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Glutamate uptake
Abstract
Brain tissue has a remarkable ability to accumulate glutamate. This ability is due to glutamate transporter proteins present in the plasma membranes of both glial cells and neurons. The transporter proteins represent the only (significant) mechanism for removal of glutamate from the extracellular fluid and their importance for the long-term maintenance of low and non-toxic concentrations of glutamate is now well documented. In addition to this simple, but essential glutamate removal role, the glutamate transporters appear to have more sophisticated functions in the modulation of neurotransmission. They may modify the time course of synaptic events, the extent and pattern of activation and desensitization of receptors outside the synaptic cleft and at neighboring synapses (intersynaptic cross-talk). Further, the glutamate transporters provide glutamate for synthesis of e.g. GABA, glutathione and protein, and for energy production. They also play roles in peripheral organs and tissues (e.g. bone, heart, intestine, kidneys, pancreas and placenta). Glutamate uptake appears to be modulated on virtually all possible levels, i.e. DNA transcription, mRNA splicing and degradation, protein synthesis and targeting, and actual amino acid transport activity and associated ion channel activities. A variety of soluble compounds (e.g. glutamate, cytokines and growth factors) influence glutamate transporter expression and activities. Neither the normal functioning of glutamatergic synapses no…
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“The astroglial cells are the main regulators of cerebral glutamate clearance and metabolism [21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36].”
From Gliovascular alterations in sporadic and familial Alzheimer's disease: APOE3 Christchurch homozygote glioprotection (2023) · cites this paper as [25]
In the citing paper
“which in turn can be reconverted into glutamate for use either as a neurotransmitter or energy substrate [21, 22, 23, 24, 25, 26, 27].”
From Gliovascular alterations in sporadic and familial Alzheimer's disease: APOE3 Christchurch homozygote glioprotection (2023) · cites this paper as [25]
In the citing paper
“Through the membrane glutamate aspartate transporter (GLAST), the astroglia dynamically remove glutamate from the extracellular milieu, restricting its signaling activity in time and space and allowing for its recycling [25, 30, 33].”
From Gliovascular alterations in sporadic and familial Alzheimer's disease: APOE3 Christchurch homozygote glioprotection (2023) · cites this paper as [25]
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Cites
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
LAEMMLI, U. K. (1970) · Nature · doi:10.1038/227680a0 · Cited by 249,961
Rosen, D. R., Siddique, T., Patterson, D., Figlewicz, D. A., Sapp, P., Hentati, A., Donaldson, D., Goto, J., O'Regan, J. P., Deng, H.-X., et al. (1993) · Nature · doi:10.1038/362059a0 · Cited by 7,062
Apoptosis in the Pathogenesis and Treatment of Disease
Thompson, C. B. (1995) · Science · doi:10.1126/science.7878464 · Cited by 6,524
Pellerin, L., & Magistretti, P. J. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.22.10625 · Cited by 2,927
Bruijn, L. I., Becher, M. W., Lee, M. K., Anderson, K. L., Jenkins, N. A., Copeland, N. G., Sisodia, S. S., Rothstein, J. D., Borchelt, D. R., Price, D. L., et al. (1997) · Neuron · doi:10.1016/s0896-6273(00)80272-x · Cited by 1,341
Superoxide Anion Radical (O·̄2), Superoxide Dismutases, and Related Matters
Fridovich, I. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.30.18515 · Cited by 1,337
Rapid Actin-Based Plasticity in Dendritic Spines
Fischer, M., Kaech, S., Knutti, D., & Matus, A. (1998) · Neuron · doi:10.1016/s0896-6273(00)80467-5 · Cited by 905
Long-term potentiation and functional synapse induction in developing hippocampus
Durand, G. M., Kovalchuk, Y., & Konnerth, A. (1996) · Nature · doi:10.1038/381071a0 · Cited by 789
Control of Kinetic Properties of AMPA Receptor Channels by Nuclear RNA Editing
Lomeli, H., Mosbacher, J., Melcher, T., Höger, T., Geiger, J. R. P., Kuner, T., Monyer, H., Higuchi, M., Bach, A., & Seeburg, P. H. (1994) · Science · doi:10.1126/science.7992055 · Cited by 746
Different modes of expression of AMPA and NMDA receptors in hippocampal synapses
Takumi, Y., Ramírez-León, V., Laake, P., Rinvik, E., & Ottersen, O. P. (1999) · Nature Neuroscience · doi:10.1038/10172 · Cited by 675
Research works printed but not linked: 1205
- Aas, 1993, Redistribution of glutamate and glutamine in slices of human neocortex exposed to combined hypoxia and glucose deprivation in vitro, J. Cereb. Blood Flow Metab., 13, 503, 10.1038/jcbfm.1993.65 · DOI
- Adams, 1997, Alzheimer's disease research: a game of connect the dots, Gerontology, 43, 8, 10.1159/000213832 · DOI
- Agostinho, 1997, Impairment of excitatory amino acid transporter activity by oxidative stress conditions in retinal cells: Effect of antioxidants, FASEB J., 11, 154, 10.1096/fasebj.11.2.9039958 · DOI
- Aihara, 2000, Molecular cloning of a novel brain-type Na+-dependent inorganic phosphate cotransporter, J. Neurochem., 74, 2622, 10.1046/j.1471-4159.2000.0742622.x · DOI
- Akbar, 1997, Expression of glial glutamate transporters GLT-1 and GLAST is unchanged in the hippocampus in fully kindled rats, Neuroscience, 78, 351, 10.1016/S0306-4522(96)00570-2 · DOI
- Akbar, 1998, Reduction of GABA and glutamate transporter messenger RNAs in the severe-seizure genetically epilepsy-prone rat, Neuroscience, 85, 1235, 10.1016/S0306-4522(97)00684-2 · DOI
- Albrecht, 1996, Glutamate: a potential mediator of inorganic mercury neurotoxicity, Metab. Brain. Dis., 11, 175, 10.1007/BF02069504 · DOI
- Albrecht, 1993, The role of sulfhydryl groups and calcium in the mercuric chloride-induced inhibition of glutamate uptake in rat primary astrocyte cultures, Brain Res., 607, 249, 10.1016/0006-8993(93)91513-R · DOI
- Alexander, 2000, Elevated cortical extracellular fluid glutamate in transgenic mice expressing human mutant (G93A) Cu/Zn superoxide dismutase, J. Neurochem., 74, 1666, 10.1046/j.1471-4159.2000.0741666.x · DOI
- Allan, 1990, Synthesis and activity of a potent N-methyl-d-aspartic acid agonist, trans-1-aminocyclobutane-1,3-dicarboxylic acid, and related phosphonic and carboxylic acids, J. Med. Chem., 33, 2905, 10.1021/jm00172a036 · DOI
- Allen, 1911, Surgery of experimental lesion of spinal cord equivalent to crush injury of fracture dislocation of spinal column, JAMA, 57, 878, 10.1001/jama.1911.04260090100008 · DOI
- Allen, 1993, Beta-N-methylamino-l-alanine in the presence of bicarbonate is an agonist at non-N-methyl-d-aspartate-type receptors, Neuroscience, 54, 567, 10.1016/0306-4522(93)90228-8 · DOI
- Alloul, 1998, Alzheimer's disease: a review of the disease, its epidemiology and economic impact, Arch. Gerontol. Geriatr., 27, 189, 10.1016/S0167-4943(98)00116-2 · DOI
- Almers, 1990, Transmitter release from synapses: does a preassembled fusion pore initiate exocytosis?, Neuron, 4, 813, 10.1016/0896-6273(90)90134-2 · DOI
- Amaral, 1981, Development of the mossy fibers of the dentate gyrus: I. A light and electron microscopic study of the mossy fibers and their expansions, J. Comp. Neurol., 195, 51, 10.1002/cne.901950106 · DOI
- Amato, 1994, Intracellular pH changes produced by glutamate uptake in rat hippocampal slices, J. Neurophysiol., 72, 1686, 10.1152/jn.1994.72.4.1686 · DOI
- Anderson, 1990, Autoradiographic characterization of putative excitatory amino acid transport sites, Neuroscience, 38, 311, 10.1016/0306-4522(90)90030-8 · DOI
- Anderson, 1991, Increased density of excitatory amino acid transport sites in the hippocampal formation following an entorhinal lesion, Brain Res., 562, 285, 10.1016/0006-8993(91)90633-7 · DOI
- Andrews, 1996, Plasmapheresis in Rasmussen's encephalitis, Neurology, 46, 242, 10.1212/WNL.46.1.242 · DOI
- Antal, 1991, Different populations of parvalbumin-D28k-immunoreactive and calbindin-D28k-immunoreactive neurons contain GABA and accumulate 3H-d-aspartate in the dorsal horn of the rat spinal cord, J. Comp. Neurol., 314, 114, 10.1002/cne.903140111 · DOI
- Aoki, 1998, Mutations in the glutamate transporter EAAT2 gene do not cause abnormal EAAT2 transcripts in amyotrophic lateral sclerosis, Ann. Neurol., 43, 645, 10.1002/ana.410430514 · DOI
- Aparicio-Legarza, 1997, Deficits of [3H]d-aspartate binding to glutamate uptake sites in striatal and accumbens tissue in patients with schizophrenia, Neurosci. Lett., 232, 13, 10.1016/S0304-3940(97)00563-6 · DOI
- Appel, 1993, Excitotoxic neuronal cell death in amyotrophic lateral sclerosis, Trends Neurosci., 16, 3, 10.1016/0166-2236(93)90039-O · DOI
- Appel, 1996, Immune-mediated cell death in neurodegenerative disease, Adv. Neurol., 69, 153
- Araque, 2000, SNARE protein-dependent glutamate release from astrocytes, J. Neurosci., 20, 666, 10.1523/JNEUROSCI.20-02-00666.2000 · DOI
- Arkwright, 1902, A family series of fatal and dangerous cases of icterus neonatorum — fourteen cases in one family, with four survivors, Edinb. Med. J., 2, 156
- Arriza, 1993, Cloning and expression of a human neutral amino acid transporter with structural similarity to the glutamate transporter gene family, J. Biol. Chem., 268, 15329, 10.1016/S0021-9258(18)82257-8 · DOI
- Arriza, 1994, Functional comparisons of three glutamate transporter subtypes cloned from human motor cortex, J. Neurosci., 14, 5559, 10.1523/JNEUROSCI.14-09-05559.1994 · DOI
- Arriza, 1997, Excitatory amino acid transporter 5, a retinal glutamate transporter coupled to a chloride conductance, Proc. Natl. Acad. Sci. USA, 94, 4155, 10.1073/pnas.94.8.4155 · DOI
- Aschner, 1990, Interactions of methylmercury with rat primary astrocyte cultures — inhibition of rubidium and glutamate uptake and induction of swelling, Brain Res., 530, 245, 10.1016/0006-8993(90)91290-W · DOI
- Aschner, 1993, Methylmercury-induced alterations in excitatory amino acid transport in rat primary astrocyte cultures, Brain Res., 602, 181, 10.1016/0006-8993(93)90680-L · DOI
- Aschner, 1995, Astrocytes as potential modulators of mercuric chloride neurotoxicity, Cell. Mol. Neurobiol., 14, 637, 10.1007/BF02088673 · DOI
- Aschner, 2000, Methylmercury alters glutamate transport in astrocytes, Neurochem. Int., 37, 199, 10.1016/S0197-0186(00)00023-1 · DOI
- Asztely, 1997, Extrasynaptic glutamate spillover in the hippocampus: dependence on temperature and the role of active glutamate uptake, Neuron, 18, 281, 10.1016/S0896-6273(00)80268-8 · DOI
- Attwell, 1994, Neurobiology-glia and neurons in dialogue, Nature, 369, 707, 10.1038/369707a0 · DOI
- Auger, 2000, Fast removal of synaptic glutamate by postsynaptic transporters, Neuron, 28, 547, 10.1016/S0896-6273(00)00132-X · DOI
- Augustine, 1996, Exocytosis: proteins and perturbations, Annu. Rev. Pharmacol. Toxicol., 36, 659, 10.1146/annurev.pa.36.040196.003303 · DOI
- Azbill, 2000, Riluzole increases high-affinity glutamate uptake in rat spinal cord synaptosomes, Brain Res., 871, 175, 10.1016/S0006-8993(00)02430-6 · DOI
- Back, 1998, Pathophysiology of the ischemic penumbra — revision of a concept, Cell. Mol. Neurobiol., 18, 621, 10.1023/A:1020265701407 · DOI
- Baddeley, 1986, Estimation of surface area from vertical sections, J. Microsc., 142, 259, 10.1111/j.1365-2818.1986.tb04282.x · DOI
- Bahn, 1994, Kainate receptor gene expression in the developing rat brain, J. Neurosci., 14, 5525, 10.1523/JNEUROSCI.14-09-05525.1994 · DOI
- Baker, 1993, Excitatory amino acids in cerebrospinal fluid following traumatic brain injury in humans, J. Neurosurg., 79, 369, 10.3171/jns.1993.79.3.0369 · DOI
- Balcar, 1992, Na+-dependent high-affinity uptake of l-glutamate in cultured fibroblasts, FEBS Lett., 300, 203, 10.1016/0014-5793(92)80846-9 · DOI
- Balcar, 1972, Glutamate uptake by brain slices and its relation to the depolarization of neurones by acidic amino acids, J. Neurobiol., 3, 295, 10.1002/neu.480030403 · DOI
- Balcar, 1972, The structural specificity of the high affinity uptake of l-glutamate and l-aspartate by rat brain slices, J. Neurochem., 19, 2657, 10.1111/j.1471-4159.1972.tb01325.x · DOI
- Balcar, 1975, High affinity uptake of l-glutamine in rat brain slices, J. Neurochem., 24, 875, 10.1111/j.1471-4159.1975.tb03650.x · DOI
- Balcar, 1992, Heterogeneity of high affinity uptake of l-glutamate and l-aspartate in the mammalian central nervous system, Life Sci., 51, 1467, 10.1016/0024-3205(92)90556-5 · DOI
- Balcar, 1977, Stereospecificity of the inhibition of l-glutamate and l-aspartate high affinity uptake in rat brain slices by threo-3-hydroxyaspartate, J. Neurochem., 28, 1145, 10.1111/j.1471-4159.1977.tb10682.x · DOI
- Balcar, 1994, Na+-dependent high affinity uptake of l-glutamate is primary cultures of human fibroblasts isolated from three different types of tissue, FEBS Lett., 339, 50, 10.1016/0014-5793(94)80382-X · DOI
- Balcar, 1995, Effects of l-trans-pyrrolidine-2,4-dicarboxylate and l-threo-3-hydroxyaspartate on the binding of [3H]l-aspartate, [3H]alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA), [3H]dl-(e)-2-amino-4-propyl-5-phosphono-3-pentenoate (CGP 39653), [3H]6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) and [3H]kainate studied by autoradiography in rat forebrain, Neurochem. Int., 26, 155, 10.1016/0197-0186(94)00120-J · DOI
- Bannai, 1984, Transport of cystine and cysteine in mammalian cells, Biochim. Biophys. Acta, 779, 289, 10.1016/0304-4157(84)90014-5 · DOI
- Bannai, 1986, Exchange of cystine and glutamate across plasma membrane of human fibroblasts, J. Biol. Chem., 261, 2256, 10.1016/S0021-9258(17)35926-4 · DOI
- Bannai, 1980, Transport interaction of l-cystine and l-glutamate in human diploid fibroblasts in culture, J. Biol. Chem., 255, 2372, 10.1016/S0021-9258(19)85901-X · DOI
- Bannai, 1981, Role of proton dissociation in the transport of cystine and glutamine in human diploid fibroblasts in culture, J. Biol. Chem., 256, 5770, 10.1016/S0021-9258(19)69273-2 · DOI
- Bannai, 1984, Amino acid transport systems, Nature, 311, 308, 10.1038/311308b0 · DOI
- Bannai, 1984, Naming plan for membrane transport systems for amino acids, Neurochem. Res., 9, 1757, 10.1007/BF00968086 · DOI
- Bar-Peled, 1997, Distribution of glutamate transporter subtypes during human brain development, J. Neurochem., 69, 2571, 10.1046/j.1471-4159.1997.69062571.x · DOI
- Barbour, 1997, Intersynaptic diffusion of neurotransmitter, Trends Neurosci., 20, 377
- Barbour, 1988, Electrogenic glutamate uptake in glial cells is activated by intracellular potassium, Nature, 335, 433, 10.1038/335433a0 · DOI
- Barbour, 1989, Arachidonic acid induces a prolonged inhibition of glutamate uptake into glial cells, Nature, 342, 918, 10.1038/342918a0 · DOI
- Barbour, 1991, Electrogenic uptake of glutamate and aspartate into glial cells isolated from the salamander (Ambystoma) retina, J. Physiol. (Lond.), 436, 169, 10.1113/jphysiol.1991.sp018545 · DOI
- Barbour, 1994, Prolonged presence of glutamate during excitatory synaptic transmission to cerebellar Purkinje cells, Neuron, 12, 1331, 10.1016/0896-6273(94)90448-0 · DOI
- Barton, 1998, An altered invariant chain protein with an antigenic peptide in place of CLIP forms SDS-stable complexes with class II alpha beta dimers and facilitates highly efficient peptide loading, Int. Immunol., 10, 1159, 10.1093/intimm/10.8.1159 · DOI
- Battaglia, 2000, Glutamine and glutamate exchange between the fetal liver and the placenta, J. Nutr., 130, 974S, 10.1093/jn/130.4.974S · DOI
- Baudry, 1981, Characterization of two [3H]glutamate binding sites in rat hippocampal membranes, J. Neurochem., 36, 811, 10.1111/j.1471-4159.1981.tb01666.x · DOI
- Baughman, 1980, Aspartate and glutamate as possible neurotransmitters of cells in layer 6 of the visual cortex, Nature, 287, 848, 10.1038/287848a0 · DOI
- Bazan, 1995, Mediators of injury in neurotrauma: intracellular signal transduction and gene expression, J. Neurotrauma, 12, 791, 10.1089/neu.1995.12.791 · DOI
- Beal, 1993, Do defects in mitochondrial energy metabolism underlie the pathology of neurodegenerative diseases, Trends Neurosci., 16, 125, 10.1016/0166-2236(93)90117-5 · DOI
- Beckman, 1998, Neurotransmitter transporters: regulators of function and functional regulation, J. Membr. Biol., 164, 1, 10.1007/s002329900388 · DOI
- Beckstrøm, 1999, Interindividual differences in the levels of the glutamate transporters GLAST and GLT, but no clear correlation with Alzheimer's disease, J. Neurosci. Res., 55, 218, 10.1002/(SICI)1097-4547(19990115)55:2<218::AID-JNR9>3.0.CO;2-L · DOI
- Behzadi, 1990, Afferents to the median raphe nucleus of the rat: retrograde cholera toxin and wheat germ conjugated horseradish peroxidase tracing, and selective d-[3H]aspartate labelling of possible excitatory amino acid inputs, Neuroscience, 37, 77, 10.1016/0306-4522(90)90194-9 · DOI
- Bellocchio, 1998, The localization of the brain-specific inorganic phosphate transporter suggests a specific presynaptic role in glutamatergic transmission, J. Neurosci., 18, 8648, 10.1523/JNEUROSCI.18-21-08648.1998 · DOI
- Bellocchio, 2000, Uptake of glutamate into synaptic vesicles by an inorganic phosphate transporter, Science, 289, 957, 10.1126/science.289.5481.957 · DOI
- Bendahan, 2000, Arginine-447 plays a pivotal role in substrate interactions in a neuronal glutamate transporter, J. Biol. Chem., 275, 37436, 10.1074/jbc.M006536200 · DOI
- Bender, 1989, Beta-dl-methylene-aspartate, an inhibitor of aspartate aminotransferase, potently inhibits l-glutamate uptake into astrocytes, Neurochem. Res., 14, 641, 10.1007/BF00964873 · DOI
- Benjamin, 1976, Cerebral uptakes and exchange diffusion in vitro of l- and d-glutamates, J. Neurochem., 26, 431, 10.1111/j.1471-4159.1976.tb01493.x · DOI
- Bennett, 1973, Amino acids as central nervous transmitters: the influence of ions, amino acid analogues and ontogeny on transport systems for l-glutamic and l-aspartic acids and glycine into central nervous synaptosomes of the rat, J. Neurochem., 21, 1533, 10.1111/j.1471-4159.1973.tb06037.x · DOI
- Benveniste, 1984, Elevation of the extracellular concentrations of glutamate and aspartate in rat hippocampus during transient cerebral ischemia monitored by intracerebral microdialysis, J. Neurochem., 43, 1369, 10.1111/j.1471-4159.1984.tb05396.x · DOI
- Benveniste, 1989, Ischemic damage in hippocampal CA1 is dependent on glutamate release and intact innervation from CA3, J. Cereb. Blood Flow Metab., 9, 629, 10.1038/jcbfm.1989.90 · DOI
- Berger, 2000, Detection and cellular localization of enterovirus RNA sequences in spinal cord of patients with ALS, Neurology, 54, 20, 10.1212/WNL.54.1.20 · DOI
- Berger, 1998, Comparative analysis of glutamate transporter expression in rat brain using differential double in situ hybridization, Anat. Embryol., 198, 13, 10.1007/s004290050161 · DOI
- Berger, 2000, Distribution of the glutamate transporters GLAST and GLT-1 in rat circumventricular organs, meninges and dorsal root ganglia, J. Comp. Neurol., 421, 385, 10.1002/(SICI)1096-9861(20000605)421:3<385::AID-CNE7>3.0.CO;2-S · DOI
- Berger, 2000, Distribution of the glutamate transporters GLAST and GLT-1 in rat circumventricular organs, meninges and dorsal root ganglia, J. Comp. Neurol., 421, 385, 10.1002/(SICI)1096-9861(20000605)421:3<385::AID-CNE7>3.0.CO;2-S · DOI
- Bergles, 1997, Synaptic activation of glutamate transporters in hippocampal astrocytes, Neuron, 19, 1297, 10.1016/S0896-6273(00)80420-1 · DOI
- Bergles, 1998, Glial contribution to glutamate uptake at Schaffer collateral-commissural synapses in the hippocampus, J. Neurosci., 18, 7709, 10.1523/JNEUROSCI.18-19-07709.1998 · DOI
- Bergles, 1997, Glutamate transporter currents in Bergmann glial cells follow the time course of extrasynaptic glutamate, Proc. Natl. Acad. Sci. USA, 94, 14821, 10.1073/pnas.94.26.14821 · DOI
- Bergles, 1999, Clearance of glutamate inside the synapse and beyond, Curr. Opin. Neurobiol., 9, 293, 10.1016/S0959-4388(99)80043-9 · DOI
- Bergles, 2000, Glutamatergic synapses on oligodendrocyte precursor cells in the hippocampus, Nature, 405, 187, 10.1038/35012083 · DOI
- Berl, 1961, Amino acid and protein metabolism. VI. Cerebral compartments of glutamic acid metabolism, J. Neurochem., 7, 186, 10.1111/j.1471-4159.1961.tb13503.x · DOI
- Berl, 1962, Metabolic compartments in vivo: ammonia and glutamic acid metabolism in brain and liver, J. Biol. Chem., 237, 2562, 10.1016/S0021-9258(19)73788-0 · DOI
- Berman, 1997, Inhibition of glutamate transport in synaptosomes by dopamine oxidation and reactive oxygen species, J. Neurochem., 69, 1185, 10.1046/j.1471-4159.1997.69031185.x · DOI
- Berman, 1997, Domoic acid neurotoxicity in cultured cerebellar granule neurons is mediated predominantly by NMDA receptors that are activated as a consequence of excitatory amino acid release, J. Neurochem., 69, 693, 10.1046/j.1471-4159.1997.69020693.x · DOI
- Bernstein, 1999, Regulation of gamma-aminobutyric acid (GABA) transporters by extracellular GABA, J. Biol. Chem., 274, 889, 10.1074/jbc.274.2.889 · DOI
- Bertrand, 1992, Evidence for a glutamate receptor of the AMPA subtype which mediates insulin release from rat perfused pancreas, Br. J. Pharmacol., 106, 354, 10.1111/j.1476-5381.1992.tb14340.x · DOI
- Bertrand, 1993, Glutamate stimulates glucagon secretion via an excitatory amino acid receptor of the AMPA subtype in rat pancreas, Eur. J. Pharmacol., 237, 45, 10.1016/0014-2999(93)90091-U · DOI
- Bertrand, 1995, Glutamate stimulates insulin secretion and improves glucose tolerance in rats, Am. J. Physiol., 32, E551
- Besson, 1999, Identification and structural characterization of two genes encoding glutamate transporter homologues differently expressed in the nervous system of Drosophila melanogaster, FEBS Lett., 443, 97, 10.1016/S0014-5793(98)01695-0 · DOI
- Bezzi, 1998, Prostaglandins stimulate calcium-dependent glutamate release in astrocytes, Nature, 391, 281, 10.1038/34651 · DOI
- Bigge, 1993, Structural requirements for the development of potent N-methyl-d-aspartic acid (NMDA) receptor antagonists, Biochem. Pharmacol., 45, 1547, 10.1016/0006-2952(93)90294-7 · DOI
- Billups, 1996, Modulation of non-vesicular glutamate release by pH, Nature, 379, 171, 10.1038/379171a0 · DOI
- Billups, 1996, Anion conductance behavior of the glutamate uptake carrier in salamander retinal glial cells, J. Neurosci., 16, 6722, 10.1523/JNEUROSCI.16-21-06722.1996 · DOI
- Billups, 1998, Patch-clamp, ion-sensing, and glutamate-sensing techniques to study glutamate transport in isolated retinal glial cells, Methods Enzymol., 296, 617, 10.1016/S0076-6879(98)96044-X · DOI
- Biziere, 1980, Characterization of specific, high-affinity binding sites for l-[3H]glutamic acid in rat brain membranes, Brain Res., 183, 421, 10.1016/0006-8993(80)90476-X · DOI
- Bjørås, 1996, Cloning and expression of a neuronal rat brain glutamate transporter, Mol. Brain Res., 36, 163, 10.1016/0169-328X(95)00279-2 · DOI
- Blackman, 1998, Oligomeric state of human erythrocyte band 3 measured by fluorescence resonance energy homotransfer, Biophys. J., 75, 1117, 10.1016/S0006-3495(98)77601-5 · DOI
- Blackstad, 1961, Special axo-dendritic synapses in the hippocampal cortex: electron and light microscopic studies of the layer of mossy fibers, J. Comp. Neurol., 117, 133, 10.1002/cne.901170202 · DOI
- Blakely, 1991, Vaccinia-T7 RNA polymerase expression system: evaluation for the expression cloning of plasma membrane transporters, Anal. Biochem., 194, 302, 10.1016/0003-2697(91)90233-J · DOI
- Blakely, 1998, Regulated phosphorylation and trafficking of antidepressant-sensitive serotonin transporter proteins, Biol. Psychiatry, 44, 169, 10.1016/S0006-3223(98)00124-3 · DOI
- Blanc, 1998, 4-Hydroxynonenal, a lipid peroxidation product, impairs glutamate transport in cortical astrocytes, Glia, 22, 149, 10.1002/(SICI)1098-1136(199802)22:2<149::AID-GLIA6>3.0.CO;2-2 · DOI
- Bleakman, 1999, Kainate receptor pharmacology and physiology, Cell. Mol. Life Sci., 56, 558, 10.1007/s000180050453 · DOI
- Blei, 1999, Pathophysiology of cerebral edema in fulminant hepatic failure, J. Hepatol., 31, 771, 10.1016/S0168-8278(99)80361-4 · DOI
- Blitzblau, 1996, The glutamate transport inhibitor l-trans-pyrrolidine-2,4-dicarboxylate indirectly evokes NMDA receptor mediated neurotoxicity in rat cortical cultures, Eur. J. Neurosci., 8, 1840, 10.1111/j.1460-9568.1996.tb01328.x · DOI
- Bonanno, 1994, Release-regulating presynaptic heterocarriers, Prog. Neurobiol., 44, 451, 10.1016/0301-0082(94)90006-X · DOI
- Bonanno, 1993, Glutamic acid and gamma-aminobutyric acid modulate each other's release through heterocarriers sited on the axon terminals of rat brain, J. Neurochem., 61, 222, 10.1111/j.1471-4159.1993.tb03558.x · DOI
- Bonanno, 1994, Heterocarrier-mediated reciprocal modulation of glutamate and glycine release in rat cerebral cortex and spinal cord synaptosomes, Eur. J. Pharmacol., 252, 61, 10.1016/0014-2999(94)90575-4 · DOI
- Bondy, 1993, Oxidative stress induced by glutamate receptor agonists, Brain Res., 610, 229, 10.1016/0006-8993(93)91405-H · DOI
- Borges, 1998, AMPA receptors: molecular and functional diversity, Prog. Brain Res., 116, 153, 10.1016/S0079-6123(08)60436-7 · DOI
- Borowsky, 1995, Neurotransmitter transporters: molecular biology, function, and regulation, Int. Rev. Neurobiol., 38, 139, 10.1016/S0074-7742(08)60526-7 · DOI
- Bouvier, 1992, The glial cell glutamate uptake carrier countertransports pH-changing anions, Nature, 360, 471, 10.1038/360471a0 · DOI
- Bradford, 1978, Glutamine — a major substrate for nerve endings, J. Neurochem., 30, 1453, 10.1111/j.1471-4159.1978.tb10477.x · DOI
- Braithwaite, 2000, Interactions between AMPA receptors and intracellular proteins, Neuropharmacology, 39, 919, 10.1016/S0028-3908(99)00171-9 · DOI
- Bramham, 1990, Distribution of glutamate-like immunoreactivity in excitatory hippocampal pathways: a semiquantitative electron microscopic study in rats, Neuroscience, 39, 405, 10.1016/0306-4522(90)90277-B · DOI
- Brandtzaeg, 1998, The increasing power of immunohistochemistry and immunocytochemistry, J. Immunol. Methods, 216, 49, 10.1016/S0022-1759(98)00070-2 · DOI
- Bräuner-Osborne, 2000, Ligands for glutamate receptors: design and therapeutic prospects, J. Med. Chem., 43, 2609, 10.1021/jm000007r · DOI
- Bräuner-Osborne, 2000, A new structural class of subtype-selective inhibitor of cloned excitatory amino acid transporter, EAAT2, Eur. J. Pharmacol., 406, 41, 10.1016/S0014-2999(00)00625-7 · DOI
- Breitkreutz, 2000, Effect of carnitine on muscular glutamate uptake and intramuscular glutathione in malignant diseases, Br. J. Cancer, 82, 399, 10.1054/bjoc.1999.0933 · DOI
- Bressan, 2000, Imaging the glutamatergic system in vivo — relevance to schizophrenia, Eur. J. Nucl. Med., 27, 1723, 10.1007/s002590000372 · DOI
- Breukel, 1997, Arachidonic acid inhibits uptake of amino acids and potentiates PKC effects on glutamate, but not GABA, exocytosis in isolated hippocampal nerve terminals, Brain Res., 773, 90, 10.1016/S0006-8993(97)00918-9 · DOI
- Brew, 1987, Electrogenic glutamate uptake is a major current carrier in the membrane of axolotal retinal glial cells, Nature, 327, 707, 10.1038/327707a0 · DOI
- Bridges, 1991, Conformationally defined neurotransmitter analogues. Selective inhibition of glutamate uptake by one pyrrolidine-2,4-dicarboxylate diastereomer, J. Med. Chem., 34, 717, 10.1021/jm00106a037 · DOI
- Bridges, 1992, Gliotoxic actions of excitatory amino acids, Neuropharmacology, 31, 899, 10.1016/0028-3908(92)90128-C · DOI
- Bridges, 1993, Conformationally restricted inhibitors of the high affinity l-glutamate transporter, Bioorg. Med. Chem. Lett., 3, 115, 10.1016/S0960-894X(00)80103-1 · DOI
- Bridges, 1994, A conformationally constrained competitive inhibitor of the sodium-dependent glutamate transporter in forebrain synaptosomes: l-anti-endo-3,4-methanopyrrolidine dicarboxylate, Neurosci. Lett., 174, 193, 10.1016/0304-3940(94)90019-1 · DOI
- Bridges, 1999, A pharmacological review of competitive inhibitors and substrates of high-affinity, sodium-dependent glutamate transport in the central nervous system, Curr. Pharm. Des., 5, 363, 10.2174/138161280505230110101259 · DOI
- Brines, 1995, The cardiac glycoside ouabain potentiates excitotoxic injury of adult neurons in rat hippocampus, Neurosci. Lett., 191, 145, 10.1016/0304-3940(95)11577-J · DOI
- Bröer, 1998, Discrimination of two amino acid transport activities in 4F2 heavy chain- expressing Xenopus laevis oocytes, Biochem. J., 333, 549, 10.1042/bj3330549 · DOI
- Bröer, 1999, The astroglial ASCT2 amino acid transporter as a mediator of glutamine efflux, J. Neurochem., 73, 2184, 10.1046/j.1471-4159.1999.02184.x · DOI
- Brookes, 1988, Specificity and reversibility of the inhibition by HgCl2 of glutamate transport in astrocyte cultures, J. Neurochem., 50, 1117, 10.1111/j.1471-4159.1988.tb10581.x · DOI
- Brooks-Kayal, 1998, The glutamate transporter, GLT-1, is expressed in cultured hippocampal neurons, Neurochem. Int., 33, 95, 10.1016/S0197-0186(98)00018-7 · DOI
- Brose, 1990, A chloride-dependent and calcium-dependent glutamate-binding protein from rat brain — identification as a ubiquitous constituent of the inner mitochondrial membrane, J. Biol. Chem., 265, 10604, 10.1016/S0021-9258(18)86989-7 · DOI
- Brown, 1995, The release of glutamate and aspartate from rat brain synaptosomes in response to domoic acid (amnesic shellfish toxin) and kainic acid, Mol. Cell. Biochem., 151, 49, 10.1007/BF01076895 · DOI
- Brown, 1998, Clinical significance of CSF glutamate concentrations following severe traumatic brain injury in humans, J. Neurotrauma, 15, 253, 10.1089/neu.1998.15.253 · DOI
- Brown, 1995, Amyotrophic lateral sclerosis: recent insights from genetics and transgenic mice, Cell, 80, 687, 10.1016/0092-8674(95)90346-1 · DOI
- Brown, 1997, Amyotrophic lateral sclerosis: insights from genetics, Arch. Neurol., 54, 1246, 10.1001/archneur.1997.00550220050013 · DOI
- Buckman, 1999, Glutamate uptake in mice bred for ethanol withdrawal severity, Psychopharmacology (Berl.), 143, 174, 10.1007/s002130050933 · DOI
- Burger, 1989, Synaptic vesicles immunoisolated from rat cerebral cortex contain high levels of glutamate, Neuron, 3, 715, 10.1016/0896-6273(89)90240-7 · DOI
- Burger, 1991, GABA and glycine in synaptic vesicles — storage and transport characteristics, Neuron, 7, 287, 10.1016/0896-6273(91)90267-4 · DOI
- Butterfield, 1997, Beta-amyloid-associated free radical oxidative stress and neurotoxicity: implications for Alzheimer's disease, Chem. Res. Toxicol., 10, 495, 10.1021/tx960130e · DOI · Paper page
- Butterworth, 1998, Effects of hyperammonaemia on brain function, J. Inherit. Metab. Dis., 21, 6, 10.1023/A:1005393104494 · DOI
- Butterworth, 1998, Pathogenesis of acute hepatic encephalopathy, Digestion, 59, 16, 10.1159/000051414 · DOI
- Cagampang, 1996, Circadian variation of EAAC1 glutamate transporter messenger RNA in the rat suprachiasmatic nuclei, Mol. Brain Res., 35, 190, 10.1016/0169-328X(95)00203-5 · DOI
- Cammack, 1996, Channel behavior in a gamma-aminobutyrate transporter, Proc. Natl. Acad. Sci. USA, 93, 723, 10.1073/pnas.93.2.723 · DOI
- Cammack, 1994, A GABA transporter operates asymmetrically and with variable stoichiometry, Neuron, 13, 949, 10.1016/0896-6273(94)90260-7 · DOI
- Canton, 1998, Glutamate uptake is decreased tardively in the spinal cord of FALS mice, Neuroreport, 9, 775, 10.1097/00001756-199803300-00001 · DOI
- Cao, 1998, Amino acid residues that control pH modulation of transport-associated current in mammalian serotonin transporters, J. Neurosci., 18, 7739, 10.1523/JNEUROSCI.18-19-07739.1998 · DOI
- Carlsson, 1997, Neurotransmitter aberrations in schizophrenia: new perspectives and therapeutic implications, Life Sci., 61, 75, 10.1016/S0024-3205(97)00228-2 · DOI
- Carlsson, 1999, A glutamatergic deficiency model of schizophrenia, Br. J. Psychiatry, 174, 2, 10.1192/S0007125000293574 · DOI
- Carpenter, 1999, The schizophrenia ketamine challenge study debate, Biol. Psychiatry, 46, 1081, 10.1016/S0006-3223(99)00194-8 · DOI
- Carrick, 1999, Protein kinase C modulation of the human excitatory amino acid transporter 2 subtype of glutamate transporter, Soc. Neurosci. Abstr., 25, 426
- Carter, 2000, Prolonged synaptic currents and glutamate spillover at the parallel fiber to stellate cell synapse, J. Neurosci., 20, 4423, 10.1523/JNEUROSCI.20-12-04423.2000 · DOI
- Casado, 1991, Activation of high-affinity uptake of glutamate by phorbol esters in primary glial cell cultures, J. Neurochem., 57, 1185, 10.1111/j.1471-4159.1991.tb08278.x · DOI
- Casado, 1993, Phosphorylation and modulation of brain glutamate transporters by protein kinase C, J. Biol. Chem., 268, 27313, 10.1016/S0021-9258(19)74251-3 · DOI
- Caspers, 1993, Alterations of cerebromicrovascular Na+,K+-ATPase activity due to fatty acids and acute hypertension, Brain Res., 602, 215, 10.1016/0006-8993(93)90685-G · DOI
- Catania, 1994, Metabotropic glutamate receptors are differentially regulated during development, Neuroscience, 61, 481, 10.1016/0306-4522(94)90428-6 · DOI
- Chalmers, 1990, Differential alterations of cortical glutamatergic binding sites in senile dementia of the Alzheimer type, Proc. Natl. Acad. Sci. USA, 87, 1352, 10.1073/pnas.87.4.1352 · DOI
- Chamberlin, 1998, Design and synthesis of conformationally constrained inhibitors of high-affinity, sodium-dependent glutamate transporters, Methods Enzymol., 296, 175, 10.1016/S0076-6879(98)96014-1 · DOI
- Chan, 1999, Evidence for an astrocytic glutamate transporter deficit in hepatic encephalopathy, Neurochem. Res., 24, 1397, 10.1023/A:1022532623281 · DOI
- Chan, 2000, Effects of ammonia on glutamate transporter (GLAST) protein and mRNA in cultured rat cortical astrocytes, Neurochem. Int., 37, 243, 10.1016/S0197-0186(00)00026-7 · DOI
- Chan, 1983, Reductions of gamma-aminobutyric acid and glutamate uptake and (Na++K+)-ATPase activity in brain slices and synaptosomes by arachidonic acid, J. Neurochem., 40, 309, 10.1111/j.1471-4159.1983.tb11284.x · DOI
- Chancellor, 1992, Adult onset motor neuron disease — worldwide mortality, incidence and distribution since 1950, J. Neurol. Neurosurg. Psychiatry, 55, 1106, 10.1136/jnnp.55.12.1106 · DOI
- Chandler, 1999, Chronic ethanol upregulates NMDA and AMPA, but not kainate receptor subunit proteins in rat primary cortical cultures, Alcohol Clin. Exp. Res., 23, 363, 10.1111/j.1530-0277.1999.tb04123.x · DOI
- Chaudhry, 1995, Glutamate transporters in glial plasma membranes: highly differentiated localizations revealed by quantitative ultrastructural immunocytochemistry, Neuron, 15, 711, 10.1016/0896-6273(95)90158-2 · DOI
- Chaudhry, 1999, Molecular analysis of system N suggests novel physiological roles in nitrogen metabolism and synaptic transmission, Cell, 99, 769, 10.1016/S0092-8674(00)81674-8 · DOI
- Chavany, 1998, Transgenic mice for interleukin 3 develop motor neuron degeneration associated with autoimmune reaction against spinal cord motor neurons, Proc. Natl. Acad. Sci. USA, 95, 11354, 10.1073/pnas.95.19.11354 · DOI
- Chenard, 1999, Antagonists selective for NMDA receptors containing the NR2b subunit, Curr. Pharm. Des., 5, 381, 10.2174/138161280504230110102541 · DOI
- Cheung, 1998, Micromolar l-glutamate induces extensive apoptosis in an apoptotic-necrotic continuum of insult-dependent, excitotoxic injury in cultured cortical neurones, Neuropharmacology, 37, 1419, 10.1016/S0028-3908(98)00123-3 · DOI
- Chicurel, 1992, Three-dimensional analysis of the structure and composition of CA3 branched dendritic spines and their synaptic relationships with mossy fiber boutons in the rat hippocampus, J. Comp. Neurol., 325, 169, 10.1002/cne.903250204 · DOI · Paper page
- Chittajallu, 1999, Kainate receptors: subunits, synaptic localization and function, Trends Pharmacol. Sci., 20, 26, 10.1016/S0165-6147(98)01286-3 · DOI
- Cho, 1990, Uptake of glutamate and cystine in C-6 glioma cells and cultured astrocytes, J. Neurochem., 55, 2091, 10.1111/j.1471-4159.1990.tb05800.x · DOI
- Choi, 1981, Radial glia of developing human fetal spinal cord: Golgi, immunohistochemical and electron microscopic study, Brain Res., 227, 249, 10.1016/0165-3806(81)90112-7 · DOI
- Choi, 1992, Excitotoxic cell death, J. Neurobiol., 23, 1261, 10.1002/neu.480230915 · DOI
- Choi, 1990, The role of glutamate neurotoxicity in hypoxic-ischemic neuronal death, Annu. Rev. Neurosci., 13, 171, 10.1146/annurev.ne.13.030190.001131 · DOI
- Choi, 1997, Expression of high-affinity neuronal and glial glutamate transporters in the rat optic nerve, Glia, 20, 184, 10.1002/(SICI)1098-1136(199707)20:3<184::AID-GLIA2>3.0.CO;2-8 · DOI
- Choi, 2000, Postfusional regulation of cleft glutamate concentration during LTP at ‘silent synapses’, Nat. Neurosci., 3, 330, 10.1038/73895 · DOI
- Christensen, 1992, Amino acid nutrition across the placenta, Nutr. Rev., 50, 13, 10.1111/j.1753-4887.1992.tb02455.x · DOI
- Christensen, 1992, The ontogeny of the uptake systems for glutamate, GABA, and glycine in synaptic vesicles isolated from rat brain, Neurochem. Res., 17, 457, 10.1007/BF00969892 · DOI
- Clements, 1996, Transmitter timecourse in the synaptic cleft: its role in central synaptic function, Trends Neurosci., 19, 163, 10.1016/S0166-2236(96)10024-2 · DOI
- Clements, 1992, The time course of glutamate in the synaptic cleft, Science, 258, 1498, 10.1126/science.1359647 · DOI
- Cohen, 1997, Sodium-dependent proline and glutamate uptake by hippocampal synaptosomes during postnatal development, Dev. Brain Res., 100, 230, 10.1016/S0165-3806(97)00045-X · DOI
- Collard, 1993, Changes in synaptosomal glutamate release during postnatal development in the rat hippocampus and cortex, Dev. Brain Res., 71, 37, 10.1016/0165-3806(93)90102-G · DOI
- Collingridge, 1989, Excitatory amino acid receptors in the vertebrate central nervous system, Pharmacol. Rev., 40, 143
- Conn, 1997, Pharmacology and functions of metabotropic glutamate receptors, Annu. Rev. Pharmacol. Toxicol., 37, 205, 10.1146/annurev.pharmtox.37.1.205 · DOI
- Conradt, 1995, Functional analysis of the high affinity, Na+-dependent glutamate transporter GLAST-1 by site-directed mutagenesis, J. Biol. Chem., 270, 25207, 10.1074/jbc.270.42.25207 · DOI
- Conradt, 1997, Inhibition of the high-affinity brain glutamate transporter GLAST-1 via direct phosphorylation, J. Neurochem., 68, 1244, 10.1046/j.1471-4159.1997.68031244.x · DOI
- Conradt, 1995, Localization of N-glycosylation sites and functional role of the carbohydrate units of GLAST-1, a cloned rat brain l-glutamate/l-aspartate transporter, Eur. J. Biochem., 229, 682, 10.1111/j.1432-1033.1995.tb20514.x · DOI
- Conti, 1998, EAAC1, a high-affinity glutamate transporter, is localized to astrocytes and GABAergic neurons besides pyramidal cells in the rat cerebral cortex, Cereb. Cortex, 8, 108, 10.1093/cercor/8.2.108 · DOI
- Conti, 1999, Neuronal and glial localization of NR1 and NR2a/b subunits of the NMDA receptor in the human cerebral cortex, Cereb. Cortex, 9, 110, 10.1093/cercor/9.2.110 · DOI
- Cookson, 1999, Oxidative stress and motor neurone disease, Brain Pathol., 9, 165, 10.1111/j.1750-3639.1999.tb00217.x · DOI
- Cooper, 1997, Multiple roles of glutathione in the central nervous system, Biol. Chem., 378, 793
- Cooper, 1998, Structural selectivity and molecular nature of l-glutamate transport in cultured human fibroblasts, Arch. Biochem. Biophys., 353, 356, 10.1006/abbi.1998.0626 · DOI
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Onwordi, E. C., Whitehurst, T., Mansur, A., Statton, B., Berry, A., Quinlan, M., O’Regan, D. P., Rogdaki, M., Marques, T. R., Rabiner, E. A., et al. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01515-3 · Cited by 55
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Krisanova, N., Kasatkina, L., Sivko, R., Borysov, A., Nazarova, A., Slenzka, K., & Borisova, T. (2013) · Astrobiology · doi:10.1089/ast.2012.0950 · Cited by 33
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Dhaher, R., Damisah, E. C., Wang, H., Gruenbaum, S. E., Ong, C., Zaveri, H. P., Gruenbaum, B. F., & Eid, T. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.03.006 · Cited by 20
Henao‐Restrepo, J., López‐Murillo, C., Valderrama‐Carmona, P., Orozco‐Santa, N., Gomez, J., Gutiérrez‐Vargas, J., Moraga, R., Toledo, J., Littau, J. L., Härtel, S., et al. (2023) · Brain Pathology · doi:10.1111/bpa.13119 · Cited by 11
Metadata
- Authors
- Danbolt, N. C.
- Affiliations
- University of Oslo (NO)
- Corresponding author
- Danbolt, Niels C
- ORCID
- Danbolt, Niels C
- Venue
- Progress in Neurobiology
- Publisher
- Elsevier BV
- Published
- 2001-09
- Volume
- 65
- Issue
- 1
- Pages
- 1-105
- ISSN
- 0301-0082 (ISSN-L)
- OpenAlex
- W4210979710
- Cited by
- 4,227
- References
- 19
- Citations by year
- 2026: 94 · 2025: 113 · 2024: 133 · 2023: 126 · 2022: 177 · 2021: 167 · 2020: 186 · 2019: 144 · 2018: 180 · 2017: 199 · 2016: 214 · 2015: 209 · 2014: 241 · 2013: 203 · 2012: 195
- FWCI
- 11.41
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Progress in Neurobiology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
- Keywords
- glutamate uptake, glutamate transporters, brain, glial cells, neurons, neurotransmission, GABA synthesis, glutathione, energy metabolism, cytokines, neurological disorders, cerebral ischemia, epilepsy, Alzheimer's disease, amyotrophic lateral sclerosis, traumatic brain injury, schizophrenia, osteoporosis
- MeSH terms
- Ethanol, Anesthetics, Animals, Bone and Bones, Brain, Carrier Proteins, Extracellular Space, Female, Gene Expression Regulation, Glutamine, Hepatic Encephalopathy, Humans, Intracellular Fluid, Ion Channels, Ischemia, Male, Mammals, Mercury Poisoning, Nerve Tissue Proteins, Nervous System Diseases, Synaptic Transmission, Neuroglia, Neurons, Organ Specificity, Placenta, Potassium, Pregnancy, Protein Conformation, Sodium, Synapses, Viscera, Ion Channel Gating, HIV Infections, Ion Transport, Receptors, Glutamate, Neurotransmitter Agents, ATP-Binding Cassette Transporters, Glutamic Acid, Amino Acid Transport System X-AG, Monocarboxylic Acid Transporters, Rats
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