The DOI matches its Crossref record; 135 of the 135 references it cites were found in a registry or an index.
Glial and neuronal control of brain blood flow
Open accessAbstract
Blood flow in the brain is regulated by neurons and astrocytes. Knowledge of how these cells control blood flow is crucial for understanding how neural computation is powered, for interpreting functional imaging scans of brains, and for developing treatments for neurological disorders. It is now recognized that neurotransmitter-mediated signalling has a key role in regulating cerebral blood flow, that much of this control is mediated by astrocytes, that oxygen modulates blood flow regulation, and that blood flow may be controlled by capillaries as well as by arterioles. These conceptual shifts in our understanding of cerebral blood flow control have important implications for the development of new therapeutic approaches.
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“This process can be adjusted on demand either through modulation of neurovascular coupling15–17 or via neuronal signaling to astrocytes18.”
From Energy paradox in REM sleep: balancing supply and consumption in brain metabolism (2026) · cites this paper as [16]
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“As neural activity elevates, local oxygen consumption and demand increases, triggering vasodilation of arterioles and capillaries to increase cerebral blood flow (124), which supplies oxygenated hemoglobin in excess of the metabolic rate of oxygen consumption (125).”
From Electrophysiological source imaging: A noninvasive window to brain dynamics (2018) · cites this paper as [124]
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“Such a cascade of metabolic and vascular events, known as the neurovascular coupling, involves complex signaling among neurons, astrocytes, and the local vasculature (124, 126, 127), and remains a topic of active research enabled by emerging tools (128).”
From Electrophysiological source imaging: A noninvasive window to brain dynamics (2018) · cites this paper as [124]
In the citing paper
“PVMs were found most abundantly in association with pial and parenchymal vessels larger than 20 μm in diameter, particularly pial arterioles, a key site for flow regulation (7), the length of which was covered 70%-80% by PVMs (Supplemental Figure 1, A-E; supplemental material available online with this article; doi:10.1172/JCI86950DS1).”
From Perivascular macrophages mediate the neurovascular and cognitive dysfunction associated with hypertension (2016) · cites this paper as [7]
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Citations
Cites
Neurophysiological investigation of the basis of the fMRI signal
Logothetis, N. K., Pauls, J., Augath, M., Trinath, T., & Oeltermann, A. (2001) · Nature · doi:10.1038/35084005 · Cited by 6,551
Interplay between Cortical Spreading Depolarization and Seizures
Kramer, D. R., Fujii, T., Ohiorhenuan, I. E., & Liu, C. Y. (2017) · Stereotactic and Functional Neurosurgery · doi:10.1159/000452841 · Cited by 3,721
An Energy Budget for Signaling in the Grey Matter of the Brain
Attwell, D., & Laughlin, S. B. (2001) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200110000-00001 · Cited by 3,543
Self-citationNonoxidative Glucose Consumption During Focal Physiologic Neural Activity
Fox, P. T., Raichle, M. E., Mintun, M. A., & Dence, C. (1988) · Science · doi:10.1126/science.3260686 · Cited by 1,796
Neuron-to-astrocyte signaling is central to the dynamic control of brain microcirculation
Zonta, M., Angulo, M. C., Gobbo, S., Rosengarten, B., Hossmann, K.-A., Pozzan, T., & Carmignoto, G. (2002) · Nature Neuroscience · doi:10.1038/nn980 · Cited by 1,446
Cerebral ischemia. II. The no-reflow phenomenon.
Ames, A., Rl, W., Kowada, M., Thurston, J. M., & Majno, G. (1968) · PubMed · Cited by 1,371
Neurovascular coupling in the normal brain and in hypertension, stroke, and Alzheimer disease
Girouard, H., & Iadecola, C. (2005) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00966.2005 · Cited by 1,311
P-450 Metabolites of Arachidonic Acid in the Control of Cardiovascular Function
Roman, R. J. (2002) · Physiological Reviews · doi:10.1152/physrev.00021.2001 · Cited by 1,307
Identification of Epoxyeicosatrienoic Acids as Endothelium-Derived Hyperpolarizing Factors
Campbell, W. B., Gebremedhin, D., Pratt, P. F., & Harder, D. R. (1996) · Circulation Research · doi:10.1161/01.res.78.3.415 · Cited by 1,221
Pathophysiology of the migraine aura: The spreading depression theory
Lauritzen, M. (1994) · Brain · doi:10.1093/brain/117.1.199 · Cited by 1,151
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Wettervik, T. S., Engquist, H., Howells, T. P., Rostami, E., Hillered, L., Enblad, P., & Lewén, A. (2020) · Journal of Critical Care · doi:10.1016/j.jcrc.2020.08.014 · Cited by 34
Maruhashi, T., & Higashi, Y. (2021) · Expert Opinion on Pharmacotherapy · doi:10.1080/14656566.2021.1912013 · Cited by 34
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Characterization of NO ‐producing neurons in the rat corpus callosum
Barbaresi, P., Fabri, M., & Mensa’, E. (2014) · Brain and Behavior · doi:10.1002/brb3.218 · Cited by 34
Collateral blood vessels in acute ischemic stroke: a physiological window to predict future outcomes
Alves, H. C. B. R., Pacheco, F. T., & da Rocha, A. J. (2016) · Arquivos de Neuro-Psiquiatria · doi:10.1590/0004-282x20160050 · Cited by 34
Helbing, C., Brocka, M., Scherf, T., Lippert, M., & Angenstein, F. (2015) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x15615535 · Cited by 34
Zanghi, C. N., & Jevtović‐Todorović, V. (2016) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2016.12.004 · Cited by 34
Lee, M. L., Martínez‐Lozada, Z., Krizman, E. N., & Robinson, M. B. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14135 · Cited by 34
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Mathias, E. J., Kenny, A., Plank, M. J., & David, T. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.03.010 · Cited by 34
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Reid, M. M., Menon, S., Liu, H., Zhou, H., Hu, Z., Frerich, S., Ding, B., Oveisgharan, S., Zhang, Z., Nelson, S., et al. (2025) · Neuron · doi:10.1016/j.neuron.2025.07.001 · Cited by 35
Developmental Switch in Neurovascular Coupling in the Immature Rodent Barrel Cortex
Zehendner, C. M., Tsohataridis, S., Luhmann, H. J., & Yang, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080749 · Cited by 36
Erythropoietin exerts cell protective effect by activating PI3K/Akt and MAPK pathways in C6 Cells
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Vascular Transdifferentiation in the CNS: A Focus on Neural and Glioblastoma Stem‐Like Cells
Guelfi, S., Duffau, H., Bauchet, L., Rothhut, B., & Hugnot, J. (2016) · Stem Cells International · doi:10.1155/2016/2759403 · Cited by 35
Aschinger, G. C., Schmetterer, L. F., Fondi, K., dos Santos, V. A., Seidel, G., Garhöfer, G., & Werkmeister, R. M. (2017) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.16-20598 · Cited by 33
Iyer, P. C., & Madhavan, S. (2018) · Clinical Neurophysiology · doi:10.1016/j.clinph.2018.09.019 · Cited by 33
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Ekstrom, A. D. (2020) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2019.0634 · Cited by 35
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Schwarz, K., & Schmitz, F. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021639 · Cited by 36
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Ryan, A. K., Rich, W. W., & Reilly, M. A. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1021152 · Cited by 33
Boorman, L. W., Harris, S., Bruyns‐Haylett, M., Kennerley, A. J., Zheng, Y., Martin, C. J., Jones, M., Redgrave, P., & Berwick, J. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2339-14.2015 · Cited by 34
Neurovascular dysfunction in dementia – human cellular models and molecular mechanisms
Parkes, I., Chintawar, S., & Cader, M. Z. (2018) · Clinical Science · doi:10.1042/cs20160720 · Cited by 33
Neurovascular and neurometabolic derailment in aging and Alzheimer's disease
Lourenço, C. F., Ledo, A., Dias, C., Barbosa, R. M., & Laranjinha, J. A. N. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00103 · Cited by 33
Garrigue, P., Giacomino, L., Bucci, C., Muzio, V., Filannino, M. A., Sabatier, F., Dignat‐George, F., Pisano, P. S., & Guillet, B. A. (2015) · International Journal of Stroke · doi:10.1177/1747493015607516 · Cited by 32
Astroglial vesicular network: evolutionary trends, physiology and pathophysiology
Zorec, R., Parpura, V., & Verkhratsky, A. (2017) · Acta Physiologica · doi:10.1111/apha.12915 · Cited by 32
Hariharan, A., Yu, J., Collie, N. D., Zhang, H., & Liu, P. (2019) · Nitric Oxide · doi:10.1016/j.niox.2019.03.006 · Cited by 34
Zheng, Y., Wu, Y., Liu, Y., Guo, Z., Bai, T., Zhou, P., Wu, J. S., Yang, Q., Liu, Z., & Lu, X. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02776-7 · Cited by 32
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Schneider, J., Weigel, J., Wittmann, M., Švehla, P., Ehrt, S., Zheng, F., Elmzzahi, T., Karpf, J., Paniagua‐Herranz, L., Başak, O., et al. (2022) · The EMBO Journal · doi:10.15252/embj.2021110409 · Cited by 34
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Moon, C., Fukuda, M., & Kim, S. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.08.064 · Cited by 32
Acute changes in neurovascular reactivity after subarachnoid hemorrhage in vivo
Balbi, M., Koide, M., Schwarzmaier, S. M., Wellman, G. C., & Plesnila, N. (2015) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x15621253 · Cited by 32
Hawkins, P. C. T., Wood, T., Vernon, A. C., Bertolino, A., Sambataro, F., Dukart, J., Merlo‐Pich, E., Risterucci, C., Silber‐Baumann, H., Walsh, E., et al. (2017) · Human Brain Mapping · doi:10.1002/hbm.23844 · Cited by 33
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Jobling, A. I., Greferath, U., Dixon, M., Quiriconi, P., Eyar, B., van Koeverden, A. K., Mills, S. A., Vessey, K. A., Bui, B. V., & Fletcher, E. L. (2025) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2025.101349 · Cited by 31
Takuwa, H., Masamoto, K., Yamazaki, K., Kawaguchi, H., Ikoma, Y., Tajima, Y., Obata, T., 冨田, 裕., Suzuki, N., Kanno, I., et al. (2013) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2013.16 · Cited by 31
Afonso‐Oramas, D., Cruz‐Muros, I., Castro‐Hernández, J., Salas-Hernández, J., Barroso‐Chinea, P., GarcÃa-Hernández, S., Lanciego, J. L., & González‐Hernández, T. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00084 · Cited by 31
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Thompson, E. G., & Sontheimer, H. W. (2016) · European Biophysics Journal · doi:10.1007/s00249-016-1154-x · Cited by 31
Roby, D. A., Ruiz, F., Kermath, B. A., Voorhees, J. R., Niehoff, M. L., Zhang, J., Morley, J. E., Musiek, E. S., Farr, S. A., & Burris, T. P. (2019) · PLoS ONE · doi:10.1371/journal.pone.0215004 · Cited by 32
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Duffin, J., Hare, G. M. T., & Fisher, J. A. (2019) · The Journal of Physiology · doi:10.1113/jp279237 · Cited by 33
Liu, J., Li, Z., Liu, Y.-S., Chu, H.-D., Hu, N.-Y., Wu, D., Huang, L., Li, S.-J., Li, X., Yang, J., et al. (2020) · Neuroscience Bulletin · doi:10.1007/s12264-020-00474-x · Cited by 31
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Jiang, Q. L., Su, D., Wang, Z., Liu, C., Sun, Y., Cheng, H., Li, X., & Yan, B. (2020) · Theranostics · doi:10.7150/thno.51550 · Cited by 31
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Institóris, Á., Rosenegger, D. G., & Gordon, G. R. (2015) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2015.141 · Cited by 31
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Iddings, J. A., Kim, K., Zhou, Y., Higashimori, H., & Filosa, J. A. (2015) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2015.31 · Cited by 32
Fan, F. (2017) · Current Research in Diabetes & Obesity Journal · doi:10.19080/crdoj.2017.02.555587 · Cited by 31
Bojesen, K. B., Andersen, K. A., Rasmussen, S. N., Baandrup, L., Madsen, L. M., Glenthoj, B. Y., Rostrup, E., & Broberg, B. V. (2018) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2018.00022 · Cited by 32
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Arbuckle, S. A., Yokoi, A., Pruszynski, J. A., & Diedrichsen, J. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.11.002 · Cited by 31
Lee, E., Lee, E.-A., Kong, E., Chon, H., Llaiqui-Condori, M., Park, C. H., Park, B. Y., Kang, N. R., Yoo, J.-S., Lee, H., et al. (2023) · Experimental & Molecular Medicine · doi:10.1038/s12276-023-00939-9 · Cited by 30
Linne, M., & Jalonen, T. O. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-397897-4.00005-x · Cited by 30
A fast neuronal signal-sensitive continuous-wave near-infrared imaging system
Zhang, Z., Sun, B., Gong, H., Zhang, L., Sun, J., Wang, B., & Luo, Q. (2012) · Review of Scientific Instruments · doi:10.1063/1.4752021 · Cited by 30
Eilam, R., Aharoni, R., Arnon, R., & Malach, R. (2016) · eLife · doi:10.7554/elife.15915 · Cited by 27
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Fondi, K., Bata, A. M., Luft, N., Witkowska, K. J., Werkmeister, R. M., Schmidl, D., Bolz, M., Schmetterer, L. F., & Garhöfer, G. (2018) · PLoS ONE · doi:10.1371/journal.pone.0207525 · Cited by 30
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Self-citationMitra, S., Devi, S., Lee, M., Jui, J., Sahu, A., & Goldman, D. J. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2211690119 · Cited by 30
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Wang, X., Liisberg, M. B., Nolt, G. L., Fu, X., Cerretani, C., Li, L., Johnson, L. A., Vosch, T., & Richards, C. I. (2023) · ACS Nano · doi:10.1021/acsnano.3c04489 · Cited by 30
Verkhratsky, A., & Butt, A. M. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-821565-4.00008-0 · Cited by 31
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Khennouf, L., Gesslein, B., Lind, B. L., van den Maagdenberg, A. M. J. M., & Lauritzen, M. (2016) · Annals of Neurology · doi:10.1002/ana.24707 · Cited by 30
Self-citationJing, B., Zhang, C., Liu, X., Zhou, L., Liu, J., Yao, Y., Yu, J., Weng, Y., Pan, M., Liu, J., et al. (2017) · Protein & Cell · doi:10.1007/s13238-017-0449-8 · Cited by 32
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Youssef, A. M., Ludwick, A., Wilcox, S. L., Lebel, A., Peng, K., Colon, É., Danehy, A. R., Burstein, R., Becerra, L. R., & Borsook, D. (2017) · Human Brain Mapping · doi:10.1002/hbm.23649 · Cited by 29
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Zhang, Y. S., Mucollari, I., Kwan, C. C., Dingillo, G., Amar, J., Schwartz, G. W., & Fawzi, A. A. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9113523 · Cited by 29
Hørlyck, S., Cai, C., Helms, H. C. C., Lauritzen, M., & Brodin, B. (2020) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00560.2020 · Cited by 30
Self-citationSzarka, N., Szellár, D., Kiss, S., Farkas, N., Szakács, Z., Czigler, A., Ungvari, Z. I., Hegyi, P. J., Büki, A., & Tóth, P. (2021) · Journal of Neurotrauma · doi:10.1089/neu.2020.7265 · Cited by 32
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Metadata
- Authors
- Attwell, D., Buchan, A. M., Charpak, S., Lauritzen, M., MacVicar, B. A., & Newman, E. A.
- Affiliations
- University College London (GB)
- John Radcliffe Hospital (GB)
- Centre National de la Recherche Scientifique (FR)
- University of Copenhagen (DK)
- University of British Columbia (CA)
- University of Minnesota (US)
- ORCID
- Venue
- Nature
- Published
- 2010-11-10
- Volume
- 468
- Issue
- 7321
- Pages
- 232-243
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3206737
- OpenAlex
- W2163234334
- Cited by
- 2,511
- References
- 135
- Citations by year
- 2026: 144 · 2025: 163 · 2024: 163 · 2023: 147 · 2022: 176 · 2021: 197 · 2020: 180 · 2019: 177 · 2018: 177 · 2017: 172 · 2016: 156 · 2015: 174 · 2014: 146 · 2013: 147 · 2012: 120
- FWCI
- 9.04
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
- Funders
- Wellcome Trust
- Canadian Institutes of Health Research
- National Eye Institute (R01EY004077, P30EY011374)
- Topics
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Health Sciences › Medicine › Clinical Neurology › Traumatic Brain Injury and Neurovascular Disturbances
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- cerebral autoregulation, astrocytes, neurons, neurotransmitter signalling, oxygen sensing, capillary blood flow, arterioles, neurovascular coupling, functional neuroimaging, neurological disorders
- MeSH terms
- Alzheimer Disease, Brain, Brain Ischemia, Cerebrovascular Circulation, Humans, Neuroglia, Neurons, Nitric Oxide, Oxygen, Signal Transduction, Neurotransmitter Agents
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