The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.
NMDA-receptor activation increases cytoplasmic calcium concentration in cultured spinal cord neurones
Abstract
Excitatory amino acids act via receptor subtypes in the mammalian central nervous system (CNS). The receptor selectively activated by N-methyl-D-aspartic acid (NMDA) has been best characterized using voltage-clamp and single-channel recording; the results suggest that NMDA receptors gate channels that are permeable to Na+, K+ and other monovalent cations. Various experiments suggest that Ca2+ flux is also associated with the activation of excitatory amino-acid receptors on vertebrate neurones. Whether Ca2+ enters through voltage-dependent Ca2+ channels or through excitatory amino-acid-activated channels of one or more subtype is unclear. Mg2+ can be used to distinguish NMDA-receptor-activated channels from voltage-dependent Ca2+ channels, because at micromolar concentrations Mg2+ has little effect on voltage-dependent Ca2+ channels while it enters and blocks NMDA receptor channels. Marked differences in the potency of other divalent cations acting as Ca2+ channel blockers compared with their action as NMDA antagonists also distinguish the NMDA channel from voltage-sensitive Ca2+ channels. However, we now directly demonstrate that excitatory amino acids acting at NMDA receptors on spinal cord neurones increase the intracellular Ca2+ activity, measured using the indicator dye arsenazo III, and that this is the result of Ca2+ influx through NMDA receptor channels. Kainic acid (KA), which acts at another subtype of excitatory amino-acid receptor, was much less effective in trigge…
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
“The discovery that NMDARs are highly permeable to Ca2+ (179, 180)”
From Synaptic memory and CaMKII (2023) · cites this paper as [179]
Citations
Cites
Hamill, O. P., Marty, A., Neher, E., Sakmann, B., & Sigworth, F. J. (1981) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00656997 · Cited by 18,436
Inositol Trisphosphate, a Novel Second Messenger in Cellular Signal Transduction
Berridge, M. J., & Irvine, R. F. (1984) · Nature · doi:10.1038/312315a0 · Cited by 6,086
Magnesium gates glutamate-activated channels in mouse central neurones
Nowak, L. M., Bregestovski, P. D., Ascher, P., Herbet, A., & Prochiantz, A. (1984) · Nature · doi:10.1038/307462a0 · Cited by 4,116
Voltage-dependent block by Mg2+ of NMDA responses in spinal cord neurones
Mayer, M. L., Westbrook, G. L., & Guthrie, P. B. (1984) · Nature · doi:10.1038/309261a0 · Cited by 2,941
Self-citationExcitatory Amino Acid Transmitters
Watkins, J. C., & Evans, R. H. (1981) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pa.21.040181.001121 · Cited by 2,497
Collingridge, G. L., Kehl, S. J., & McLennan, H. (1983) · The Journal of Physiology · doi:10.1113/jphysiol.1983.sp014478 · Cited by 2,413
Hagiwara, S., & Byerly, L. (1981) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.04.030181.000441 · Cited by 1,193
Intracellular injections of EGTA block induction of hippocampal long-term potentiation
Lynch, G., Larson, J., Kelso, S., Barrionuevo, G., & Schottler, F. (1983) · Nature · doi:10.1038/305719a0 · Cited by 1,116
Glutamate stimulates inositol phosphate formation in striatal neurones
Sladeczek, F. A. J., Pin, J., Récasens, M., Bockaert, J., & Weiss, S. (1985) · Nature · doi:10.1038/317717a0 · Cited by 752
Fabiato, A., & Fabiato, F. (1978) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1978.tb41979.x · Cited by 467
Flagged first, then by citations
Research works printed but not linked: 8
- Lansman, J. B., Hess, P. & Tsien, R. W. J. gen. Physiol. (in the press).
- Cull-Candy, S. G. & Ogden, D. C. Proc. R. Soc. B224, 367–373 (1985).
- Evans, R. H. & Watkins, J. C. J. Physiol., Lond. 277, 57P (1977).
- Nowak, L. M. & Ascher, P. Soc. Neurosci. Abstr. 10, 23 (1984).
- Mayer, M. L. & Westbrook, G. L. Soc. Neurosci. Abstr. 11, 785 (1985).
- Ascher, P. & Nowak, L. J. Physiol., Lond. Proc. (in the press).
- Nowak, L. M. & Ascher, P. Soc. Neurosci. Abstr. 11, 953 (1985).
- Miledi, R. Proc. R. Soc. B209, 447–452 (1980).
Cited by
Sorted by citations
Items 601–700 of 1,002
Propofol attenuates pancreatic cancer malignant potential via inhibition of NMDA receptor
Chen, X., Wu, Q., Li, Y., Chen, S., Zhu, M., & Miao, C. (2016) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2016.12.017 · Cited by 61
Luzzi, S., Zilletti, L., Franchi‐Micheli, S., Gori, A. M., & Moroni, F. (1988) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1988.tb11764.x · Cited by 61
Foster, A. C., & Kemp, J. A. (1989) · Nature · doi:10.1038/338377a0 · Cited by 61
Molecular mechanism of ligand gating and opening of NMDA receptor
Chou, T., Epstein, M., Fritzemeier, R. G., Akins, N. S., Paladugu, S., Ullman, E. Z., Liotta, D. C., Traynelis, S. F., & Furukawa, H. (2024) · Nature · doi:10.1038/s41586-024-07742-0 · Cited by 62
Kölker, S., Köhr, G., Ahlemeyer, B., Okun, J. G., Pawlak, V., Hörster, F., Mayatepek, E., Krieglstein, J., & Hoffmann, G. F. (2002) · Pediatric Research · doi:10.1203/00006450-200208000-00011 · Cited by 60
Interactions between excitatory amino acids and tachykinins in the rat spinal dorsal horn
Rusin, K. I., Jiang, M. C., Cerne, R., & Randić, M. (1993) · Brain Research Bulletin · doi:10.1016/0361-9230(93)90261-9 · Cited by 60
Direct stimulation of pituitary prolactin release by glutamate
Login, I. S. (1990) · Life Sciences · doi:10.1016/0024-3205(90)90158-n · Cited by 60
raises cytosolic calcium concentration in rat cerebellar granule cells in culture
Burgoyne, R. D., Pearce, I. A., & Cambray-Deakin, M. A. (1988) · Neuroscience Letters · doi:10.1016/0304-3940(88)90247-9 · Cited by 60
Regulation of AMPA receptor dephosphorylation by glutamate receptor agonists
Snyder, G. L., Galdi, S., Fienberg, A. A., Allen, P. B., Nairn, A. C., & Greengard, P. (2003) · Neuropharmacology · doi:10.1016/s0028-3908(03)00319-8 · Cited by 60
Abdi, A., Tahoori, M. B., & Emamian, E. S. (2008) · Science Signaling · doi:10.1126/scisignal.2000008 · Cited by 59
Saito, Y., & Isa, T. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-13-05854.2003 · Cited by 59
The Interphase Nucleus as a Dynamic Structure
Boni, U. D. (1994) · International review of cytology · doi:10.1016/s0074-7696(08)61541-7 · Cited by 59
Calcium-dependent, slow desensitization distinguishes different types of glutamate receptors
Zorumski, C. F., Yang, J., & Fischbach, G. D. (1989) · Cellular and Molecular Neurobiology · doi:10.1007/bf00711446 · Cited by 59
Activation of N-Methyl-d-Aspartate Receptor Attenuates Acute Responsiveness of δ-Opioid Receptors
Cai, Y.-C., Ma, L., Fan, G.-H., Zhao, J., Jiang, L., & Pei, G. (1997) · Molecular Pharmacology · doi:10.1124/mol.51.4.583 · Cited by 59
Long-term potentiation in rat hippocampal slices is impaired following acute lead perfusion.
Altmann, L., Sveinsson, K., & Wiegand, H. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90771-k · Cited by 59
Andiné, P., Jacobson, I., & Hagberg, H. (1992) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1992.108 · Cited by 59
Didier, M., Roux, P., Piechaczyk, M., Verrier, B., Bockaert, J., & Pin, J. (1989) · Neuroscience Letters · doi:10.1016/0304-3940(89)90790-8 · Cited by 59
Rao, J. S., Ertley, R. N., Rapoport, S. I., Bazinet, R. P., & Lee, H. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04648.x · Cited by 59
RetractedTransducer of regulated CREB and late phase long‐term synaptic potentiation
Wu, H., Zhou, Y., & Xiong, Z. (2007) · FEBS Journal · doi:10.1111/j.1742-4658.2007.05891.x · Cited by 59
Low concentrations of inhibit the induction of long-term potentiation in rat hippocampal slices
Izumi, Y., Clifford, D. B., & Zorumski, C. F. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90414-3 · Cited by 58
Guo, H., & Huang, L. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.0115k.x · Cited by 58
Westergaard, N., Banke, T. G., Wahl, P., Sonnewald, U., & Schousboe, A. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.8.3367 · Cited by 58
Choi, D. W., & Viseskul, V. (1988) · European Journal of Pharmacology · doi:10.1016/0014-2999(88)90399-8 · Cited by 58
Long-term potentiation during whole-cell recording in rat hippocampal slices
Kato, K., Clifford, D. B., & Zorumski, C. F. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90282-k · Cited by 51
Verheul, H. B., Balázs, R., van der Sprenkel, J. W. B., Tulleken, C. A. F., Nicolay, K., & Campagne, M. V. L. (1993) · Brain Research · doi:10.1016/0006-8993(93)91267-v · Cited by 58
He, Y., Janssen, W. G. M., Vissavajjhala, P., & Morrison, J. H. (1998) · Experimental Neurology · doi:10.1006/exnr.1997.6720 · Cited by 58
Imaging of calcium variations in living dendritic spines of cultured rat hippocampal neurons.
Segal, M. (1995) · The Journal of Physiology · doi:10.1113/jphysiol.1995.sp020811 · Cited by 58
Excitotoxicity and N‐methyl‐D‐Aspartate receptors
Olney, J. W. (1989) · Drug Development Research · doi:10.1002/ddr.430170406 · Cited by 58
Bénavidès, J., Claustre, Y., & Scatton, B. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-10-03607.1988 · Cited by 58
Tse, Y. C., Bagot, R. C., Hutter, J. A., Wong, A. S., & Wong, T. P. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027215 · Cited by 59
Schizophrenia and the D1 receptor: Focus on negative symptoms
Lynch, M. R. (1992) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/0278-5846(92)90102-k · Cited by 58
Arvin, B. M., Neville, L. F., Pan, J. B., & Roberts, P. (1989) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1989.tb16886.x · Cited by 57
Monosialoganglioside GM1 protects against anoxia-induced neuronal death in vitro
Skaper, S. D., Facci, L., Milani, D., & Leon, A. (1989) · Experimental Neurology · doi:10.1016/0014-4886(89)90163-5 · Cited by 57
The α7nACh–NMDA receptor complex is involved in cue-induced reinstatement of nicotine seeking
Li, S., Li, Z., Pei, L., Lê, A. D., & Liu, F. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20121270 · Cited by 56
Rivera-Cervantes, M. C., Torres, J. S., Feria‐Velasco, A., Armendáriz‐Borunda, J., & Beas‐Zárate, C. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20103 · Cited by 57
Suárez, L. M., Suárez, F., Olmo, N. D., Ruiz, M., González-Escalada, J. R., & Solís, J. M. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03832.x · Cited by 56
Coordination of Head and Eyes during the Performance of Natural (and Unnatural) Visual Tasks
Kowler, E., Pizlo, Z., Zhu, G.-L., Erkelens, C. J., Steinman, R. M., & Collewijn, H. (1992) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195068207.003.0065 · Cited by 56
Desmond, N. L., Colbert, C. M., Zhang, D. X., & Levy, W. B. (1991) · Brain Research · doi:10.1016/0006-8993(91)90664-h · Cited by 56
L-Glutamate Receptors on the Cell Body Membrane of an Identified Insect Motor Neurone
Wafford, K. A., & Sattelle, D. B. (1989) · Journal of Experimental Biology · doi:10.1242/jeb.144.1.449 · Cited by 56
Pregnenolone sulfate exacerbates NMDA-induced death of hippocampal neurons
Weaver, C. E., Wu, F., Gibbs, T. T., & Farb, D. H. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00640-4 · Cited by 56
Chittajallu, R., Alford, S. T., & Collingridge, G. L. (1998) · Cell Calcium · doi:10.1016/s0143-4160(98)90061-6 · Cited by 56
Mechanisms of epileptogenicity in cortical dysplasias
Najm, I., Ying, Z., Babb, T. L., Crino, P. B., Macdonald, R. L., Mathern, G. W., & Spreafico, R. (2004) · Neurology · doi:10.1212/01.wnl.0000114506.49267.bb · Cited by 56
Gerber, G., Cerne, R., & Randić, M. (1991) · Brain Research · doi:10.1016/0006-8993(91)91600-6 · Cited by 56
Toporikova, N., & Chacron, M. J. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00282.2009 · Cited by 55
Hounoum, B. M., Vourc’h, P., Félix, R., Corcia, P., Patin, F., Guéguinou, M., Potier‐Cartereau, M., Vandier, C., Raoul, C., Andres, C. R., et al. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00118 · Cited by 63
PET studies of binding competition between endogenous dopamine and the D1 radiotracer [11C]NNC 756
Abi‐Dargham, A., Simpson, N. R., Kegeles, L. S., Parsey, R. V., Hwang, D., Anjilvel, S., Zea‐Ponce, Y., Lombardo, I., Heertum, R. V., Mann, J. J., et al. (1999) · Synapse · doi:10.1002/(sici)1098-2396(199905)32:2 · Cited by 115
Extracellular Acidity Potentiates AMPA Receptor-Mediated Cortical Neuronal Death
McDonald, J. W., Bhattacharyya, T., Sensi, S. L., Lobner, D., Ying, H. S.-C., Canzoniero, L. M. T., & Choi, D. W. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-16-06290.1998 · Cited by 55
Nadler, V., Mechoulam, R., & Sokolovsky, M. (1993) · Brain Research · doi:10.1016/0006-8993(93)90804-v · Cited by 55
The pharmacology of segmental transmission in the spinal cord
Evans, R. H. (1989) · Progress in Neurobiology · doi:10.1016/0301-0082(89)90003-8 · Cited by 55
Pharmacology of N‐methyl‐D‐aspartate‐induced brain injury in an in vivo perinatal rat model
McDonald, J. W., & Johnston, M. V. (1990) · Synapse · doi:10.1002/syn.890060210 · Cited by 55
Alford, S. T., & Grillner, S. E. (1990) · Brain Research · doi:10.1016/0006-8993(90)91266-j · Cited by 55
N-methyl-d-aspartate (NMDA) receptors are inactivated by trypsin
Allen, C. N., Brady, R. J., Swann, J. W., Hori, N., & Carpenter, D. O. (1988) · Brain Research · doi:10.1016/0006-8993(88)90507-0 · Cited by 55
Linn, C., & Christensen, B. N. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-06-02156.1992 · Cited by 55
Kiskin, N. I., Krishtal, O., & Tsyndrenko, A. Y. (1990) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1990.tb00437.x · Cited by 55
Ketamine inhibits colorectal cancer cells malignant potential via blockage of NMDA receptor
Duan, W., Hu, J., & Liu, Y. (2019) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2019.02.004 · Cited by 54
Interactions between two divalent ion binding sites in N -methyl- d -aspartate receptor channels
Sharma, G., & Stevens, C. F. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.24.14170 · Cited by 55
Memory systems in the chick: Dissociations and neuronal analysis
Horn, G., & Johnson, M. H. (1989) · Neuropsychologia · doi:10.1016/0028-3932(89)90086-9 · Cited by 54
Minato, H., Kikuta, C., Fujitani, B., & Masuda, Y. (1997) · Epilepsia · doi:10.1111/j.1528-1157.1997.tb01479.x · Cited by 54
Singh, T. D., Basham, M. E., Nordeen, E. J., & Nordeen, K. W. (2000) · Journal of Neurobiology · doi:10.1002/1097-4695(200007)44:1 · Cited by 54
Pharmacological effects of the non‐competitive NMDA antagonist CNS 1102 in normal volunteers.
Muir, K. W., Grosset, D. G., Gamzu, E., & Lees, K. R. (1994) · British Journal of Clinical Pharmacology · doi:10.1111/j.1365-2125.1994.tb04318.x · Cited by 54
Localization of glutamate receptors at a complex synapse
Brandstätter, J. H., & Hack, I. (2001) · Cell and Tissue Research · doi:10.1007/s004410000304 · Cited by 54
Borowitz, J. L., Gunasekar, P. G., & Isom, G. E. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00659-8 · Cited by 53
Glasgow, S. D., Ruthazer, E. S., & Kennedy, T. E. (2021) · The Journal of Physiology · doi:10.1113/jp278704 · Cited by 51
NMDA Receptor-Mediated Control of Presynaptic Calcium and Neurotransmitter Release
Cochilla, A. J., & Alford, S. T. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-01-00193.1999 · Cited by 53
Neuronal fodrin proteolysis occurs independently of excitatory amino acid-induced neurotoxicity
Stasi, A. M. M. D., Gallo, V., Ceccarini, M., & Petrucci, T. C. (1991) · Neuron · doi:10.1016/0896-6273(91)90252-u · Cited by 53
Antibodies to ependymin block the sharpening of the regenerating retinotectal projection in goldfish
Schmidt, J. T., & Shashoua, V. E. (1988) · Brain Research · doi:10.1016/0006-8993(88)90886-4 · Cited by 53
Fink, K., Schultheiß, R., & Göthert, M. (1992) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1992.tb14294.x · Cited by 53
Garthwaite, G., & Garthwaite, J. (1986) · Neuroscience Letters · doi:10.1016/0304-3940(86)90256-9 · Cited by 53
Colwell, C. S., & Levine, M. S. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90429-4 · Cited by 53
Lontay, B., Kiss, A., Virág, L., & Tar, K. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21124282 · Cited by 55
Glutamate Neurotoxicity, Calcium, and Zinca
Choi, D. W., Weiss, J. H., Koh, J., Christine, C. W., & Kurth, M. (1989) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1989.tb12511.x · Cited by 52
Genesis of spontaneous rhythmic motor patterns in the lumbosacral spinal cord of neonate mouse
Bonnot, A., Morin, D., & Viala, D. (1998) · Developmental Brain Research · doi:10.1016/s0165-3806(98)00033-9 · Cited by 52
Blockade of N- response in enzyme-treated rat hippocampal neurons
Akaike, N., Kaneda, M., Hori, N., & Krishtal, O. (1988) · Neuroscience Letters · doi:10.1016/0304-3940(88)90148-6 · Cited by 52
Chapter 27. Plasticity of excitatory synaptic transmission in the spinal cord dorsal horn
Randić, M. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)61104-8 · Cited by 52
Spinal dorsal horn synaptic plasticity: involvement of Group I metabotropic glutamate receptors
Gerber, G., Youn, D., Hsu, C. H., Isaev, D. S., & Randić, M. (2000) · Progress in brain research · doi:10.1016/s0079-6123(00)29009-2 · Cited by 52
Lyden, P. D., Jackson-Friedman, C., Shin, C., & Hassid, S. (2000) · Experimental Neurology · doi:10.1006/exnr.2000.7394 · Cited by 52
Ramoa, A. S., & Prusky, G. T. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(97)00061-8 · Cited by 52
Heterosynaptic correlates of long-term potentiation induction in hippocampal CA3 neurons
Bradler, J. E., & Barrionuevo, G. (1990) · Neuroscience · doi:10.1016/0306-4522(90)90080-n · Cited by 52
Fujikawa, D. G. (2019) · Epilepsia · doi:10.1111/epi.14676 · Cited by 51
Glutamate receptors and synaptic plasticity: The impact of Evans and Watkins
Collingridge, G. L., & Abraham, W. C. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108922 · Cited by 52
Hall, C. W., & Behbehani, M. M. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00648-9 · Cited by 51
Solomon, I. C. (2000) · Respiration Physiology · doi:10.1016/s0034-5687(00)00122-5 · Cited by 51
Nowak, L. M., & Wright, J. M. (1992) · Neuron · doi:10.1016/0896-6273(92)90119-x · Cited by 51
Comparison of Head Movement Strategies among Mammals
Fuller, J. H. (1992) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195068207.003.0013 · Cited by 51
Yuzaki, M., Forrest, D., Verselis, L. M., Sun, S. C., Curran, T., & Connor, J. A. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-15-04651.1996 · Cited by 52
Becker, C. G., Artola, A., Gerardy‐Schahn, R., Becker, T., Welzl, H., & Schachner, M. (1996) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19960715)45:2 · Cited by 306
Excitatory amino acids and intracellular pH in motoneurons of the isolated frog spinal cord
Endres, W., Ballanyi, K., Serve, G., & Grafe, P. (1986) · Neuroscience Letters · doi:10.1016/0304-3940(86)90617-8 · Cited by 51
Ca2+ channels from the sea urchin sperm plasma membrane.
Liévano, A., Vega-Saenzdemiera, E. C., & Darszon, A. (1990) · The Journal of General Physiology · doi:10.1085/jgp.95.2.273 · Cited by 51
Calbindin‐D28K and ischemic damage of pyramidal cells in rat hippocampus
Rami, A., Rabié, A., THOMASSET, M., & Krieglstein, J. (1992) · Journal of Neuroscience Research · doi:10.1002/jnr.490310113 · Cited by 51
Didier, M., Héaulme, M., Soubrié, P., Bockaert, J., & Pin, J. (1990) · Journal of Neuroscience Research · doi:10.1002/jnr.490270105 · Cited by 51
Mulkeen, D., Anwyl, R., & Rowan, M. J. (1987) · Neuroscience Letters · doi:10.1016/0304-3940(87)90481-2 · Cited by 51
Selective vulnerability of brain: New insights from the excitatory synapse
Collins, R. C. (1986) · Metabolic Brain Disease · doi:10.1007/bf00999353 · Cited by 51
Su, C., Hsia, S.-C., & Sun, Y. (2014) · Analytica Chimica Acta · doi:10.1016/j.aca.2014.06.037 · Cited by 50
Nakamichi, N., Ohno, H., Nakamura, Y., Hirai, T., Kuramoto, N., & Yoneda, Y. (2002) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2002.01042.x · Cited by 50
Murdoch, J. D., & Hall, R. (1990) · Canadian Journal of Anesthesia/Journal canadien d anesthésie · doi:10.1007/bf03006487 · Cited by 50
Role of nitric oxide in zymosan induced paw inflammation and thermal hyperalgesia
Gühring, H., Tegeder, I., Lötsch, J., Pahl, A. M., Werner, U., Reeh, P. W., Rehse, K., Brune, K., & Geißlinger, G. (2001) · Inflammation Research · doi:10.1007/s000110050728 · Cited by 50
The Pharmacology of Vertebrate Spinal Central Pattern Generators
Alford, S. T., Schwartz, E., & Prisco, G. V. D. (2003) · The Neuroscientist · doi:10.1177/1073858403009003014 · Cited by 50
Different receptors mediate motor neuron death induced by short and long exposures to excitotoxicity
Bosch, L. V. D., & Robberecht, W. (2000) · Brain Research Bulletin · doi:10.1016/s0361-9230(00)00371-3 · Cited by 51
ClineP, H. T., & Tsien, R. W. (1991) · Neuron · doi:10.1016/0896-6273(91)90361-3 · Cited by 50
The Role of Glutamate in Physical Dependence on Opioids
Zhu, H., Rockhold, R. W., & Ho, I. K. (1998) · The Japanese Journal of Pharmacology · doi:10.1254/jjp.76.1 · Cited by 50
Metadata
- Authors
- MacDermott, A. B., Mayer, M. L., Westbrook, G. L., Smith, S. J., & Barker, J. L.
- Affiliations
- National Institutes of Health (US)
- Yale University (US)
- Venue
- Nature
- Published
- 1986-05
- Volume
- 321
- Issue
- 6069
- Pages
- 519-522
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2010926499
- Cited by
- 1,835
- References
- 30
- Citations by year
- 2026: 8 · 2025: 11 · 2024: 14 · 2023: 12 · 2022: 13 · 2021: 15 · 2020: 18 · 2019: 22 · 2018: 15 · 2017: 17 · 2016: 19 · 2015: 20 · 2014: 29 · 2013: 23 · 2012: 24
- FWCI
- 40.51
- Type
- journal article
- Language
- en
- Update notices
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Keywords
- NMDA receptor, glutamate receptors, intracellular calcium, calcium influx, spinal cord neurons, kainic acid, voltage-gated calcium channels, magnesium block, arsenazo III, excitatory amino acid antagonists
- MeSH terms
- Animals, Aspartic Acid, Calcium, Cells, Cultured, Cytoplasm, Embryo, Mammalian, Neurons, Spinal Cord, Receptors, N-Methyl-D-Aspartate, N-Methylaspartate, Receptors, Neurotransmitter, Mice
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