The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
Nonoxidative Glucose Consumption During Focal Physiologic Neural Activity
Abstract
Brain glucose uptake, oxygen metabolism, and blood flow in humans were measured with positron emission tomography, and a resting-state molar ratio of oxygen to glucose consumption of 4.1:1 was obtained. Physiological neural activity, however, increased glucose uptake and blood flow much more (51 and 50 percent, respectively) than oxygen consumption (5 percent) and produced a molar ratio for the increases of 0.4:1. Transient increases in neural activity cause a tissue uptake of glucose in excess of that consumed by oxidative metabolism, acutely consume much less energy than previously believed, and regulate local blood flow for purposes other than oxidative metabolism.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
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?
In the citing paper
“Supporting this glycolytic shift hypothesis, PET studies in humans have reported increased cerebral blood flow and glucose utilization without a corresponding rise in oxygen consumption during REM sleep69.”
From Energy paradox in REM sleep: balancing supply and consumption in brain metabolism (2026) · cites this paper as [69]
In the citing paper
“Curiously, AG persists for at least 40 minutes following cognitive demanding task performance, despite the return of blood flow and lactate production to control levels”
From Aerobic glycolysis in the human brain is associated with development and neotenous gene expression (2014) · cites this paper as Fox et al., 1988
In the citing paper
“Uncoupling of glucose metabolism from oxygen consumption is characteristic of the brain’s response to imposed tasks (‘activation’)”
From Aerobic glycolysis in the human brain is associated with development and neotenous gene expression (2014) · cites this paper as Fox et al., 1988
In the citing paper
“The drop in OGI during brain stimulation was the first indication of some transient uncoupling of glycolysis and oxphos in the brain (Fox et al., 1988).”
From Fueling thought: Management of glycolysis and oxidative phosphorylation in neuronal metabolism (2018) · cites this paper as Fox et al., 1988
In the citing paper
“However, with brain activation, glucose consumption increases much more than oxygen consumption (Fox and Raichle, 1986; Fox et al., 1988).”
From Neuronal Stimulation Triggers Neuronal Glycolysis and Not Lactate Uptake (2017) · cites this paper as Fox et al., 1988
In the citing paper
“PET studies also show that blood flow and glucose consumption are dramatically increased by brain activation, but oxygen consumption barely increases (Fox and Raichle, 1986; Fox et al., 1988).”
From Neuronal Stimulation Triggers Neuronal Glycolysis and Not Lactate Uptake (2017) · cites this paper as Fox et al., 1988
In the citing paper
“Despite the fact that both glycolysis and oxidative metabolism are elevated after stimulation, there is ample evidence that immediately after brain activation, oxygen consumption does not rise commensurate with the increases in blood flow and glucose consumption.”
From Neuronal Stimulation Triggers Neuronal Glycolysis and Not Lactate Uptake (2017) · cites this paper as Fox et al., 1988
In the citing paper
“This relationship is altered in the normal brain only when areas briefly change their activity during specific behaviors (4, 13).”
From A default mode of brain function (2001) · cites this paper as [13]
Citations
Cites
Fox, P. T., & Raichle, M. E. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.4.1140 · Cited by 2,056
Self-citationSiesjö, B. K. (1978) · Medical Entomology and Zoology · Cited by 1,426
Brain blood flow measured with intravenous H2(15)O. II. Implementation and validation.
Raichle, M. E., Martin, W. R. W., Herscovitch, P., Mintun, M. A., & Markham, J. (1983) · PubMed · Cited by 1,015
Self-citationBrain blood flow measured with intravenous H2(15)O. I. Theory and error analysis.
Herscovitch, P., Markham, J., & Raichle, M. E. (1983) · PubMed · Cited by 835
Self-citationBrain oxygen utilization measured with O-15 radiotracers and positron emission tomography.
Mintun, M. A., Raichle, M. E., Martin, W. R. W., & Herscovitch, P. (1984) · PubMed · Cited by 608
Self-citationFox, P. T., & Raichle, M. E. (1984) · Journal of Neurophysiology · doi:10.1152/jn.1984.51.5.1109 · Cited by 500
Self-citationReivich, M., Alavi, A. A., Wolf, A. P., Fowler, J. S., Russell, J. A. G., Arnett, C. D., MacGregor, R. R., Shiue, C., Atkins, H. L., Anand, A., et al. (1985) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1985.24 · Cited by 415
Does the Release of Potassium from Astrocyte Endfeet Regulate Cerebral Blood Flow?
Paulson, O. B., & Newman, E. A. (1987) · Science · doi:10.1126/science.3616619 · Cited by 414
Retinotopic organization of human visual cortex mapped with positron- emission tomography
Fox, P. T., Miezin, F. M., Allman, J. M., Essen, D. C. V., & Raichle, M. E. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-03-00913.1987 · Cited by 364
Self-citationCerebral Metabolic and Circulatory Responses to Induced Convulsions in Animals
Plum, F., Posner, J. B., & Troy, B. P. (1968) · Archives of Neurology · doi:10.1001/archneur.1968.00470310015001 · Cited by 326
Flagged first, then by citations
Research works printed but not linked: 5
- Creutzfeldt, O., Brain Work: The Coupling of Function, Metabolism, and Blood Flow in the Brain: 22 (1975).
- HOSSMANN, K. A., JOURNAL OF CEREBRAL BLOOD FLOW & METABOLISM 7: S297 (1987).
- PENFIELD, W, RESEARCH PUBLICATIONS - ASSOCIATION FOR RESEARCH IN NERVOUS AND MENTAL DISEASE 18: 605 (1937).
- SWANSON, R.A., SOCIETY FOR NEUROSCIENCE. ABSTRACTS 13: 649 (1987).
- Van den Berg, C., Energetics and Human Information Processing: 131 (1986).
Cited by
Sorted by citations
Items 701–800 of 1,003
Smith, S. K., Lee, C. A., Dausch, M. E., Horman, B. M., Patisaul, H. B., McCarty, G. S., & Sombers, L. A. (2016) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.6b00363 · Cited by 47
Buxton, R. B. (2020) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2019.0624 · Cited by 48
Cerebral non‐oxidative carbohydrate consumption in humans driven by adrenaline
Seifert, T. S., Brassard, P., Jørgensen, T. B., Hamada, A. J., Rasmussen, P., Quistorff, B., Secher, N. H., & Nielsen, H. B. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.162073 · Cited by 47
A comparison of FDG PET and IQNB SPECT in normal subjects and in patients with dementia
Weinberger, D. R., Jones, D., Reba, R. C., Mann, U. M., Coppola, R., Gibson, R. E., Gorey, J. G., Braun, A., & Chase, T. N. (1992) · Journal of Neuropsychiatry · doi:10.1176/jnp.4.3.239 · Cited by 47
Hunter, R., Wyper, D., Patterson, J. C., Hansen, M. T., & Goodwin, G. M. (1991) · The British Journal of Psychiatry · doi:10.1192/bjp.158.3.351 · Cited by 47
Lactate as a determinant of neuronal excitability, neuroenergetics and beyond
Cauli, B., Dusart, I., & Li, D. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106207 · Cited by 50
Cardiovascular effects of xenon and nitrous oxide in patients during fentanyl‐midazolam anaesthesia*
Goto, T., Hanne, P., Ishiguro, Y., Ichinose, F., Niimi, Y., & Morita, S. (2004) · Anaesthesia · doi:10.1111/j.1365-2044.2004.03900.x · Cited by 47
Sakadžić, S., Yaseen, M. A., Jaswal, R. S., Roussakis, E., Dale, A. M., Buxton, R. B., Vinogradov, S. A., Boas, D. A., & Devor, A. (2016) · Neurophotonics · doi:10.1117/1.nph.3.4.045005 · Cited by 46
Neural inhibition can explain negative BOLD responses: A mechanistic modelling and fMRI study
Sten, S., Lundengård, K., Witt, S. T., Cedersund, G., Elinder, F., & Engström, M. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.07.002 · Cited by 51
Advances in simultaneous PET/MR for imaging neuroreceptor function
Sander, C. Y. M., Hansen, H. D., & Wey, H. (2020) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x20910038 · Cited by 46
Functional Magnetic Resonance Imaging
Lin, A., & Way, H.-Y. M. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-386456-7.07610-3 · Cited by 47
Thompson, J. K., Peterson, M. R., & Freeman, R. D. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2127-05.2005 · Cited by 46
The BOLD onset transient: identification of novel functional differences in schizophrenia
Fox, M., Snyder, A. Z., McAvoy, M. P., Barch, D. M., & Raichle, M. E. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2004.12.025 · Cited by 46
Self-citationGJEDDE, A. H. (2002) · NeuroImage · doi:10.1006/nimg.2002.1272 · Cited by 42
Predicting performance from functional imaging data: methods matter
Sidtis, J. J., Strother, S. C., & Rottenberg, D. A. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00349-5 · Cited by 46
Yamane, K., Yokono, K., & Okada, Y. (2000) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(00)00312-5 · Cited by 46
Hackländer, T., Hofer, M., Reichenbach, J. R., Rascher, K., Fürst, G., & Mödder, U. (1996) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-199607000-00006 · Cited by 46
Viñas, F. C., Zamorano, L. J., Mueller, R.-A., Jiang, Z., Chugani, H. T., Fuerst, D. R., Muzik, O., Mangner, T. J., & Diaz, F. (1997) · Neurological Research · doi:10.1080/01616412.1997.11740867 · Cited by 46
Miller, A., York, E. M., Stopka, S. A., Martínez‐François, J. R., Hossain, M. A., Baquer, G., Regan, M. S., Agar, N. Y. R., & Yellen, G. (2023) · Nature Metabolism · doi:10.1038/s42255-023-00890-z · Cited by 45
Tissue-type plasminogen activator mediates neuroglial coupling in the central nervous system
An, J., Haile, W. B., Wu, F., Torre, E. R., & Yepes, M. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.10.060 · Cited by 45
Brain Tissue Oxygen: In Vivo Monitoring with Carbon Paste Electrodes
Bolger, F. B., & Lowry, J. P. (2005) · Sensors · doi:10.3390/s5110473 · Cited by 45
Kato, T. (2004) · International Congress Series · doi:10.1016/j.ics.2004.05.052 · Cited by 45
Lubow, J. M., Pinon, I., Avogaro, A., Cobelli, C., Treeson, D. M., Mandeville, K. A., TOFFOLO, G. M., & Boyle, P. J. (2005) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00049.2005 · Cited by 45
Transient global cerebral ischemia induces rapid and sustained reorganization of synaptic structures
Zhu, L., Wang, L., Ju, F., Ran, Y., Wang, C., & Zhang, S. (2016) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x16674736 · Cited by 43
APOE genotype-dependent pharmacogenetic responses to rapamycin for preventing Alzheimer's disease
Lin, A., Parikh, I. J., Yanckello, L. M., White, R. S., Hartz, A. M. S., Taylor, C. E., McCulloch, S. D., Thalman, S. W., Xia, M., McCarty, K. L., et al. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.104834 · Cited by 45
Blomqvist, G., Seitz, R. J., SJÖGREN, I., Halldin, C., Stone‐Elander, S., Widén, L., Solin, O. H., & Haaparanta‐Solin, M. (1994) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1994.tb09718.x · Cited by 45
Functional Study of the Brain by NMR
Prichard, J. W., & Rosen, B. R. (1994) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1994.47 · Cited by 45
Functional imaging, affective disorder and dementia
Goodwin, G. M. (1996) · British Medical Bulletin · doi:10.1093/oxfordjournals.bmb.a011563 · Cited by 45
Chen, W., Zhu, X., Kato, T., Andersen, P., & Uǧurbil, K. (1998) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910390404 · Cited by 45
Functional MRI : Methods and Applications
Clare, S. (1997) · Cited by 45
Mazuel, L., Blanc, J., Repond, C., Bouchaud, V., Raffard, G., Déglon, N., Bonvento, G., Pellerin, L., & Bouzier-Sore, A.-K. (2017) · PLoS ONE · doi:10.1371/journal.pone.0174990 · Cited by 44
Metabolic Recruitment in Brain Tissue
Barros, L. F., Ruminot, I., Sotelo-Hitschfeld, T., Lerchundi, R., & Fernández‐Moncada, I. (2022) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021422-091035 · Cited by 43
Cerebral oxygen delivery and consumption during evoked neural activity
Vazquez, A. L. (2010) · Frontiers in Neuroenergetics · doi:10.3389/fnene.2010.00011 · Cited by 48
Hypocapnia induced vasoconstriction significantly inhibits the neurovascular coupling in humans
Szabó, K., Lako, E., Juhasz, T., Rosengarten, B., Csiba, L., & Oláh, L. (2011) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2011.07.026 · Cited by 42
Emmanuel, Y., Cochlin, L. E., Tyler, D. J., de Jager, C. A., Smith, A. D., & Clarke, K. (2013) · Brain and Behavior · doi:10.1002/brb3.124 · Cited by 44
Shibuya, K., Sadamoto, T., Sato, K., Moriyama, M., & Iwadate, M. (2008) · Brain Research · doi:10.1016/j.brainres.2008.03.009 · Cited by 44
1H-MRS metabolites in adults with Down syndrome: Effects of dementia
Lin, A., Powell, D. K., Caban‐Holt, A., Jicha, G. A., Robertson, W. C., Gold, B. T., Davis, R., Abner, E. L., Wilcock, D. M., Schmitt, F. A., et al. (2016) · NeuroImage Clinical · doi:10.1016/j.nicl.2016.06.001 · Cited by 42
Effects of salicylate on serotoninergic activities in rat inferior colliculus and auditory cortex
Liu, J., Li, X., Wang, L., Dong, Y., Han, H., & Liu, G. (2003) · Hearing Research · doi:10.1016/s0378-5955(02)00708-6 · Cited by 44
Magnetic Resonance Imaging of Human Brain Function
Bandettini, P. A., & Wong, E. C. (1997) · Neurosurgery Clinics of North America · doi:10.1016/s1042-3680(18)30309-7 · Cited by 44
Functional Studies of the Human Brain Using High‐speed Magnetic Resonance Imaging
Belliveau, J. W., Cohen, M. S., Weisskoff, R. M., Buchbinder, B. R., & Rosen, B. R. (1991) · Journal of Neuroimaging · doi:10.1111/jon19911136 · Cited by 44
Cerebral blood oxygenation changes induced by visual stimulation in humans
Wenzel, R., Obrig, H., Ruben, J. L., Villringer, K., Thiel, A., Bernarding, J., Dirnagl, U., & Villringer, A. (1996) · Journal of Biomedical Optics · doi:10.1117/12.251465 · Cited by 44
Febo, M. (2011) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2011.00043 · Cited by 43
A trade-off between cognitive and physical performance, with relative preservation of brain function
Longman, D. P., Stock, J. T., & Wells, J. C. K. (2017) · Scientific Reports · doi:10.1038/s41598-017-14186-2 · Cited by 46
Rasmussen, P., Vedel, J. ‐., Olesen, J., Adser, H., Pedersen, M. V., Hart, E. C., Secher, N. H., & Pilegaard, H. (2010) · Acta Physiologica · doi:10.1111/j.1748-1716.2010.02223.x · Cited by 44
Dienel, G. A., & Cruz, N. F. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1427.011 · Cited by 45
Safaeian, N., & David, T. (2013) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2013.119 · Cited by 43
Functional Magnetic Resonance Imaging of the Spinal Cord: Current Status and Future Developments
Cohen‐Adad, J. (2016) · Seminars in Ultrasound CT and MRI · doi:10.1053/j.sult.2016.07.007 · Cited by 43
The CSF and arterial to internal jugular venous hormonal differences during exercise in humans
Dalsgaard, M. K., Ott, P., Dela, F., Juul, A., Pedersen, B. K., Warberg, J., Fahrenkrug, J., & Secher, N. H. (2004) · Experimental Physiology · doi:10.1113/expphysiol.2003.026922 · Cited by 43
On the role of anesthesia on the body/brain temperature differential in rats
Zhu, M., Nehra, D., Ackerman, J. J. H., & Yablonskiy, D. A. (2004) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2004.08.029 · Cited by 43
Mapping cortical columnar structures using fMRI
KIM, S., & Duong, T. Q. (2002) · Physiology & Behavior · doi:10.1016/s0031-9384(02)00901-0 · Cited by 43
Tsukada, H., Kakiuchi, T., Ando, I., & Ouchi, Y. (1997) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)36742-4 · Cited by 43
Effect of photic stimulation on energy metabolism in the human brain measured by 31P-MR spectroscopy
Kato, T., Murashita, J., Shioiri, T., Hamakawa, H., & Inubushi, T. (1996) · Journal of Neuropsychiatry · doi:10.1176/jnp.8.4.417 · Cited by 43
Diminished cerebral metabolic response to motor stimulation in schizophrenics: a PET study
Guenther, W., Brodie, J. D., Bartlett, E. J., Dewey, S. L., Henn, F. A., Volkow, N. D., Alper, K., Wolkin, A., Cancro, R., & Wolf, A. P. (1994) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/bf02191884 · Cited by 43
Smart, K., Liu, H., Matuskey, D., Chen, M.-K., Torres, K., Nabulsi, N., Labaree, D., Ropchan, J., Hillmer, A. T., Huang, Y., et al. (2021) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x20946198 · Cited by 42
Dennis, A., Thomas, A. G., Rawlings, N. B., Near, J., Nichols, T. E., Clare, S., Johansen-Berg, H., & Stagg, C. J. (2015) · Frontiers in Physiology · doi:10.3389/fphys.2015.00351 · Cited by 43
Event-related functional magnetic resonance spectroscopy
Koolschijn, R. S., Clarke, W. T., Ip, I. B., Emir, U. E., & Barron, H. C. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120194 · Cited by 43
Autologous mitochondrial transplant for acute cerebral ischemia: Phase 1 trial results and review
Walker, M., Levitt, M. R., Federico, E. M., Miralles, F. J., Lévy, S., Prijoles, K. L., Winter, A., Swicord, J. K., & Sancak, Y. (2024) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x241305230 · Cited by 44
Bolaños, J. P., & Magistretti, P. J. (2025) · Nature Metabolism · doi:10.1038/s42255-025-01404-9 · Cited by 46
Baseline CBF , and BOLD, CBF , and CMRO 2 fMRI of Visual and Vibrotactile Stimulations in Baboons
Wey, H., Wang, D. J. J., & Duong, T. Q. (2010) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2010.154 · Cited by 42
Functional MRI using steady‐state arterial water labeling
Talagala, S. L., & Noll, D. C. (1998) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910390203 · Cited by 42
Principles of BOLD Functional MRI
Chen, W., & Ogawa, S. (2000) · Medical radiology · doi:10.1007/978-3-642-58716-0_10 · Cited by 42
Increased oxygen consumption in human visual cortex: response to visual stimulation
Vafaee, M. S., Marrett, S., Meyer, E., Evans, A. C., & GJEDDE, A. H. (2009) · Acta Neurologica Scandinavica · doi:10.1111/j.1600-0404.1998.tb01724.x · Cited by 42
BOLD signal changes can oppose oxygen metabolism across the human cortex
Epp, S. M., Castrillón, G., Yuan, B., Andrews-Hanna, J., Preibisch, C., & Riedl, V. (2026) · Nature Neuroscience · doi:10.1038/s41593-025-02132-9 · Cited by 41
Muramoto, S., Yamada, H., Sadato, N., Kimura, H., Konishi, Y., Kimura, K., Tanaka, M., Kochiyama, T., Yonekura, Y., & Ito, H. (2002) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-200211000-00007 · Cited by 41
Tsukada, H., Kakiuchi, T., Ando, I., Shizuno, H., Nakanishi, S., & Ouchi, Y. (1997) · Brain Research · doi:10.1016/s0006-8993(96)01028-1 · Cited by 41
The Na(+)/K(+) pump dominates control of glycolysis in hippocampal dentate granule cells
Meyer, D. J., Díaz-García, C. M., Nathwani, N., Rahman, M., & Yellen, G. (2022) · eLife · doi:10.7554/elife.81645 · Cited by 40
DiNuzzo, M., Dienel, G. A., Behar, K. L., Petroff, O. A. C., Benveniste, H., Hyder, F., Giove, F., Michaeli, S., Mangia, S., Herculano‐Houzel, S., et al. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15839 · Cited by 40
Hahn, A., Gryglewski, G., Nics, L., Rischka, L., Ganger, S., Sigurdardottir, H., Vraka, C., Silberbauer, L., Vanicek, T., Kautzky, A., et al. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1558-0 · Cited by 44
Agarwal, S., Sair, H. I., Gujar, S. K., & Pillai, J. J. (2019) · Topics in Magnetic Resonance Imaging · doi:10.1097/rmr.0000000000000216 · Cited by 40
Blin, J., Ivanoiu, A., Coppens, A., Volder, A. D., Labar, D., Michel, C. J., & Laterre, E.-C. (1997) · NeuroImage · doi:10.1006/nimg.1997.0296 · Cited by 40
Vaucher, E., Borredon, J., Bonvento, G., Seylaz, J., & Lacombe, P. M. (1997) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-199706000-00010 · Cited by 40
Nitrous oxide-oxygen or oral midazolam for pediatric outpatient sedation
Hulland, S. A., Freilich, M. M., & Sándor, G. K. B. (2002) · Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology · doi:10.1067/moe.2002.124763 · Cited by 40
Functional Magnetic Resonance Imaging
Sexton, J. A., Deshpande, G., Li, Z., Glielmi, C. B., & Hu, X. P. (2012) · Springer eBooks · doi:10.1007/978-1-4614-5227-0_11 · Cited by 41
Chapter 30: Density of perfused capillaries in living human brain during functional activation
Kuwabara, H., Ohta, S., Brust, P., Meyer, E., & GJEDDE, A. H. (1992) · Progress in brain research · doi:10.1016/s0079-6123(08)62337-7 · Cited by 40
Local and dynamic regulation of neuronal glycolysis in vivo
Wolfe, A. D., Koberstein, J. N., Smith, C. B., Stewart, M. L., Gonzalez, I. J., Hammarlund, M., Hyman, A. A., Stork, P. A., Goodman, R. H., & Colón‐Ramos, D. A. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2314699121 · Cited by 38
PET in Cerebrovascular Disease
Powers, W. J., & Zazulia, A. R. (2010) · PET Clinics · doi:10.1016/j.cpet.2009.12.007 · Cited by 38
MCA Vmean and the arterial lactate-to-pyruvate ratio correlate during rhythmic handgrip
Rasmussen, P., Plomgaard, P., Krogh‐Madsen, R., Kim, Y.-S., LIESHOUT, J. J. V., Secher, N. H., & Quistorff, B. (2006) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00423.2006 · Cited by 39
Zhu, X., Du, F., Zhang, N., Zhang, Y., Lei, H. C., Zhang, X., Qiao, H., Uǧurbil, K., & Chen, W. (2008) · Methods in molecular biology · doi:10.1007/978-1-59745-543-5_15 · Cited by 41
Levodopa-induced local cerebral blood flow changes in Parkinson's disease and related disorders
Kobari, M., Fukuuchi, Y., Shinohara, T., Obara, K., & Nogawa, S. (1995) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(94)00237-i · Cited by 39
Lactate: a major and crucial player in normal function of both muscle and brain
Schurr, A. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.155416 · Cited by 39
The physiology and metabolism of neuronal activation: in vivo studies by NMR and other methods
Giove, F., Mangia, S., Bianciardi, M., Garreffa, G., Salle, F. D., Morrone, R., & Maraviglia, B. (2003) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2003.08.028 · Cited by 39
Sandberg, A. (2011) · Wiley eBooks · doi:10.1002/9781444393552.ch5 · Cited by 40
Dietary supplementation of creatine monohydrate reduces the human fMRI BOLD signal
Hammett, S. T., Wall, M. B., Edwards, T. C., & Smith, A. T. (2010) · Neuroscience Letters · doi:10.1016/j.neulet.2010.05.054 · Cited by 38
Shibuya, K., Kuboyama, N., & Tanaka, J. (2014) · Physiological Measurement · doi:10.1088/0967-3334/35/3/417 · Cited by 40
Moro, N., Ghavim, S. S., Harris, N. G., Hovda, D. A., & Sutton, R. L. (2013) · Brain Research · doi:10.1016/j.brainres.2013.08.044 · Cited by 38
Strelnikov, K. (2010) · Brain and Cognition · doi:10.1016/j.bandc.2009.12.008 · Cited by 38
Quantitative measurements of cerebral blood flow with near-infrared spectroscopy
Pham, T., Tgavalekos, K. T., Sassaroli, A., Blaney, G. P., & Fantini, S. (2019) · Biomedical Optics Express · doi:10.1364/boe.10.002117 · Cited by 38
Marcar, V. L., Straessle, A., Loenneker, T., Schwarz, U., & Martin, E. (2004) · Pediatric Research · doi:10.1203/01.pdr.0000145296.24669.a5 · Cited by 38
Correlational Imaging of Thalamocortical Coupling in the Primary Visual Pathway of the Human Brain
Kleinschmidt, A. K., Merboldt, K., Hänicke, W., Steinmetz, H., & Frahm, J. (1994) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1994.127 · Cited by 38
Functional MRI in Human Motor Control Studies and Clinical Applications
Toma, K., & Nakai, T. (2002) · Magnetic Resonance in Medical Sciences · doi:10.2463/mrms.1.109 · Cited by 37
Schnorr, J., Taupitz, M., Wagner, S., Pilgrimm, H., Hansel, J., & Hamm, B. (2000) · Journal of Magnetic Resonance Imaging · doi:10.1002/1522-2586(200011)12:5 · Cited by 15
The application of functional magnetic resonance imaging to neuropharmacology
Shah, Y. B., & Marsden, C. A. (2004) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2004.06.002 · Cited by 38
Duncan, G. E., & Stumpf, W. E. (1991) · Progress in Neurobiology · doi:10.1016/0301-0082(91)90023-t · Cited by 38
Regional cerebral blood flow during hypoglycaemia in children with IDDM
Jarjour, I. T., Ryan, C. M., & Becker, D. J. (1995) · Diabetologia · doi:10.1007/bf00402180 · Cited by 38
Chronic cerebrospinal venous insufficiency and venous stenoses in multiple sclerosis
Blinkenberg, M., Åkeson, P., Sillesen, H. H., Lövgaard, S., Sellebjerg, F. T., Paulson, O. B., Siebner, H. R., & Sørensen, P. S. (2012) · Acta Neurologica Scandinavica · doi:10.1111/j.1600-0404.2012.01671.x · Cited by 37
Holper, L., Shalóm, D. E., Wolf, M., & Sigman, M. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07720.x · Cited by 37
The neurobiology of Alzheimer disease defined by neuroimaging
Masdeu, J. C., Kreisl, W. C., & Berman, K. F. (2012) · Current Opinion in Neurology · doi:10.1097/wco.0b013e3283557b36 · Cited by 39
Seidel-Marzi, O., Carius, D., Roediger, J., Rumpf, S., & Ragert, P. (2019) · Experimental Brain Research · doi:10.1007/s00221-019-05646-4 · Cited by 40
Memory recall involves a transient break in excitatory-inhibitory balance
Koolschijn, R. S., Shpektor, A., Ip, I. B., Clarke, W. T., Dupret, D., Emir, U. E., & Barron, H. C. (2021) · eLife · doi:10.7554/elife.70071 · Cited by 40
Liu, X., Li, C., Falck, J. R., Harder, D. R., & Koehler, R. C. (2011) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00794.2011 · Cited by 37
Metadata
- Authors
- Fox, P. T., Raichle, M. E., Mintun, M. A., & Dence, C.
- Affiliations
- Washington University in St. Louis (US)
- Venue
- Science
- Published
- 1988-07-22
- Volume
- 241
- Issue
- 4864
- Pages
- 462-464
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W1993303421
- Cited by
- 1,796
- References
- 27
- Citations by year
- 2026: 24 · 2025: 32 · 2024: 34 · 2023: 30 · 2022: 29 · 2021: 69 · 2020: 29 · 2019: 37 · 2018: 58 · 2017: 50 · 2016: 46 · 2015: 46 · 2014: 59 · 2013: 56 · 2012: 56
- FWCI
- 19.19
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Heart, Lung, and Blood Institute (HL 13851)
- National Institute of Neurological Disorders and Stroke (NS-07025, NS 06833)
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Medical Imaging Techniques and Applications
- Keywords
- brain glucose uptake, oxygen consumption, cerebral blood flow, neuronal activity, brain energy metabolism, local blood flow regulation
- MeSH terms
- Brain, Cerebrovascular Circulation, Energy Metabolism, Glucose, Humans, Neurons, Oxygen, Tomography, Emission-Computed, Visual Cortex, Visual Perception
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