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Impulse activity of locus coeruleus neurons in awake rats and monkeys is a function of sensory stimulation and arousal
Open accessAbstract
By means of extracellular recordings, individual norepinephrine-containing neurons in the locus coeruleus of unanesthetized behaviorally responsive rats and squirrel monkeys were found to respond to specific sensory and behavioral conditions. In rats, distinct clusters of action potentials followed the presentation of various nonnoxious auditory, visual, or somatosensory stimuli at latencies of 15-60 msec. Increased discharge rates were also seen during periods of spontaneous electroencephalogram arousal in both species. In monkeys, these cells responded most vigorously to complex arousing stimuli such as a preferred food. Because the noradrenergic innervation of most forebrain regions arises from the locus coeruleus, these results allow prediction of situations under which this massive projection system would be active and suggest a physiological role for this chemically identified network in specific behavioral processes.
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“Low arousal conditions are associated with very low levels of NE cell firing (Aston-Jones et al., 2000; Foote et al., 1980).”
From Catecholamine influences on prefrontal cortical function: Relevance to treatment of attention deficit/hyperactivity disorder and related disorders (2011) · cites this paper as Foote et al., 1980
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Cites
Applied Nonparametric Statistics
Wozniak, P. J., & Daniel, W. W. (1991) · Technometrics · doi:10.2307/1268795 · Cited by 5,008
Sleep Cycle Oscillation: Reciprocal Discharge by Two Brainstem Neuronal Groups
Hobson, J. A., McCarley, R. W., & Wyzinski, P. (1975) · Science · doi:10.1126/science.1094539 · Cited by 1,238
Raphe unit activity in freely moving cats: correlation with level of behavioral arousal.
Trulson, M., & Jacobs, B. (1979) · Brain Research · doi:10.1016/0006-8993(79)90157-4 · Cited by 815
II. New evidence for a locus coeruleus-norepinephrine connection with anxiety
Redmond, D. E., & Huang, Y. H. (1979) · Life Sciences · doi:10.1016/0024-3205(79)90087-0 · Cited by 662
The locus coeruleus: A cytoarchitectonic, golgi and immunohistochemical study in the albino rat
Swanson, L. W. (1976) · Brain Research · doi:10.1016/0006-8993(76)90207-9 · Cited by 518
The locus coeruleus: neurobiology of a central noradrenergic nucleus
Amaral, D. G., & Sinnamon, H. M. (1977) · Progress in Neurobiology · doi:10.1016/0301-0082(77)90016-8 · Cited by 497
Effects of putative neurotransmitters on neuronal activity in monkey auditory cortex
Foote, S. L., Freedman, R., & Oliver, A. P. (1975) · Brain Research · doi:10.1016/0006-8993(75)90699-x · Cited by 458
Self-citationNoradrenergic neurons: Morphine inhibition of spontaneous activity
Korf, J., Bunney, B. S., & Aghajanian, G. K. (1974) · European Journal of Pharmacology · doi:10.1016/0014-2999(74)90045-4 · Cited by 432
Neuronal activity during the sleep-waking cycle
Steriade, M., & Hobson, J. A. (1976) · Progress in Neurobiology · doi:10.1016/0301-0082(76)90013-7 · Cited by 386
Cedarbaum, J. M., & Aghajanian, G. K. (1978) · Life Sciences · doi:10.1016/0024-3205(78)90398-3 · Cited by 382
Research works printed but not linked: 3
- [19]Foote, S. & Bloom, F. (1979) in Catecholamines: Basic and Clinical Frontiers, eds. Usdin, E., Kopin, I. & Barchas, J. (Pergamon, Elmsford, NY), pp. 625–627.
- [20]Jones, G., Segal, M., Foote, S. & Bloom, F. (1979) in Catecholamines: Basic and Clinical Frontiers, eds. Usdin, E., Kopin, I. & Barchas, J. (Pergamon, Elmsford, NY), pp. 643–645.
- [21]Siegel, S. (1956) Nonparametric Statistics (McGraw-Hill, New York).
Cited by
Sorted by citations
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Curtis, A. L., Leiser, S. C., Snyder, K., & Valentino, R. J. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.11.020 · Cited by 120
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Isaac, S. O., & Berridge, C. W. (2003) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.103.053918 · Cited by 120
Dunn, A. J., & Kramarcy, N. R. (1984) · Springer eBooks · doi:10.1007/978-1-4615-7178-0_8 · Cited by 120
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Nelson, K. R., Mattingly, M., Lee, S. A., & Schmitt, F. A. (2006) · Neurology · doi:10.1212/01.wnl.0000204296.15607.37 · Cited by 115
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Hirata, A., Aguilar, J., & Castro-Alamancos, M. A. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.5298-05.2006 · Cited by 118
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Coull, J. T., Frith, C., Dolan, R. J., Frackowiak, R. S. J., & Grasby, P. M. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01635.x · Cited by 117
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Eschenko, O., & Sara, S. J. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn020 · Cited by 115
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Fort, P., Khateb, A., Pegna, A. J., Mühlethaler, M., & Jones, B. E. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb01145.x · Cited by 115
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The influence of alertness on spatial and nonspatial components of visual attention.
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Jonkman, L. M., van Melis, J. J. M., Kemner, C., & Markus, C. R. (2007) · Biological Psychology · doi:10.1016/j.biopsycho.2007.08.004 · Cited by 111
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Haug, T. M., & Storm, J. F. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.4.2071 · Cited by 110
Brain aminergic axons exhibit marked variability in conduction velocity
Aston‐Jones, G., Segal, M., & Bloom, F. E. (1980) · Brain Research · doi:10.1016/0006-8993(80)90880-x · Cited by 110
Self-citationAltered locus coeruleus–norepinephrine function following single prolonged stress
George, S. A., Knox, D., Curtis, A. L., Aldridge, J. W., Valentino, R. J., & Liberzon, I. (2012) · European Journal of Neuroscience · doi:10.1111/ejn.12095 · Cited by 108
Brainstem Modulation of the Hippocampus
Vertes, R. P. (1986) · Springer eBooks · doi:10.1007/978-1-4615-8024-9_2 · Cited by 109
Novitskaya, Y., Sara, S. J., Logothetis, N. K., & Eschenko, O. (2016) · Learning & Memory · doi:10.1101/lm.040923.115 · Cited by 116
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Page, M. E., Berridge, C. W., Foote, S. L., & Valentino, R. J. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90862-f · Cited by 107
Self-citationKiyashchenko, L. I., Mileykovskiy, B. Y., Lai, Y.-Y., & Siegel, J. M. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.5.2008 · Cited by 105
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Veyrac, A., Sacquet, J., Nguyen, V., Marien, M. R., Jourdan, F., & Didier, A. (2008) · Neuropsychopharmacology · doi:10.1038/npp.2008.191 · Cited by 105
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Zhang, Z., Matos, S. C., Jego, S., Adamantidis, A., & Séguéla, P. (2013) · PLoS ONE · doi:10.1371/journal.pone.0066122 · Cited by 110
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Waterhouse, B. D., & Navarra, R. L. (2018) · Brain Research · doi:10.1016/j.brainres.2018.08.032 · Cited by 121
Baumgartner, A., Dietzel, M., Saletu, B., Wolf, R. W., Campos‐Barros, Á., Gräf, K.-J., Kürten, I., & Mannsmann, U. (1993) · Psychiatry Research · doi:10.1016/0165-1781(93)90039-j · Cited by 103
Feenstra, M. G. P. (2000) · Progress in brain research · doi:10.1016/s0079-6123(00)26012-3 · Cited by 103
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Morilak, D. A., Fornal, C. A., & Jacobs, B. L. (1987) · Brain Research · doi:10.1016/0006-8993(87)90535-x · Cited by 102
Spronk, M., Jonkman, L. M., & Kemner, C. (2008) · Clinical Neurophysiology · doi:10.1016/j.clinph.2008.09.010 · Cited by 108
Page, M. E., & Abercrombie, E. D. (1999) · Synapse · doi:10.1002/(sici)1098-2396(19990915)33:4 · Cited by 100
West, C. H. K., Ritchie, J., Boss-Williams, K. A., & Weiss, J. M. (2008) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145708009474 · Cited by 103
Catecholamines and cognition after traumatic brain injury
Jenkins, P. O., Mehta, M. A., & Sharp, D. J. (2016) · Brain · doi:10.1093/brain/aww128 · Cited by 102
Activation of locus coeruleus by prefrontal cortex is mediated by excitatory amino acid inputs
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Lee, H. S., Kim, M., & Waterhouse, B. D. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20365 · Cited by 99
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Gonon, F., Buda, M., de Simoni, G., & Pujol, J. F. (1983) · Brain Research · doi:10.1016/0006-8993(83)90845-4 · Cited by 97
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Guyenet, P. G., Bayliss, D. A., Stornetta, R. L., Ludwig, M., Kumar, N. N., Shi, Y., Burke, P. G. R., Kanbar, R., Basting, T. M., Holloway, B. B., et al. (2016) · The Journal of Physiology · doi:10.1113/jp271480 · Cited by 98
Opp, M. R. (1995) · Advances in Neuroimmunology · doi:10.1016/0960-5428(95)00004-l · Cited by 96
Jordan, R., & Keller, G. B. (2023) · eLife · doi:10.7554/elife.85111 · Cited by 127
Moises, H. C., Waterhouse, B. D., & Woodward, D. J. (1981) · Brain Research · doi:10.1016/0006-8993(81)90939-2 · Cited by 95
Nakamura, S., & Sakaguchi, T. (1990) · Progress in Neurobiology · doi:10.1016/0301-0082(90)90018-c · Cited by 94
Behavior during hippocampal microinfusions. I. Norepinephrine and diversive exploration
Flicker, C., & Geyer, M. A. (1982) · Brain Research Reviews · doi:10.1016/0165-0173(82)90006-6 · Cited by 94
Marzo, A., Totah, N. K. B., Neves, R. M., Logothetis, N. K., & Eschenko, O. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00920.2013 · Cited by 90
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Page, M. E., Akaoka, H., Aston‐Jones, G., & Valentino, R. J. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90295-d · Cited by 92
Self-citationKalwani, R. M., Joshi, S., & Gold, J. I. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2566-14.2014 · Cited by 96
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Berridge, C. W. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301159 · Cited by 91
Kössl, M., & Vater, M. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-12-04169.1989 · Cited by 91
Hahn, M. K., & Bannon, M. J. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00319-x · Cited by 90
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España, R. A., & Berridge, C. W. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20946 · Cited by 90
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Vitrac, C., & Benoit‐Marand, M. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00072 · Cited by 94
The neuroanatomical basis of anxiety
Pratt, J. A. (1992) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(92)90014-q · Cited by 89
Psychiatric symptoms of noradrenergic dysfunction: A pathophysiological view
Yamamoto, K., Shinba, T., & Yoshii, M. (2014) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.12126 · Cited by 88
Mefford, I. N., & Potter, W. Z. (1989) · Medical Hypotheses · doi:10.1016/0306-9877(89)90164-3 · Cited by 89
Bari, A., & Aston-Jones, G. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.07.020 · Cited by 85
Self-citationNeurobiology of ADHD: A Review
Mehta, T., Monegro, A. F., Nene, Y., Fayyaz, M., & Bollu, P. C. (2019) · Current Developmental Disorders Reports · doi:10.1007/s40474-019-00182-w · Cited by 98
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Privitera, M., Ferrari, K. D., von Ziegler, L., Sturman, O., Duss, S. N., Floriou‐Servou, A., Germain, P., Vermeiren, Y., Wyss, M. T., Deyn, P. P. D., et al. (2020) · Nature Protocols · doi:10.1038/s41596-020-0324-6 · Cited by 86
The cholinergic nucleus basalis: A key structure in neocortical arousal
Buzsáki, G., & Gage, F. H. (1989) · Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions · doi:10.1007/978-3-0348-9138-7_16 · Cited by 86
Berridge, C. W., & Stalnaker, T. A. (2002) · Synapse · doi:10.1002/syn.10131 · Cited by 86
Locus coeruleus activation by physiological challenges
Page, M. E., & Valentino, R. J. (1994) · Brain Research Bulletin · doi:10.1016/0361-9230(94)90169-4 · Cited by 86
Weil, R. S., Nicholas Furl, A., Ruff, C. C., Symmonds, M., Flandin, G., Dolan, R. J., Driver, J., & Rees, G. E. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00870.2009 · Cited by 84
Escanilla, O., Arellanos, A., Karnow, A., Ennis, M. J., & Linster, C. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07297.x · Cited by 85
Britton, K. T., Segal, D. S., Kuczenski, R. T., & Hauger, R. (1992) · Brain Research · doi:10.1016/0006-8993(92)90808-m · Cited by 86
Mileykovskiy, B. Y., Kiyashchenko, L. I., Kodama, T., Lai, Y., & Siegel, J. M. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-22-08551.2000 · Cited by 85
Role of the locus coeruleus and basal forebrain in arousal and attention
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The bladder–brain connection: putative role of corticotropin-releasing factor
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Berridge, C. W., Arnsten, A. F. T., & Foote, S. L. (1993) · Psychological Medicine · doi:10.1017/s0033291700025332 · Cited by 83
Self-citationSimson, P. E., & Weiss, J. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-06-01732.1987 · Cited by 83
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Olpe, H. R., Jones, R. S. G., & Steinmann, M. (1983) · Cellular and Molecular Life Sciences · doi:10.1007/bf01955287 · Cited by 81
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Castelino, C. B., & Ball, G. F. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04028.x · Cited by 78
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Zampese, E., & Surmeier, D. J. (2020) · Cells · doi:10.3390/cells9092045 · Cited by 79
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Chamberlain, S. R., Müller, U., Robbins, T. W., & Sahakian, B. J. (2006) · Current Opinion in Neurology · doi:10.1097/01.wco.0000247613.28859.77 · Cited by 80
Excitatory effects of adenosine 5′-triphosphate on rat locus coeruleus neurones
Tschöpl, M., Harms, L., Nörenberg, W., & Illés, P. (1992) · European Journal of Pharmacology · doi:10.1016/0014-2999(92)90234-u · Cited by 79
Song, A. H., Kucyi, A., Napadow, V., Brown, E. N., Loggia, M. L., & Akeju, O. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0446-17.2017 · Cited by 83
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Harley, C. W., & Milway, J. S. (1986) · Experimental Brain Research · doi:10.1007/bf00235656 · Cited by 77
Sustained vigilance and animal performance
Dukas, R., & Clark, C. (1995) · Animal Behaviour · doi:10.1006/anbe.1995.0158 · Cited by 77
Metadata
- Authors
- Foote, S. L., Aston-Jones, G., & Bloom, F. E.
- Affiliations
- Salk Institute for Biological Studies (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1980-05
- Volume
- 77
- Issue
- 5
- Pages
- 3033-3037
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC349541
- OpenAlex
- W2016014417
- Cited by
- 857
- References
- 22
- Citations by year
- 2026: 16 · 2025: 13 · 2024: 18 · 2023: 29 · 2022: 28 · 2021: 26 · 2020: 23 · 2019: 22 · 2018: 22 · 2017: 17 · 2016: 21 · 2015: 23 · 2014: 22 · 2013: 19 · 2012: 25
- FWCI
- 4.34
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Rutgers University Community Repository (Rutgers University) (submittedVersion)
- CaltechAUTHORS (California Institute of Technology) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroscience of respiration and sleep
- Keywords
- locus coeruleus, noradrenergic neurons, neuronal firing rate, sensory stimulation, arousal, auditory stimuli, visual stimuli, somatosensory stimuli, food reward, rats, squirrel monkey
- MeSH terms
- Action Potentials, Adrenergic Fibers, Animals, Haplorhini, Arousal, Auditory Perception, Evoked Potentials, Locus Coeruleus, Male, Nociceptors, Norepinephrine, Sleep, Visual Perception, Wakefulness, Rats
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 ›
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