The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index.
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.
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?
The cited source says what the claim attributes to it.
In the citing paper
“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
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
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
Predictive reward signal of dopamine neurons
Schultz, W. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.1.1 · Cited by 4,564
Aston-Jones, G., & Cohen, J. D. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135709 · Cited by 4,472
Self-citationGetting formal with dopamine and reward
Schultz, W. (2002) · Neuron · doi:10.1016/s0896-6273(02)00967-4 · Cited by 2,574
Berridge, C. W., & Waterhouse, B. D. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(03)00143-7 · Cited by 2,529
Aston-Jones, G., & Bloom, F. (1981) · The Journal of Neuroscience · doi:10.1523/jneurosci.01-08-00876.1981 · Cited by 1,960
Self-citationCircuitry of Primate Prefrontal Cortex and Regulation of Behavior by Representational Memory
Goldman‐Rakic, P. S. (1987) · Comprehensive Physiology · doi:10.1002/cphy.cp010509 · Cited by 1,960
Nucleus locus ceruleus: new evidence of anatomical and physiological specificity
Foote, S. L., Bloom, F. E., & Aston-Jones, G. (1983) · Physiological Reviews · doi:10.1152/physrev.1983.63.3.844 · Cited by 1,901
Self-citationDecision making, the P3, and the locus coeruleus–norepinephrine system
Nieuwenhuis, S., Aston-Jones, G., & Cohen, J. D. (2005) · Psychological Bulletin · doi:10.1037/0033-2909.131.4.510 · Cited by 1,678
Self-citationNeuronal Coding of Prediction Errors
Schultz, W., & Dickinson, A. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.473 · Cited by 1,427
The cognitive neuroscience of sustained attention: where top-down meets bottom-up.
Sarter, M., Givens, B., & Bruno, J. P. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00044-3 · Cited by 1,194
Selective neuronal vulnerability in Parkinson disease
Surmeier, D. J., Obeso, J. A., & Halliday, G. M. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.178 · Cited by 1,116
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
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
Clinical and Biochemical Manifestations of Depression
Gold, P. W., Goodwin, F. K., & Chrousos, G. P. (1988) · New England Journal of Medicine · doi:10.1056/nejm198808183190706 · Cited by 1,057
Meerlo, P., Sgoifo, A., & Suchecki, D. (2008) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2007.07.007 · Cited by 948
Role of locus coeruleus in attention and behavioral flexibility
Aston-Jones, G., Rajkowski, J., & Cohen, J. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(99)00140-7 · Cited by 900
Self-citationMechanisms of stress: A dynamic overview of hormonal and behavioral homeostasis
Johnson, E. O., Kamilaris, T. C., Chrousos, G. P., & Gold, P. W. (1992) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(05)80175-7 · Cited by 899
Network reset: a simplified overarching theory of locus coeruleus noradrenaline function
Bouret, S., & Sara, S. J. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.09.002 · Cited by 862
Gilzenrat, M. S., Nieuwenhuis, S., Jepma, M., & Cohen, J. D. (2010) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/cabn.10.2.252 · Cited by 873
The Brain Nucleus Locus Coeruleus: Restricted Afferent Control of a Broad Efferent Network
Aston‐Jones, G., Ennis, M. J., Pieribone, V. A., Nickell, W. T., & Shipley, M. T. (1986) · Science · doi:10.1126/science.3775363 · Cited by 778
Self-citationSamuels, E., & Szabadi, E. (2008) · Current Neuropharmacology · doi:10.2174/157015908785777229 · Cited by 766
Sex differences in stress-related psychiatric disorders: neurobiological perspectives
Bangasser, D. A., & Valentino, R. J. (2014) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.03.008 · Cited by 737
The role of locus coeruleus in the regulation of cognitive performance
Usher, M., Cohen, J. D., Servan-Schreiber, D., Rajkowski, J., & Aston-Jones, G. (1999) · Science · doi:10.1126/science.283.5401.549 · Cited by 715
Self-citationMather, M., Clewett, D., Sakaki, M., & Harley, C. W. (2016) · Behavioral and Brain Sciences · doi:10.1017/s0140525x15000667 · Cited by 695
CRH Engagement of the Locus Coeruleus Noradrenergic System Mediates Stress-Induced Anxiety
McCall, J. G., Al-Hasani, R., Siuda, E. R., Hong, D. Y., Norris, A. J., Ford, C. P., & Bruchas, M. R. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.002 · Cited by 666
Locus coeruleus neurons in monkey are selectively activated by attended cues in a vigilance task
Aston-Jones, G., Rajkowski, J., Kubiak, P., & Alexinsky, T. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-07-04467.1994 · Cited by 637
Self-citationAdaptive 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
Self-citationCellular mechanisms of brain state-dependent gain modulation in visual cortex
Polack, P.-O., Friedman, J., & Golshani, P. (2013) · Nature Neuroscience · doi:10.1038/nn.3464 · Cited by 628
Charney, D. S. (1984) · Archives of General Psychiatry · doi:10.1001/archpsyc.1984.01790190025003 · Cited by 599
Androgen modulates N-methyl-D-aspartate-mediated depolarization in CA1 hippocampal pyramidal cells
Pouliot, W. A., Handa, R. J., & Beck, S. G. (1996) · Synapse · doi:10.1002/(sici)1098-2396(199605)23:1 · Cited by 128
Aston‐Jones, G., Chiang, C., & Alexinsky, T. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)63830-3 · Cited by 589
Self-citationAdrenergic 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
Effects of sleep and arousal on the processing of visual information in the cat
Livingstone, M. S., & Hubel, D. H. (1981) · Nature · doi:10.1038/291554a0 · Cited by 583
Organization of the Locus Coeruleus-Norepinephrine System
Schwarz, L. A., & Luo, L. (2015) · Current Biology · doi:10.1016/j.cub.2015.09.039 · Cited by 578
Role of norepinephrine in the pathophysiology and treatment of posttraumatic stress disorder
Southwick, S. M., Bremner, J. D., Rasmusson, A., Morgan, C. A., Arnsten, A., & Charney, D. S. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(99)00219-x · Cited by 573
Convergent regulation of locus coeruleus activity as an adaptive response to stress
Valentino, R. J., & Van Bockstaele, E. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.11.062 · Cited by 569
Pupillometry and P3 index the locus coeruleus-noradrenergic arousal function in humans
Murphy, P. R., Robertson, I. H., Balsters, J. H., & O'connell, R. G. (2011) · Psychophysiology · doi:10.1111/j.1469-8986.2011.01226.x · Cited by 519
Norepinephrine Controls Astroglial Responsiveness to Local Circuit Activity
Paukert, M., Agarwal, A., Cha, J., Doze, V. A., Kang, J. U., & Bergles, D. E. (2014) · Neuron · doi:10.1016/j.neuron.2014.04.038 · Cited by 556
Clinical and Biochemical Manifestations of Depression
Gold, P. W., Goodwin, F. K., & Chrousos, G. P. (1988) · New England Journal of Medicine · doi:10.1056/nejm198808113190606 · Cited by 547
Brain mechanisms of insomnia: new perspectives on causes and consequences
Someren, E. J. W. V. (2020) · Physiological Reviews · doi:10.1152/physrev.00046.2019 · Cited by 578
Neurobiology of REM and NREM sleep
McCarley, R. W. (2007) · Sleep Medicine · doi:10.1016/j.sleep.2007.03.005 · Cited by 538
Paus, T., Zatorre, R. J., Hofle, N., Caramanos, Z., Gotman, J., Petrides, M., & Evans, A. C. (1997) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1997.9.3.392 · Cited by 514
The control of retinogeniculate transmission in the mammalian lateral geniculate nucleus
Sherman, S. M., & Christof Koch, A. (1986) · Experimental Brain Research · doi:10.1007/bf00235642 · Cited by 513
Xu, Y.-L., Reinscheid, R. K., Huitrón‐Reséndiz, S., Clark, S. D., Wang, Z., Lin, S. H., Brücher, F., Zeng, J., Ly, N. K., Henriksen, S. J., et al. (2004) · Neuron · doi:10.1016/j.neuron.2004.08.005 · Cited by 514
Extrathalamic Modulation Of Cortical Function
Foote, S. L., & Morrison, J. (1987) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.10.030187.000435 · Cited by 489
Self-citationNeural mechanisms of selective visual attention.
Moore, T., & Zirnsak, M. (2017) · Annual Review of Psychology · doi:10.1146/annurev-psych-122414-033400 · Cited by 471
Paus, T., Koski, L. M., Caramanos, Z., & Westbury, C. F. (1998) · Neuroreport · doi:10.1097/00001756-199806220-00001 · Cited by 460
Varazzani, C., San‐Galli, A., Gilardeau, S., & Bouret, S. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0454-15.2015 · Cited by 482
Samuels, E., & Szabadi, E. (2008) · Current Neuropharmacology · doi:10.2174/157015908785777193 · Cited by 454
Loughlin, S. E., Foote, S. L., & Grzanna, R. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90156-9 · Cited by 437
Self-citationBerridge, C. W., & Foote, S. L. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-10-03135.1991 · Cited by 434
Self-citationAghajanian, G. K., & VanderMaelen, C. P. (1982) · Science · doi:10.1126/science.6278591 · Cited by 431
Goodman, A. (2007) · Biochemical Pharmacology · doi:10.1016/j.bcp.2007.07.030 · Cited by 445
Locus coeruleus and regulation of behavioral flexibility and attention
(2000) · Progress in Brain Research · doi:10.1016/s0079-6123(00)26013-5 · Cited by 400
Self-citationMorrison, J. H., & Foote, S. L. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902430110 · Cited by 392
Self-citationBrainstem projections to spinal motoneurons: An update
Holstege, J. C., & Kuypers, H. G. J. M. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90160-6 · Cited by 389
Arnsten, A. F. T., & Pliszka, S. R. (2011) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2011.01.020 · Cited by 383
Abercrombie, E., & Jacobs, B. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-09-02837.1987 · Cited by 377
“…electrophysiological studies of LC neurons in unanesthetized animals have shown that these neurons are activated by a wide variety of environmental stimuli of many modalities (Foote and Bloom, 1979; Foote et al., 1980; Aston-Jones and Bloom, 198 lb; Rasmussen et al., 1986).”
BackgroundThe reticular-activating hypofrontality (RAH) model of acute exercise
Dietrich, A., & Audiffren, M. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.02.001 · Cited by 365
Locus coeruleus activity in monkey: Phasic and tonic changes are associated with altered vigilance
Rajkowski, J., Kubiak, P., & Aston‐Jones, G. (1994) · Brain Research Bulletin · doi:10.1016/0361-9230(94)90175-9 · Cited by 359
Self-citationNoradrenergic modulation of arousal
Berridge, C. W. (2008) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.10.013 · Cited by 368
Buchsbaum, M. S., Wu, J. C., DeLisi, L. E., Holcomb, H. H., KESSLER, R. M., Johnson, J., King, A. C., Hazlett, E., Langston, K. C., & Post, R. M. (1986) · Journal of Affective Disorders · doi:10.1016/0165-0327(86)90036-4 · Cited by 368
A new three-dimensional model for emotions and monoamine neurotransmitters
Lövheim, H. (2011) · Medical Hypotheses · doi:10.1016/j.mehy.2011.11.016 · Cited by 396
Thiele, A., & Bellgrove, M. A. (2018) · Neuron · doi:10.1016/j.neuron.2018.01.008 · Cited by 350
Webster, H. H., & Jones, B. E. (1988) · Brain Research · doi:10.1016/0006-8993(88)90471-4 · Cited by 350
Noradrenergic modulation of wakefulness/arousal
Berridge, C. W., Schmeichel, B. E., & España, R. A. (2012) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2011.12.003 · Cited by 360
Baldo, B. A., Daniel, R. A., Berridge, C. W., & Kelley, A. E. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10783 · Cited by 346
Arnsten, A. F. T., & Goldman-Rakic, P. S. (1984) · Brain Research · doi:10.1016/0006-8993(84)90351-2 · Cited by 333
Recognition memory: neuronal substrates of the judgement of prior occurrence
Brown, M. W., & Xiang, J. ‐. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00002-1 · Cited by 337
Svensson, T. H. (1987) · Psychopharmacology · doi:10.1007/bf00215471 · Cited by 334
Long Road to Ruin: Noradrenergic Dysfunction in Neurodegenerative Disease
Weinshenker, D. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.01.010 · Cited by 339
Single unit activity of locus coeruleus neurons in the freely moving cat
Rasmussen, K., Morilak, D. A., & Jacobs, B. L. (1986) · Brain Research · doi:10.1016/0006-8993(86)90370-7 · Cited by 324
Potent excitatory influence of prefrontal cortex activity on noradrenergic locus coeruleus neurons
Jodoj, E., Chiang, C., & Aston-Jones, G. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00372-2 · Cited by 321
Self-citationEvolving concepts of sleep cycle generation: From brain centers to neuronal populations
Hobson, J. A., Lydic, R., & Baghdoyan, H. A. (1986) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00046215 · Cited by 317
Hunt, R. D., Minderaa, R. B., & Cohen, D. J. (1985) · Journal of the American Academy of Child Psychiatry · doi:10.1016/s0002-7138(09)60065-0 · Cited by 313
Wake-promoting and sleep-suppressing actions of hypocretin (orexin): basal forebrain sites of action
España, R. A., Baldo, B. A., Kelley, A. E., & Berridge, C. W. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00319-0 · Cited by 311
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
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
Charney, D. S., Woods, S. W., Goodman, W. K., & Heninger, G. R. (1987) · American Journal of Psychiatry · doi:10.1176/ajp.144.8.1030 · Cited by 301
Phasic norepinephrine: A neural interrupt signal for unexpected events
Dayan, P., & Yu, A. J. (2006) · Network Computation in Neural Systems · doi:10.1080/09548980601004024 · Cited by 319
Abnormal Regulation of Noradrenergic Function in Panic Disorders
Charney, D. S. (1986) · Archives of General Psychiatry · doi:10.1001/archpsyc.1986.01800110028005 · Cited by 300
Valentino, R. J., Foote, S. L., & Page, M. E. (1993) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1993.tb49931.x · Cited by 292
Self-citationSurprisingly rich projection from locus coeruleus to the olfactory bulb in the rat
Shipley, M. T., Halloran, F. J., & de la Torre, J. (1985) · Brain Research · doi:10.1016/0006-8993(85)90537-2 · Cited by 292
Codispoti, M., Ferrari, V., & Bradley, M. M. (2007) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2007.19.4.577 · Cited by 288
Maloney, K. J., Mainville, L., & Jones, B. E. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-08-03057.1999 · Cited by 284
Identification of a brainstem circuit regulating visual cortical state in parallel with locomotion
Lee, A. M., Hoy, J. L., Bonci, A., Wilbrecht, L., Stryker, M. P., & Niell, C. M. (2014) · Neuron · doi:10.1016/j.neuron.2014.06.031 · Cited by 282
Sleep Neurobiology from a Clinical Perspective
España, R. A., & Scammell, T. E. (2011) · SLEEP · doi:10.5665/sleep.1112 · Cited by 294
Neuronal Gene Expression in the Waking State: A Role for the Locus Coeruleus
Cirelli, C., Pompeiano, M., & Tononi, G. (1996) · Science · doi:10.1126/science.274.5290.1211 · Cited by 270
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-citationPedarzani, P., & Storm, J. F. (1993) · Neuron · doi:10.1016/0896-6273(93)90216-e · Cited by 272
Xu, Y., Gall, C. M., Jackson, V. R., Civelli, O., & Reinscheid, R. K. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21159 · Cited by 272
Sex differences in the locus coeruleus-norepinephrine system and its regulation by stress
Bangasser, D. A., Wiersielis, K., & Khantsis, S. (2015) · Brain Research · doi:10.1016/j.brainres.2015.11.021 · Cited by 278
Timing is not everything: neuromodulation opens the STDP gate
Pawlak, V. (2010) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2010.00146 · Cited by 267
Neuronal Basis of Behavioral State Control
Hobson, J. A., & Steriade, M. (1986) · Comprehensive physiology · doi:10.1002/cphy.cp010414 · Cited by 256
Chapter 23 Role of the locus coeruleus in emotional activation
Aston‐Jones, G., Rajkowski, J., Kubiak, P., Valentino, R. J., & Shipley, M. T. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)61877-4 · Cited by 256
Self-citationLocus 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
Locus coeruleus neuronal activity during the sleep-waking cycle in mice
Takahashi, K., Kayama, Y., Lin, J., & Sakai, K. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.06.009 · Cited by 251
Nash Unsworth, A., & Robison, M. K. (2017) · Psychonomic Bulletin & Review · doi:10.3758/s13423-016-1220-5 · Cited by 277
Valentino, R. J., Page, M. E., & Curtis, A. L. (1991) · Brain Research · doi:10.1016/0006-8993(91)90855-p · Cited by 246
REM sleep and depression: common neurobiological control mechanisms
McCarley, R. W. (1982) · American Journal of Psychiatry · doi:10.1176/ajp.139.5.565 · Cited by 246
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 ›
Are you an author, or do you see a problem with this page? Request a review