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Norepinephrine ignites local hotspots of neuronal excitation: How arousal amplifies selectivity in perception and memory
Open accessAbstract
Emotional arousal enhances perception and memory of high-priority information but impairs processing of other information. Here, we propose that, under arousal, local glutamate levels signal the current strength of a representation and interact with norepinephrine (NE) to enhance high priority representations and out-compete or suppress lower priority representations. In our "glutamate amplifies noradrenergic effects" (GANE) model, high glutamate at the site of prioritized representations increases local NE release from the locus coeruleus (LC) to generate "NE hotspots." At these NE hotspots, local glutamate and NE release are mutually enhancing and amplify activation of prioritized representations. In contrast, arousal-induced LC activity inhibits less active representations via two mechanisms: 1) Where there are hotspots, lateral inhibition is amplified; 2) Where no hotspots emerge, NE levels are only high enough to activate low-threshold inhibitory adrenoreceptors. Thus, LC activation promotes a few hotspots of excitation in the context of widespread suppression, enhancing high priority representations while suppressing the rest. Hotspots also help synchronize oscillations across neural ensembles transmitting high-priority information. Furthermore, brain structures that detect stimulus priority interact with phasic NE release to preferentially route such information through large-scale functional brain networks. A surge of NE before, during, or after encoding enhances synaptic plasticity at NE hotspots, triggering local protein synthesis processes that enhance selective memory consolidation. Together, these noradrenergic mechanisms promote selective attention and memory under arousal. GANE not only reconciles apparently contradictory findings in the emotion-cognition literature but also extends previous influential theories of LC neuromodulation by proposing specific mechanisms for how LC-NE activity increases neural gain.
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“These neurotransmitters play a key role in mood regulation (Ressler and Nemeroff, 1999), cognition(Hoshino, 2005) and perception (Mather et al., 2016).”
From Efficacy, acceptability and side-effects of oral versus long-acting- injectables antipsychotics: Systematic review and network meta-analysis (2024) · cites this paper as Mather et al., 2016
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“Release of norepinephrine by the locus coeruleus influences arousal levels and has been shown to prioritize processing of goal-relevant information and to promote memory formation in the hippocampus (Clewett et al., 2018; Mather et al., 2016).”
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Cites
A synaptic model of memory: long-term potentiation in the hippocampus
Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566
Neural Mechanisms of Selective Visual Attention
Desimone, R., & Duncan, J. (1995) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.18.030195.001205 · Cited by 8,388
The free-energy principle: a unified brain theory?
Friston, K. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2787 · Cited by 8,120
Dissociable intrinsic connectivity networks for salience processing and executive control
Seeley, W. W., Menon, V., Schatzberg, A. F., Keller, J., Glover, G. H., Kenna, H., Reiss, A. L., & Greicius, M. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5587-06.2007 · Cited by 7,426
How do you feel — now? The anterior insula and human awareness
(Bud) Craig, A. D. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2555 · Cited by 6,657
Cognitive and emotional influences in anterior cingulate cortex
Bush, G., Luu, P., & Posner, M. I. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01483-2 · Cited by 6,259
Saliency, switching, attention and control: a network model of insula function
Menon, V., & Uddin, L. Q. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0262-0 · Cited by 5,592
Anxiety and cognitive performance: Attentional control theory
Eysenck, M. W., Derakshan, N., Santos, R., & Calvo, M. G. (2007) · Emotion · doi:10.1037/1528-3542.7.2.336 · Cited by 5,289
Aston-Jones, G., & Cohen, J. D. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135709 · Cited by 4,472
Memory - A century of consolidation
McGaugh, J. L. (2000) · Science · doi:10.1126/science.287.5451.248 · Cited by 4,250
Research works printed but not linked: 3
- Sutherland M. R. & Mather M. (under review) Both positive and negative arousing sounds increase the impact of visual salience.
- Easterbrook, 1982, This week's citation classic, Current Contents, 20
- Sutherland M. R. , Lee T. H. & Mather M. (under review) Arousal impairs top-down prioritization in selective attention.
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Fortin, S. M., Chen, J. C., Petticord, M. C., Ragozzino, F. J., Peters, J. H., & Hayes, M. R. (2023) · Science Advances · doi:10.1126/sciadv.adh0980 · Cited by 32
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Baraly, K. T. A., Hot, P., Davidson, P. S. R., & Talmi, D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21051-1 · Cited by 32
Swallow, K. M., Jiang, Y. V., & Riley, E. (2019) · Scientific Reports · doi:10.1038/s41598-019-41658-4 · Cited by 32
Bast, N., Boxhoorn, S., Supèr, H., Helfer, B., Polzer, L., Klein, C., Cholemkery, H., & Freitag, C. M. (2021) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2021.04.010 · Cited by 32
Abdallah, C. G., Averill, L. A., Krystal, J. H., Southwick, S. M., & Arnsten, A. F. T. (2016) · Behavioral and Brain Sciences · doi:10.1017/s0140525x15001727 · Cited by 30
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Self-citationKafkas, A. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107412 · Cited by 30
He, H., Hong, L., & Sajda, P. (2023) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011081 · Cited by 30
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Ghosh, A., Massaeli, F., Power, K. D., Omoluabi, T., Torraville, S. E., Pritchett, J. B., Sepahvand, T., Strong, V., Reinhardt, C., Chen, X., et al. (2021) · Cerebral Cortex Communications · doi:10.1093/texcom/tgab026 · Cited by 29
Self-citationYi, Y., Lüsebrink, F., Ludwig, M., Maaß, A., Ziegler, G., Yakupov, R., Kreissl, M. C., Betts, M. J., Speck, O., Düzel, E., et al. (2021) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2023.04.007 · Cited by 29
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Kruijne, W., Olivers, C. N. L., & van Rijn, H. (2021) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01705 · Cited by 28
Ritchey, M., McCullough, A. M., Ranganath, C., & Yonelinas, A. P. (2016) · Hippocampus · doi:10.1002/hipo.22674 · Cited by 27
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Wichary, S., Magnuski, M., Oleksy, T., & Brzezicka, A. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00401 · Cited by 27
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Kim, D., Lokey, S., & Ling, S. (2017) · Journal of Vision · doi:10.1167/17.2.14 · Cited by 27
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Kleberg, J. L., Bianco, T. D., & Falck‐Ytter, T. (2018) · Child Development · doi:10.1111/cdev.13198 · Cited by 27
Yamashita, J., Terashima, H., Yoneya, M., Maruya, K., Koya, H., Oishi, H., Nakamura, H., & Kumada, T. (2021) · PLoS ONE · doi:10.1371/journal.pone.0256953 · Cited by 26
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Jiang, M., & Zeng, Z. (2023) · IEEE Transactions on Biomedical Circuits and Systems · doi:10.1109/tbcas.2023.3324574 · Cited by 25
Sun, L., Wang, Q., & Ai, J. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102265 · Cited by 25
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David, M., & Malhotra, P. (2022) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.51539 · Cited by 22
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Episodic retrieval for model-based evaluation in sequential decision tasks.
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Xin, Z., Gu, S., Lei, Y., Li, H., & Wang, F. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.544540 · Cited by 21
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Wang, J., Zhou, Y., Li, K., Li, X., Guo, M., & Peng, M. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.752838 · Cited by 20
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Self-citationBast, N., Mason, L., Ecker, C., Baumeister, S., Banaschewski, T., Jones, E. J. H., Murphy, D., Buitelaar, J. K., Loth, E., Pandina, G., et al. (2023) · Molecular Autism · doi:10.1186/s13229-023-00537-6 · Cited by 16
Zeng, Y., Xiong, B., Gao, H., Liu, C., Chen, C., Wu, J., & Qin, S. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2405850121 · Cited by 16
Aberg, K. C., Müller, J., & Schwartz, S. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00056 · Cited by 16
Multisensory deficits in dyslexia may result from a locus coeruleus attentional network dysfunction
Kershner, J. R. (2021) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2021.108023 · Cited by 16
Upadhyay, J., Verrico, C. D., Cay, M., Kodele, S., Yammine, L., Koob, G. F., & Schreiber, R. (2021) · The Lancet Psychiatry · doi:10.1016/s2215-0366(21)00008-0 · Cited by 16
Metadata
- Authors
- Mather, M., Clewett, D., Sakaki, M., & Harley, C. W.
- Affiliations
- University of Southern California (US)
- Kochi University of Technology (JP)
- Memorial University of Newfoundland (CA)
- Venue
- Behavioral and Brain Sciences
- Publisher
- Cambridge University Press (CUP)
- Published
- 2015-07-01
- Volume
- 39
- Pages
- e200-e200
- ISSN
- 0140-525X (ISSN-L)
- 1469-1825
- PMC
- PMC5830137
- OpenAlex
- W2126712529
- Cited by
- 695
- References
- 399
- Citations by year
- 2026: 70 · 2025: 79 · 2024: 59 · 2023: 86 · 2022: 66 · 2021: 87 · 2020: 65 · 2019: 49 · 2018: 53 · 2017: 43 · 2016: 32 · 2015: 5
- FWCI
- 26.68
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Behavioral and Brain Sciences (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- CentAUR (University of Reading) (acceptedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- National Institute on Aging (R01AG025340)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- norepinephrine, locus coeruleus, emotional arousal, glutamate, neural gain, selective attention, memory consolidation, lateral inhibition, adrenergic receptors, neural oscillations, synaptic plasticity, emotion-cognition interaction
- MeSH terms
- Arousal, Attention, Humans, Locus Coeruleus, Memory, Norepinephrine
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.
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