A., McGuire, K. L., Sferrazza, C. E., Field, B. C., Rabinowitz, G. S., Sawicka, K., Liang, Y., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.03.048 · Cited by 94
Locus Coeruleus and Dopamine-Dependent Memory Consolidation
Yamasaki, M., & Takeuchi, T. (2017) · Neural Plasticity · doi:10.1155/2017/8602690 · Cited by 91
Differences in neurotropism and neurotoxicity among retrograde viral tracers
Sun, L., Tang, Y., Yan, K., Yu, J., Zou, Y., Xu, W., Xiao, K., Zhang, Z., Li, W., Wu, B., et al. (2019) · Molecular Neurodegeneration · doi:10.1186/s13024-019-0308-6 · Cited by 91
A noradrenergic-hypothalamic neural substrate for stress-induced sleep disturbances
Antila, H., Kwak, I., Choi, A., Pisciotti, A., Covarrubias, I., Baik, J., Eisch, A., Beier, K., Thomas, S., Weber, F., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2123528119 · Cited by 92
Self-citationA whole-brain monosynaptic input connectome to neuron classes in mouse visual cortex
Yao, S., Wang, Q., Hirokawa, K. E., Ouellette, B., Ahmed, R., Bomben, J., Brouner, K., Casal, L., Caldejon, S., Cho, A., et al. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01219-x · Cited by 91
Uematsu, A., Tan, B. Z., & Johansen, J. P. (2015) · Learning & Memory · doi:10.1101/lm.037283.114 · Cited by 89
Mapping mesoscale axonal projections in the mouse brain using a 3D convolutional network
Friedmann, D., Pun, A., Adams, E. L., Lui, J. H., Kebschull, J. M., Grutzner, S. M., Castagnola, C., Tessier‐Lavigne, M., & Luo, L. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1918465117 · Cited by 97
Self-citationZhang, H., Chaudhury, D., Nectow, A. R., Friedman, A. K., Zhang, S., Juarez, B., Liu, H., Pfau, M. L., Aleyasin, H., Jiang, C., et al. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.08.020 · Cited by 88
A thalamo-amygdalar circuit underlying the extinction of remote fear memories
Silva, B. A., Astori, S., Burns, A. M., Heiser, H., van den Heuvel, L., Santoni, G., Martínez-Reza, M. F., Sandi, C., & Gräff, J. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00856-y · Cited by 91
Collins, L. N., Francis, J., Emanuel, B., & McCormick, D. A. (2023) · eLife · doi:10.7554/elife.81826 · Cited by 87
Noncanonical connections between the subiculum and hippocampal CA1
Xu, X., Sun, Y., Holmes, T. C., & López, A. J. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.24024 · Cited by 88
Yang, F., Liu, Y., Chen, S., Dai, Z., Yang, D., Gao, D., Shao, J., Wang, Y., Wang, T., Zhang, Z., et al. (2020) · Journal of Clinical Investigation · doi:10.1172/jci136105 · Cited by 87
Wang, Q., Cheng, S., Qin, F., Fu, A., & Fu, C. (2021) · RSC Advances · doi:10.1039/d1ra00550b · Cited by 85
Distribution, physiology and pharmacology of relaxin‐3/RXFP3 systems in brain
Ma, S., Smith, C. M., Błasiak, A., & Gundlach, A. L. (2016) · British Journal of Pharmacology · doi:10.1111/bph.13659 · Cited by 85
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
Hypothalamic regulation of the sleep/wake cycle
Ono, D., & Yamanaka, A. (2017) · Neuroscience Research · doi:10.1016/j.neures.2017.03.013 · 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
Catecholaminergic 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
Chandler, D. J. (2015) · Brain Research · doi:10.1016/j.brainres.2015.11.022 · Cited by 87
Sexual rejection via a vomeronasal receptor-triggered limbic circuit
Osakada, T., Ishii, K. K., Mori, H., Eguchi, R., Ferrero, D. M., Yoshihara, Y., Liberles, S. D., Miyamichi, K., & Touhara, K. (2018) · Nature Communications · doi:10.1038/s41467-018-07003-5 · Cited by 78
Self-citationvan der Heijden, M. E., & Sillitoe, R. V. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.06.010 · Cited by 81
Glypicans and Heparan Sulfate in Synaptic Development, Neural Plasticity, and Neurological Disorders
Kamimura, K., & Maeda, N. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.595596 · Cited by 81
Noradrenergic and cholinergic systems take centre stage in neuropsychiatric diseases of ageing
Orlando, I. F., Shine, J. M., Robbins, T. W., Rowe, J. B., & O’Callaghan, C. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105167 · Cited by 81
The locus coeruleus as a global model failure system
Jordan, R. (2023) · Trends in Neurosciences · doi:10.1016/j.tins.2023.11.006 · Cited by 82
Lateral hypothalamic circuits for sleep–wake control
Yamashita, T., & Yamanaka, A. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.03.020 · Cited by 80
Azizi, S. A. (2020) · The Neuroscientist · doi:10.1177/1073858420974336 · Cited by 81
Pinto, D. F. C., Yang, H., Dorocic, I. P., de Jong, J. W., Han, V. J., Peck, J. R., Zhu, Y., Liu, C. J., Beier, K. T., Smidt, M. P., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-12392-2 · Cited by 80
Self-citationAscending noradrenergic excitation from the locus coeruleus to the anterior cingulate cortex
Koga, K., Yamada, A., Song, Q., Li, X., Chen, Q., Liu, R., Ge, J., Zhan, C., Furue, H., Zhuo, M., et al. (2020) · Molecular Brain · doi:10.1186/s13041-020-00586-5 · Cited by 78
Moreno-Rius, J. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.100774 · Cited by 77
Locus coeruleus anchors a trisynaptic circuit controlling fear-induced suppression of feeding
Yang, B., Sánchez-Padilla, J., Kondapalli, J., Morison, S. L., Delpire, E. J., Awatramani, R. B., & Surmeier, D. J. (2021) · Neuron · doi:10.1016/j.neuron.2020.12.023 · Cited by 80
Novello, M., Bosman, L. W. J., & Zeeuw, C. I. D. (2022) · The Cerebellum · doi:10.1007/s12311-022-01499-w · Cited by 78
Sánchez-Bellot, C., AlSubaie, R., Mishchanchuk, K., Wee, R. W. S., & MacAskill, A. F. (2022) · Nature Communications · doi:10.1038/s41467-022-27977-7 · Cited by 78
Zeng, H. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.03.003 · Cited by 76
The role of the serotonergic system in motor control
Kawashima, T. (2017) · Neuroscience Research · doi:10.1016/j.neures.2017.07.005 · Cited by 72
A novel cortico-intrathalamic circuit for flight behavior
Dong, P., Wang, H., Shen, X., Jiang, P., Zhu, X., Li, Y., Gao, J., Lin, S., Huang, Y., He, X., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0391-6 · Cited by 71
Gao, W., Yang, S.-S., Mack, N. R., & Chamberlin, L. A. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01196-w · Cited by 74
Li, S.-J., Vaughan, A., Sturgill, J. F., & Kepecs, Á. (2018) · Neuron · doi:10.1016/j.neuron.2018.05.028 · Cited by 74
Sleep and Sedative States Induced by Targeting the Histamine and Noradrenergic Systems
Yu, X., Franks, N. P., & Wisden, W. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00004 · Cited by 69
Satoh, A., & Iijima, K. (2017) · Brain Research · doi:10.1016/j.brainres.2017.12.027 · Cited by 72
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
Weisenhorn, D. M. V., Giesert, F., & Wurst, W. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13670 · Cited by 73
Lee, C., Lavoie, A., Liu, J., Chen, S. X., & Liu, B. (2020) · Frontiers in Neural Circuits · doi:10.3389/fncir.2020.00018 · Cited by 74
Sensory cortical control of movement
Karadimas, S. K., Satkunendrarajah, K., Laliberté, A. M., Ringuette, D., Weisspapir, I., Li, L., Gosgnach, S., & Fehlings, M. G. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0536-7 · Cited by 66
Koba, S., Inoue, R., & Watanabe, T. (2016) · Physiological Reports · doi:10.14814/phy2.12831 · Cited by 65
Runegaard, A. H., Sørensen, A. T., Fitzpatrick, C. M., Jørgensen, S. H., Petersen, A. V., Hansen, N. W., Weikop, P., Andreasen, J. T., Mikkelsen, J. D., Perrier, J., et al. (2018) · eNeuro · doi:10.1523/eneuro.0345-17.2018 · Cited by 69
Salay, L. D., & Huberman, A. D. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109792 · Cited by 65
Henrich, M. T., Geibl, F. F., Lee, B., Chiu, W., Koprich, J. B., Brotchie, J. M., Timmermann, L., Decher, N., Matschke, L. A., & Oertel, W. H. (2018) · Acta Neuropathologica Communications · doi:10.1186/s40478-018-0541-1 · Cited by 70
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
Properties and modulation of excitatory inputs to the locus coeruleus
Barcomb, K., Olah, S. S., Kennedy, M. J., & Ford, C. (2022) · The Journal of Physiology · doi:10.1113/jp283605 · Cited by 77
Neuroinflammation and Post-Stroke Depression: Focus on the Microglia and Astrocytes
Lu, W., & Wen, J. (2024) · Aging and Disease · doi:10.14336/ad.2024.0214-1 · Cited by 64
Social transmission of food safety depends on synaptic plasticity in the prefrontal cortex
Loureiro, M., Achargui, R., Flakowski, J., van Zessen, R., Stefanelli, T., Pascoli, V., & Lüscher, C. (2019) · Science · doi:10.1126/science.aaw5842 · Cited by 63
Raber, J., Arzy, S., Bertolus, J. B., Depue, B., Haas, H. E., Hofmann, S. G., Kangas, M., Kensinger, E., Lowry, C. A., Marusak, H. A., et al. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.03.015 · Cited by 62
“…of cortical NE (Giustino and Maren, 2018) and highly relevant for fear and learning because of the many LC projections (Schwarz and Luo, 2015; Schwarz et al., 2015) that extend to the medial prefrontal cortex, the basolateral amygdala (all nuclei), the central amygdala and the hippocampus…”
BackgroundInfluentialSong, J. H., Choi, W., Song, Y.-H., Kim, J., Jeong, D., Lee, S., & Paik, S. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107682 · Cited by 63
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
Dissociable Roles of Pallidal Neuron Subtypes in Regulating Motor Patterns
Cui, Q., Pamukcu, A., Cherian, S., Chang, I. Y. M., Berceau, B. L., Xenias, H. S., Higgs, M. H., Rajamanickam, S., Chen, Y., Du, X., et al. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2210-20.2021 · Cited by 62
Luchsinger, J. R., Fetterly, T. L., Williford, K. M., Salimando, G. J., Doyle, M. A., Maldonado, J. A., Simerly, R. B., Winder, D. G., & Centanni, S. W. (2021) · Nature Communications · doi:10.1038/s41467-021-23674-z · Cited by 64
Anteromedial thalamus gates the selection and stabilization of long-term memories
Toader, A. C., Regalado, J. M., Li, Y. R., Terceros, A. A., Yadav, N., Kumar, S., Satow, S., Hollunder, F., Bonito-Oliva, A., & Rajasethupathy, P. (2023) · Cell · doi:10.1016/j.cell.2023.02.024 · Cited by 68
Cocaine-Induced Structural Plasticity in Input Regions to Distinct Cell Types in Nucleus Accumbens
Barrientos, C., Knowland, D., Wu, M. M. J., Lilascharoen, V., Huang, K. W., Malenka, R. C., & Lim, B. K. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.04.019 · Cited by 63
Self-citationExtended amygdala-parabrachial circuits alter threat assessment and regulate feeding
Luskin, A. T., Bhatti, D. L., Mulvey, B., Pedersen, C. E., Girven, K. S., Oden-Brunson, H., Kimbell, K., Blackburn, T., Sawyer, A., Gereau, R. W., et al. (2021) · Science Advances · doi:10.1126/sciadv.abd3666 · Cited by 63
Sadacca, B. F., Wikenheiser, A. M., & Schoenbaum, G. M. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.04.017 · Cited by 59
Hashimoto, M., Yamanaka, A., Kato, S., Tanifuji, M., Kobayashi, K., & Yaginuma, H. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00006 · Cited by 61
Orexin as a modulator of fear-related behavior: Hypothalamic control of noradrenaline circuit
Soya, S., & Sakurai, T. (2018) · Brain Research · doi:10.1016/j.brainres.2018.11.032 · Cited by 63
An, J. J., Kinney, C. E., Tan, J., Liao, G., Kremer, E. J., & Xu, B. (2020) · Nature Communications · doi:10.1038/s41467-020-15537-w · Cited by 59
Self-citationCalretinin positive neurons form an excitatory amplifier network in the spinal cord dorsal horn
Smith, K. M., Browne, T. J., Davis, O. C., Coyle, A., Boyle, K. A., Watanabe, M., Dickinson, S. A., Iredale, J. A., Gradwell, M. A., Jobling, P., et al. (2019) · eLife · doi:10.7554/elife.49190 · Cited by 57
Tsuneoka, Y., Tsukahara, S., Yoshida, S., Takase, K., Oda, S., Kuroda, M., & Funato, H. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00026 · Cited by 58
Wang, X., Jia, W.-B., Xu, X. M., Chen, R., Wang, L., Su, X.-J., Xu, P., Liu, X., Wen, J., Song, X., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-40860-3 · Cited by 59
Lubejko, S. T., Livrizzi, G., Buczynski, S. A., Patel, J. R., Yung, J. C., Yaksh, T. L., & Banghart, M. R. (2024) · Science Advances · doi:10.1126/sciadv.adj9581 · Cited by 58
Bacon, T., Pickering, A. E., & Mellor, J. R. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa159 · Cited by 56
Reward from bugs to bipeds: a comparative approach to understanding how reward circuits function
Scaplen, K. M., & Kaun, K. R. (2016) · Journal of Neurogenetics · doi:10.1080/01677063.2016.1180385 · Cited by 60
Pomeranz, L. E., Ekstrand, M. I., Latcha, K. N., Smith, G. A., Enquist, L. W., & Friedman, J. M. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3193-16.2017 · Cited by 54
Metadata
- Authors
- 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., & Luo, L.
- Affiliations
- Howard Hughes Medical Institute (US)
- Centre National de la Recherche Scientifique (FR)
- Stanford Medicine (US)
- Corresponding author
- Luo, Liqun
- ORCID
- Venue
- Nature
- Published
- 2015-07-01
- Volume
- 524
- Issue
- 7563
- Pages
- 88-92
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC4587569
- OpenAlex
- W2099401565
- Cited by
- 744
- References
- 40
- Citations by year
- 2026: 48 · 2025: 74 · 2024: 64 · 2023: 85 · 2022: 67 · 2021: 77 · 2020: 85 · 2019: 78 · 2018: 55 · 2017: 55 · 2016: 38 · 2015: 16
- FWCI
- 25.50
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Science Foundation
- Howard Hughes Medical Institute
- Agence Nationale de la Recherche (ANR-10-LABX-0012)
- Stanford Bio-X
- National Institute of Mental Health
- National Institute on Drug Abuse (F32DA038913, P01DA008227)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
- Keywords
- locus coeruleus, noradrenergic neurons, norepinephrine, rabies virus tracing, transsynaptic tracing, Purkinje cells, neuronal projection patterns, mice, brain states, spinal cord projections, sensory gating
- MeSH terms
- Animals, Axons, Brain, Female, Locus Coeruleus, Male, Neural Pathways, Neurons, Norepinephrine, Pilot Projects, Purkinje Cells, Rabies virus, Synapses, Reproducibility of Results, Rats, Wistar, Mice, Rats, Neuroanatomical Tract-Tracing 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