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Energy metabolism of the visual system

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Wong-Riley, Margaret·2010·Eye and Brain

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Abstract

The visual system is one of the most energetically demanding systems in the brain. The currency of energy is ATP, which is generated most efficiently from oxidative metabolism in the mitochondria. ATP supports multiple neuronal functions. Foremost is repolarization of the membrane potential after depolarization. Neuronal activity, ATP generation, blood flow, oxygen consumption, glucose utilization, and mitochondrial oxidative metabolism are all interrelated. In the retina, phototransduction, neurotransmitter utilization, and protein/organelle transport are energy-dependent, yet repolarization-after-depolarization consumes the bulk of the energy. Repolarization in photoreceptor inner segments maintains the dark current. Repolarization by all neurons along the visual pathway following depolarizing excitatory glutamatergic neurotransmission preserves cellular integrity and permits reactivation. The higher metabolic activity in the magno- versus the parvo-cellular pathway, the ON- versus the OFF-pathway in some (and the reverse in other) species, and in specialized functional representations in the visual cortex all reflect a greater emphasis on the processing of specific visual attributes. Neuronal activity and energy metabolism are tightly coupled processes at the cellular and even at the molecular levels. Deficiencies in energy metabolism, such as in diabetes, mitochondrial DNA mutation, mitochondrial protein malfunction, and oxidative stress can lead to retinopathy, visual deficits, neuronal degeneration, and eventual blindness.

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Sequence and organization of the human mitochondrial genome
Anderson, S., Bankier, A. T., Barrell, B. G., de Bruijn, M. H. L., Coulson, A. R., Drouin, J., Eperon, I. C., Nierlich, D. P., Roe, B. A., Sanger, F., et al. (1981) · Nature · doi:10.1038/290457a0 · Cited by 9,636
Distributed hierarchical processing in the primate cerebral cortex
Felleman, D. J., & Van Essen, D. C. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1 · Cited by 7,783
THE [ 14 C]DEOXYGLUCOSE METHOD FOR THE MEASUREMENT OF LOCAL CEREBRAL GLUCOSE UTILIZATION: THEORY, PROCEDURE, AND NORMAL VALUES IN THE CONSCIOUS AND ANESTHETIZED ALBINO RAT 1
Sokoloff, L., Reivich, M., Kennedy, C., Rosiers, M. H. D., Patlak, C. S., Pettigrew, K. D., Sakurada, O., & Shinohara, M. (1977) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1977.tb10649.x · Cited by 6,000
Principles of biochemistry
(1978) · Biochemical Education · doi:10.1016/0307-4412(78)90049-3 · Cited by 5,046
What we can do and what we cannot do with fMRI
Logothetis, N. K. (2008) · Nature · doi:10.1038/nature06976 · Cited by 3,612
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
Object vision and spatial vision: Two cortical pathways
Mishkin, M., Ungerleider, L. G., & Macko, K. A. (1983) · Trends in Neurosciences · doi:10.1016/0166-2236(83)90190-x · Cited by 2,947
Ferrier lecture. Functional architecture of macaque monkey visual cortex
Hubel, D. H., & Wiesel, T. N. (1977) · Proceedings of the Royal Society of London. Series B. Biological Sciences · doi:10.1098/rspb.1977.0085 · Cited by 2,608
Mitochondrial DNA mutation associated with Leber’s hereditary optic neuropathy
Wallace, D. C., Singh, G., Lott, M. T., Hodge, J. A., Schurr, T. G., Lezza, A. M. S., Elsas, L. J., & Nikoskelainen, E. K. (1988) · Science · doi:10.1126/science.3201231 · Cited by 2,440
Glutamate, nitric oxide and cell-cell signalling in the nervous system
Garthwaite, J. (1991) · Trends in Neurosciences · doi:10.1016/0166-2236(91)90022-m · Cited by 2,402
The influence of some cations on an adenosine triphosphatase from peripheral nerves
Skou, J. C. (1957) · Biochimica et Biophysica Acta · doi:10.1016/0006-3002(57)90343-8 · Cited by 2,247
Cellular energy utilization and molecular origin of standard metabolic rate in mammals
Rolfe, D. F., & Brown, G. C. (1997) · Physiological Reviews · doi:10.1152/physrev.1997.77.3.731 · Cited by 2,021
The Molecular Motor Toolbox for Intracellular Transport
Vale, R. D. (2003) · Cell · doi:10.1016/s0092-8674(03)00111-9 · Cited by 1,982
‘What’ and ‘where’ in the human brain
Ungerleider, L. G., & Haxby, J. V. (1994) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(94)90066-3 · Cited by 1,913
Changes in the visual system of monocularly sutured or enucleated cats demonstrable with cytochrome oxidase histochemistry
Wong-Riley, M. (1979) · Brain Research · doi:10.1016/0006-8993(79)90728-5 · Cited by 1,858
Self-citation
The physiology of excitatory amino acids in the vertebrate central nervous system
Mayer, M. L., & Westbrook, G. L. (1987) · Progress in Neurobiology · doi:10.1016/0301-0082(87)90011-6 · Cited by 1,717
Diabetic retinopathy
Antonetti, D. A., Klein, R., & Gardner, T. W. (2012) · New England Journal of Medicine · doi:10.1056/nejmra1005073 · Cited by 1,659
Anatomy and physiology of a color system in the primate visual cortex
Livingstone, M., & Hubel, D. (1984) · The Journal of Neuroscience · doi:10.1523/jneurosci.04-01-00309.1984 · Cited by 1,628
Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy
Delettre, C., Lenaers, G., Griffoin, J.-M., Gigarel, N., Lorenzo, C., Belenguer, P., Pelloquin, L., Grosgeorge, J., Turc-Carel, C., Perret, E., et al. (2000) · Nature Genetics · doi:10.1038/79936 · Cited by 1,446
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophy
Allikmets, R., Singh, N., Sun, H., Shroyer, N. F., Hutchinson, A., Chidambaram, A., Gerrard, B., Baird, L., Stauffer, D., Peiffer, A., et al. (1997) · Nature Genetics · doi:10.1038/ng0397-236 · Cited by 1,435 · cited 1×
“More than 180 mutations of the ABCR gene (ABCA4) have been implicated in a number of retinal degenerative diseases,(83,84) notably early onset autosomal recessive Stargardt macular dystrophy,(85,86) fundus flavimaculatus,(87) autosomal recessive retinitis pigmentosa,(88) cone-rod dystrophy,(89) and increased risk for…”
Cytochrome oxidase: an endogenous metabolic marker for neuronal activity
Wong-Riley, M. T. T. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90165-3 · Cited by 1,238
Self-citation
PARTICIPATION OF THE RETINAL PIGMENT EPITHELIUM IN THE ROD OUTER SEGMENT RENEWAL PROCESS
Young, R. W., & Bok, D. (1969) · The Journal of Cell Biology · doi:10.1083/jcb.42.2.392 · Cited by 1,187
The metabolic cost of neural information
Laughlin, S. B., de Ruyter van Steveninck, R. R., & Anderson, J. C. (1998) · Nature Neuroscience · doi:10.1038/236 · Cited by 1,166
Concurrent processing streams in monkey visual cortex
DeYoe, E. A., & Van Essen, D. C. (1988) · Trends in Neurosciences · doi:10.1016/0166-2236(88)90130-0 · Cited by 1,118
Molecular and cellular physiology of intracellular calcium stores
Pozzan, T., Rizzuto, R., Volpe, P., & Meldolesi, J. (1994) · Physiological Reviews · doi:10.1152/physrev.1994.74.3.595 · Cited by 1,114
Energy limitation as a selective pressure on the evolution of sensory systems
Niven, J. E., & Laughlin, S. B. (2008) · Journal of Experimental Biology · doi:10.1242/jeb.017574 · Cited by 1,056
Calibrated functional MRI: Mapping the dynamics of oxidative metabolism
Davis, T. L., Kwong, K. K., Weisskoff, R. M., & Rosen, B. R. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.4.1834 · Cited by 1,052
Hierarchical organization and functional streams in the visual cortex
Van Essen, D. C., & Maunsell, J. H. R. (1983) · Trends in Neurosciences · doi:10.1016/0166-2236(83)90167-4 · Cited by 962
Excitatory amino acid transporter 5, a retinal glutamate transporter coupled to a chloride conductance
Arriza, J. L., Eliasof, S., Kavanaugh, M. P., & Amara, S. G. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.8.4155 · Cited by 912
Stoichiometric coupling of brain glucose metabolism and glutamatergic neuronal activity.
Sibson, N. R., Dhankhar, A., Mason, G. F., Rothman, D. L., Behar, K. L., & Shulman, R. G. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.1.316 · Cited by 897
Mitochondrial dysfunction as a cause of optic neuropathies
Carelli, V., Ross-Cisneros, F. N., & Sadun, A. A. (2004) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2003.10.003 · Cited by 839
Segregation of form, color, and stereopsis in primate area 18
Hubel, D., & Livingstone, M. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-11-03378.1987 · Cited by 834
Neuron-glia metabolic coupling and plasticity
Magistretti, P. J. (2011) · Experimental Physiology · doi:10.1113/expphysiol.2010.053157 · Cited by 747
Diabetic Retinopathy
Antonetti, D. A., Barber, A. J., Bronson, S. K., Freeman, W. M., Gardner, T. W., Jefferson, L. S., Kester, M., Kimball, S. R., Krady, J. K., LaNoue, K. F., et al. (2006) · Diabetes · doi:10.2337/db05-1635 · Cited by 746
Circulation and Energy Metabolism of the Brain
Clarke, D. D., & Sokoloff, L. (1999) · Cited by 732
Aging-Dependent Large Accumulation of Point Mutations in the Human mtDNA Control Region for Replication
Michikawa, Y., Mazzucchelli, F., Bresolin, N., Scarlato, G., & Attardi, G. (1999) · Science · doi:10.1126/science.286.5440.774 · Cited by 725
CNS energy metabolism as related to function
Ames, A. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(00)00038-2 · Cited by 663
Oxygen Distribution and Consumption within the Retina in Vascularised and Avascular Retinas and in Animal Models of Retinal Disease
Yu, D.-Y., & Cringle, S. J. (2001) · Progress in Retinal and Eye Research · doi:10.1016/s1350-9462(00)00027-6 · Cited by 653
SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome
Zhu, Z., Yao, J., Johns, T., Fu, K., Bie, I. D., Macmillan, C., Cuthbert, A. P., Newbold, R. F., Wang, J.-C., Chevrette, M., et al. (1998) · Nature Genetics · doi:10.1038/3804 · Cited by 623
Regulation of retinal blood flow in health and disease
Pournaras, C. J., Rungger-Brändle, E., Riva, C. E., Hardarson, S. H., & Stefansson, E. (2008) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2008.02.002 · Cited by 618
Tissue oxygen tension and brain sensitivity to hypoxia
Erecińska, M., & Silver, I. A. (2001) · Respiration Physiology · doi:10.1016/s0034-5687(01)00306-1 · Cited by 615
A Direct Repeat Is a Hotspot for Large-Scale Deletion of Human Mitochondrial DNA
Schon, E. A., Rizzuto, R., Moraes, C. T., Nakase, H., Zeviani, M., & DiMauro, S. (1989) · Science · doi:10.1126/science.2711184 · Cited by 567
Linear coupling between cerebral blood flow and oxygen consumption in activated human cortex
Hoge, R. D., Atkinson, J., Gill, B., Crelier, G. R., Marrett, S., & Pike, G. B. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.16.9403 · Cited by 563
Dark Current and Photocurrent in Retinal Rods
Hagins, W. A., Penn, R. D., & Yoshikami, S. (1970) · Biophysical Journal · doi:10.1016/s0006-3495(70)86308-1 · Cited by 556
Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR
Cremers, F. (1998) · Human Molecular Genetics · doi:10.1093/hmg/7.3.355 · Cited by 548
Functional Organization of Primate Visual Cortex Revealed by High Resolution Optical Imaging
Ts'o, D. Y., Frostig, R. D., Lieke, E. E., & Grinvald, A. (1990) · Science · doi:10.1126/science.2165630 · Cited by 524
Single-Channel Properties of Recombinant AMPA Receptors Depend on RNA Editing, Splice Variation, and Subunit Composition
Swanson, G. T., Kamboj, S. K., & Cull-Candy, S. G. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-01-00058.1997 · Cited by 489
Functional analysis of primary visual cortex (V1) in humans
Tootell, R. B. H., Hadjikhani, N. K., Vanduffel, W., Liu, A. K., Mendola, J. D., Sereno, M. I., & Dale, A. M. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.3.811 · Cited by 488
Positron Emission Tomography: Human Brain Function and Biochemistry
Phelps, M. E., & Mazziotta, J. C. (1985) · Science · doi:10.1126/science.2860723 · Cited by 469
Energy metabolism of rabbit retina as related to function: high cost of Na+ transport
Ames, A., Li, Y., Heher, E., & Kimble, C. (1992) · The Journal of Neuroscience · doi:10.1523/jneurosci.12-03-00840.1992 · Cited by 458
Propagation of Intercellular Calcium Waves in Retinal Astrocytes and Müller Cells
Newman, E. A. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-07-02215.2001 · Cited by 449
Energy-Efficient Action Potentials in Hippocampal Mossy Fibers
Alle, H., Roth, A., & Geiger, J. R. P. (2009) · Science · doi:10.1126/science.1174331 · Cited by 429
Lactate released by Muller glial cells is metabolized by photoreceptors from mammalian retina
Poitry-Yamate, C., Poitry, S., & Tsacopoulos, M. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-07-05179.1995 · Cited by 410
Cytochrome oxidase patches: a new cytoarchitectonic feature of monkey visual cortex
Horton, J. C. (1984) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1984.0021 · Cited by 406
Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.
Howell, N., Bindoff, L. A., McCullough, D. A., Kubacka, I., Poulton, J., Mackey, D. A., Taylor, L., & Turnbull, D. M. (1991) · PubMed · Cited by 404
ATP Consumption by Mammalian Rod Photoreceptors in Darkness and in Light
Okawa, H., Sampath, A. P., Laughlin, S. B., & Fain, G. L. (2008) · Current Biology · doi:10.1016/j.cub.2008.10.029 · Cited by 404
Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR
Martínez-Mir, A., Paloma, E., Allikmets, R., Ayuso, C., Río, T. D., Dean, M., Vilageliu, L., Gonzàlez-Duarte, R., & Balcells, S. (1998) · Nature Genetics · doi:10.1038/ng0198-11 · Cited by 402
An ND-6 mitochondrial DNA mutation associated with leber hereditary optic neuropathy
Johns, D. R., Neufeld, M. J., & Park, R. D. (1992) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(92)90479-5 · Cited by 347
New images from human visual cortex
Tootell, R. B. H., Dale, A. M., Sereno, M. I., & Malach, R. (1996) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)10053-9 · Cited by 345
Cytochrome oxidase : a synthesis
Wikström, M. K. F., Krab, K., & Saraste, M. (1981) · Andalas University Repository (Andalas University) · Cited by 329
Immunocytochemical localization of glutamic acid decarboxylase in monkey striate cortex
Hendrickson, A. E., Hunt, S. P., & Wu, J.-Y. (1981) · Nature · doi:10.1038/292605a0 · Cited by 320
How Does the Eye Breathe?
Schmidt, M., Giessl, A., Laufs, T., Hankeln, T., Wolfrum, U., & Burmester, T. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m209909200 · Cited by 316
The 220-kDa Rim Protein of Retinal Rod Outer Segments Is a Member of the ABC Transporter Superfamily
Illing, M., Molday, L. L., & Molday, R. S. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.15.10303 · Cited by 304
Energy metabolism in mammalian brain during development
Erecinska, M., Cherian, S., & Silver, I. A. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.06.003 · Cited by 297
The blood-retinal barriers
Cunha-Vaz, J. G. (1976) · Documenta Ophthalmologica · doi:10.1007/bf00146764 · Cited by 281
The Microvascular System of the Striate and Extrastriate Visual Cortex of the Macaque
Weber, B., Keller, A. L., Reichold, J., & Logothetis, N. K. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm259 · Cited by 279
Mitochondrial Dysfunction and Glaucoma
Kong, G. Y. X., Van Bergen, N. J., Trounce, I. A., & Crowston, J. G. (2009) · Journal of Glaucoma · doi:10.1097/ijg.0b013e318181284f · Cited by 261
Microtubule-associated protein 1C from brain is a two-headed cytosolic dynein
Vallee, R. B., Wall, J. S., Paschal, B. M., & Shpetner, H. S. (1988) · Nature · doi:10.1038/332561a0 · Cited by 261
Stargardt's ABCR is localized to the disc membrane of retinal rod outer segments
Sun, H., & Nathans, J. (1997) · Nature Genetics · doi:10.1038/ng0997-15 · Cited by 251
The toxicity of methanol
Tephly, T. R. (1991) · Life Sciences · doi:10.1016/0024-3205(91)90504-5 · Cited by 251
Beyond Counting Photons: Trials and Trends in Vertebrate Visual Transduction
Burns, M. E., & Arshavsky, V. Y. (2005) · Neuron · doi:10.1016/j.neuron.2005.10.014 · Cited by 250
What is the function of neuroglobin?
Burmester, T., & Hankeln, T. (2009) · Journal of Experimental Biology · doi:10.1242/jeb.000729 · Cited by 244
Functional anatomy of macaque striate cortex. V. Spatial frequency
Tootell, R., Silverman, M., Hamilton, S., Switkes, E., & De Valois, R. (1988) · The Journal of Neuroscience · doi:10.1523/jneurosci.08-05-01610.1988 · Cited by 244
Effect of impulse blockage on cytochrome oxidase activity in monkey visual system
Wong-Riley, M., & Carroll, E. W. (1984) · Nature · doi:10.1038/307262a0 · Cited by 243
Self-citation
Immunocytochemical localization of a large intrinsic membrane protein to the incisures and margins of frog rod outer segment disks.
Papermaster, D. S., Schneider, B. G., Zorn, M. A., & Kraehenbuhl, J. P. (1978) · The Journal of cell biology · doi:10.1083/jcb.78.2.415 · Cited by 237
Assessment of Visual Impairment in Patients With Alzheimer's Disease
Sadun, A. A., Borchert, M., DeVita, E., Hinton, D. R., & Bassi, C. J. (1987) · American Journal of Ophthalmology · doi:10.1016/0002-9394(87)90001-8 · Cited by 225
In vivo nuclear magnetic resonance spectroscopy studies of the relationship between the glutamate--glutamine neurotransmitter cycle and functional neuroenergetics
Rothman, D. L., Sibson, N. R., Hyder, F., Shen, J., Behar, K. L., & Shulman, R. G. (1999) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.1999.0472 · Cited by 225
Metabolic anatomy of brain: A comparison of regional capillary density, glucose metabolism, and enzyme activities
Borowsky, I. W., & Collins, R. C. (1989) · Journal of Comparative Neurology · doi:10.1002/cne.902880304 · Cited by 221
Neuroenergetics and the kinetic design of excitatory synapses
Attwell, D., & Gibb, A. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1784 · Cited by 191
Cytochrome oxidase: A synthesis
Leslie Dutton, P. (1982) · Trends in Biochemical Sciences · doi:10.1016/0968-0004(82)90019-6 · Cited by 189
Nuclear Respiratory Factor 1 Regulates All Ten Nuclear-encoded Subunits of Cytochrome c Oxidase in Neurons
Dhar, S. S., Ongwijitwat, S., & Wong-Riley, M. T. T. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m707587200 · Cited by 188
Self-citation
The influence of some cations on an adenosine triphosphatase from peripheral nerves.
Skou, J. C. (1998) · Journal of the American Society of Nephrology · doi:10.1681/asn.v9112170 · Cited by 187
Rod and cone photoreceptors: Molecular basis of the difference in their physiology
Kawamura, S., & Tachibanaki, S. (2008) · Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2008.04.600 · Cited by 182
The Na,K-ATPase of nervous tissue
Stahl, W. L. (1986) · Neurochemistry International · doi:10.1016/0197-0186(86)90179-8 · Cited by 175
Energy metabolism in human retinal Müller cells.
Winkler, B. S., Arnold, M. J., Brassell, M. A., & Puro, D. G. (2000) · PubMed · Cited by 174
Membrane Topology of the ATP Binding Cassette Transporter ABCR and Its Relationship to ABC1 and Related ABCA Transporters
Bungert, S., Molday, L. L., & Molday, R. S. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m101902200 · Cited by 173
How kinesin waits between steps
Mori, T., Vale, R. D., & Tomishige, M. (2007) · Nature · doi:10.1038/nature06346 · Cited by 171
Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle
Hartong, D. T., Dange, M., McGee, T. L., Berson, E. L., Dryja, T. P., & Colman, R. F. (2008) · Nature Genetics · doi:10.1038/ng.223 · Cited by 171
GLUT1 glucose transporter expression in the diabetic and nondiabetic human eye.
Kumagai, A. K., Glasgow, B. J., & Pardridge, W. M. (1994) · PubMed · Cited by 170
Mouse Cones Require an Arrestin for Normal Inactivation of Phototransduction
Nikonov, S. S., Brown, B. M., Davis, J. A., Zuniga, F. I., Bragin, A., Pugh, E. N., & Craft, C. M. (2008) · Neuron · doi:10.1016/j.neuron.2008.06.011 · Cited by 168
Light adaptation and photopigment bleaching in cone photoreceptors in situ in the retina of the turtle
Burkhardt, D. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-03-01091.1994 · Cited by 167
Multiple Phosphorylation of Rhodopsin and the In Vivo Chemistry Underlying Rod Photoreceptor Dark Adaptation
Kennedy, M. J., Lee, K. A., Niemi, G. A., Craven, K. B., Garwin, G. G., Saari, J. C., & Hurley, J. B. (2001) · Neuron · doi:10.1016/s0896-6273(01)00340-3 · Cited by 159
Concurrent downregulation of a glutamate transporter and receptor in glaucoma.
Naskar, R., Vorwerk, C. K., & Dreyer, E. B. (2000) · PubMed · Cited by 156
Complex experience promotes capillary formation in young rat visual cortex
Black, J., Sirevaag, A. M., & Greenough, W. T. (1987) · Neuroscience Letters · doi:10.1016/0304-3940(87)90113-3 · Cited by 154
Retinopathy in Parkinson disease
Bodis-Wollner, I. G. (2009) · Journal of Neural Transmission · doi:10.1007/s00702-009-0292-z · Cited by 150
Retinal Oxygen Utilization Measured by Hyperbaric Blackout
ANDERSON, B., & Saltzman, H. A. (1964) · Archives of Ophthalmology · doi:10.1001/archopht.1964.00970020794009 · Cited by 150
A Stop-Codon Mutation in the Human mtDNA Cytochrome c Oxidase I Gene Disrupts the Functional Structure of Complex IV
Bruno, C., Martinuzzi, A., Tang, Y., Andreu, A. L., Pallotti, F., Bonilla, E., Shanske, S., Fu, J., Sue, C. M., Angelini, C. I., et al. (1999) · The American Journal of Human Genetics · doi:10.1086/302546 · Cited by 147
Synaptic organization of the inner plexiform layer in the retina of the tiger salamander
Wong‐Riley, M. T. T. (1974) · Journal of Neurocytology · doi:10.1007/bf01111929 · Cited by 145
Self-citation
Three-dimensional analysis of mouse rod and cone mitochondrial cristae architecture: bioenergetic and functional implications.
Perkins, G. A., Ellisman, M. H., & Fox, D. A. (2003) · PubMed · Cited by 145
Depression of retinal glutamate transporter function leads to elevated intravitreal glutamate levels and ganglion cell death.
Vorwerk, C. K., Naskar, R., Schuettauf, F., Quinto, K., Zurakowski, D., Gochenauer, G. E., Robinson, M. B., Mackler, S. A., & Dreyer, E. B. (2000) · PubMed · Cited by 143
Mass spectrometric identification of phosphorylation sites in bleached bovine rhodopsin
Papac, D. I., Oatis, J. E., Crouch, R. K., & Knapp, D. R. (1993) · Biochemistry · doi:10.1021/bi00074a002 · Cited by 139
Specialized vascularization of the primate visual cortex
Zheng, D., LaMantia, A., & Purves, D. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-08-02622.1991 · Cited by 138
The histochemical localization of cytochrome oxidase in the retina and lateral geniculate nucleus of the ferret, cat, and monkey, with particular reference to retinal mosaics and ON/OFF-center visual channels
Kageyama, G. H., & Wong-Riley, M. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-10-02445.1984 · Cited by 138
Self-citation
Comparative study of the fine structure of retinal Müller cells in various vertebrates.
Uga, S., & Smelser (1973) · PubMed · Cited by 134
A photoreceptor cell-specific ATP-binding trans- porter gene (ABCR) is mutated in recessive Star- gardt macular dystrophy.
Grossniklaus, H. E. (1998) · American Journal of Ophthalmology · doi:10.1016/s0002-9394(99)80261-x · Cited by 131
Light adaptation in cone photoreceptors of the salamander: a role for cytoplasmic calcium.
Matthews, H. R., Fain, G., Murphy, R. L., & Lamb, T. D. (1990) · The Journal of Physiology · doi:10.1113/jphysiol.1990.sp017922 · Cited by 130
Characterization of glucose transporter isoforms in the adult and developing human eye
Mantych, G. J., Hageman, G. S., & Devaskar, S. U. (1993) · Endocrinology · doi:10.1210/en.133.2.600 · Cited by 130
Mapping the Primate Visual System with [2- 14 C]Deoxyglucose
Macko, K. A., Jarvis, C. D., Kennedy, C., Miyaoka, M., Shinohara, M., Sololoff, L., & Mishkin, M. (1982) · Science · doi:10.1126/science.7123241 · Cited by 128
The effect of impulse blockage on cytochrome oxidase activity in the cat visual system
Wong‐Riley, M. T. T., & Riley, D. A. (1983) · Brain Research · doi:10.1016/0006-8993(83)90622-4 · Cited by 125
Self-citation
Mouse MCT3 gene is expressed preferentially in retinal pigment and choroid plexus epithelia
Philp, N. J., Yoon, H., & Lombardi, L. (2001) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2001.280.5.c1319 · Cited by 125
Glucose metabolism in pig outer retina in light and darkness
Wang, L., Törnquist, P., & Bill, A. (1997) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.1997.00131.x · Cited by 122
Spatial-frequency organization in primate striate cortex.
Silverman, M. S., Grosof, D. H., Valois, R. L. D., & Elfar, S. D. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.2.711 · Cited by 120
Biochemical phenotypes associated with the mitochondrial ATP6 gene mutations at nt8993
Baracca, A., Sgarbi, G., Mattiazzi, M., Casalena, G., Pagnotta, E., Valentino, M. L., Moggio, M. G., Lenaz, G., Carelli, V., & Solaini, G. (2007) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2007.05.005 · Cited by 116
Mitochondrial and nuclear gene expression for cytochrome oxidase subunits are disproportionately regulated by functional activity in neurons
Hevner, R., & Wong-Riley, M. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-05-01805.1993 · Cited by 113
Self-citation
Release of ATP by a human retinal pigment epithelial cell line: potential for autocrine stimulation through subretinal space
Mitchell, C. H. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.00193.x · Cited by 109
Pharmacological insights obtained from structure–function studies of ionotropic glutamate receptors
Chen, P. E., & Wyllie, D. J. A. (2006) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0706689 · Cited by 103
Degenerative diseases, oxidative stress and cytochrome c oxidase function
Kadenbach, B., Ramzan, R., & Vogt, S. K. (2009) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2009.02.004 · Cited by 103
Glycolytic enzymes and a GLUT-1 glucose transporter in the outer segments of rod and cone photoreceptor cells.
Hsu, S.-C., & Molday, R. S. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)54699-8 · Cited by 102
Progressive failure of cerebral angiogenesis supporting neural plasticity in aging rats
Black, J., Polinsky, M. N., & Greenough, W. T. (1989) · Neurobiology of Aging · doi:10.1016/0197-4580(89)90048-1 · Cited by 102
Mapping of the rod photoreceptor ABC transporter (ABCR) to 1p21-p22.1 and identification of novel mutations in Stargardt's disease
Nasonkin, I. O., Illing, M., Koehler, M. R., Schmid, M., Molday, R. S., & Weber, B. H. F. (1998) · Human Genetics · doi:10.1007/s004390050649 · Cited by 99
Coordination of ATP production and consumption in brain: Parallel regulation of cytochrome oxidase and Na+, K+-ATPase
Hevner, R. F., Duff, R. S., & Wong‐Riley, M. T. T. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90502-x · Cited by 98
Self-citation
Diversity of glutamate transporter expression and function in the mammalian retina
Rauen, T. (2000) · Amino Acids · doi:10.1007/s007260070033 · Cited by 97
High-altitude retinopathy and altitude illness
Wiedman, M., & Tabin, G. C. (1999) · Ophthalmology · doi:10.1016/s0161-6420(99)90402-5 · Cited by 97
Clinical and molecular findings in a patient with a novel mutation in the deafness-dystonia peptide (DDP1) gene
Binder, J., Hofmann, S., Kreisel, S., Wöhrle, J. C., Bäzner, H., Krauss, J. K., Hennerici, M. G., & Bauer, M. F. (2003) · Brain · doi:10.1093/brain/awg174 · Cited by 96
Limited Roles of Rdh8, Rdh12, and Abca4 in all- trans -Retinal Clearance in Mouse Retina
Maeda, A., Golczak, M., Maeda, T., & Palczewski, K. (2009) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.09-3944 · Cited by 95
Cytochrome oxidase in the human visual cortex: Distribution in the developing and the adult brain
Wong‐Riley, M. T. T., Hevner, R. F., Cutlan, R. T., Earnest, M., Egan, R. A., Frost, J. A., & Nguyen, T. (1993) · Visual Neuroscience · doi:10.1017/s0952523800003217 · Cited by 95
Self-citation
Circulation and axonal transport in the optic nerve
Morgan, J. E. (2004) · Eye · doi:10.1038/sj.eye.6701574 · Cited by 94
ABCR, the ATP-binding Cassette Transporter Responsible for Stargardt Macular Dystrophy, Is an Efficient Target of All-trans-retinal-mediated Photooxidative Damage in Vitro
Sun, H., & Nathans, J. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m010152200 · Cited by 94
Coupling of Energy Metabolism and Synaptic Transmission at the Transcriptional Level: Role of Nuclear Respiratory Factor 1 in Regulating both CytochromecOxidase and NMDA Glutamate Receptor Subunit Genes
Dhar, S. S., & Wong‐Riley, M. T. T. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3704-08.2009 · Cited by 87
Self-citation
Plasma membrane calcium ATPases as critical regulators of calcium homeostasis during neuronal cell function
Michael, L. G. (1999) · Frontiers in bioscience · doi:10.2741/garcia · Cited by 87
A Circadian Clock and Light/Dark Adaptation Differentially Regulate Adenosine in the Mammalian Retina
Ribelayga, C., & Mangel, S. C. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3138-04.2005 · Cited by 85
The [14C]Deoxyglucose Method for the Measurement of Local Cerebral Glucose Utilization: Theory, Procedure, and Normal Values in the Conscious and Anesthetized Albino Rat
Sokoloff, L., Reivich, M., Kennedy, C., Des Rosiers, M. H., Patlak, C. S., Pettigrew, K. D., Sakurada, O., & Shinohara, M. (1977) · Cited by 85
Hemoglobin Expression and Regulation in Glaucoma: Insights into Retinal Ganglion Cell Oxygenation
Tezel, G., Yang, X., Luo, C., Cai, J., Kain, A. D., Powell, D. W., Kuehn, M. H., & Pierce, W. M. J. (2010) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.09-4014 · Cited by 82
Fast axonal transport in permeabilized lobster giant axons is inhibited by vanadate
Forman, D. S., Brown, K., & Livengood, D. R. (1983) · Journal of Neuroscience · doi:10.1523/jneurosci.03-06-01279.1983 · Cited by 78
Altered visual function in monocarboxylate transporter 3 (Slc16a8) knockout mice
Daniele, L. L., Sauer, B., Gallagher, S. M., Pugh, E. N., & Philp, N. J. (2008) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00124.2008 · Cited by 76
Energy sources for glutamate neurotransmission in the retina: absence of the aspartate/glutamate carrier produces reliance on glycolysis in glia
Xu, Y., Ola, M. S., Berkich, D. A., Gardner, T. W., Barber, A. J., Palmieri, F., Hutson, S. M., & LaNoue, K. F. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04349.x · Cited by 73
Effect of retinal impulse blockage on cytochrome oxidase-rich zones in the macaque striate cortex: I. Quantitative electron-microscopic (EM) analysis of neurons
Wong‐Riley, M. T. T., Tripathi, S. C., Trusk, T. C., & Hoppe, D. A. (1989) · Visual Neuroscience · doi:10.1017/s0952523800012384 · Cited by 73
Self-citation
Glucose dependence of glycolysis, hexose monophosphate shunt activity, energy status, and the polyol pathway in retinas isolated from normal (nondiabetic) rats.
Winkler, B. S., Arnold, M. J., Brassell, M. A., & Sliter, D. R. (1997) · PubMed · Cited by 70
Are neuronal transporters relevant in retinal glutamate homeostasis?
Pow, D. V., Barnett, N. L., & Penfold, P. (2000) · Neurochemistry International · doi:10.1016/s0197-0186(00)00022-x · Cited by 70
Laminar variation in the microvascular architecture of normal human visual cortex (area 17)
Bell, M. A., & Ball, M. J. (1985) · Brain Research · doi:10.1016/0006-8993(85)90284-7 · Cited by 65
Diabetic retinopathy: a growing concern in an aging population.
Paulus, Y. M., & Gariano, R. F. (2009) · PubMed · Cited by 64
Neurochemical organization of the macaque striate cortex: Correlation of cytochrome oxidase with Na+K+ATPase, NADPH-diaphorase, nitric oxide synthase, and N-methyl-d-aspartate receptor subunit 1
Wong‐Riley, M. T. T., Anderson, B. D., Liebl, W., & Huang, Z. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00432-6 · Cited by 63
Self-citation
Genetics of age-related macular degeneration
Ting, A., Lee, T. K. M., & MacDonald, I. M. (2009) · Current Opinion in Ophthalmology · doi:10.1097/icu.0b013e32832f8016 · Cited by 58
Activity correlates of cytochrome oxidase-defined compartments in granular and supragranular layers of primary visual cortex of the macaque monkey
DeYoe, E. A., Trusk, T. C., & Wong-Riley, M. T. T. (1995) · Visual Neuroscience · doi:10.1017/s0952523800008920 · Cited by 56
Self-citation
Highly efficient retinal metabolism in cones
Miyazono, S., Shimauchi-Matsukawa, Y., Tachibanaki, S., & Kawamura, S. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806593105 · Cited by 55
Neurochemical organization of the macaque retina: effect of TTX on levels and gene expression of cytochrome oxidase and nitric oxide synthase and on the immunoreactivity of Na+K+ATPase and NMDA receptor subunit I
Wong‐Riley, M. T. T., Huang, Z., Liebl, W., Nie, F., Xu, H., & Zhang, C. (1998) · Vision Research · doi:10.1016/s0042-6989(98)00001-7 · Cited by 52
Self-citation
Metabolic mapping in mammalian retina: a biochemical and 3H-2-deoxyglucose autoradiographic study
Winkler, B. S., Pourcho, R. G., Starnes, C. A., Slocum, J. L., & Slocum, N. K. (2003) · Experimental Eye Research · doi:10.1016/s0014-4835(03)00147-7 · Cited by 51
OPA1 , the Disease Gene for Autosomal Dominant Optic Atrophy, Is Specifically Expressed in Ganglion Cells and Intrinsic Neurons of the Retina
Pesch, U. E. A., Fries, J. E., Bette, S. J., Kalbacher, H., Wissinger, B., Alexander, C., & Köhler, K. (2004) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.03-1261 · Cited by 50
Hypoglycemia induces general neuronal death, whereas hypoxia and glutamate transport blockade lead to selective retinal ganglion cell death in vitro.
Luo, X., Lambrou, G. N., Sahel, J., et al. (2001) · PubMed · Cited by 48
Cytochrome-c-oxidase redox changes during visual stimulation measured by near-infrared spectroscopy cannot be explained by a mere cross talk artefact
Uludaǧ, K., Steinbrink, J. M., Kohl‐Bareis, M., Wenzel, R., Villringer, A., & Obrig, H. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.09.053 · Cited by 48
Nuclear respiratory factor 1 co‐regulates AMPA glutamate receptor subunit 2 and cytochrome c oxidase: tight coupling of glutamatergic transmission and energy metabolism in neurons
Dhar, S. S., Liang, H., & Wong‐Riley, M. T. T. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.05929.x · Cited by 48
Self-citation
Visual perception in prediagnostic and early stage Huntington's disease
O’Donnell, B. F., Blekher, T., Weaver, M. R., White, K., Marshall, J. D., Beristaín, X., Stout, J. C., Jackson, J. G., Wojcieszek, J., & Foroud, T. (2008) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617708080405 · Cited by 44
A Novel Relationship Between Creatine Transport at the Blood-Brain and Blood-Retinal Barriers, Creatine Biosynthesis, And its Use for Brain and Retinal Energy Homeostasis
Tachikawa, M., Hosoya, K., Ohtsuki, S., & Terasaki, T. (2007) · Springer eBooks · doi:10.1007/978-1-4020-6486-9_5 · Cited by 44
Differential glutamatergic innervation in cytochrome oxidase-rich and -poor regions of the macaque striate cortex: Quantitative EM analysis of neurons and neuropil
Nie, F., & Wong-Riley, M. T. T. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960610)369:4<571::aid-cne7>3.0.co;2-1 · Cited by 43
Self-citation
Bioenergetic‐based neuroprotection and glaucoma
Schober, M. S., Chidlow, G., Wood, J. P. M., & Casson, R. J. (2008) · Clinical and Experimental Ophthalmology · doi:10.1111/j.1442-9071.2008.01740.x · Cited by 40
Localization and ontogeny of GLUT3 expression in the rat retina
Watanabe, T., Matsushima, S., Okazaki, M., Nagamatsu, S., Hirosawa, K., Uchimura, H., & Nakahara, K. (1996) · Developmental Brain Research · doi:10.1016/0165-3806(96)00044-2 · Cited by 37
Initial observations on the isolated retinal pigment epithelium-choroid of the cat.
Steinberg, R. H., Miller, S. S., & Stern, W. H. (1978) · PubMed · Cited by 36
Ophthalmological Effects of High Altitude
Karaküçük, S., & Mirza, G. E. (2000) · Ophthalmic Research · doi:10.1159/000055584 · Cited by 34
Transcriptional coupling of synaptic transmission and energy metabolism: Role of nuclear respiratory factor 1 in co-regulating neuronal nitric oxide synthase and cytochrome c oxidase genes in neurons
Dhar, S. S., Liang, H., & Wong‐Riley, M. T. T. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2009.07.001 · Cited by 30
Self-citation
A novel ABCR nonsense mutation responsible for late-onset fundus flavimaculatus.
Souied, E. H., Ducroq, D., Rozet, J., Gerber, S., Perrault, I., Sterkers, M., Benhamou, N., Münnich, A., COSCAS, G. J., Soubrane, G., et al. (1999) · PubMed · Cited by 30
Effect of anoxia on the electroretinogram of three anoxia-tolerant vertebrates
Stensløkken, K., Milton, S., Lutz, P. L., Sundin, L., Renshaw, G. M. C., Stecyk, J. A. W., & Nilsson, G. (2008) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2008.03.022 · Cited by 23
Genetics of Age-related Macular Degeneration
DeAngelis, M. M., & Ji, F. (2008) · Elsevier eBooks · doi:10.1016/b978-1-4160-0016-7.50146-6 · Cited by 23
Energy-efficient action potentials in hippocampal mossy fibers
Alle, H., Roth, A., & Geiger, J. R. P. (2009) · e-Neuroforum · doi:10.1515/nf-2009-0405 · Cited by 22
How Does the Eye Breathe? Evidence for Neuroglobin-mediated Oxygen Supply in the Mammalian Retina
Uwe Wolfrum, B., Gießl, A., Schmidt, M., Laufs, T., Hankeln, T., & Burmester, T. (2003) · Investigative Ophthalmology & Visual Science · Cited by 21
Parvalbumin immunoreactivity is enhanced by brain-derived neurotrophic factor in organotypic cultures of rat retina
Rickman, D. W. (1999) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(19991115)41:3<340::aid-neu3>3.0.co;2-8 · Cited by 21
Effect of retinal impulse blockage on cytochrome oxidase-poor interpuffs in the macaque striate cortex: quantitative EM analysis of neurons
Wong‐Riley, M. T. T., Trusk, T. C., Kaboord, W. S., & Huang, Z. (1994) · Journal of Neurocytology · doi:10.1007/bf01262055 · Cited by 16
Self-citation

Basal Mitophagy Occurs Independently of PINK1 in Mouse Tissues of High Metabolic Demand
McWilliams, T. G., Prescott, A. R., Montava-Garriga, L., Ball, G., Singh, F., Barini, E., Muqit, M. M. K., Brooks, S. P., & Ganley, I. G. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2017.12.008 · Cited by 591
Principles of Neural Design
Sterling, P., & Laughlin, S. (2015) · doi:10.7551/mitpress/9780262028707.001.0001 · Cited by 482
Retinal lipid and glucose metabolism dictates angiogenesis through the lipid sensor Ffar1
Joyal, J.-S., Sun, Y., Gantner, M. L., Shao, Z., Evans, L. P., Saba, N., Fredrick, T., Burnim, S., Kim, J. S., Patel, G., et al. (2016) · Nature Medicine · doi:10.1038/nm.4059 · Cited by 264
Inherited Retinal Degenerations: Current Landscape and Knowledge Gaps
Duncan, J. L., Pierce, E. A., Laster, A. M., Daiger, S. P., Birch, D. G., Ash, J. D., Iannaccone, A., Flannery, J. G., Sahel, J. A., Zack, D. J., et al. (2018) · Translational Vision Science & Technology · doi:10.1167/tvst.7.4.6 · Cited by 257
Pathological angiogenesis in retinopathy engages cellular senescence and is amenable to therapeutic elimination via BCL-xL inhibition
Crespo-Garcia, S., Tsuruda, P. R., Dejda, A., Ryan, R. D., Fournier, F., Chaney, S. Y., Pilon, F., Dogan, T., Cagnone, G., Patel, P., et al. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.01.011 · Cited by 182

See all 461

Authors: Wong-Riley, M.
Venue: Eye and Brain
Publisher: Informa UK Limited
Published: 2010-07
Volume: 2
Pages: 99
ISSN: 1179-2744 (ISSN-L)
DOI: 10.2147/eb.s9078
OpenAlex: W1964267325
Cited by: 461
References: 166
FWCI: 1.18
Type: journal article
Language: en
Open access: gold

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Energy metabolism of the visual system

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