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Intracellular injections of EGTA block induction of hippocampal long-term potentiation
Abstract
Hippocampal long-term potentiation (LTP) is a remarkably stable facilitation of synaptic responses resulting from very brief trains of high-frequency stimulation. Because of its persistence and modest induction conditions, LTP represents a promising candidate for a substrate of memory. Some progress has been made in localizing the changes responsible for the effect; for example, it has been shown that LTP is not accompanied by changes in the fibre volleys of the test afferents or by generalized alterations of the dendrites of their target cells. However, it is unknown whether the potentiation is due to pre- or postsynaptic changes and there is evidence in favour of each (for example, see refs 5, 6). We now report that intracellular injections of the calcium chelator EGTA block the development of LTP. These results strongly suggest that LTP is caused by a modification of the postsynaptic neurone and that its induction depends on the level of free calcium.
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“loading postsynaptic cells with the Ca2+ chelator EGTA blocked LTP (176), suggesting that Ca2+ is necessary for LTP.”
From Synaptic memory and CaMKII (2023) · cites this paper as [176]
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Cites
Bliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,424
A calcium-activated hyperpolarization follows repetitive firing in hippocampal neurons
Hotson, J. R., & Prince, D. A. (1980) · Journal of Neurophysiology · doi:10.1152/jn.1980.43.2.409 · Cited by 569
Dunwiddie, T. V., & LYNCH, G. S. (1978) · The Journal of Physiology · doi:10.1113/jphysiol.1978.sp012239 · Cited by 479
Self-citationAlger, B. E., & Nicoll, R. A. (1980) · Science · doi:10.1126/science.7444438 · Cited by 421
Afterpotential generation in hippocampal pyramidal cells.
Wong, R. K. S., & Prince, D. A. (1981) · Journal of Neurophysiology · doi:10.1152/jn.1981.45.1.86 · Cited by 391
Long-term potentiation of the perforant path in vivo is associated with increased glutamate release
DOLPHIN, A. C., Errington, M. L., & Bliss, T. V. P. (1982) · Nature · doi:10.1038/297496a0 · Cited by 389
Andersen, P. N., Sundberg, S. H., Sveen, O., Swann, J. W., & Wigström, H. (1980) · The Journal of Physiology · doi:10.1113/jphysiol.1980.sp013256 · Cited by 366
Effects of EGTA on the Calcium-Activated Afterhyperpolarization in Hippocampal CA3 Pyramidal Cells
Schwartzkroin, P. A., & Stafstrom, C. E. (1980) · Science · doi:10.1126/science.6777871 · Cited by 275
Dunwiddie, T. V., & LYNCH, G. S. (1979) · Brain Research · doi:10.1016/0006-8993(79)90377-9 · Cited by 234
Self-citationMicromolar Calcium Stimulates Proteolysis and Glutamate Binding in Rat Brain Synaptic Membranes
Baudry, M., Bundman, M. C., Smith, E. K., & LYNCH, G. S. (1981) · Science · doi:10.1126/science.7015504 · Cited by 181
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Flagged first, then by citations
Research works printed but not linked: 2
- Bliss, T. V. P. & Lomo, T. J. Physiol., Lond. 232, 331–356 (1973). · DOI · Paper page
- Lee, K., Oliver, M., Schottler, F. & Lynch, G. in Electrical Activity in Isolated Mammalian CNS Preparations (eds Kerkut, G. & Wheal, H. V.) 189–212 (Academic, New York, 1981).
Cited by
Sorted by citations
Items 301–400 of 1,000
Opposing Effects of Neuronal Activity on Structural Plasticity
Fauth, M. J., & Tetzlaff, C. (2016) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2016.00075 · Cited by 110
Cruikshank, S. J., & Weinberger, N. M. (1996) · Brain Research Reviews · doi:10.1016/s0165-0173(96)00015-x · Cited by 102
Huber, K. M., Mauk, M. D., & Kelly, P. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.73.1.270 · Cited by 102
The substrates of memory: Defects, treatments, and enhancement
LYNCH, G. S., Rex, C. S., Chen, L. Y., & Gall, C. M. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.11.082 · Cited by 103
Self-citationRison, R. A., & Stanton, P. K. (1995) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(95)00017-8 · Cited by 102
Sah, P., & Nicoll, R. A. (1991) · The Journal of Physiology · doi:10.1113/jphysiol.1991.sp018446 · Cited by 122
Unpredictable and uncontrollable stress impairs neuronal plasticity in the rat hippocampus
Shors, T. J., Foy, M. R., Levine, S., & Thompson, R. F. (1990) · Brain Research Bulletin · doi:10.1016/0361-9230(90)90005-k · Cited by 100
Dendritic Spines: Convergence of Theory and Experiment
Christof Koch, A., Zador, A. M., & Brown, T. H. (1992) · Science · doi:10.1126/science.1589781 · Cited by 99
Ishiyama, J., Saitō, H., & Abe, K. (1991) · Neuroscience Research · doi:10.1016/0168-0102(91)90071-6 · Cited by 99
Hirsch, J. C., & Crépel, F. (1992) · Synapse · doi:10.1002/syn.890100211 · Cited by 99
Nitric oxide and hippocampal synaptic plasticity.
Zorumski, C., & Izumi, Y. (1993) · Biochemical Pharmacology · doi:10.1016/0006-2952(93)90484-e · Cited by 102
Activity Shapes Neural Circuit Form and Function: A Historical Perspective
Pan, Y., & Monje, M. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0740-19.2019 · Cited by 98
Wang, Y., Wu, J., Rowan, M. J., & Anwyl, R. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021631 · Cited by 98
Calcium flux-independent NMDA receptor activity is required for Aβ oligomer-induced synaptic loss
Birnbaum, J. H., Bali, J., Rajendran, L., Nitsch, R. M., & Tackenberg, C. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.160 · Cited by 101
Multideterminant role of calcium in hippocampal synaptic plasticity
Teyler, T. J., Cavus, I., Coussens, C., DiScenna, P. G., Grover, L. M., Lee, Y. P., & Little, Z. (1994) · Hippocampus · doi:10.1002/hipo.450040602 · Cited by 98
A spike-timing-dependent plasticity rule for dendritic spines
Tazerart, S., Mitchell, D. E., Miranda‐Rottmann, S., & Araya, R. (2020) · Nature Communications · doi:10.1038/s41467-020-17861-7 · Cited by 95
Metabotropic Glutamate Receptor-Mediated LTD Involves Two Interacting Ca2+ Sensors, NCS-1 and PICK1
Jo, J., Seok, H., Kim, M. J., Son, G. H., Park, Y., Henley, J. M., Weiss, J. L., Sheng, M., Collingridge, G. L., & Cho, K. (2008) · Neuron · doi:10.1016/j.neuron.2008.10.050 · Cited by 99
Mutational and biophysical studies suggest RC3/neurogranin regulates calmodulin availability.
Gerendasy, D. D., Herron, S. R., Watson, J. B., & Sutcliffe, J. G. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)31806-9 · Cited by 96
Benke, T. A., Jones, O., Collingridge, G. L., & Angelides, K. J. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.16.7819 · Cited by 97
Complexity of calcium signaling in synaptic spines
Franks, K. M., & B, T. J. S. A. (2002) · BioEssays · doi:10.1002/bies.10193 · Cited by 98
Vitórica, J., & Satrústegui, J. (1986) · Brain Research · doi:10.1016/0006-8993(86)90284-2 · Cited by 95
Bengtson, C. P., & Bading, H. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-3-7091-0932-8_17 · Cited by 101
Staubli, U. V., Larson, J., Thibault, O., Baudry, M., & LYNCH, G. S. (1988) · Brain Research · doi:10.1016/0006-8993(88)90922-5 · Cited by 94
Self-citationNeurophysiology and pharmacology of long‐term potentiation in the rat sympathetic ganglion.
Briggs, C. A., Brown, T. H., & McAfee, D. A. (1985) · The Journal of Physiology · doi:10.1113/jphysiol.1985.sp015599 · Cited by 94
Glial Cell Line-derived Neurotrophic Factor Increases Intracellular Calcium Concentration
Pérez‐García, M. J., Ceña, V., de Pablo, Y., Llovera, M., Comella, J. X., & Soler, R. M. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m308367200 · Cited by 93
Onset Characteristics of Long‐Term Potentiation in the Guinea‐Pig Hippocampal CA1 Region in Vitro
Gustafsson, B., Asztély, F., Hanse, E., & Wigström, H. (1989) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1989.tb00803.x · Cited by 93
Anoxia reveals a vulnerable period in the development of long-term potentiation
Arai, A., Larson, J., & LYNCH, G. S. (1990) · Brain Research · doi:10.1016/0006-8993(90)90184-d · Cited by 93
Self-citationLong-Term Potentiation in Two Synaptic Systems of the Hippocampal Brain Slice
Brown, T. H., Ganong, A. H., Kairiss, E. W., Keenan, C. L., & Kelso, S. R. (1989) · Elsevier eBooks · doi:10.1016/b978-0-12-148955-7.50018-7 · Cited by 92
Self-citationDlx1andDlx2Promote Interneuron GABA Synthesis, Synaptogenesis, and Dendritogenesis
Pla, R., Stanco, A., Howard, M. A., Rubin, A. N., Vogt, D. L., Mortimer, N., Cobos, I., Potter, G. B., Lindtner, S., Price, J. D., et al. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx241 · Cited by 103
Long‐term potentiation requires activation of calcium‐independent phospholipase A2
Wolf, M. J., Izumi, Y., Zorumski, C. F., & Gross, R. W. (1995) · FEBS Letters · doi:10.1016/0014-5793(95)01371-7 · Cited by 92
Müller, W. S., & Connor, J. A. (1991) · Neuron · doi:10.1016/0896-6273(91)90230-w · Cited by 92
O’Carroll, C., & Morris, R. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.04.005 · Cited by 95
Is backpropagation biologically plausible?
Stork (1989) · International Joint Conference on Neural Networks (IJCNN) · doi:10.1109/ijcnn.1989.118705 · Cited by 91
Dissecting the Components of Long-Term Potentiation
Blundon, J. A., & Zakharenko, S. S. (2008) · The Neuroscientist · doi:10.1177/1073858408320643 · Cited by 91
Synaptic changes induced by melanocortin signalling
Caruso, V., Lagerström, M. C., Olszewski, P. K., Fredriksson, R., & Schiöth, H. B. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3657 · Cited by 90
Sick, T. J., Pérez‐Pinzón, M. A., & Feng, Z.-Z. (1998) · Brain Research · doi:10.1016/s0006-8993(97)01418-2 · Cited by 89
The protease inhibitor leupeptin interferes with the development of LTP in hippocampal slices
Oliver, M. W., Baudry, M., & LYNCH, G. S. (1989) · Brain Research · doi:10.1016/0006-8993(89)91448-0 · Cited by 88
Self-citationCavazzini, M., Bliss, T., & Emptage, N. J. (2005) · Cell Calcium · doi:10.1016/j.ceca.2005.06.013 · Cited by 93
Kim, Y., Hsu, C.-L., Cembrowski, M. S., Mensh, B. D., & Spruston, N. (2015) · eLife · doi:10.7554/elife.06414 · Cited by 90
Toxic effects of aluminium on nerve cells and synaptic transmission
Meiri, H., Banin, E., Roll, M., & ROUSSEAU, A. (1993) · Progress in Neurobiology · doi:10.1016/0301-0082(93)90049-x · Cited by 91
Free radicals accelerate the decay of long-term potentiation in field CA1 of guinea-pig hippocampus.
Pellmar, T., Hollinden, G., & Sarvey, J. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90060-2 · Cited by 94
Stanton, P. K., Módy, I., & Heinemann, U. (1989) · Experimental Brain Research · doi:10.1007/bf00249605 · Cited by 88
Mizuno, T., Kanazawa, I., & Sakurai, M. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01679.x · Cited by 87
ATP-induced synaptic potentiation in hippocampal slices
Wieraszko, A., & Seyfried, T. N. (1989) · Brain Research · doi:10.1016/0006-8993(89)90070-x · Cited by 87
Xiong, H., Zeng, Y., Lewis, T. B., Zheng, J., Persidsky, Y., & Gendelman, H. E. (2000) · PubMed · Cited by 85
Cummings, J., Nicola, S. M., & Malenka, R. C. (1994) · Neuroscience Letters · doi:10.1016/0304-3940(94)90883-4 · Cited by 85
Taurine Regulates Mitochondrial Calcium Homeostasis
Idrissi, A. E., & Trenkner, E. (2003) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-0077-3_63 · Cited by 84
Geometry of Dendritic Spines Affects Calcium Dynamics in Hippocampal Neurons: Theory and Experiments
Volfovsky, N., Parnas, H., Segal, M., & Korkotian, E. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.1.450 · Cited by 84
Massicotte, G., Oliver, M. W., LYNCH, G. S., & Baudry, M. (1990) · Brain Research · doi:10.1016/0006-8993(90)90338-c · Cited by 84
Self-citationInduction and expression of GluA1 (GluR‐A)‐independent LTP in the hippocampus
Romberg, C., Raffel, J., Martin, L., Sprengel, R., Seeburg, P. H., Rawlins, J. N. P., Bannerman, D. M., & Paulsen, O. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06677.x · Cited by 82
Signaling in dendritic spines and spine microdomains
Chen, Y., & Sabatini, B. L. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.03.003 · Cited by 83
Smeets, W. J. A. J., Alonso, J. R., & Gonz�lez, A. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970106)377:1 · Cited by 71
Gold, J. I., & Bear, M. F. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.9.3941 · Cited by 84
Derivation of Encoding Characteristics of Layer II Cerebral Cortex
Granger, R., Ambros‐Ingerson, J., & LYNCH, G. S. (1989) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1989.1.1.61 · Cited by 82
Self-citationModulation of synaptic plasticity by exercise
Bettio, L. E. B., Thacker, J. S., Hutton, C. P., & Christie, B. R. (2019) · International review of neurobiology · doi:10.1016/bs.irn.2019.07.002 · Cited by 87
Stable and functional expression of the CIC-3 chloride channel in somatic cell lines
Kawasaki, M., Suzuki, M., Uchida, S., Sasaki, S., & Marumo, F. (1995) · Neuron · doi:10.1016/0896-6273(95)90275-9 · Cited by 81
Presynaptic enhancement of synaptic transmission in hippocampal cell cultures by phorbol esters
Finch, D. M., & Jackson, M. B. (1990) · Brain Research · doi:10.1016/0006-8993(90)90979-l · Cited by 81
Regehr, W. G., & Tank, D. W. (1991) · Neuron · doi:10.1016/0896-6273(91)90297-d · Cited by 80
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O’Donnell, C., Nolan, M. F., & van Rossum, M. C. W. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2520-11.2011 · Cited by 78
Yoshii, M., & Watabe, S. (1994) · Brain Research · doi:10.1016/0006-8993(94)90913-x · Cited by 79
Chen, N., Chen, X., & Wang, J. (2008) · Journal of Cell Science · doi:10.1242/jcs.022368 · Cited by 73
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Wang, J., Ko, G. Y. ‐., & Kelly, P. T. (1997) · Journal of Clinical Neurophysiology · doi:10.1097/00004691-199707000-00002 · Cited by 74
Jeon, S. J., Rhee, S. Y., Seo, J. E., Bak, H.-R., Lee, S. H., Ryu, J. H., Cheong, J. H., Shin, C. Y., Kim, G., Lee, Y. S., et al. (2010) · Neuroscience Research · doi:10.1016/j.neures.2010.11.008 · Cited by 77
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Fitzjohn, S. M., & Collingridge, G. L. (2002) · Cell Calcium · doi:10.1016/s0143416002001999 · Cited by 77
Cooke, S. F., Wu, J., Plattner, F., Errington, M., Rowan, M., Peters, M., Hirano, A., Bradshaw, K. D., Anwyl, R., Bliss, T. V. P., et al. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.111559 · Cited by 77
Coan, E. J., & Collingridge, G. L. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90192-8 · Cited by 78
Doy�re, V., Errington, M. L., Laroche, S., & Bliss, T. V. P. (1996) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:1 · Cited by 79
Self-citationRegehr, W. G., & Tank, D. W. (1994) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(94)90099-x · Cited by 74
Inuzuka, T., Tamura, A., Sato, S., Kirino, T., Yanagisawa, K., Toyoshima, I., & Miyatake, T. (1990) · Stroke · doi:10.1161/01.str.21.6.917 · Cited by 77
Furuya, S., Ohmori, H., Shigemoto, T., & Sugiyama, H. (1989) · The Journal of Physiology · doi:10.1113/jphysiol.1989.sp017702 · Cited by 77
A model of bidirectional synaptic plasticity: From signaling network to channel conductancePreprint
Castellani, G., Quinlan, E. M., Bersani, F., Cooper, L. N., & Shouval, H. Z. (2005) · Learning & Memory · doi:10.1101/lm.80705 · Cited by 77
Cooke, S. F., & Bear, M. F. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.09.006 · Cited by 77
The calcium sensor Copine-6 regulates spine structural plasticity and learning and memory
Reinhard, J. R., Kriz, A., Galic, M., Angliker, N., Rajalu, M., Vogt, K. E., & Rüegg, M. A. (2016) · Nature Communications · doi:10.1038/ncomms11613 · Cited by 77
Long-term potentiation: Persisting problems and recent results
LYNCH, G. S., Müller, D., Seubert, P. A., & Larson, J. (1988) · Brain Research Bulletin · doi:10.1016/0361-9230(88)90148-7 · Cited by 77
Self-citationWigström, H., Gustafsson, B., & Huang, Y.-Y. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90080-1 · Cited by 76
Cellular investigations of behavioral reinforcement
Stein, L., & Belluzzi, J. D. (1989) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(89)80014-4 · Cited by 76
Caruana, D. A., Alexander, G. M., & Dudek, S. M. (2012) · Learning & Memory · doi:10.1101/lm.025304.111 · Cited by 81
Costello, D. A., Claret, M., Al‐Qassab, H., Plattner, F., Irvine, E. E., Choudhury, A. I., Giese, K.-P., Withers, D. J., & Pedarzani, P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031124 · Cited by 73
Integrins Modulate Fast Excitatory Transmission at Hippocampal Synapses
Kramár, E. A., Bernard, J. A., Gall, C. M., & LYNCH, G. S. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m210225200 · Cited by 75
Self-citationA Role For Glial Cells in Activity-Dependent Central Nervous Plasticity? Review and Hypothesis
Müller, C. M. (1992) · International review of neurobiology · doi:10.1016/s0074-7742(08)60099-9 · Cited by 77
Modulation of Neuronal Signal Transduction Systems by Extracellular ATP
Ehrlich, Y. H., Snider, R. M., Kornecki, E., Garfield, M. G., & Lenox, R. H. (1988) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1988.tb13263.x · Cited by 75
Oxidation-induced persistent activation of protein kinase C in hippocampal homogenates.
Palumbo, E., Sweatt, J., Chen, S.-J. J., & Klann, E. (1992) · Biochemical and Biophysical Research Communications - BBRC · doi:10.1016/0006-291x(92)90463-u · Cited by 80
Horizontal long-term potentiation of responses in rat somatosensory cortex
Lee, S. M., Weisskopf, M. G., & Ebner, F. F. (1991) · Brain Research · doi:10.1016/0006-8993(91)90069-8 · Cited by 75
Calcium, Reactive Oxygen Species, and Synaptic Plasticity
Hidalgo, C., & Arias‐Cavieres, A. (2016) · Physiology · doi:10.1152/physiol.00038.2015 · Cited by 75
Jester, J. M., Campbell, L. W., & B, T. J. S. A. (1995) · The Journal of Physiology · doi:10.1113/jphysiol.1995.sp020696 · Cited by 74
Tsubokawa, H., Oguro, K., Robinson, H. P. C., Masuzawa, T., Kirino, T., & Kawai, N. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90358-9 · Cited by 74
Degeneracy in hippocampal physiology and plasticity
Rathour, R. K., & Narayanan, R. (2019) · Hippocampus · doi:10.1002/hipo.23139 · Cited by 78
Up‐regulation of NMDAR1 subunit gene expression in cortical neurons via a PKA‐dependent pathway
Lau, G. C., Saha, S., Faris, R., & Russek, S. J. (2004) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.02156.x · Cited by 72
Modulation of Synaptic Plasticity by Exercise Training as a Basis for Ischemic Stroke Rehabilitation
Nie, J., & Yang, X. (2016) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-016-0348-1 · Cited by 73
Lestienne, R., & Strehler, B. L. (1987) · Brain Research · doi:10.1016/0006-8993(87)91638-6 · Cited by 71
Katsuki, H., Kaneko, S., Tajima, A., & Satoh, M. (1991) · Neuroscience Research · doi:10.1016/0168-0102(91)90070-f · Cited by 72
Belfield, J. L., Whittaker, C., Cader, M. Z., & Chawla, S. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m601485200 · Cited by 69
Freir, D. B., & Herron, C. E. (2003) · Brain Research · doi:10.1016/s0006-8993(02)04190-2 · Cited by 69
Nuclear calcium: a key regulator of gene expression
Hardingham, G. E., & Bading, H. (1998) · BioMetals · doi:10.1023/a:1009257909785 · Cited by 69
Ramakers, G. M. J., Pasinelli, P., Hens, J. J. H., Gispen, W. H., & Graan, P. N. E. D. (1997) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(97)00013-4 · Cited by 68
Lynch, M. A., Errington, M. L., & Bliss, T. (1985) · Neuroscience Letters · doi:10.1016/0304-3940(85)90295-2 · Cited by 69
Calcium-Sensing Receptor: A Key Target for Extracellular Calcium Signaling in Neurons
Jones, B., & Smith, S. M. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00116 · Cited by 67
Bramham, C. R., Milgram, N. W., & Srebro, B. (1991) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1991.tb00062.x · Cited by 67
Drago, A., Crisafulli, C., Sidoti, A., & Serretti, A. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.05.009 · Cited by 71
Cellular, molecular, and genetic substrates underlying the impact of nicotine on learning
Gould, T. J., & Leach, P. T. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.08.004 · Cited by 72
Metadata
- Authors
- Lynch, G., Larson, J., Kelso, S., Barrionuevo, G., & Schottler, F.
- Affiliations
- University of California, Irvine (US)
- ORCID
- Lynch, Gary
- Venue
- Nature
- Published
- 1983-10
- Volume
- 305
- Issue
- 5936
- Pages
- 719-721
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2031739172
- Cited by
- 1,116
- References
- 16
- Citations by year
- 2026: 6 · 2025: 9 · 2024: 11 · 2023: 7 · 2022: 10 · 2021: 9 · 2020: 9 · 2019: 25 · 2018: 18 · 2017: 14 · 2016: 16 · 2015: 19 · 2014: 17 · 2013: 19 · 2012: 28
- FWCI
- 6.65
- Type
- journal article
- Language
- en
- 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 › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- long-term potentiation, hippocampus, EGTA, calcium chelation, intracellular injection, free calcium, synaptic plasticity, memory substrate, high-frequency stimulation
- MeSH terms
- Animals, Calcium, Egtazic Acid, Electric Stimulation, Ethylene Glycols, Evoked Potentials, Hippocampus, Membrane Potentials, Time Factors, Rats
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 ›
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