The DOI matches its Crossref record; 2,576 of the 2,576 references it cites were found in a registry or an index.
Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels
Open accessAbstract
Many physiologic effects of l-glutamate, the major excitatory neurotransmitter in the mammalian central nervous system, are mediated via signaling by ionotropic glutamate receptors (iGluRs). These ligand-gated ion channels are critical to brain function and are centrally implicated in numerous psychiatric and neurologic disorders. There are different classes of iGluRs with a variety of receptor subtypes in each class that play distinct roles in neuronal functions. The diversity in iGluR subtypes, with their unique functional properties and physiologic roles, has motivated a large number of studies. Our understanding of receptor subtypes has advanced considerably since the first iGluR subunit gene was cloned in 1989, and the research focus has expanded to encompass facets of biology that have been recently discovered and to exploit experimental paradigms made possible by technological advances. Here, we review insights from more than 3 decades of iGluR studies with an emphasis on the progress that has occurred in the past decade. We cover structure, function, pharmacology, roles in neurophysiology, and therapeutic implications for all classes of receptors assembled from the subunits encoded by the 18 ionotropic glutamate receptor genes. SIGNIFICANCE STATEMENT: Glutamate receptors play important roles in virtually all aspects of brain function and are either involved in mediating some clinical features of neurological disease or represent a therapeutic target for treatment. Therefore, understanding the structure, function, and pharmacology of this class of receptors will advance our understanding of many aspects of brain function at molecular, cellular, and system levels and provide new opportunities to treat patients.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The cited source says what the claim attributes to it.
In the citing paper
“NMDARs are heterotetrameric ligand-gated ionotropic receptors”
From Mechanisms of ketamine and its metabolites as antidepressants (2022) · cites this paper as Hansen et al., 2021
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Items 2,401–2,576 of 2,576
Delaney, A., Power, J., & Sah, P. (2011) · Journal of Neurophysiology · doi:10.1152/jn.01066.2011 · Cited by 17
Benedetto, D. D., Musumeci, S. A., Avola, E., Alberti, A., Buono, S., Scuderi, C., Grillo, L., Galesi, O., Spalletta, A., Giudice, M. L., et al. (2014) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.36570 · Cited by 17
Sheng, Z., Prorok, M., & Castellino, F. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.07.056 · Cited by 17
Sheng, Z., Liang, Z., Geiger, J. H., et al. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.04.014 · Cited by 17
Li, M., Zhang, D., Wang, X., et al. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.06.170 · Cited by 17
Lim, K. S., Cheong, K.-L., & Tan, C. (2010) · Lupus · doi:10.1177/0961203309351539 · Cited by 17
Cao, J., Qiu, S., Zhang, J., Wang, J., Zhang, X., & Luo, J. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.235333 · Cited by 17
Distinct regions within the GluN2C subunit regulate the surface delivery of NMDA receptors
Hemelíková, K., Kaniaková, M., Skřenková, K., Vyklický, L., & Hořák, M. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00375 · Cited by 17
Mesic, I., Madry, C., Geider, K., et al. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.01.014 · Cited by 17
GluA1 signal peptide determines the spatial assembly of heteromeric AMPA receptors
He, X.-Y., Li, Y., Kalyanaraman, C., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1524358113 · Cited by 17
Tamborini, L., Chen, Y., Foss, C. A., et al. (2016) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.6b01344 · Cited by 17
Sapkota, K., Irvine, M. W., Fang, G., Burnell, E. S., Bannister, N. J., Volianskis, A., Culley, G. R., Dravid, S. M., Collingridge, G. L., Jane, D. E., et al. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.07.007 · Cited by 17
Unitary Properties of AMPA Receptors with Reduced Desensitization
Zhang, W., Eibl, C., Weeks, A. M., et al. (2017) · Biophysical Journal · doi:10.1016/j.bpj.2017.07.030 · Cited by 17
NRAP-1 Is a Presynaptically Released NMDA Receptor Auxiliary Protein that Modifies Synaptic Strength
Lei, N., Mellem, J. E., Brockie, P. J., Madsen, D. M., & Maricq, A. V. (2017) · Neuron · doi:10.1016/j.neuron.2017.11.019 · Cited by 17
Neto-α Controls Synapse Organization and Homeostasis at the Drosophila Neuromuscular Junction
Han, T. H., Vicidomini, R., Ramos, C. I., Wang, Q., Nguyen, P., Jarník, M., Lee, C., Stawarski, M., Hernandez, R. X., Macleod, G. T., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107866 · Cited by 17
D-Serine Potently Drives Ligand-Binding Domain Closure in the Ionotropic Glutamate Receptor GluD2
Chin, A. C., Yovanno, R. A., Wied, T. J., Gershman, A., & Lau, A. Y. (2020) · Structure · doi:10.1016/j.str.2020.07.005 · Cited by 17
Perszyk, R. E., Zheng, Z., Banke, T. G., Zhang, J., Xie, L., McDaniel, M. J., Katzman, B. M., Pelly, S. C., Yuan, H., Liotta, D. C., et al. (2021) · Molecular Pharmacology · doi:10.1124/molpharm.120.000218 · Cited by 17
Self-citationSchlesinger, F., Tammena, D., Krampfl, K., & Bufler, J. (2005) · Synapse · doi:10.1002/syn.20110 · Cited by 16
TARP γ-8 glycosylation regulates the surface expression of AMPA receptors
Zheng, C.-Y., Chang, K., Suh, Y. H., & Roche, K. W. (2014) · Biochemical Journal · doi:10.1042/bj20140806 · Cited by 16
Jensen, A. A., Christesen, T., Bølcho, U., Greenwood, J. R., Postorino, G., Vogensen, S. B., Johansen, T. N., Egebjerg, J., Bräuner‐Osborne, H., & Clausen, R. P. (2007) · Journal of Medicinal Chemistry · doi:10.1021/jm070532r · Cited by 16
Glutamate escape from a tortuous synaptic cleft of the hippocampal mossy fibre synapse
Savtchenko, L. P., & Rusakov, D. A. (2004) · Neurochemistry International · doi:10.1016/j.neuint.2003.11.008 · Cited by 16
Probing Intersubunit Interfaces in AMPA-subtype Ionotropic Glutamate Receptors
Yelshanskaya, M. V., Saotome, K., Singh, A. K., et al. (2016) · Scientific Reports · doi:10.1038/srep19082 · Cited by 16
Pathogenic role of autoantibodies against inhibitory synapses
Prüß, H., & Kirmse, K. (2018) · Brain Research · doi:10.1016/j.brainres.2018.09.009 · Cited by 16
Channel-Opening Kinetic Mechanism for Human Wild-Type GluK2 and the M867I Mutant Kainate Receptor
Han, Y., Wang, C., Park, J. S., & Niu, L. (2010) · Biochemistry · doi:10.1021/bi100819v · Cited by 16
The mouse cornichon gene family
Hwang, S.-Y., Oh, B., Zhang, Z., et al. (1999) · Development Genes and Evolution · doi:10.1007/s004270050234 · Cited by 16
Dynamics of the Ligand Binding Domain Layer during AMPA Receptor Activation
Baranovic, J., Chebli, M., Salazar, H., et al. (2016) · Biophysical Journal · doi:10.1016/j.bpj.2015.12.033 · Cited by 16
Slavı́ková, B., Chodounská, H., Nekardová, M., Vyklický, V., Ladislav, M., Hubálková, P., Krausová, B. H., Vyklický, L., & Kudová, E. (2016) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.6b00079 · Cited by 16
Gaynor, S. C., Breen, M. E., Monson, E. T., de Klerk, K., Parsons, M. G., DeLuca, A. P., Scheetz, T. E., Zandi, P. P., Potash, J. B., & Willour, V. L. (2016) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32479 · Cited by 16
Structure and Affinity of Two Bicyclic Glutamate Analogues at AMPA and Kainate Receptors
Møllerud, S., Pinto, A., Marconi, L., Frydenvang, K., Thorsen, T. S., Laulumaa, S., Venskutonytė, R., Winther, S., Moral, A. M. C., Tamborini, L., et al. (2017) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.7b00201 · Cited by 16
Nouhi, M., Zhang, X., Yao, N., & Chergui, K. (2017) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12784 · Cited by 16
Beckwith‐Cohen, B., Holzhausen, L. C., Wang, T.-M., Rajappa, R., & Krämer, R. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1541-18.2018 · Cited by 16
Mechanisms underlying the synaptic trafficking of the glutamate delta receptor GluD1
Tao, W., Ma, C., Bemben, M. A., Li, K. H., Burlingame, A. L., Zhang, M., & Nicoll, R. A. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0378-4 · Cited by 16
The structural arrangement at intersubunit interfaces in homomeric kainate receptors
Litwin, D. B., Carrillo, E. C., Shaikh, S. A., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-43360-x · Cited by 16
Litwin, D. B., Paudyal, N., Carrillo, E. C., Berka, V., & Jayaraman, V. (2019) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2019.05.023 · Cited by 16
Self-citationKainic Acid-Based Agonists of Glutamate Receptors: SAR Analysis and Guidelines for Analog Design
Tian, Z., Clark, B. L. M., & Ménard, F. (2019) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.9b00349 · Cited by 16
Ward, S. E., Harries, M. H., Aldegheri, L., Bradford, A. M., Ballini, E., Dawson, L. A., Lacroix, L. P., Pardoe, J., Starr, K. R., Weil, A., et al. (2019) · Journal of Psychopharmacology · doi:10.1177/0269881119872198 · Cited by 16
AMPAR/TARP stoichiometry differentially modulates channel properties
Míguez‐Cabello, F., Sánchez-Fernández, N., Yefimenko, N., Gasull, X., Gratacòs‐Batlle, E., & Soto, D. (2020) · eLife · doi:10.7554/elife.53946 · Cited by 16
Strong, K. L., Epplin, M. P., Ogden, K. K., Burger, P. B., Kaiser, T. M., Wilding, T. J., Kusumoto, H., Camp, C. R., Shaulsky, G. H., Bhattacharya, S., et al. (2020) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.0c00561 · Cited by 16
Self-citationBuck, D. P., Howitt, S. M., & Clements, J. D. (2000) · Biophysical Journal · doi:10.1016/s0006-3495(00)76488-5 · Cited by 15
Valeš, K., Rambousek, L., Holubová, K., Svoboda, J., Bubeníková-Valešová, V., Chodounská, H., Vyklický, L., & Stuchlík, A. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.07.020 · Cited by 15
Tsuang, D. W., Greenwood, T. A., Jayadev, S., Davis, M. Y., Shutes‐David, A., & Bird, T. D. (2018) · Journal of Huntington s Disease · doi:10.3233/jhd-170277 · Cited by 15
Abdallah, C. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-0668-1 · Cited by 15
Ziolkowski, L. H., Mordukhovich, I., Chen, D. M., Chisari, M., Shu, H.-J., Lambert, P. M., Qian, M., Zorumski, C. F., Covey, D. F., & Mennerick, S. J. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.108358 · Cited by 15
Kainate Receptor Modulation by Sodium and Chloride
Plested, A. J. R. (2011) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-9557-5_9 · Cited by 15
A novel 47.2Mb duplication on chromosomal bands Xq21.1–25 associated with mental retardation
Jin, Z., Yu, L., Geng, J., et al. (2015) · Gene · doi:10.1016/j.gene.2015.04.083 · Cited by 15
A New Mouse Allele of Glutamate Receptor Delta 2 with Cerebellar Atrophy and Progressive Ataxia
Miyoshi, Y., Yoshioka, Y., Suzuki, K., Miyazaki, T., Koura, M., Saigoh, K., Kajimura, N., Monobe, Y., Kusunoki, S., Matsuda, J., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0107867 · Cited by 15
Manita, S., Miyazaki, K.-I., & Ross, W. N. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.216564 · Cited by 15
Seong, H. J., Behnia, R., & Carter, A. G. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00590.2013 · Cited by 15
Advanced Fluorescence Protein-Based Synapse-Detectors
Lee, H., Oh, W. C., Seong, J., & Kim, J. (2016) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2016.00016 · Cited by 15
Lomash, R. M., Sheng, N., Li, Y., Nicoll, R. A., & Roche, K. W. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.787903 · Cited by 15
Chisari, M., Wilding, T. J., Brunwasser, S. J., Krishnan, K., Qian, M., Benz, A. M., Huettner, J. E., Zorumski, C. F., Covey, D. F., & Mennerick, S. J. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.10.015 · Cited by 15
Krampfl, K., Schlesinger, F., Wolfes, H., Dengler, R., & Bufler, J. (2001) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(01)00626-8 · Cited by 14
Cations But Not Anions Regulate the Responsiveness of Kainate Receptors
MacLean, D. M., Wong, A. Y. C., Fay, A.-M. L., et al. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4314-10.2011 · Cited by 14
Zanjani, H., Vogel, M. W., & Mariani, J. (2015) · The Cerebellum · doi:10.1007/s12311-015-0748-7 · Cited by 14
Retour aux sources: defining the structural basis of glutamate receptor activation
Dawe, G. B., Aurousseau, M. R. P., Daniels, B. A., & Bowie, D. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.277921 · Cited by 14
Self-citationPrenatal development of NMDA receptor composition and function in trigeminal neurons.
Ishihama, K., Kogo, M., Wakisaka, S., & Turman, J. (2005) · Archives of histology and cytology · doi:10.1679/aohc.68.321 · Cited by 14
Puddifoot, C., Chen, P. E., Schoepfer, R., & Wyllie, D. J. A. (2009) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2008.00040.x · Cited by 14
Mechanism-Based Mathematical Model for Gating of Ionotropic Glutamate Receptors
Dai, J., Wollmuth, L. P., & Zhou, H. (2015) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.5b00521 · Cited by 14
Self-citationKlein, R. C., Warder, S. E., Galdzicki, Z., et al. (2001) · Neuropharmacology · doi:10.1016/s0028-3908(01)00119-8 · Cited by 14
Noncompetitive, Voltage-Dependent NMDA Receptor Antagonism by Hydrophobic Anions
Linsenbardt, A. J., Chisari, M., Yu, A., Shu, H., Zorumski, C. F., & Mennerick, S. J. (2012) · Molecular Pharmacology · doi:10.1124/mol.112.081794 · Cited by 14
Haglerød, C., Hussain, S., Nakamura, Y., Xia, J., Haug, F. Š., Ottersen, O. P., Henley, J. M., & Davanger, S. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2016.12.042 · Cited by 14
Cummings, K. A., Belin, S., & Popescu, G. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.03.031 · Cited by 14
A Rare Syndrome of GRID2 Deletion in 2 Siblings
Veerapandiyan, A., Enner, S., Thulasi, V., et al. (2017) · Child Neurology Open · doi:10.1177/2329048x17726168 · Cited by 14
Taghdiri, M., Kashef, A., Abbassi, G. M., et al. (2019) · Clinical Case Reports · doi:10.1002/ccr3.2020 · Cited by 14
Zampieri, D., Fortuna, S., Calabretti, A., Romano, M., Menegazzi, R., Schepmann, D., Wünsch, B., Collina, S., Zanon, D., & Mamolo, M. G. (2019) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2019.07.012 · Cited by 14
AMPA Receptor Noncompetitive Inhibitors Occupy a Promiscuous Binding Site
Narangoda, C., Sakipov, S. N., & Kurnikova, M. G. (2019) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.9b00344 · Cited by 14
Kainate receptor regulation of synaptic inhibition in the hippocampus
Pressey, J. C., & Woodin, M. A. (2020) · The Journal of Physiology · doi:10.1113/jp279645 · Cited by 14
Myers, S. J., Ruppa, K. P., Wilson, L., Tahirovic, Y., Lyuboslavsky, P., Menaldino, D., Dentmon, Z. W., Koszalka, G. W., Zaczek, R., Dingledine, R., et al. (2021) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.120.000370 · Cited by 14
Self-citationBunch, L., Gefflaut, T., Alaux, S., Sagot, E., Nielsen, B., & Pickering, D. S. (2009) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2009.03.011 · Cited by 13
Henle, F., Dehmel, M., Leemhuis, J., Fischer, C., & Meyer, D. (2011) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-011-0701-3 · Cited by 13
Distinct mechanisms of Up state maintenance in the medial entorhinal cortex and neocortex
Digby, R. J., Bravo, D. S., Paulsen, O., & Magloire, V. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.11.009 · Cited by 13
Yamashita, M., Kawaguchi, S., & Hirano, T. (2013) · The Cerebellum · doi:10.1007/s12311-013-0474-y · Cited by 13
From molecular phylogeny towards differentiating pharmacology for NMDA receptor subtypes
Platt, R. J., Curtice, K. J., Twede, V., Watkins, M., Gruszczyński, P., Bulaj, G. W., Horvath, M. P., & Olivera, B. M. (2014) · Toxicon · doi:10.1016/j.toxicon.2014.01.016 · Cited by 13
Thalhammer, A. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2002.1137 · Cited by 13
GluK2-Mediated Excitability within the Superficial Layers of the Entorhinal Cortex
Beed, P. S., Salmen, B., & Schmitz, D. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005576 · Cited by 13
The expression of the NR1-subunit of the NMDA receptor during mouse and early chicken development
Bennett, G. D., Moser, K., Chaudoin, T. R., et al. (2006) · Reproductive Toxicology · doi:10.1016/j.reprotox.2006.03.010 · Cited by 13
Glutamate Receptor Agonists: Stereochemical Aspects
Vogensen, S. B., Greenwood, J. R., Bunch, L., et al. (2011) · Current Topics in Medicinal Chemistry · doi:10.2174/156802611795164990 · Cited by 13
Miyata, M., & Imoto, K. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2008.164996 · Cited by 13
Kristensen, O., Kristensen, L. B., Møllerud, S., Frydenvang, K., Pickering, D. S., & Kastrup, J. S. (2016) · Structure · doi:10.1016/j.str.2016.06.019 · Cited by 13
Pallesen, J. S., Møllerud, S., Frydenvang, K., et al. (2019) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.8b00726 · Cited by 13
Banerjee, P., Donello, J., Hare, B. D., & Duman, R. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.112706 · Cited by 13
TARPs Modulate Receptor-Mediated Paired-Pulse Depression and Recovery from Desensitization
Devi, S. P. S., Cheng, Y., Tomita, S., Howe, J. R., & Zhang, W. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.3026-19.2020 · Cited by 13
Fukushima, T., Shingai, R., Ogurusu, T., & Ichinose, M. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(03)00805-x · Cited by 12
Role of Cross-Cleft Contacts in NMDA Receptor Gating
Paganelli, M. A., Kussius, C. L., & Popescu, G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080953 · Cited by 12
Juknaitė, L., Venskutonytė, R., Assaf, Z., et al. (2012) · Journal of Structural Biology · doi:10.1016/j.jsb.2012.07.001 · Cited by 12
Matsuda, K., Kondo, T., Iijima, T., Matsuda, S., Watanabe, M., & Yuzaki, M. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06639.x · Cited by 12
Terhag, J., Gottschling, K., & Hollmann, M. (2010) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2010.00117 · Cited by 12
Chopra, D. A., Monaghan, D. T., & Dravid, S. M. (2015) · Molecular Pharmacology · doi:10.1124/mol.115.100396 · Cited by 12
NMDA-induced burst firing in a model subthalamic nucleus neuron
Kubota, S., & Rubin, J. E. (2011) · Journal of Neurophysiology · doi:10.1152/jn.01127.2010 · Cited by 12
Design and Synthesis of Selurampanel, a Novel Orally Active and Competitive AMPA Receptor Antagonist
Orain, D., Tasdelen, E., Haessig, S., Koller, M., Picard, A., Dubois, C., Lingenhoehl, K., Desrayaud, S., Floersheim, P., Carcache, D. A., et al. (2016) · ChemMedChem · doi:10.1002/cmdc.201600467 · Cited by 12
Irvine, M. W., Fang, G., Sapkota, K., et al. (2018) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2018.12.054 · Cited by 12
Mayer, M. L. (2020) · The Journal of Physiology · doi:10.1113/jp279026 · Cited by 12
Cross-subunit interactions that stabilize open states mediate gating in NMDA receptors
Iacobucci, G. J., Wen, H., Helou, M., Liu, B., Zheng, W., & Popescu, G. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2007511118 · Cited by 12
Zhang, Y., Nayeem, N., & Green, T. (2008) · Molecular Pharmacology · doi:10.1124/mol.108.048819 · Cited by 11
Kreitzer, M. A., Birnbaum, A. D., Qian, H., & Malchow, R. P. (2009) · Visual Neuroscience · doi:10.1017/s0952523809990149 · Cited by 11
Akgül, G., & McBain, C. J. (2020) · Scientific Reports · doi:10.1038/s41598-020-58068-6 · Cited by 11
Self-citationSun, Y., Jiang, X., Liu, X., et al. (2010) · Brain Research · doi:10.1016/j.brainres.2009.12.068 · Cited by 11
The mechanisms of Zn2+ effects on Ca2+-permeable AMPA receptors on carp retinal horizontal cells
Sun, Y., Zhang, Y., Gong, H.-Q., et al. (2010) · Brain Research · doi:10.1016/j.brainres.2010.05.033 · Cited by 11
Inoue, S., Kamiyama, H., Matsumoto, M., Yanagawa, Y., Hiraide, S., Saito, Y., Shimamura, K., & Togashi, H. (2013) · Journal of Pharmacological Sciences · doi:10.1254/jphs.13123fp · Cited by 11
Tikhonov, D. B., & Zhorov, B. S. (2020) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2020.183401 · Cited by 11
Šmídková, M., Hájek, M., Adla, S. K., Slavı́ková, B., Chodounská, H., Matoušová, M., Mertlíková‐Kaiserová, H., & Kudová, E. (2019) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2019.03.007 · Cited by 10
Akgül, G., Abebe, D. T., Yuan, X. Q., Auville, K., & McBain, C. J. (2019) · Scientific Reports · doi:10.1038/s41598-019-41920-9 · Cited by 10
Self-citationBuemi, M. R., Luca, L. D., Ferro, S., et al. (2014) · Archiv der Pharmazie · doi:10.1002/ardp.201400061 · Cited by 10
Bekkers, J. M., Vidovic, M., & Ymer, S. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00586-2 · Cited by 10
Risgaard, R., Nielsen, S. D., Hansen, K. B., et al. (2013) · Journal of Medicinal Chemistry · doi:10.1021/jm400346a · Cited by 10
Self-citationCalcium-Impermeable NMDA Receptor: A Novel Target for Addiction
Huang, X., Wei, N., & Zhang, C. (2017) · Neuroscience Bulletin · doi:10.1007/s12264-017-0121-6 · Cited by 10
A single-channel mechanism for pharmacological potentiation of GluN1/GluN2A NMDA receptors
Chopra, D. A., Sapkota, K., Irvine, M. W., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-07292-8 · Cited by 10
Laulumaa, S., Hansen, K. V., Masternak, M., Drapier, T., Francotte, P., Pirotte, B., Frydenvang, K., & Kastrup, J. S. (2018) · ACS Medicinal Chemistry Letters · doi:10.1021/acsmedchemlett.8b00369 · Cited by 10
Self-citationSchönrock, M., Thiel, G., & Laube, B. (2019) · Communications Biology · doi:10.1038/s42003-019-0320-y · Cited by 10
NETO1 Regulates Postsynaptic Kainate Receptors in CA3 Interneurons During Circuit Maturation
Orav, E., Dowavic, I., Huupponen, J., Taira, T., & Lauri, S. E. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-1612-4 · Cited by 10
Zhang, L., Quan, J., Zhao, Y., et al. (2019) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2019.111654 · Cited by 10
Zinc Modulates Olfactory Bulb Kainate Receptors
Blakemore, L. J., & Trombley, P. Q. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.11.041 · Cited by 10
Li, C., Yan, J., Tang, D., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-62192-8 · Cited by 10
Common Binding Site for Externally and Internally Applied AMPA Receptor Channel Blockers
Tikhonova, T. B., Tikhonov, D. B., & Magazanik, L. G. (2009) · Journal of Molecular Neuroscience · doi:10.1007/s12031-008-9172-5 · Cited by 9
An Unusual Suspect in Cocaine Addiction
Huang, Y. H., Schlüter, O. M., & Dong, Y. (2013) · Neuron · doi:10.1016/j.neuron.2013.11.001 · Cited by 9
Wee, K. S.-L., Wee, Z.-N., Chow, N. B.-H., et al. (2010) · Neurochemistry International · doi:10.1016/j.neuint.2010.05.003 · Cited by 9
Fiszman, M. L., Erdélyi, F., Szabó, G., et al. (2007) · Neuropharmacology · doi:10.1016/j.neuropharm.2007.03.010 · Cited by 9
Zhang, Q., Huang, X., Chen, X., Li, S., Yao, T., & Wu, J. (2020) · Journal of Attention Disorders · doi:10.1177/1087054720905089 · Cited by 9
Santangelo, R., Ogden, K. K., Strong, K. L., Khatri, A., Chepiga, K. M., Jensen, H. S., Traynelis, S. F., & Liotta, D. C. (2014) · Journal of Medicinal Chemistry · doi:10.1021/jm500710w · Cited by 9
Self-citationSierra, R. O., Nítola, L. P., Duran, J. M., Prieto, D. R., León, L. A., & Cárdenas, F. P. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.08.021 · Cited by 9
Bunk, E. C., König, H., Prehn, J. H. M., & Kirby, B. P. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23347 · Cited by 9
Ambrogini, P., Minelli, A., Lattanzi, D., Ciuffoli, S., Fanelli, M., & Cuppini, R. (2006) · PubMed · Cited by 9
Role of Stoichiometry in the Dimer-Stabilizing Effect of AMPA Receptor Allosteric Modulators
Ptak, C. P., Hsieh, C., Weiland, G. A., & Oswald, R. E. (2013) · ACS Chemical Biology · doi:10.1021/cb4007166 · Cited by 9
Venskutonytė, R., Larsen, A. P., Frydenvang, K., et al. (2014) · ChemMedChem · doi:10.1002/cmdc.201402204 · Cited by 9
Partial Agonists and Subunit Selectivity at NMDA Receptors
Risgaard, R., Hansen, K. B., & Clausen, R. P. (2010) · Chemistry - A European Journal · doi:10.1002/chem.201001366 · Cited by 9
Self-citationGao, J., Stevenson, T. J., Douglass, A. D., Barrios, J. P., & Bonkowsky, J. L. (2018) · eNeuro · doi:10.1523/eneuro.0389-17.2018 · Cited by 9
Tarps differentially affect the pharmacology of ampakines
Radin, D. P., Li, Y., Rogers, G. A., Purcell, R., & LIPPA, A. S. (2018) · Biochemical Pharmacology · doi:10.1016/j.bcp.2018.06.013 · Cited by 9
Zscherp, R., Baumeister, S., Schepmann, D., & Wünsch, B. (2018) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2018.08.003 · Cited by 9
Phosphorylation Induces Conformational Rigidity at the C-Terminal Domain of AMPA Receptors
Chatterjee, S., Ade, C., Nurik, C. E., Carrejo, N. C., Dutta, C., Jayaraman, V., & Landes, C. F. (2018) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.8b10749 · Cited by 9
Self-citationBowers, M. S., Cacheaux, L. P., Sahu, S. U., Schmidt, M. E., Sennello, J. A., Leaderbrand, K., Khan, M. A., Kroes, R. A., & Moskal, J. R. (2019) · Journal of Neurochemistry · doi:10.1111/jnc.14845 · Cited by 9
Møllerud, S., Hansen, R. B., Pallesen, J. S., et al. (2019) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.9b00479 · Cited by 9
Li, W., & Pozzo‐Miller, L. D. (2019) · eNeuro · doi:10.1523/eneuro.0118-19.2019 · Cited by 9
Kayser, S., Hansen, J. C., Staudt, M., Moroz, A., Larsen, Y., Temperini, P., Yi, F., Syrenne, J. T., Krogsgaard‐Larsen, N., Iliadis, S., et al. (2020) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.0c00003 · Cited by 9
Self-citationEngineering a high-affinity allosteric binding site for divalent cations in kainate receptors
Plested, A. J. R., & Mayer, M. L. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.07.013 · Cited by 8
Kumamoto, E. (1996) · PubMed · Cited by 8
Saver, J. L. (2013) · Stroke · doi:10.1161/strokeaha.113.001070 · Cited by 8
Elger, C. E., Hong, S. B., Brandt, C., et al. (2017) · Epilepsia · doi:10.1111/epi.13771 · Cited by 8
High Conformational Variability in the GluK2 Kainate Receptor Ligand-Binding Domain
Wied, T. J., Chin, A. C., & Lau, A. Y. (2018) · Structure · doi:10.1016/j.str.2018.09.008 · Cited by 8
Cadmium opens GluK2 kainate receptors with cysteine substitutions at the M3 helix bundle crossing
Wilding, T. J., & Huettner, J. E. (2018) · The Journal of General Physiology · doi:10.1085/jgp.201812234 · Cited by 8
Nofziger, J., Paxos, C., Emshoff, J., & Mullen, C. (2019) · Mental Health Clinician · doi:10.9740/mhc.2019.03.076 · Cited by 8
Callahan, P. M., Terry, A. V., Nelson, F. R., Volkmann, R. A., Vinod, A., Zainuddin, M., & Menniti, F. S. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.107994 · Cited by 8
Self-citationIzumi, Y., Mennerick, S. J., Doherty, J., & Zorumski, C. F. (2021) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.120.000376 · Cited by 8
Antipsychotic-like profile of CIQ isomers in animal models of schizophrenia
Gawai, P., Upadhyay, R., Gakare, S. G., Sarode, L. P., Dravid, S. M., & Ugale, R. R. (2019) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000532 · Cited by 7
Nakamura, M., Choi, K.-H., Choi, S.-K., et al. (2010) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2010.03.004 · Cited by 7
McIntyre, C. J., McCauley, J. A., Bednár̂, B., et al. (2009) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2009.07.028 · Cited by 7
Dey, S., Schepmann, D., & Wünsch, B. (2017) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2017.12.010 · Cited by 7
Woodhams, S. G., Markus, R., Gowler, P. R. W., Self, T. J., & Chapman, V. (2019) · Pain · doi:10.1097/j.pain.0000000000001672 · Cited by 7
Hetzelt, K. L. M. L., Kraus, C. S., Kusnik, S., Thiel, C. T., Uebe, S., Ekici, A. B., Trollmann, R., Reis, A., & Zweier, C. (2020) · European Journal of Medical Genetics · doi:10.1016/j.ejmg.2020.103998 · Cited by 7
Pharmacology of NMDA Receptors
Jane, D. E., & Monaghan, D. T. (2008) · Frontiers in neuroscience · doi:10.1201/9781420044157.ch12 · Cited by 7
Li‐Smerin, Y., Aizenman, E., & Johnson, J. W. (2000) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)35395-9 · Cited by 6
Shypshyna, M. S., & Veselovsky, N. S. (2014) · Neuroscience Letters · doi:10.1016/j.neulet.2014.11.015 · Cited by 6
Activation-induced structural change in the GluN1/GluN3A excitatory glycine receptor
Balasuriya, D., Takahashi, H., Srivats, S., et al. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.07.009 · Cited by 6
The neurotoxin domoate causes long-lasting inhibition of the kainate receptor GluK5 subunit
Fisher, J. L. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.05.003 · Cited by 6
Krogsgaard‐Larsen, N., Delgar, C. G., Koch, K., et al. (2016) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.6b01516 · Cited by 6
Configurational Preference of the Glutamate Receptor Ligand Binding Domain Dimers
Yonkunas, M. J., Maiti, B., Flores‐Canales, J. C., et al. (2017) · Biophysical Journal · doi:10.1016/j.bpj.2017.04.042 · Cited by 6
Stargazin differentially modulates ampakine gating kinetics and pharmacology
Radin, D. P., Li, Y., Rogers, G. A., et al. (2018) · Biochemical Pharmacology · doi:10.1016/j.bcp.2018.01.019 · Cited by 6
Thum, S., Schepmann, D., Kalinin, D. V., et al. (2018) · ChemMedChem · doi:10.1002/cmdc.201800566 · Cited by 6
Stargazin and γ4 slow the channel opening and closing rates of GluA4 AMPA receptors
Pierce, V. D., & Niu, L. (2019) · Scientific Reports · doi:10.1038/s41598-019-45870-0 · Cited by 6
Fava, V. A. R., Sarin, L. M., Lucchese, A. C., Sant, L. C. D., Magalhães, E. T. P., Delfino, R. S., Tuena, M. A., Nakahira, C., Jackowski, A. P., Abdo, G. L., et al. (2020) · Revista de Psiquiatría y Salud Mental · doi:10.1016/j.rpsm.2020.10.003 · Cited by 6
Kistler, T. M., & Fleck, M. W. (2007) · Channels · doi:10.4161/chan.1.6.5589 · Cited by 5
Ihle, E. C., & Patneau, D. K. (2000) · Molecular Pharmacology · doi:10.1016/s0026-895x(24)12689-2 · Cited by 5
Inhibition of AMPA Receptors by Polyamine Toxins is Regulated by Agonist Efficacy and Stargazin
Poulsen, M. H., Lucas, S., Strømgaard, K., & Kristensen, A. S. (2014) · Neurochemical Research · doi:10.1007/s11064-014-1258-6 · Cited by 5
Zhou, H. (2017) · Accounts of Chemical Research · doi:10.1021/acs.accounts.6b00598 · Cited by 5
A novel function for the ER retention signals in the C-terminus of kainate receptor subunit, GluK5
Hong, X., Jeyifous, O., Ronilo, M., et al. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2018.10.009 · Cited by 5
NMDA受容体は効率的なシナプス活性のための複数の前開口ゲーティング段階を必要とする【JST・京大機械翻訳】
Johansen, B. A., Aaron, G., Miaomiao, H., et al. (2021) · Neuron · Cited by 5
The human δ2 glutamate receptor gene is not mutated in patients with spinocerebellar ataxia
Wang, C., Huang, J., Lin, A., et al. (2014) · Neural Regeneration Research · doi:10.4103/1673-5374.133173 · Cited by 4
Thalamic Reticular Neurons Are Unexcited by New Stargazer Seizure Mechanism
Chetkovich, D. M. (2009) · Epiliepsy currents/Epilepsy currents · doi:10.1111/j.1535-7511.2008.01293.x · Cited by 4
Ghafari, M., Falsafi, S. K., Höger, H., Bennett, K. L., & Lübec, G. (2015) · PROTEOMICS - CLINICAL APPLICATIONS · doi:10.1002/prca.201400057 · Cited by 3
Cadmium activates AMPA and NMDA receptors with M3 helix cysteine substitutions
Wilding, T. J., & Huettner, J. E. (2020) · The Journal of General Physiology · doi:10.1085/jgp.201912537 · Cited by 3
Chvojková, M., Rambousek, L., Chodounská, H., Kudová, E., & Valeš, K. (2020) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2020.173187 · Cited by 3
Mayer, M. L., & Jegla, T. J. (2018) · eLife · doi:10.7554/elife.43815 · Cited by 2
Correction: GluK2-Mediated Excitability within the Superficial Layers of the Entorhinal Cortex
Beed, P. S., Salmen, B., & Schmitz, D. (2009) · PLoS ONE · doi:10.1371/annotation/40012908-73d7-4bfc-8731-d24ec701dca4 · Cited by 2
Ligand-Dependent Opening of the Multiple AMPA Receptor Conductance States: A Concerted Model
Roy, R. D., Rosenmund, C., Edelstein, S. J., & Novère, N. G. L. (2015) · PLoS ONE · doi:10.1371/journal.pone.0116616 · Cited by 2
Fava, V. A. R., Sarin, L. M., Lucchese, A. C., et al. (2021) · Revista de Psiquiatría y Salud Mental (English Edition) · doi:10.1016/j.rpsmen.2021.11.003 · Cited by 1
Broca's region revisited: Cytoarchitecture and intersubject variability
Amunts, K., Schleicher, A., B�rgel, U., Mohlberg, H., Uylings, H. B. M., & Zilles, K. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990920)412:2
?imi?, G., Kostovi?, I., Winblad, B., & Bogdanovi?, N. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970324)379:4
Flagged first, then by citations
Cited by
Sorted by citations
Mechanisms of ketamine and its metabolites as antidepressants
Hess, E. M., Riggs, L. M., Michaelides, M., & Gould, T. D. (2022) · Biochemical Pharmacology · doi:10.1016/j.bcp.2021.114892 · Cited by 175
Coombs, I. D., Ziobro, J., Krotov, V., Surtees, T., Cull‐Candy, S. G., & Farrant, M. (2022) · Epilepsia · doi:10.1111/epi.17419 · Cited by 32
Cryo-EM structure of the human Asc-1 transporter complex
Li, Y., Guo, Y., Bröer, A., Dai, L., Brӧer, S., & Yan, R. (2024) · Nature Communications · doi:10.1038/s41467-024-47468-1 · Cited by 12
Glutamate receptor 4 as a fluid biomarker for the diagnosis of psychiatric disorders
Gómez de San José, N., Goossens, J., Al Shweiki, M. R., Halbgebauer, S., Oeckl, P., Steinacker, P., Danzer, K. M., Graf, H., Schönfeldt-Lecuona, C., Belbin, O., et al. (2022) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2022.10.010 · Cited by 9
Metadata
- Authors
- Hansen, K. B., Wollmuth, L. P., Bowie, D., Furukawa, H., Menniti, F. S., Sobolevsky, A. I., Swanson, G. T., Swanger, S. A., Greger, I. H., Nakagawa, T., McBain, C. J., Jayaraman, V., Low, C.-M., Dell’Acqua, M. L., Diamond, J. S., Camp, C. R., Perszyk, R. E., Yuan, H., & Traynelis, S. F.
- Affiliations
- Northwestern University (US)
- Corresponding author
- Traynelis, Stephen F.
- ORCID
- Hansen, Kasper B.
- Wollmuth, Lonnie P.
- Bowie, Derek
- Furukawa, Hiro
- Menniti, Frank S.
- Sobolevsky, Alexander I.
- Swanson, Geoffrey T.
- Swanger, Sharon A.
- Greger, Ingo H.
- Nakagawa, Terunaga
- McBain, Chris J.
- Jayaraman, Vasanthi
- Low, Chian-Ming
- Dell’Acqua, Mark L.
- Diamond, Jeffrey S.
- Camp, Chad R.
- Perszyk, Riley E.
- Yuan, Hongjie
- Traynelis, Stephen F.
- Venue
- Pharmacological Reviews
- Publisher
- Elsevier BV
- Published
- 2021-10
- Volume
- 73
- Issue
- 4
- Pages
- 1469-1658
- ISSN
- 0031-6997 (ISSN-L)
- PMC
- PMC8626789
- OpenAlex
- W3214054678
- Cited by
- 686
- References
- 2,576
- Citations by year
- 2026: 123 · 2025: 198 · 2024: 160 · 2023: 115 · 2022: 81 · 2021: 9
- FWCI
- 13.86
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Pharmacological Reviews (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
- Funders
- National Institutes of Health (5f31ns113530-02)
- Biotechnology and Biological Sciences Research Council (BB/N002113/1)
- National Institute of Mental Health (R56MH123474, R21MH127404, R01MH085926, R01MH123474)
- National Cancer Institute (R01CA206573)
- National Institute of General Medical Sciences (P20GM103546, R35GM122528)
- National Institute of Neurological Disorders and Stroke (F31‐NS113530, R01NS105804, R56NS040701, R01NS083660, R01NS040701, R01NS088479, R01NS111745, RF1NS113632, R01NS105502, R01NS107253, R35NS111619, R37NS083660, R01NS116055, R01NS097536)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD082373)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Keywords
- ionotropic glutamate receptors, ligand-gated ion channels, glutamate, receptor subtypes, receptor structure, receptor pharmacology, excitatory neurotransmission, neurophysiology, neurological disorders, mental illness, therapeutic target
- MeSH terms
- Animals, Central Nervous System, Humans, Receptors, Glutamate, Neurotransmitter Agents, Glutamic Acid, Receptors, Ionotropic Glutamate
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