Cocaine triggered AMPA receptor redistribution is reversed in vivo by mGluR-dependent long-term depression

The neural basis of drug craving: An incentive-sensitization theory of addiction

Robinson, T. (1993) · Brain Research Reviews · doi:10.1016/0165-0173(93)90013-p · Cited by 7,346

Glutamate receptor ion channels

Mayer, M. L. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.05.004 · Cited by 3,655

The Glutamate Receptor Ion Channels

Dingledine, R., Borges, K., Bowie, D., & Traynelis, S. F. (1999) · Pharmacological Reviews · doi:10.1016/s0031-6997(24)01394-2 · Cited by 3,554

Is there a common molecular pathway for addiction?

Nestler, E. J. (2005) · Nature Neuroscience · doi:10.1038/nn1578 · Cited by 1,388

Drugs of Abuse and Stress Trigger a Common Synaptic Adaptation in Dopamine Neurons

Saal, D., Dong, Y., Bonci, A., & Malenka, R. C. (2003) · Neuron · doi:10.1016/s0896-6273(03)00021-7 · Cited by 1,147

Single cocaine exposure in vivo induces long-term potentiation in dopamine neurons

Ungless, M. A., Whistler, J. L., Malenka, R. C., & Bonci, A. (2001) · Nature · doi:10.1038/35079077 · Cited by 1,106

The mesolimbic dopamine system: The final common pathway for the reinforcing effect of drugs of abuse?

Pierce, R. C., & Kumaresan, V. (2006) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2005.04.016 · Cited by 913

GRIP: a synaptic PDZ domain-containing protein that interacts with AMPA receptors

Dong, H., O’Brien, R., Fung, E. T., Lanahan, A. A., Worley, P. F., & Huganir, R. L. (1997) · Nature · doi:10.1038/386279a0 · Cited by 888

Postsynaptic signaling and plasticity mechanisms

Sheng, M., & Kim, M. J. (2002) · Science · doi:10.1126/science.1075333 · Cited by 731

Tat peptide-mediated cellular delivery: back to basics

Brooks, H., Lebleu, B., & Vivès, É. (2005) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2004.12.001 · Cited by 676

Two types of neurone in the rat ventral tegmental area and their synaptic inputs.

Johnson, S. W., & NORTH, R. A. (1992) · The Journal of Physiology · doi:10.1113/jphysiol.1992.sp019136 · Cited by 672

Kainate receptors mediate a slow postsynaptic current in hippocampal CA3 neurons

Castillo, P. E., Malenka, R. C., & Nicoll, R. A. (1997) · Nature · doi:10.1038/40645 · Cited by 568

Clustering of AMPA Receptors by the Synaptic PDZ Domain–Containing Protein PICK1

Xia, J., Zhang, X., Staudinger, J. L., & Huganir, R. L. (1999) · Neuron · doi:10.1016/s0896-6273(00)80689-3 · Cited by 561

Phosphorylation of the AMPA receptor subunit GluR2 differentially regulates its interaction with PDZ domain-containing proteins

Chung, H. J., Xia, J., Scannevin, R. H., Zhang, X., & Huganir, R. L. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-19-07258.2000 · Cited by 558

Reinforcing and locomotor stimulant effects of cocaine are absent in mGluR5 null mutant mice

Chiamulera, C., Epping-Jordan, M. P., Zocchi, A., Marcon, C., Cottiny, C., Tacconi, S., Corsi, M., Orzi, F., & Conquet, F. (2001) · Nature Neuroscience · doi:10.1038/nn0901-873 · Cited by 554

NSF Binding to GluR2 Regulates Synaptic Transmission

Nishimune, A., Isaac, J. T. R., Molnár, E., Noël, J., Nash, S. R., Tagaya, M., Collingridge, G. L., Nakanishi, S., & Henley, J. M. (1998) · Neuron · doi:10.1016/s0896-6273(00)80517-6 · Cited by 545

Behavioral Sensitization to Cocaine Is Associated with Increased AMPA Receptor Surface Expression in the Nucleus Accumbens

Boudreau, A. C., & Wolf, M. E. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2252-05.2005 · Cited by 481

In vivo protein transduction: intracellular delivery of biologically active proteins, compounds and DNA

Schwarze, S. R., & Dowdy, S. F. (2000) · Trends in Pharmacological Sciences · doi:10.1016/s0165-6147(99)01429-7 · Cited by 454

Synaptic activity at calcium-permeable AMPA receptors induces a switch in receptor subtype

Liu, S. J., & Cull-Candy, S. G. (2000) · Nature · doi:10.1038/35013064 · Cited by 452

I h Channels Contribute to the Different Functional Properties of Identified Dopaminergic Subpopulations in the Midbrain

Neuhoff, H., Neu, A. D., Liss, B., & Roeper, J. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-04-01290.2002 · Cited by 400

Interaction of the N-Ethylmaleimide–Sensitive Factor with AMPA Receptors

Song, I., Kamboj, S. K., Xia, J., Dong, H., Liao, D., & Huganir, R. L. (1998) · Neuron · doi:10.1016/s0896-6273(00)80548-6 · Cited by 399

Bi-directional effects of GABAB receptor agonists on the mesolimbic dopamine system

Cruz, H. G., Ivanova, T., Lunn, M.-L., Stoffel, M., Slesinger, P. A., & Lüscher, C. (2004) · Nature Neuroscience · doi:10.1038/nn1181 · Cited by 367

Glutamate systems in cocaine addiction

Kalivas, P. W. (2003) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2003.11.002 · Cited by 367

Interaction of the AMPA receptor subunit GluR2/3 with PDZ domains regulates hippocampal long-term depression

Kim, C., Chung, H. J., Lee, H., & Huganir, R. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.211132798 · Cited by 364

Novel Anchorage of GluR2/3 to the Postsynaptic Density by the AMPA Receptor–Binding Protein ABP

Srivastava, S., Osten, P., Vilim, F. S., Khatri, L., Inman, G. J., States, B. A., Daly, C., deSouza, S., Abagyan, R. A., Valtschanoff, J. G., et al. (1998) · Neuron · doi:10.1016/s0896-6273(00)80568-1 · Cited by 360

PICK1 Targets Activated Protein Kinase Cα to AMPA Receptor Clusters in Spines of Hippocampal Neurons and Reduces Surface Levels of the AMPA-Type Glutamate Receptor Subunit 2

Perez, J. L., Khatri, L., Chang, C., Srivastava, S., Osten, P., & Ziff, E. B. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-15-05417.2001 · Cited by 330

PDZ Proteins Interacting with C-Terminal GluR2/3 Are Involved in a PKC-Dependent Regulation of AMPA Receptors at Hippocampal Synapses

Daw, M. I., Chittajallu, R., Bortolotto, Z. A., Dev, K. K., Duprat, F., Henley, J. M., Collingridge, G. L., & Isaac, J. T. R. (2000) · Neuron · doi:10.1016/s0896-6273(00)00160-4 · Cited by 323

Repeated cocaine exposure in vivo facilitates LTP induction in midbrain dopamine neurons

Liu, Q.-S., Pu, L., & Poo, M. (2005) · Nature · doi:10.1038/nature04050 · Cited by 305

Differential Dependence on GluR2 Expression of Three Characteristic Features of AMPA Receptors

Washburn, M. S., Numberger, M., Zhang, S., & Dingledine, R. J. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-24-09393.1997 · Cited by 302

Acute and Chronic Cocaine-Induced Potentiation of Synaptic Strength in the Ventral Tegmental Area: Electrophysiological and Behavioral Correlates in Individual Rats

Borgland, S. L., Malenka, R. C., & Bonci, A. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1312-04.2004 · Cited by 289

Glutamate mediates an inhibitory postsynaptic potential in dopamine neurons

Fiorillo, C. D., & Williams, J. T. (1998) · Nature · doi:10.1038/27919 · Cited by 285

Elevated levels of GluR1 in the midbrain: a trigger for sensitization to drugs of abuse?

Carlezon, W. A., & Nestler, E. J. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02289-0 · Cited by 281

Sensitization to Morphine Induced by Viral-Mediated Gene Transfer

Carlezon, W. A., Boundy, V. A., Haile, C. N., Lane, S. B., Kalb, R. G., Neve, R. L., & Nestler, E. J. (1997) · Science · doi:10.1126/science.277.5327.812 · Cited by 279

The AMPAR subunit GluR2: still front and center-stage11Published on the World Wide Web on 30 October 2000.

Tanaka, H., Grooms, S. Y., Bennett, M. V. L., & Zukin, R. S. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02951-6 · Cited by 247

Calcium-Permeable AMPA Receptor Plasticity Is Mediated by Subunit-Specific Interactions with PICK1 and NSF

Gardner, S. M., Takamiya, K., Xia, J., Suh, J., Johnson, R. C., Yu, S., & Huganir, R. L. (2005) · Neuron · doi:10.1016/j.neuron.2005.02.026 · Cited by 245

Positive allosteric modulators of metabotropic glutamate 1 receptor: Characterization, mechanism of action, and binding site

Knoflach, F., Mutel, V., Jolidon, S., Kew, J. N. C., Malherbe, P., Vieira, E., Wichmann, J., & Kemp, J. A. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.231358298 · Cited by 241

Learning Mechanisms in Addiction: Synaptic Plasticity in the Ventral Tegmental Area as a Result of Exposure to Drugs of Abuse

Kauer, J. A. (2004) · Annual Review of Physiology · doi:10.1146/annurev.physiol.66.032102.112534 · Cited by 232

The protein kinase Cα binding protein PICK1 interacts with short but not long form alternative splice variants of AMPA receptor subunits

Dev, K. K., Nishimune, A., Henley, J. M., & Nakanishi, S. (1999) · Neuropharmacology · doi:10.1016/s0028-3908(98)00230-5 · Cited by 212

The AMPA Receptor Subunits GluR-A and GluR-B Reciprocally Modulate Spinal Synaptic Plasticity and Inflammatory Pain

Hartmann, B., Ahmadi, S., Heppenstall, P. A., Lewin, G. R., Schott, C., Borchardt, T., Seeburg, P. H., Zeilhofer, H. U., Sprengel, R., & Kuner, R. (2004) · Neuron · doi:10.1016/j.neuron.2004.10.029 · Cited by 201

NSF ATPase and α-/β-SNAPs Disassemble the AMPA Receptor-PICK1 Complex

Hanley, J. G., Khatri, L., Hanson, P. I., & Ziff, E. B. (2002) · Neuron · doi:10.1016/s0896-6273(02)00638-4 · Cited by 197

Regulation of Synaptic Strength and AMPA Receptor Subunit Composition by PICK1

Terashima, A. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4378-03.2004 · Cited by 183

Subunit interaction with PICK and GRIP controls Ca2+ permeability of AMPARs at cerebellar synapses

Liu, S. J., & Cull-Candy, S. G. (2005) · Nature Neuroscience · doi:10.1038/nn1468 · Cited by 162

Cocaine-induced potentiation of synaptic strength in dopamine neurons: Behavioral correlates in GluRA(–/–) mice

Dong, Y., Saal, D., Thomas, M., Faust, R., Bonci, A., Robinson, T., & Malenka, R. C. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401553101 · Cited by 158

Synaptic plasticity in the mesolimbic dopamine system

Thomas, M. J., & Malenka, R. C. (2003) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1236 · Cited by 137

mGluRs induce a long‐term depression in the ventral tegmental area that involves a switch of the subunit composition of AMPA receptors

Bellone, C., & Lüscher, C. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.03979.x · Cited by 129

Facilitation of currents through rat Ca2+‐permeable AMPA receptor channels by activity‐dependent relief from polyamine block

Rozov, A., Zilberter, Y., Wollmuth, L. P., & Burnashev, N. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.361bh.x · Cited by 114

Restless AMPA receptors: implications for synaptic transmission and plasticity

Lüscher, C., & Frerking, M. E. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01959-7 · Cited by 101

Rapid Synaptic Plasticity of Glutamatergic Synapses on Dopamine Neurons in the Ventral Tegmental Area in Response to Acute Amphetamine Injection

Faleiro, L. J., Jones, S., & Kauer, J. A. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300495 · Cited by 77

Changes in AMPA receptor currents following LTP induction on rat CA1 pyramidal neurones

Andrásfalvy, B. K., & Magee, J. C. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.065219 · Cited by 71

Sensitization to cocaine's motor activating properties produced by electrical kindling of the medial prefrontal cortex but not of the hippocampus

Schenk, S., & Snow, S. (1994) · Brain Research · doi:10.1016/0006-8993(94)90858-3 · Cited by 70

Evidence for a Relationship between Group 1 mGluR Hypofunction and Increased Cocaine and Ethanol Sensitivity in Homer2 Null Mutant Mice

Szumlinski, K. K., Toda, S., Middaugh, L. D., Worley, P. F., & Kalivas, P. W. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1300.055 · Cited by 27

Synaptic Plasticity: Multiple Forms, Functions, and Mechanisms

Citri, A., & Malenka, R. C. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301559 · Cited by 2,323

Synaptic plasticity and addiction

Kauer, J. A., & Malenka, R. C. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2234 · Cited by 1,397

NMDA receptor-dependent long-term potentiation and long-term depression (LTP/LTD).

Luscher, C., & Malenka, R. C. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005710 · Cited by 1,110

Drug-evoked synaptic plasticity in addiction: from molecular changes to circuit remodeling

Lüscher, C., & Malenka, R. C. (2011) · Neuron · doi:10.1016/j.neuron.2011.01.017 · Cited by 1,105

Synaptic AMPA receptor plasticity and behavior

Kessels, H. W., & Malinow, R. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.015 · Cited by 993

Correcting Cocaine-Induced Plasticity

Stern, P. (2007) · Science s STKE · doi:10.1126/stke.3972007tw277

Cocaine inverts rules for synaptic plasticity of glutamate transmission in the ventral tegmental area

Mameli, M., Bellone, C., Brown, M. T. C., & Lüscher, C. (2011) · Nature Neuroscience · doi:10.1038/nn.2763 · Cited by 177

Single cocaine exposure in vivo induces long-term potentiation in dopamine neurons

Ungless, M. A., Whistler, J. L., Malenka, R. C., & Bonci, A. (2001) · Nature · doi:10.1038/35079077 · Cited by 1,106

Loss of mGluR1-LTD following cocaine exposure accumulates Ca2+-permeable AMPA receptors and facilitates synaptic potentiation in the prefrontal cortex

Ruan, H., & Yao, W. (2021) · Journal of Neurogenetics · doi:10.1080/01677063.2021.1931180 · Cited by 13

Cocaine Enhances NMDA Receptor-Mediated Currents in Ventral Tegmental Area Cells via Dopamine D5Receptor-Dependent Redistribution of NMDA Receptors

Schilström, B., Yaka, R., Argilli, E., Suvarna, N. U., Schumann, J., Chen, B. T., Carman, M., Singh, V., Mailliard, W. S., Dorit Ron, A., et al. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5179-05.2006 · Cited by 147