The locus ceruleus norepinephrine system: Functional organization and potential clinical significance
Abstract
IL-9–producing Th cells, termed Th9 cells, contribute to immunity against parasites and cancers but have detrimental roles in allergic disease and colitis. Th9 cells differentiate in response to IL-4 and TGF-β, but these signals are insufficient to drive Th9 differentiation in the absence of IL-2. IL-2–induced STAT5 activation is required for chromatin accessibility within Il9 enhancer and promoter regions and directly transactivates the Il9 locus. STAT5 also suppresses gene expression during Th9 cell development, but these roles are less well defined. In this study, we demonstrate that human allergy-associated Th9 cells exhibited a signature of STAT5-mediated gene repression that is associated with the silencing of a Th17-like transcriptional signature. In murine Th9 cell differentiation, blockade of IL-2/STAT5 signaling induced the expression of IL-17 and the Th17-associated transcription factor Rorγt. However, IL-2–deprived Th9 cells did not exhibit a significant Th17- or STAT3-associated transcriptional signature. Consistent with these observations, differentiation of IL-17–producing cells under these conditions was STAT3-independent but did require Rorγt and BATF. Furthermore, ectopic expression of Rorγt and BATF partially rescued IL-17 production in STAT3-deficient Th17 cells, highlighting the importance of these factors in this process. Although STAT3 was not required for the differentiation of IL-17–producing cells under IL-2–deprived Th9 conditions, their prolonged survival was STAT3-dependent, potentially explaining why STAT3-independent IL-17 production is not commonly observed in vivo. Together, our data suggest that IL-2/STAT5 signaling plays an important role in controlling the balance of a Th9 versus a Th17-like differentiation program in vitro and in allergic disease.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
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?
NE modulates multiple functions, including arousal, attention, stress, and learning and memory.
“NE modulates multiple functions, including arousal, attention, stress, and learning and memory”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Benarroch, 2009
The locus coeruleus located in the brainstem is a cluster of adrenergic neurons that release NE across the central nervous system.
“The locus coeruleus located in the brainstem is a cluster of adrenergic neurons that release NE across the central nervous system.”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Benarroch, 2009
Cites
Aston-Jones, G., & Cohen, J. D. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135709 · Cited by 4,472 · see citing works
The reorienting system of the human brain: from environment to theory of mind
Corbetta, M., Patel, G., & Shulman, G. L. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.017 · Cited by 3,889 · see citing works
Berridge, C. W., & Waterhouse, B. D. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(03)00143-7 · Cited by 2,529 · see citing works
The locus coeruleus and noradrenergic modulation of cognition
Sara, S. J. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2573 · Cited by 1,848 · see citing works
Zarow, C., Lyness, S. A., Mortimer, J. A., & Chui, H. C. (2003) · Archives of Neurology · doi:10.1001/archneur.60.3.337 · Cited by 1,003 · see citing works
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 806 · see citing works
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 · see citing works
Fuller, P. M., Gooley, J. J., & Saper, C. B. (2006) · Journal of Biological Rhythms · doi:10.1177/0748730406294627 · Cited by 596 · see citing works
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 · see citing works
Disease‐specific patterns of locus coeruleus cell loss
German, D. C., Manaye, K. F., White, C. L., Woodward, D. J., McIntire, D. D., Smith, W. K., Kalaria, R. N., & Mann, D. M. A. (1992) · Annals of Neurology · doi:10.1002/ana.410320510 · Cited by 512 · see citing works
Grudzien, A., Shaw, P., Weintraub, S., Bigio, E., Mash, D. C., & Mesulam, M. M. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.02.007 · Cited by 396 · see citing works
Noradrenergic modulation of arousal
Berridge, C. W. (2008) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.10.013 · Cited by 368 · see citing works
Heneka, M. T., Ramanathan, M., Jacobs, A. H., Dumitrescu-Ozimek, L., Bilkei-Gorzo, A., Debeir, T., Sastre, M., Galldiks, N., Zimmer, A., Hoehn, M., et al. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4236-05.2006 · Cited by 305 · see citing works
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 302 · see citing works
Locus Coeruleus α-Adrenergic–Mediated Activation of Cortical Astrocytes In Vivo
Bekar, L. K., He, W., & Nedergaard, M. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn040 · Cited by 286 · see citing works
Norepinephrine: The redheaded stepchild of Parkinson's disease
Rommelfanger, K. S., & Weinshenker, D. (2007) · Biochemical Pharmacology · doi:10.1016/j.bcp.2007.01.036 · Cited by 255 · see citing works
Drug enhancement of memory consolidation: historical perspective and neurobiological implications
McGaugh, J. L., & Roozendaal, B. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1285-6 · Cited by 250 · see citing works
Szot, P., White, S. S., Greenup, J. L., Leverenz, J. B., Peskind, E. R., & Raskind, M. A. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4265-05.2006 · Cited by 249 · see citing works
The Locus Ceruleus Is Involved in the Successful Retrieval of Emotional Memories in Humans
Sterpenich, V., D'Argembeau, A., Desseilles, M., Balteau, E., Albouy, G., Vandewalle, G., Degueldre, C., Luxen, A., Collette, F., & Maquet, P. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1001-06.2006 · Cited by 245 · see citing works
Modulators in concert for cognition: Modulator interactions in the prefrontal cortex
Briand, L. A., Gritton, H., Howe, W. M., Young, D. A., & Sarter, M. (2007) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2007.06.007 · Cited by 216 · see citing works
The pontine REM switch: past and present
Fuller, P. M., Saper, C. B., & Lu, J. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.140160 · Cited by 211 · see citing works
Kalinin, S., Gavrilyuk, V., Polak, P. E., Vasser, R., Zhao, J. J., Heneka, M. T., & Feinstein, D. L. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.06.003 · Cited by 202 · see citing works
Functional Consequences of Locus Coeruleus Degeneration in Alzheimers Disease
Weinshenker, D. (2008) · Current Alzheimer Research · doi:10.2174/156720508784533286 · Cited by 180 · see citing works
Idazoxan, an alpha‐2 antagonist, and L‐DOPA‐induced dyskinesias in patients with Parkinson's disease
Rascol, O., Arnulf, I., Paul, H. P., Brefel‐Courbon, C., Vidailhet, M., Thalamas, C., Bonnet, A. M., Descombes, S., Bejjani, B.-P. W., Fabre, N., et al. (2001) · Movement Disorders · doi:10.1002/mds.1143 · Cited by 149 · see citing works
Noradrenoceptor antagonism with idazoxan improves l-dopa-induced dyskinesias in MPTP monkeys
Grondin, R., Tahar, A. H., Doan, V. D., Ladure, P., & Bédard, P. J. (2000) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s002109900167 · Cited by 91 · see citing works
Haglund, M., Sjöbeck, M., & Englund, E. M. (2006) · Neuropathology · doi:10.1111/j.1440-1789.2006.00725.x · Cited by 81 · see citing works
Waterhouse, B. D., Devilbiss, D. M., Fleischer, D., Sessler, F. M., & Simpson, K. L. (1997) · Advances in pharmacology · doi:10.1016/s1054-3589(08)60856-x · Cited by 33 · see citing works
Neuropharmacological Treatment of Mental Dysfunction in Parkinson’s Disease
McNamara, P., & Durso, R. (2006) · Behavioural Neurology · doi:10.1155/2006/138263 · Cited by 17 · see citing works
Chemically Coded Transmitter Systems
Bloom, F. E. (1979) · Progress in brain research · doi:10.1016/s0079-6123(08)61300-x · Cited by 7 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
The pathological process underlying Alzheimer’s disease in individuals under thirty
Braak, H., & Del Tredici, K. (2011) · Acta Neuropathologica · doi:10.1007/s00401-010-0789-4 · Cited by 812 · see citing works
The preclinical phase of the pathological process underlying sporadic Alzheimer’s disease
Braak, H., & Del Tredici, K. (2015) · Brain · doi:10.1093/brain/awv236 · Cited by 540 · see citing works
Sleep and anxiety: From mechanisms to interventions
Chellappa, S. L., & Aeschbach, D. (2022) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2021.101583 · Cited by 509 · see citing works
Review: Sporadic Parkinson's disease: development and distribution ofα‐synuclein pathology
Tredici, K. D., & Braak, H. (2015) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12298 · Cited by 396 · see citing works
Locus coeruleus imaging as a biomarker for noradrenergic dysfunction in neurodegenerative diseases
Betts, M. J., Kirilina, E. P., Otaduy, M. C. G., Ivanov, D., Acosta‐Cabronero, J., Callaghan, M. F., Lambert, C., Cárdenas‐Blanco, A., Pine, K., Passamonti, L., et al. (2019) · Brain · doi:10.1093/brain/awz193 · Cited by 349 · see citing works
Alzheimer’s pathogenesis: is there neuron-to-neuron propagation?
Braak, H., & Tredici, K. D. (2011) · Acta Neuropathologica · doi:10.1007/s00401-011-0825-z · Cited by 359 · see citing works
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 362 · see citing works
A primer on investigating the after effects of acute bouts of physical activity on cognition
Pontifex, M. B., McGowan, A. L., Chandler, M. C., Gwizdala, K. L., Parks, A. C., Fenn, K., & Kamijo, K. (2019) · Psychology of Sport and Exercise · doi:10.1016/j.psychsport.2018.08.015 · Cited by 339 · see citing works
Arousal Effects on Pupil Size, Heart Rate, and Skin Conductance in an Emotional Face Task
Wang, C., Baird, T., Huang, J. C. H., Coutinho, J., Brien, D. C., & Munoz, D. P. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.01029 · Cited by 312 · see citing works
Where, when, and in what form does sporadic Alzheimerʼs disease begin?
Braak, H., & Tredici, K. D. (2012) · Current Opinion in Neurology · doi:10.1097/wco.0b013e32835a3432 · Cited by 252 · see citing works
Tredici, K. D., & Braak, H. (2012) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2011-301817 · Cited by 237 · see citing works
Norepinephrine deficiency in Parkinson's disease: The case for noradrenergic enhancement
Espay, A. J., LeWitt, P. A., & Kaufmann, H. (2014) · Movement Disorders · doi:10.1002/mds.26048 · Cited by 237 · see citing works
Noradrenaline and Parkinson's Disease
Delaville, C., Deurwaerdère, P. D., & Benazzouz, A. (2011) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2011.00031 · Cited by 229 · see citing works
The influence of acute stress on attention mechanisms and its electrophysiological correlates
Sänger, J., Bechtold, L., Schoofs, D., Blaszkewicz, M., & Wascher, E. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00353 · Cited by 218 · see citing works
Benarroch, E. E. (2017) · Cell and Tissue Research · doi:10.1007/s00441-017-2649-1 · Cited by 218 · see citing works
Self-citationThe Brain Circuitry Underlying the Temporal Evolution of Nausea in Humans
Napadow, V., Sheehan, J. D., Kim, J., LaCount, L. T., Park, K., Kaptchuk, T. J., Rosen, B. R., & Kuo, B. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs073 · Cited by 215 · see citing works
Ross, J. A., & Bockstaele, E. J. V. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.601519 · Cited by 223 · see citing works
Shared Mechanisms of Neurodegeneration in Alzheimer’s Disease and Parkinson’s Disease
Xie, A., Gao, J., Xu, L., & Meng, D.-M. (2014) · BioMed Research International · doi:10.1155/2014/648740 · Cited by 196 · see citing works
PTSD and gene variants: new pathways and new thinking
Skelton, K., Ressler, K. J., Norrholm, S. D., Jovanovic, T., & Bradley-Davino, B. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.02.013 · Cited by 191 · see citing works
Lewy pathology and neurodegeneration in premotor Parkinson's disease
Tredici, K. D., & Braak, H. (2012) · Movement Disorders · doi:10.1002/mds.24921 · Cited by 184 · see citing works
Neurobehavioral foundation of environmental reactivity.
Moore, S. R., & Depue, R. A. (2015) · Psychological Bulletin · doi:10.1037/bul0000028 · Cited by 181 · see citing works
Feinstein, D. L., Kalinin, S., & Braun, D. J. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13447 · Cited by 178 · see citing works
Betts, M. J., Cárdenas‐Blanco, A., Kanowski, M., Jessen, F., & Düzel, E. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.09.042 · Cited by 165 · see citing works
Chao, O. Y., de Souza Silva, M. A., Yang, Y.-M., & Huston, J. P. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.007 · Cited by 158 · see citing works
Neuronal circuitry for recognition memory of object and place in rodent models
Chao, O. Y.-H., Nikolaus, S., Yang, Y., & Huston, J. P. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104855 · Cited by 157 · see citing works
Niu, L., Zhang, F., Xu, X., Yang, Y., Li, S., Liu, H., & Le, W. (2021) · Brain Pathology · doi:10.1111/bpa.13028 · Cited by 150 · see citing works
Role of adrenergic receptor signalling in neuroimmune communication
Chhatar, S., & Lal, G. (2021) · Current Research in Immunology · doi:10.1016/j.crimmu.2021.11.001 · Cited by 143 · see citing works
Blue‐blocking glasses as additive treatment for mania: a randomized placebo‐controlled trial
Henriksen, T. E., Skrede, S., Fasmer, O. B., Schoeyen, H., Leskauskaite, I., Bjørke‐Bertheussen, J., Assmus, J., Hamre, B., Grønli, J., & Lund, A. (2016) · Bipolar Disorders · doi:10.1111/bdi.12390 · Cited by 139 · see citing works
Braak, H., & Tredici, K. D. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a023630 · Cited by 129 · see citing works
The clinical spectrum of anxiety in Parkinson's disease
Dissanayaka, N. N. N. W., White, E., O'Sullivan, J. D., Marsh, R., Pachana, N. A., & Byrne, G. J. (2014) · Movement Disorders · doi:10.1002/mds.25937 · Cited by 124 · see citing works
The influence of acute stress on the regulation of conditioned fear
Raio, C. M., & Phelps, E. A. (2015) · Neurobiology of Stress · doi:10.1016/j.ynstr.2014.11.004 · Cited by 121 · see citing works
Vermeiren, Y., & Deyn, P. P. D. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2016.11.009 · Cited by 119 · see citing works
Masilamoni, G. J., Bogenpohl, J. W., Alagille, D., Delevich, K. M., Tamagnan, G. D., Votaw, J. R., Wichmann, T., & Smith, Y. (2011) · Brain · doi:10.1093/brain/awr137 · Cited by 118 · see citing works
Hong, L., Walz, J. M., & Sajda, P. (2014) · PLoS ONE · doi:10.1371/journal.pone.0091321 · Cited by 116 · see citing works
White Matter Atrophy and Cognitive Dysfunctions in Neuromyelitis Optica
Blanc, F., Noblet, V., Jung, B., Rousseau, F., Renard, F., Bourre, B., Longato, N., Cremel, N., Bitonto, L. D., Kleitz, C., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0033878 · Cited by 112 · see citing works
Polak, P. E., Kalinin, S., & Feinstein, D. L. (2011) · Brain · doi:10.1093/brain/awq362 · Cited by 108 · see citing works
Brain energy metabolism: A roadmap for future research
Rae, C. D., Baur, J. A., Borges, K., Dienel, G. A., Díaz‐García, C. M., Douglass, S. R., Drew, K. L., Duarte, J. M. N., Durán, J., Kann, O., et al. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16032 · Cited by 109 · see citing works
Microglia as Central Protagonists in the Chronic Stress Response
Schramm, E., & Waisman, A. (2022) · Neurology Neuroimmunology & Neuroinflammation · doi:10.1212/nxi.0000000000200023 · Cited by 107 · see citing works
Aldridge‐Waddon, L., Vanova, M., Munneke, J., Puzzo, I., & Kumari, V. (2020) · Clinical Psychology Review · doi:10.1016/j.cpr.2020.101942 · Cited by 103 · see citing works
Go with the flow: A neuroscientific view on being fully engaged
van der Linden, D., Mattie Tops, A., & Bakker, A. B. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.15014 · Cited by 102 · see citing works
Astroglia in Alzheimer’s Disease
Verkhratsky, A., Parpura, V., Rodriguez, J. J., & Zorec, R. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-981-13-9913-8_11 · Cited by 94 · see citing works
Metabolic Plasticity of Astrocytes and Aging of the Brain
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 · see citing works
Huang, X., Ng, S. Y., Chia, N. S. Y., Setiawan, F., Tay, K. Y., Au, W., Tan, E., & Tan, L. C. S. (2018) · European Journal of Neurology · doi:10.1111/ene.13803 · Cited by 88 · see citing works
Bittar, T. P., & Labonté, B. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.699592 · Cited by 87 · see citing works
Effects of Noradrenaline and Dopamine on Supraspinal Fatigue in Well-Trained Men
Klass, M., Roelands, B., Lévénez, M., Fontenelle, V., Pattyn, N., MEEUSEN, R. R., & Duchateau, J. (2012) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e318265f356 · Cited by 82 · see citing works
Noradrenergic Responsiveness Supports Selective Attention across the Adult Lifespan
Dahl, M. J., Mather, M., Sander, M. C., & Werkle-Bergner, M. (2020) · The Journal of Neuroscience · doi:10.1523/jneurosci.0398-19.2020 · Cited by 72 · see citing works
Excitable Astrocytes: Ca2+- and cAMP-Regulated Exocytosis
Vardjan, N., & Zorec, R. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1545-x · Cited by 70 · see citing works
Jardanhazi‐Kurutz, D., Kummer, M. P., Terwel, D., Vogel, K., Thiele, A., & Heneka, M. T. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.11.052 · Cited by 72 · see citing works
Neuromelanin-sensitive MRI as a promising biomarker of catecholamine function
Trujillo, P., Aumann, M. A., & Claassen, D. O. (2023) · Brain · doi:10.1093/brain/awad300 · Cited by 71 · see citing works
Memory Formation Shaped by Astroglia
Zorec, R., Horvat, A., Vardjan, N., & Verkhratsky, A. (2015) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2015.00056 · Cited by 70 · see citing works
Hougaard, A., Amin, F. M., Larsson, H. B. W., Rostrup, E., & Ashina, M. (2017) · Human Brain Mapping · doi:10.1002/hbm.23548 · Cited by 71 · see citing works
Satoh, A., & Iijima, K. (2017) · Brain Research · doi:10.1016/j.brainres.2017.12.027 · Cited by 68 · see citing works
Pamphlett, R. (2013) · Medical Hypotheses · doi:10.1016/j.mehy.2013.11.016 · Cited by 67 · see citing works
Cox, A., Kohls, G., Naples, A. J., Mukerji, C., Coffman, M. C., Rutherford, H. J. V., Mayes, L. C., & McPartland, J. C. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv024 · Cited by 68 · see citing works
Monoaminergic and Histaminergic Strategies and Treatments in Brain Diseases
Giovanni, G. D., Štrac, D. Š., Solé, M., Unzeta, M., Tipton, K. F., Mück‐Šeler, D., Bolea, I., Corte, L., Perković, M. N., Pivac, N., et al. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00541 · Cited by 71 · see citing works
Ahn, H., Seo, S. W., Chin, J., Suh, M. K., Lee, B. H., Kim, S. T., Im, K., Lee, J. M., Lee, J. H., Heilman, K. M., et al. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2011.10.010 · Cited by 66 · see citing works
Abdelhamid, R. E., Kovács, K. J., Nunez, M. G., & Larson, A. A. (2013) · Pharmacological Research · doi:10.1016/j.phrs.2013.10.006 · Cited by 66 · see citing works
The Neural Mechanism Underlying Cognitive and Emotional Processes in Creativity
Gu, S., Gao, M., Yan, Y., Wang, F., Tang, Y., & Huang, J. H. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.01924 · Cited by 63 · see citing works
Wilson, C. B., McLaughlin, L. D., Ebenezer, P. J., Nair, A. R., Dange, R. B., Harre, J. G., Shaak, T. L., Diamond, D. M., & Francis, J. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00256 · Cited by 62 · see citing works
A Brief Review of the Pharmacology of Amitriptyline and Clinical Outcomes in Treating Fibromyalgia
Lawson, K. (2017) · Biomedicines · doi:10.3390/biomedicines5020024 · Cited by 61 · see citing works
Locus coeruleus in memory formation and Alzheimer's disease
James, T., Kula, B., Choi, S., Khan, S. S., Bekar, L. K., & Smith, N. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.15045 · Cited by 61 · see citing works
Direct Neuronal Reprogramming: Bridging the Gap Between Basic Science and Clinical Application
Vasan, L., Park, E., David, L. A., Fleming, T., & Schuurmans, C. J. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.681087 · Cited by 60 · see citing works
Hou, L., Sun, F., Sun, W., Zhang, L., & Wang, Q. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.09.006 · Cited by 59 · see citing works
The Neuroscience of the Flow State: Involvement of the Locus Coeruleus Norepinephrine System
van der Linden, D., Mattie Tops, A., & Bakker, A. B. (2021) · Frontiers in Psychology · doi:10.3389/fpsyg.2021.645498 · Cited by 61 · see citing works
Sleep disturbances in Lewy body dementia: A systematic review
Elder, G. J., Lázár, A. S., Alfonso‐Miller, P., & Taylor, J. (2022) · International Journal of Geriatric Psychiatry · doi:10.1002/gps.5814 · Cited by 56 · see citing works
Oshaghi, M., Kourosh‐Arami, M., & Roozbehkia, M. (2022) · Neurological Sciences · doi:10.1007/s10072-022-06413-0 · Cited by 55 · see citing works
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 · see citing works
Chávez-Castillo, M., Núñez, V., Nava, M., Ortega, Á., Rojas, M., Bermúdez, V., & Rojas, J. (2019) · Advances in Pharmacological Sciences · doi:10.1155/2019/7943481 · Cited by 56 · see citing works
Noradrenergic Dysfunction in Alzheimer's and Parkinson's Diseases—An Overview of Imaging Studies
Peterson, A. C., & Li, C. R. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00127 · Cited by 54 · see citing works
Xia, Y. F., Kou, L., Zhang, G., Han, C., Hu, J., Wan, F. J., Yin, S., Sun, Y., Wu, J., Li, Y., et al. (2020) · Sleep Medicine · doi:10.1016/j.sleep.2020.09.011 · Cited by 52 · see citing works
Quantitative magnetization transfer imaging of the human locus coeruleus
Trujillo, P., Petersen, K. J., Cronin, M. J., Lin, Y., Kang, H., Donahue, M. J., Smith, S. A., & Claassen, D. O. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.06.049 · Cited by 52 · see citing works
Brain structure and function related to headache: Brainstem structure and function in headache
Vila‐Pueyo, M., Hoffmann, J., Romero‐Reyes, M., & Akerman, S. (2018) · Cephalalgia · doi:10.1177/0333102418784698 · Cited by 50 · see citing works
The locus coeruleus: Another vulnerability target in Parkinson's disease
Oertel, W. H., Henrich, M. T., Janzen, A., & Geibl, F. F. (2019) · Movement Disorders · doi:10.1002/mds.27785 · Cited by 51 · see citing works
Recent Advances in the Understanding of Specific Efferent Pathways Emerging From the Cerebellum
Kang, S., Jun, S., Baek, S. J., Park, H., Yamamoto, Y., & Tanaka, K. (2021) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2021.759948 · Cited by 53 · see citing works
Yang, J. H., Lee, E. O., Kim, S. E., Suh, Y.-H., & Chong, Y. H. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.05.008 · Cited by 51 · see citing works
Janitzky, K. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.00371 · Cited by 50 · see citing works
Norepinephrine: the next therapeutics frontier for Parkinson's disease
LeWitt, P. A. (2012) · Translational Neurodegeneration · doi:10.1186/2047-9158-1-4 · Cited by 49 · see citing works
Neural, physiological, and behavioral correlates of visuomotor cognitive load
Hosseini, S. M. H., Bruno, J. L., Baker, J. M., Gundran, A., Harbott, L. K., Gerdes, J. C., & Reiss, A. L. (2017) · Scientific Reports · doi:10.1038/s41598-017-07897-z · Cited by 51 · see citing works
Kelberman, M. A., Rorabaugh, J. M., Anderson, C. R., Marriott, A., DePuy, S. D., Rasmussen, K., McCann, K. E., Weiss, J. M., & Weinshenker, D. (2022) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2023.01.016 · Cited by 48 · see citing works
Molecular Mechanisms of Stress-Induced Increases in Fear Memory Consolidation within the Amygdala
Aubry, A., Serrano, P. A., & Burghardt, N. S. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2016.00191 · Cited by 47 · see citing works
Cercignani, M., Dipasquale, O., Bogdan, I., Carandini, T., Scott, J., Rashid, W., Sabri, O., Hesse, S., Rullmann, M., Lopiano, L., et al. (2021) · Brain Communications · doi:10.1093/braincomms/fcab023 · Cited by 46 · see citing works
Pamphlett, R., & Jew, S. K. (2013) · Acta Neuropathologica Communications · doi:10.1186/2051-5960-1-13 · Cited by 47 · see citing works
Du, X., Yin, M., Yuan, L., Zhang, G., Fan, Y., Li, Z., Yuan, N., Lv, X., Zhao, X., Zou, S., et al. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-0808-8 · Cited by 46 · see citing works
Carandini, T., Cercignani, M., Galimberti, D., Scarpini, E. A., & Bozzali, M. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.02.030 · Cited by 46 · see citing works
Cai, D., Yue, Y., Su, X., Liu, M., Wang, Y., You, L., Xie, F., Deng, F., Chen, F., Luo, M., et al. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhy115 · Cited by 45 · see citing works
Dopaminergic Input to the Inferior Colliculus in Mice
Nevue, A. A., Elde, C. J., Perkel, D. J., & Portfors, C. V. (2016) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00168 · Cited by 45 · see citing works
Vriend, C. (2018) · Cell and Tissue Research · doi:10.1007/s00441-017-2771-0 · Cited by 45 · see citing works
Cognitive impairment in Parkinson's disease: A clinical and pathophysiological overview
Brandão, P. R. D. P., Munhoz, R. P., Grippe, T. C., Cardoso, F., Castro, B. M. D. A. E., Titze‐de‐Almeida, R., Tomaz, C. A. B., & Tavares, M. C. H. (2020) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2020.117177 · Cited by 47 · see citing works
Clinical Markers of Anxiety Subtypes in Parkinson Disease
Broen, M. P. G., Leentjens, A. F. G., Hinkle, J. T., Moonen, A. J. H., Kuijf, M. L., Fischer, N. M., Perepezko, K. M., Bakker, A., & Pontone, G. M. (2018) · Journal of Geriatric Psychiatry and Neurology · doi:10.1177/0891988718757369 · Cited by 44 · see citing works
Laurencin, C., Lancelot, S., Brosse, S., Mérida, I., Redouté, J., Greusard, E., Lamberet, L., Liotier, V., Bars, D. L., Costes, N., et al. (2023) · Brain · doi:10.1093/brain/awad338 · Cited by 43 · see citing works
Ulke, C., Rullmann, M., Huang, J., Luthardt, J., Becker, G.-A., Patt, M., Meyer, P. M., Tiepolt, S., Hesse, S., Sabri, O., et al. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0619-y · Cited by 43 · see citing works
Huang, Y., Zhang, Y., Hodges, S., Li, H., Yan, Z., Liu, X., Hou, X., Chen, W., Chai‐Zhang, T. C., Kong, J., et al. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1160006 · Cited by 41 · see citing works
Carandini, T., Mancini, M., Bogdan, I., Rae, C., Barritt, A. W., Sethi, A., Harrison, N., Rashid, W., Scarpini, E., Galimberti, D., et al. (2021) · NeuroImage: Clinical · doi:10.1016/j.nicl.2021.102587 · Cited by 36 · see citing works
Matschke, L. A., Rinné, S., Snutch, T. P., Oertel, W. H., Dolga, A. M., & Decher, N. (2018) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2018.03.002 · Cited by 40 · see citing works
Preventing neurodegeneration by adrenergic astroglial excitation
Zorec, R., Parpura, V., & Verkhratsky, A. (2018) · FEBS Journal · doi:10.1111/febs.14456 · Cited by 39 · see citing works
Plini, E. R. G., O’Hanlon, E., Boyle, R. T., Sibilia, F., Rikhye, G., Kenney, J. P. M., Whelan, R., Melnychuk, M. C., Robertson, I. H., & Dockree, P. M. (2021) · Cells · doi:10.3390/cells10071829 · Cited by 39 · see citing works
The Endocannabinoid/Endovanilloid System and Depression
Smaga, I., Bystrowska, B., Gawliński, D., Przegaliński, E., & Filip, M. (2014) · Current Neuropharmacology · doi:10.2174/1570159x12666140923205412 · Cited by 39 · see citing works
Sex-specific Effects of Endocrine-disrupting Chemicals on Brain Monoamines and Cognitive Behavior
Hilz, E. N., & Gore, A. C. (2022) · Endocrinology · doi:10.1210/endocr/bqac128 · Cited by 38 · see citing works
The toxic metal hypothesis for neurological disorders
Pamphlett, R., & Bishop, D. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1173779 · Cited by 39 · see citing works
Han, S., Wang, J., Zhang, W., & Tian, X. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04073-z · Cited by 37 · see citing works
- Authors
- Benarroch, E. E.
- Affiliations
- Mayo Clinic (US)
- Corresponding author
- Benarroch, Eduardo E.
- Venue
- Neurology
- Published
- 2009-11-17
- Volume
- 73
- Issue
- 20
- Pages
- 1699-1704
- ISSN
- 0028-3878 (ISSN-L)
- 1526-632X
- OpenAlex
- W1969610953
- Cited by
- 317
- References
- 29
- Citations by year
- 2026: 14 · 2025: 17 · 2024: 17 · 2023: 32 · 2022: 23 · 2021: 24 · 2020: 32 · 2019: 22 · 2018: 32 · 2017: 17 · 2016: 16 · 2015: 13 · 2014: 19 · 2013: 9 · 2012: 13
- FWCI
- 4.31
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Health Sciences › Medicine › Oncology › Cytokine Signaling Pathways and Interactions
- Keywords
- locus coeruleus, norepinephrine, noradrenergic neurons, noradrenergic neurotransmission
- MeSH terms
- Alzheimer Disease, Animals, Arousal, Attention, Brain, Humans, Locus Coeruleus, Memory, Neural Pathways, Neurons, Norepinephrine, Parkinson Disease, Stress, Psychological, Prosencephalon
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