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Reduced hippocampal long-term potentiation and context-specific deficit in associative learning in mGluR1 mutant mice.
Abstract
We generated a novel strain of mutant mouse with a deletion in the gene encoding metabotropic glutamate receptor 1 (mGluR1). Gross anatomy of the hippocampus, excitatory synaptic transmission, long-term depression, and short-term potentiation in the hippocampal CA1 region are all apparently normal in the mutant mice. In contrast, long-term potentiation (LTP) is substantially reduced, and a moderate level of impairment is observed in context-specific associative learning. We propose that mGluR1 is not "in line" in LTP production, but rather modulates the plasticity process, and hence affects context-specific associative learning.
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“It is important to point out that the only exceptional case, namely that of the mGluR1 mutant mice, is complicated by the fact that two groups have generated and analyzed these mutants independently and have obtained opposing results (Aiba et al., 1994; Conquet et al., 1994; Chen and Tonegawa, 1997).”
From The essential role of hippocampal CA1 NMDA receptor-dependent synaptic plasticity in spatial memory. (1996) · cites this paper as Aiba et al., 1994
In the citing paper
“Numerous studies, using lesioning (Kim and Fanselow, 1992;Phillips and LeDoux, 1992) and genetic (Aiba et al., 1994;Tsien et al., 1996) strategies, indicated that the hippocampus plays a crucial role in context-dependent fear conditioning.”
From Modulation of learning and anxiety by corticotropin-releasing factor (CRF) and stress: differential roles of CRF receptors 1 and 2 (1999) · cites this paper as Aiba et al., 1994
Citations
Cites
Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction
Chomczynski, P., & Sacchi, N. (1987) · Analytical Biochemistry · doi:10.1006/abio.1987.9999 · Cited by 65,515
Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans.
Squire, L. R. (1992) · Psychological Review · doi:10.1037/0033-295x.99.2.195 · Cited by 5,376
Morris, R. G. M., Anderson, E., Lynch, G. S., & Baudry, M. (1986) · Nature · doi:10.1038/319774a0 · Cited by 3,640
Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning.
Phillips, R. G., & LeDoux, J. E. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.2.274 · Cited by 3,292
Molecular diversity of glutamate receptors and implications for brain function
Nakanishi, S. (1992) · Science · doi:10.1126/science.1329206 · Cited by 2,543
Modality-Specific Retrograde Amnesia of Fear
Kim, J. J., & Fanselow, M. S. (1992) · Science · doi:10.1126/science.1585183 · Cited by 2,483
Dudek, S. M., & Bear, M. F. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.10.4363 · Cited by 1,708
Deficient Hippocampal Long-Term Potentiation in α-Calcium-Calmodulin Kinase II Mutant Mice
Silva, A. J., Stevens, C. F., Tonegawa, S., & Wang, Y. (1992) · Science · doi:10.1126/science.1378648 · Cited by 1,472
Impaired Spatial Learning in α-Calcium-Calmodulin Kinase II Mutant Mice
Silva, A. J., Paylor, R. E., Wehner, J. M., & Tonegawa, S. (1992) · Science · doi:10.1126/science.1321493 · Cited by 1,366
Sequence and expression of a metabotropic glutamate receptor
Masu, M., Tanabe, Y., Tsuchida, K., Shigemoto, R., & Nakanishi, S. (1991) · Nature · doi:10.1038/349760a0 · Cited by 1,216
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Long-Term Potentiation and Memory
Lynch, M. A. (2004) · Physiological Reviews · doi:10.1152/physrev.00014.2003 · Cited by 2,074
Metabotropic Glutamate Receptors: Physiology, Pharmacology, and Disease
Niswender, C. M., & Conn, P. J. (2010) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.011008.145533 · Cited by 1,889
The essential role of hippocampal CA1 NMDA receptor-dependent synaptic plasticity in spatial memory.
Tsien, J. Z., Huerta, P. T., & Tonegawa, S. (1996) · Cell · doi:10.1016/s0092-8674(00)81827-9 · Cited by 1,782
Glutamate receptors in the mammalian central nervous system
Ozawa, S., Kamiya, H., & Tsuzuki, K. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(97)00085-3 · Cited by 1,133
Shigemoto, R., Kinoshita, A., Wada, E., Nomura, S., Ohishi, H., Takada, M., Flor, P. J., Neki, A., Abe, T., Nakanishi, S., et al. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-19-07503.1997 · Cited by 1,116
Coupling of mGluR/Homer and PSD-95 Complexes by the Shank Family of Postsynaptic Density Proteins
Tu, J. C., Xiao, B., Naisbitt, S. R., Yuan, J. P., Petralia, R. S., Brakeman, P., Doan, A., Aakalu, V. K., Lanahan, A. A., Sheng, M., et al. (1999) · Neuron · doi:10.1016/s0896-6273(00)80810-7 · Cited by 1,079
Glutamate receptor function in learning and memory
Riedel, G. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00272-3 · Cited by 993
Deficient cerebellar long-term depression and impaired motor learning in mGluR1 mutant mice
Aiba, A., Kano, M., Chen, C., Stanton, M. E., Fox, G. D., Herrup, K., Zwingman, T. A., & Tonegawa, S. (1994) · Cell · doi:10.1016/0092-8674(94)90205-4 · Cited by 930
Self-citationGene-targeting studies of mammalian behavior: is it the mutation or the background genotype?
Gerlai, R. (1996) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)20020-7 · Cited by 881
Tu, J. C., Xiao, B., Yuan, J. P., Lanahan, A. A., Leoffert, K., Li, M., Linden, D. J., & Worley, P. F. (1998) · Neuron · doi:10.1016/s0896-6273(00)80589-9 · Cited by 862
Metabotropic glutamate receptors: electrophysiological properties and role in plasticity
Anwyl, R. (1999) · Brain Research Reviews · doi:10.1016/s0165-0173(98)00050-2 · Cited by 799
The Neuroscience of Mammalian Associative Learning
Fanselow, M. S., & Poulos, A. M. (2005) · Annual Review of Psychology · doi:10.1146/annurev.psych.56.091103.070213 · Cited by 683
Evolution, structure, and activation mechanism of family 3/C G-protein-coupled receptors
Pin, J.-P., Galvez, T., & Prézeau, L. (2003) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(03)00038-x · Cited by 662
Metabotropic glutamate receptors: From the workbench to the bedside
Nicoletti, F., Bockaert, J., Collingridge, G. L., Conn, P. J., Ferraguti, F., Schoepp, D. D., Wroblewski, J. T., & Pin, J. (2010) · Neuropharmacology · doi:10.1016/j.neuropharm.2010.10.022 · Cited by 680
Metabotropic glutamate receptors
Ferraguti, F., & Shigemoto, R. (2006) · Cell and Tissue Research · doi:10.1007/s00441-006-0266-5 · Cited by 682
Lu, Y.-M., Jia, Z., Janus, C., Henderson, J. T., Gerlai, R., Wojtowicz, J. M., & Roder, J. C. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-13-05196.1997 · Cited by 634
Ataxia and epileptic seizures in mice lacking type 1 inositol 1,4,5-trisphosphate receptor
Matsumoto, M., Nakagawa, T., Inoue, T., Nagata, E., Tanaka, K., Takano, H., Kuno, J., Sakakibara, S., Yamada, M., Yoneshima, H., et al. (1996) · Nature · doi:10.1038/379168a0 · Cited by 485
Distributed synergistic plasticity and cerebellar learning
Gao, Z., van Beugen, B. J., & De Zeeuw, C. I. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3312 · Cited by 479
Cerebellum-dependent learning: the role of multiple plasticity mechanisms
Boyden, E. S., Katoh, A., & Raymond, J. L. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144238 · Cited by 448
Paraneoplastic Cerebellar Ataxia Due to Autoantibodies against a Glutamate Receptor
Smitt, P. A. E. S., Kinoshita, A., de Leeuw, B., Moll, W., Coesmans, M., Jaarsma, D., Henzen-Logmans, S. C., Vecht, C. J., Zeeuw, C. I. D., Sekiyama, N., et al. (2000) · New England Journal of Medicine · doi:10.1056/nejm200001063420104 · Cited by 450
Spatiotemporal firing patterns in the cerebellum
Zeeuw, C. I. D., Hoebeek, F. E., Bosman, L. W. J., Schonewille, M., Witter, L., & Koekkoek, S. K. E. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn3011 · Cited by 411
Motor discoordination and increased susceptibility to cerebellar injury in GLAST mutant mice
Watase, K., Hashimoto, K., Kano, M., Yamada, K., Watanabe, M., Inoue, Y., Okuyama, S., Sakagawa, T., Ogawa, S., Kawashima, N., et al. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00108.x · Cited by 408
A new class of synaptic response involving calcium release in dendritic spines
Takechi, H., Eilers, J., & Konnerth, A. (1998) · Nature · doi:10.1038/25547 · Cited by 409
Ichise, T., Kano, M., Hashimoto, K., Yanagihara, D., Nakao, K., Shigemoto, R., Katsuki, M., & Aiba, A. (2000) · Science · doi:10.1126/science.288.5472.1832 · Cited by 413
Self-citationRadulovic, J., Rühmann, A., Liepold, T., & Spiess, J. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-12-05016.1999 · Cited by 402
Hermans, E., & Challiss, R. A. J. (2001) · Biochemical Journal · doi:10.1042/0264-6021:3590465 · Cited by 414
Logue, S. F., Paylor, R., & Wehner, J. M. (1997) · Behavioral Neuroscience · doi:10.1037/0735-7044.111.1.104 · Cited by 385
Cerebellar circuits and synaptic mechanisms involved in classical eyeblink conditioning
Kim, J. J., & Thompson, R. F. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)10081-3 · Cited by 358
Bosio, A., Binczek, E., & Stoffel, W. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.23.13280 · Cited by 347
Activation of the TRPC1 cation channel by metabotropic glutamate receptor mGluR1
Kim, S. J., Kim, Y. S., Yuan, J. P., Petralia, R. S., Worley, P. F., & Linden, D. J. (2003) · Nature · doi:10.1038/nature02162 · Cited by 350
Kamiya, H., Shinozaki, H., & Yamamoto, C. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021395 · Cited by 327
Can molecules explain long-term potentiation?
Sanes, J. R., & Lichtman, J. W. (1999) · Nature Neuroscience · doi:10.1038/10154 · Cited by 336
Induction of long‐term potentiation at spinal synapses by noxious stimulation or nerve injury
Sandkühler, J., & Liu, X. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00278.x · Cited by 321
Pisani, A., Gubellini, P., Bonsi, P., Conquet, F., Picconi, B., Centonze, D., Bernardi, G., & Calabresi, P. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00297-4 · Cited by 316
Miyazaki, T., Fukaya, M., Shimizu, H., & Watanabe, M. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02698.x · Cited by 310
Phospholipase C isozymes selectively couple to specific neurotransmitter receptors
Kim, D., Jun, K. S., Lee, S. B., Kang, N.-G., Min, D. S., Kim, Y.-H., Ryu, S. H., Suh, P.-G., & Shin, H.-S. (1997) · Nature · doi:10.1038/38508 · Cited by 305
Biased Receptor Signaling in Drug Discovery
Kenakin, T. (2019) · Pharmacological Reviews · doi:10.1124/pr.118.016790 · Cited by 321
Persistent Multiple Climbing Fiber Innervationof Cerebellar Purkinje Cellsin Mice Lacking mGluR1
Kano, M., Hashimoto, K., Kurihara, H., Watanabe, M., Inoue, Y., Aiba, A., & Tonegawa, S. (1997) · Neuron · doi:10.1016/s0896-6273(01)80047-7 · Cited by 308
Self-citationMelanoma mouse model implicates metabotropic glutamate signaling in melanocytic neoplasia
Pollock, P. M., Cohen-Solal, K., Sood, R. B., Namkoong, J., Martino, J. J., Koganti, A., Zhu, H., Robbins, C. M., Makałowska, I., Shin, S., et al. (2003) · Nature Genetics · doi:10.1038/ng1148 · Cited by 306
Chen, C., & Tonegawa, S. (1997) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.20.1.157 · Cited by 300
Group I metabotropic glutamate receptors: implications for brain diseases
Bordi, F., & Ugolini, A. (1999) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00095-1 · Cited by 294
Memory systems in the brain and localization of a memory
Thompson, R. F., & Kim, J. J. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.24.13438 · Cited by 300
The molecular organization of cerebellar long-term depression
Ito, M. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn962 · Cited by 294
PI3 kinase enhancer–Homer complex couples mGluRI to PI3 kinase, preventing neuronal apoptosis
Rong, R., Ahn, J.-Y., Huang, H., Nagata, E., Kalman, D., Kapp, J. A., Tu, J., Worley, P. F., Snyder, S. H., & Ye, K. (2003) · Nature Neuroscience · doi:10.1038/nn1134 · Cited by 285
Complex interactions between mGluRs, intracellular Ca2+ stores and ion channels in neurons
Fagni, L., Chavis, P., Ango, F., & Bockaert, J. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(99)01492-7 · Cited by 285
staggerer phenotype in retinoid-related orphan receptor α-deficient mice
Steinmayr, M., André, É., Conquet, F., Rondi‐Reig, L., Delhaye‐Bouchaud, N., Auclair, N., Daniel, H., Crépel, F., Mariani, J., Sotelo, C., et al. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.7.3960 · Cited by 275
Nicotinic Stimulation Produces Multiple Forms of Increased Glutamatergic Synaptic Transmission
Radcliffe, K. A., & Dani, J. A. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-18-07075.1998 · Cited by 271
Offermanns, S., Hashimoto, K., Watanabe, M., Sun, W. Y., Kurihara, H., Thompson, R. F., Inoue, Y., Kano, M., & Simon, M. I. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.25.14089 · Cited by 265
On climbing fiber signals and their consequence(s)
Simpson, J. I., WYLIE, D. R. W., & Zeeuw, C. I. D. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081486 · Cited by 252
Disruption of the Oxysterol 7α-Hydroxylase Gene in Mice
Li-Hawkins, J., Lund, E. G., Turley, S. D., & Russell, D. W. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m001811200 · Cited by 241
Manahan‐Vaughan, D. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-09-03303.1997 · Cited by 235
Disruption of Cholesterol 7α-Hydroxylase Gene in Mice
Ishibashi, S., Schwarz, M., Frykman, P. K., Herz, J., & Russell, D. W. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.30.18017 · Cited by 233
Selective Abolition of the NMDA Component of Long-Term Potentiation in Mice Lacking mGluR5Preprint
Jia, Z., Lu, Y., Henderson, J., Taverna, F. A., Romano, C., Abramow-Newerly, W., Wojtowicz, J. M., & Roder, J. (1998) · Learning & Memory · doi:10.1101/lm.5.4.331 · Cited by 240
Foster, D. J., & Conn, P. J. (2017) · Neuron · doi:10.1016/j.neuron.2017.03.016 · Cited by 231
Rose, C. R., & Konnerth, A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00402-0 · Cited by 228
Becker, E. B. E., Oliver, P. L., Glitsch, M. D., Banks, G. T., Achilli, F., Hardy, A., Nolan, P. M., Fisher, E., & Davies, K. E. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0810599106 · Cited by 223
Heidinger, V., Manzerra, P., Wang, X. Q., Strasser, U., Yu, S. P., Choi, D. W., & Behrens, M. M. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-13-05452.2002 · Cited by 223
Patterned expression of Purkinje cell glutamate transporters controls synaptic plasticity
Wadiche, J. I., & Jahr, C. E. (2005) · Nature Neuroscience · doi:10.1038/nn1539 · Cited by 220
Metabotropic glutamate receptor ligands as possible anxiolytic and antidepressant drugs
Pałucha-Poniewiera, A., & Pilc, A. (2007) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2007.04.007 · Cited by 225
LONG-TERM POTENTIATION AND LEARNING
Martinez, J. L., & Derrick, B. E. (1996) · Annual Review of Psychology · doi:10.1146/annurev.psych.47.1.173 · Cited by 219
PLC-β1, activated via mGluRs, mediates activity-dependent differentiation in cerebral cortex
Hannan, A. J., Blakemore, C. B., Katsnelson, A., Vitalis, T., Huber, K. M., Bear, M. F., Roder, J., Kim, D., Shin, H., & Kind, P. C. (2001) · Nature Neuroscience · doi:10.1038/85132 · Cited by 214
Metabotropic Glutamate 1 Receptor: Current Concepts and Perspectives
Ferraguti, F., Crepaldi, L., & Nicoletti, F. (2008) · Pharmacological Reviews · doi:10.1124/pr.108.000166 · Cited by 218
Structural Basis for a Ca 2+ -Sensing Function of the Metabotropic Glutamate Receptors
Kubo, Y., Miyashita, T., & Murata, Y. (1998) · Science · doi:10.1126/science.279.5357.1722 · Cited by 212
Reexamination of the effects of MCPG on hippocampal LTP, LTD, and depotentiation
Selig, D. K., Lee, H., Bear, M. F., & Malenka, R. C. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.74.3.1075 · Cited by 211
Regulation of metabotropic glutamate receptor signaling, desensitization and endocytosis
Dhami, G. K., & Ferguson, S. S. G. (2006) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2005.01.008 · Cited by 219
Metabotropic Glutamate Receptor Ligands as Potential Therapeutics for Addiction
Olive, M. F. (2009) · Current Drug Abuse Reviews · doi:10.2174/1874473710902010083 · Cited by 207
Boulware, M. I., Heisler, J. D., & Frick, K. M. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1716-13.2013 · Cited by 196
Regional distribution of neurotrophin receptors in the developing auditory brainstem
Hafidi, A., Moore, T., & Sanes, D. H. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960408)367:3 · Cited by 51
Kano, M., Hashimoto, K., Watanabe, M., Kurihara, H., Offermanns, S., Jiang, H., Wu, Y., Jun, K., Shin, H., Inoue, Y., et al. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.26.15724 · Cited by 194
Roles of metabotropic glutamate receptors in LTP and LTD in
Bortolotto, Z. A., Fitzjohn, S. M., & Collingridge, G. L. (1999) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(99)80044-0 · Cited by 193
Brain dystrophin, neurogenetics and mental retardation
Mehler, M. F. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00090-9 · Cited by 192
Varney, M. A., Cosford, N. D. P., Jachec, C., Rao, S. P., Sacaan, A. I., Lin, F., Bleicher, L. S., Santori, E. M., Flor, P. J., Allgeier, H., et al. (1999) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)34881-5 · Cited by 189
Arendt, T. (2003) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2003.09.007 · Cited by 189
Toward a Molecular Explanation for Long-Term PotentiationPreprint
Sweatt, J. D. (1999) · Learning & Memory · doi:10.1101/lm.6.5.399 · Cited by 193
Using Knockout and Transgenic Mice to Study Neurophysiology and Behavior
Picciotto, M. R., & Wickman, K. (1998) · Physiological Reviews · doi:10.1152/physrev.1998.78.4.1131 · Cited by 189
Mechanisms underlying cerebellar motor deficits due to mGluR1‐autoantibodies
Coesmans, M., Smitt, P. A. E. S., Linden, D. J., Shigemoto, R., Hirano, T., Yamakawa, Y., van Alphen, A. M., Luo, C., van der Geest, J. N., Kros, J. M., et al. (2002) · Annals of Neurology · doi:10.1002/ana.10451 · Cited by 188
Phenylglycine derivatives discriminate between mGluR1- and mGluR5-mediated responses
Brabet, I., Mary, S., Bockaert, J., & Pin, J. (1995) · Neuropharmacology · doi:10.1016/0028-3908(95)00079-l · Cited by 178
Spooren, W. P. J. M., Ballard, T. M., Gasparini, F., Amalric, M., Mutel, V., & Schreiber, R. (2003) · Behavioural Pharmacology · doi:10.1097/01.fbp.0000081783.35927.8f · Cited by 178
Pharmacological Characterization of 1-Aminoindan-1,5-dicarboxylic Acid, a Potent mGluR1 Antagonist
Moroni, F., Lombardi, G., Thomsen, C., Leonardi, P., Attucci, S., Peruginelli, F., Albani-Torregrossa, S., Pellegrini-Giampietro, D. E., Luneia, R., & Pellicciari, R. (1997) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)36672-8 · Cited by 177
Cerebellar long-term depression might normalize excitation of Purkinje cells: a hypothesis
Schutter, E. D. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)93916-l · Cited by 168
Qi, M., Zhuo, M., Skålhegg, B. S., Brandon, E. P., Kandel, E. R., McKnight, G. S., & Idzerda, R. L. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.4.1571 · Cited by 169
Quantitative trait locus analysis of contextual fear conditioning in mice
Wehner, J. M., Radcliffe, R. A., Rosmann, S. T., Christensen, S. C., Rasmussen, D. L., Fulker, D. W., & Wiles, M. (1997) · Nature Genetics · doi:10.1038/ng1197-331 · Cited by 163
Ligand-induced rearrangement of the dimeric metabotropic glutamate receptor 1α
Tateyama, M., Abe, H., Nakata, H., Saito, O., & Kubo, Y. (2004) · Nature Structural & Molecular Biology · doi:10.1038/nsmb770 · Cited by 166
Turco, E., Tang, W., Topham, M. K., Sakane, F., Marcheselli, V. L., Chen, C., Taketomi, A., Prescott, S. M., & Bazan, N. G. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.081536298 · Cited by 166
Komatsu, Y. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-20-06342.1996 · Cited by 159
Fitzjohn, S. M., Bortolotto, Z. A., Palmer, M. J., Doherty, A., Ornstein, P. L., Schoepp, D. D., Kingston, A. E., Lodge, D., & Collingridge, G. L. (1998) · Neuropharmacology · doi:10.1016/s0028-3908(98)00145-2 · Cited by 161
Naie, K. (2003) · Cerebral Cortex · doi:10.1093/cercor/bhg118 · Cited by 160
Cerebellar plasticity and motor learning deficits in a copy-number variation mouse model of autism
Piochon, C., Kloth, A. D., Grasselli, G., Titley, H. K., Nakayama, H., Hashimoto, K., Wan, V., Simmons, D. H., Eissa, T. L., Nakatani, J., et al. (2014) · Nature Communications · doi:10.1038/ncomms6586 · Cited by 163
Application of an optogenetic byway for perturbing neuronal activity via glial photostimulation
Sasaki, T., Beppu, K., Tanaka, K. F., Fukazawa, Y., Shigemoto, R., & Matsui, K. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1213458109 · Cited by 156
Long-Term Depression: A Cellular Basis for Learning?
Braunewell, K., & Manahan‐Vaughan, D. (2001) · Reviews in the Neurosciences · doi:10.1515/revneuro.2001.12.2.121 · Cited by 160
Get receptive to metabotropic glutamate receptors
Pin, J., & Bockaert, J. (1995) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(95)80047-6 · Cited by 160
Volk, L. J., Daly, C. A., & Huber, K. M. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00383.2005 · Cited by 153
Quantitative trait loci analysis affecting contextual conditioning in mice
Caldarone, B. J., Saavedra, C., Tartaglia, K., Wehner, J. M., Dudek, B. C., & Flaherty, L. A. (1997) · Nature Genetics · doi:10.1038/ng1197-335 · Cited by 148
Role of metabotropic glutamate receptors in persistent forms of hippocampal plasticity and learning
Mukherjee, S., & Manahan‐Vaughan, D. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.06.005 · Cited by 151
Book Review: Metabotropic Glutamate Receptors: Electrical and Chemical Signaling Properties
Coutinho, V., & Knöpfel, T. (2002) · The Neuroscientist · doi:10.1177/1073858402238514 · Cited by 144
Gerlai, R. T., Wojtowicz, J. M., Marks, A., & Roder, J. (1995) · Learning & Memory · doi:10.1101/lm.2.1.26 · Cited by 144
Neyman, S., & Manahan‐Vaughan, D. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06109.x · Cited by 149
Hippocampal lesions impair contextual fear conditioning in two strains of mice.
Chen, C., Kim, J. J., Thompson, R. F., & Tonegawa, S. (1996) · Behavioral Neuroscience · doi:10.1037/0735-7044.110.5.1177 · Cited by 148
Behavioural performance in three substrains of mouse strain 129
Montkowski, A., Poettig, M., Mederer, A., & Holsboer, F. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00370-3 · Cited by 144
Bagot, R. C., Zhang, T.-Y., Wen, X., Nguyen, T. T. T., Nguyen, H.-B., Diorio, J., Wong, T. P., & Meaney, M. J. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1204599109 · Cited by 141
Metadata
- Authors
- Aiba, A.
- Affiliations
- Howard Hughes Medical Institute (US)
- Corresponding author
- Aiba, A
- ORCID
- Aiba, A
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 1994-10-21
- Volume
- 79
- Issue
- 2
- Pages
- 365-375
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W1983956991
- Cited by
- 614
- References
- 49
- Citations by year
- 2026: 3 · 2025: 2 · 2024: 1 · 2023: 7 · 2022: 10 · 2021: 13 · 2020: 14 · 2019: 11 · 2018: 5 · 2017: 9 · 2016: 14 · 2015: 14 · 2014: 13 · 2013: 12 · 2012: 21
- FWCI
- 16.15
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Rare & Special e-Zone (The Hong Kong University of Science and Technology) (submittedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01 NS32925, R01NS020591, NS20591, R01NS032925)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Keywords
- metabotropic glutamate receptor 1, hippocampal long-term potentiation, hippocampal CA1, synaptic plasticity, long-term depression, short-term potentiation, excitatory synaptic transmission, learning disabilities
- MeSH terms
- Animals, Base Sequence, Electric Stimulation, Female, Genes, Hippocampus, Male, Mice, Inbred C57BL, Molecular Sequence Data, Synaptic Transmission, Neuronal Plasticity, Restriction Mapping, Receptors, Glutamate, Long-Term Potentiation, DNA Primers, Mice, Knockout, Mice, In Vitro Techniques
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