Removal of Perineuronal Nets in the Medial Prefrontal Cortex Impairs the Acquisition and Reconsolidation of a Cocaine-Induced Conditioned Place Preference Memory
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Pyramidal neurons in the medial prefrontal cortex (mPFC) critically contribute to cocaine-seeking behavior in humans and rodents. Activity of these neurons is significantly modulated by GABAergic, parvalbumin-containing, fast-spiking interneurons, the majority of which are enveloped by specialized structures of extracellular matrix called perineuronal nets (PNNs), which are integral to the maintenance of many types of plasticity. Using a conditioned place preference (CPP) procedure, we found that removal of PNNs primarily from the prelimbic region of the mPFC of adult, male, Sprague Dawley rats impaired the acquisition and reconsolidation of a cocaine-induced CPP memory. This impairment was accompanied by a decrease in the number of c-Fos-positive cells surrounded by PNNs. Following removal of PNNs, the frequency of inhibitory currents in mPFC pyramidal neurons was decreased; but following cocaine-induced CPP, both frequency and amplitude of inhibitory currents were decreased. Our findings suggest that cocaine-induced plasticity is impaired by removal of prelimbic mPFC PNNs and that PNNs may be a therapeutic target for disruption of cocaine CPP memories.
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The mPFC has reward-regulated mechanisms of spatial learning.
“The mPFC has an integrative role in object, place and time information [114, 115] as well as reward-regulated mechanisms of spatial learning [116, 117].”
From The extracellular matrix and perineuronal nets in memory (2022) · cites this paper as [117]
The Discussion reports that perineuronal nets in the prelimbic mPFC contribute to acquiring and reconsolidating a cocaine-associated conditioned place preference memory. This supports a role in reward-associated place learning in rats, but not the broader claim about reward-regulated mechanisms of spatial learning generally. (LLM, conf=0.83)
Experimental — accuracy not yet measuredRemoval of PNNs with ChABC in the mPFC or lateral hypothalamus prior to CPP training attenuates acquisition of the CPP memory, and removal after CPP training attenuates memory reconsolidation.
“For example, removal of PNNs with ChABC in the mPFC or lateral hypothalamus prior to training for conditioned place preference (CPP) attenuates acquisition of the CPP memory [117, 159], and removal after CPP training also attenuates memory reconsolidation [117].”
From The extracellular matrix and perineuronal nets in memory (2022) · cites this paper as [117]
Removal of PNNs with ChABC alters behavioural responses to drugs.
“Several studies have demonstrated that removal of PNNs with ChABC alters behavioural responses to drugs.”
From The extracellular matrix and perineuronal nets in memory (2022) · cites this paper as [117]
Degrading PNNs with Ch-ABC in the mPFC reduces the acquisition and/or maintenance (reconsolidation) of cocaine memory in a conditioned place preference model of addiction in rats.
“degrading PNNs with Ch--ABC in the mPFC reduced the acquisition and/or maintenance (reconsolidation) of cocaine memory in a conditioned place preference model of addiction in rats (Slaker et al., 2015)”
From Casting a Wide Net: Role of Perineuronal Nets in Neural Plasticity (2016) · cites this paper as Slaker et al., 2015
ChABC-induced removal of perineuronal nets in the medial prefrontal cortex impaired acquisition and reconsolidation of conditioned place preference memory after its impairment by cocaine.
“Moreover, the ChABC-induced removal of PNs in the medial prefrontal cortex impaired acquisition and reconsolidation of conditioned place preference memory after its impairment by cocaine (Slaker et al., 2015).”
From Damaged Neocortical Perineuronal Nets Due to Experimental Focal Cerebral Ischemia in Mice, Rats and Sheep (2017) · cites this paper as Slaker et al., 2015
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Cites
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works
AChE-stained horizontal sections of the rat brain in stereotaxic coordinates
Paxinos, G., WATSON, C. R. R., & Emson, P. C. (1980) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(80)90021-7 · Cited by 4,501 · see citing works
Bardo, M. T., & Hammer, R. P. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90226-e · Cited by 3,229 · see citing works
Interneurons of the neocortical inhibitory system
Markram, H., Toledo-Rodriguez, M., Wang, Y., Gupta, A., Silberberg, G., & Wu, C. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1519 · Cited by 2,954 · see citing works
The Neural Basis of Addiction: A Pathology of Motivation and Choice
Kalivas, P. W., & Volkow, N. D. (2005) · American Journal of Psychiatry · doi:10.1176/appi.ajp.162.8.1403 · Cited by 2,757 · see citing works
Dysfunction of the prefrontal cortex in addiction: neuroimaging findings and clinical implications
Goldstein, R. Z., & Volkow, N. D. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3119 · Cited by 2,749 · see citing works
Reactivation of Ocular Dominance Plasticity in the Adult Visual Cortex
Pizzorusso, T., Medini, P., Berardi, N., Chierzi, S., Fawcett, J. W., & Maffei, L. (2002) · Science · doi:10.1126/science.1072699 · Cited by 1,679 · see citing works
Jentsch, J. D., & Taylor, J. R. (1999) · Psychopharmacology · doi:10.1007/pl00005483 · Cited by 1,545 · see citing works
Limbic Activation During Cue-Induced Cocaine Craving
Childress, A. R., Mozley, P. D., McElgin, W., Fitzgerald, J., Reivich, M., & O’Brien, C. P. (1999) · American Journal of Psychiatry · doi:10.1176/ajp.156.1.11 · Cited by 1,513 · see citing works
Prefrontal executive and cognitive functions in rodents: neural and neurochemical substrates
Dalley, J. W., Cardinal, R. N., & Robbins, T. W. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.09.006 · Cited by 1,329 · see citing works
Activation of memory circuits during cue-elicited cocaine craving.
Grant, S., London, E. D., Newlin, D. B., Villemagne, V. L., Liu, X., Contoreggi, C., Phillips, R. L., Kimes, A. S., & Margolin, A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.21.12040 · Cited by 936 · see citing works
The circuitry mediating cocaine-induced reinstatement of drug-seeking behavior
McFarland, K., & Kalivas, P. W. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-21-08655.2001 · Cited by 905 · see citing works
Perineuronal Nets Protect Fear Memories from Erasure
Gogolla, N., Caroni, P., Lüthi, A., & Herry, C. (2009) · Science · doi:10.1126/science.1174146 · Cited by 760 · see citing works
Extinction circuits for fear and addiction overlap in prefrontal cortex
Peters, J., Kalivas, P. W., & Quirk, G. J. (2009) · Learning & Memory · doi:10.1101/lm.1041309 · Cited by 736 · see citing works
Molecular mechanisms of memory acquisition, consolidation and retrieval
Abel, T. G., & Lattal, K. M. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00194-x · Cited by 689 · see citing works
Brain circuitry and the reinstatement of cocaine-seeking behavior
Kalivas, P., & McFarland, K. (2003) · Psychopharmacology · doi:10.1007/s00213-003-1393-2 · Cited by 613 · see citing works
Neural activity related to drug craving in cocaine addiction
Kilts, C. D., Schweitzer, J. B., Quinn, C. K., Gross, R. E., Faber, T. L., Muhammad, F., Ely, T. D., Hoffman, J. M., & Drexler, K. P. G. (2001) · Archives of General Psychiatry · doi:10.1001/archpsyc.58.4.334 · Cited by 556 · see citing works
Brain extracellular matrix affects AMPA receptor lateral mobility and short-term synaptic plasticity
Frischknecht, R., Heine, M., Perrais, D., Seidenbecher, C. I., Choquet, D., & Gundelfinger, E. D. (2009) · Nature Neuroscience · doi:10.1038/nn.2338 · Cited by 554 · see citing works
Fuchs, R. A., Evans, K. A., Ledford, C. C., Parker, M. P., Case, J. M., Mehta, R. H., & See, R. E. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300579 · Cited by 517 · see citing works
Drug Addiction and the Memory Systems of the Brain
Robbins, T. W., Ersche, K. D., & Everitt, B. J. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1441.020 · Cited by 447 · see citing works
Wisteria floribunda agglutinin-labelled nets surround parvalbumin-containing neurons
Härtig, W., Brauer, K., & Brückner, G. (1992) · NeuroReport · doi:10.1097/00001756-199210000-00012 · Cited by 440 · see citing works
Functional Magnetic Resonance Imaging of Human Brain Activation During Cue-Induced Cocaine Craving
Maas, L. C., Lukas, S. E., Kaufman, M. J., Weiss, R. D., Daniels, S. L., Rogers, V. W., Kukes, T. J., & Renshaw, P. F. (1998) · American Journal of Psychiatry · doi:10.1176/ajp.155.1.124 · Cited by 434 · see citing works
Chondroitinase ABC Promotes Sprouting of Intact and Injured Spinal Systems after Spinal Cord Injury
Barritt, A. W., Davies, M., Marchand, F., Hartley, R., Grist, J., Yip, P., McMahon, S. B., & Bradbury, E. J. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.2980-06.2006 · Cited by 413 · see citing works
Ciccocioppo, R., Sanna, P. P., & Weiss, F. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.4.1976 · Cited by 371 · see citing works
Dityatev, A., Brückner, G., Dityateva, G., Grosche, J., Kleene, R., & Schachner, M. (2007) · Developmental Neurobiology · doi:10.1002/dneu.20361 · Cited by 365 · see citing works
Brückner, G., Brauer, K., Härtig, W., Wolff, J. R., Rickmann, M. J., Derouiche, A., Delpech, B., Girard, N., Oertel, W. H., & Reichenbach, A. (1993) · Glia · doi:10.1002/glia.440080306 · Cited by 358 · see citing works
Deepa, S. S., Umehara, Y., Higashiyama, S., Itoh, N., & Sugahara, K. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m207105200 · Cited by 332 · see citing works
Mauney, S. A., Athanas, K. M., Pantazopoulos, H., Shaskan, N., Passeri, E., Berretta, S., & Woo, T.-U. W. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.05.007 · Cited by 291 · see citing works
Very long-term memories may be stored in the pattern of holes in the perineuronal net
Tsien, R. Y. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1310158110 · Cited by 244 · see citing works
Optogenetic inhibition of cocaine seeking in rats
Stefanik, M. T., Moussawi, K., Kupchik, Y. M., Smith, K. C., Miller, R. L., Huff, M. L., Deisseroth, K. A., Kalivas, P. W., & LaLumiere, R. T. (2012) · Addiction Biology · doi:10.1111/j.1369-1600.2012.00479.x · Cited by 241 · see citing works
Happel, M. F. K., Niekisch, H., Castiblanco Rivera, L. L., Ohl, F. W., Deliano, M., & Frischknecht, R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1310272111 · Cited by 176 · see citing works
Depletion of Perineuronal Nets in the Amygdala to Enhance the Erasure of Drug Memories
Xue, Y.-X., Xue, L.-F., Liu, J.-F., He, J., Deng, J.-H., Sun, S.-C., Han, H.-B., Luo, Y.-X., Xu, L.-Z., Wu, P., et al. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.5390-13.2014 · Cited by 176 · see citing works
The infralimbic cortex regulates the consolidation of extinction after cocaine self-administrationPreprint
LaLumiere, R. T., Niehoff, K. E., & Kalivas, P. W. (2010) · Learning & Memory · doi:10.1101/lm.1576810 · Cited by 175 · see citing works
Ridder, D. D., Vanneste, S., Kovacs, S., Sunaert, S. G., & Dom, G. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.03.074 · Cited by 165 · see citing works
Memory Reconsolidation Mediates the Updating of Hippocampal Memory Content
Lee, J. L. C. (2010) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2010.00168 · Cited by 153 · see citing works
Hylin, M. J., Orsi, S. A., Moore, A. N., & Dash, P. K. (2013) · Learning & Memory · doi:10.1101/lm.030197.112 · Cited by 143 · see citing works
Corvetti, L., & Rossi, F. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.0683-05.2005 · Cited by 138 · see citing works
Dong, Y., Nasif, F. J., Tsui, J. J., Ju, W. Y. H., Cooper, D., Hu, X., Malenka, R. C., & White, F. J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4715-04.2005 · Cited by 129 · see citing works
van den Oever, M. C., Lubbers, B. R., Goriounova, N. A., Li, K. W., van der Schors, R. C., Loos, M., Riga, D., Wiskerke, J., Binnekade, R., Stegeman, M., et al. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.90 · Cited by 126 · see citing works
Sparta, D. R., Hovelsø, N., Mason, A. O., Kantak, P. A., Ung, R. L., Decot, H., & Stuber, G. D. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0235-13.2014 · Cited by 123 · see citing works
Brown, T. E., Forquer, M. R., Cocking, D. L., Jansen, H. T., Harding, J. W., & Sorg, B. A. (2007) · Learning & Memory · doi:10.1101/lm.476207 · Cited by 121 · see citing works
Self-citationRepeated Cocaine Weakens GABAB-Girk Signaling in Layer 5/6 Pyramidal Neurons in the Prelimbic Cortex
Hearing, M. C., Kotecki, L., de Velasco, E. M. F., Fajardo‐Serrano, A., Chung, H. J., Luján, R., & Wickman, K. D. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.019 · Cited by 117 · see citing works
Sun, W., & Rebec, G. V. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1413-06.2006 · Cited by 116 · see citing works
Neurosciences in the Third Millennium: A Tribute to Mimo Costa
Murray, T. F. (2004) · Critical Reviews in Neurobiology · doi:10.1615/critrevneurobiol.v16.i12.10 · Cited by 111 · see citing works
Nasif, F. J., Hu, X., & White, F. J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0010-05.2005 · Cited by 107 · see citing works
Altered Prelimbic Cortex Output during Cue-Elicited Drug Seeking
Miller, C. A., & Marshall, J. F. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1685-04.2004 · Cited by 102 · see citing works
Combination treatment with chondroitinase ABC in spinal cord injury—breaking the barrier
Zhao, R., & Fawcett, J. W. (2013) · Neuroscience Bulletin · doi:10.1007/s12264-013-1359-2 · Cited by 100 · see citing works
Nasif, F. J., Sidiropoulou, K., Hu, X., & White, F. J. (2005) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.104.075184 · Cited by 100 · see citing works
Robinson, M. J. F., & Franklin, K. B. J. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.04.056 · Cited by 99 · see citing works
Gherardini, L. M., Gennaro, M., & Pizzorusso, T. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht217 · Cited by 86 · see citing works
Huang, C., Lin, H., & Hsu, K. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhl096 · Cited by 84 · see citing works
Huang, C., Yang, P.-C., Lin, H.-J., & Hsu, K. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4247-06.2007 · Cited by 68 · see citing works
Prefrontal cortex and the organization of recent and remote memories: An alternative viewPreprint
Rudy, J. W., Biedenkapp, J. C., & O'Reilly, R. C. (2005) · Learning & Memory · doi:10.1101/lm.97905 · Cited by 67 · see citing works
Baclofen enhances extinction of opiate conditioned place preference
Heinrichs, S. C., Leite‐Morris, K. A., Carey, R. J., & Kaplan, G. B. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.10.013 · Cited by 60 · see citing works
Steullet, P., Cabungcal, J.-H., Cuénod, M., & Do, K. Q. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00244 · Cited by 49 · see citing works
Jayaram, P., & Steketee, J. D. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04000.x · Cited by 47 · see citing works
Schüppel, K., Brauer, K., Härtig, W., Grosche, J., Earley, B., Leonard, B. E., & Brückner, G. (2002) · Brain Research · doi:10.1016/s0006-8993(02)03569-2 · Cited by 47 · see citing works
Plasticity of L‐type Ca2+ channels after cocaine withdrawal
Ford, K. A., Wolf, M. E., & Hu, X. (2009) · Synapse · doi:10.1002/syn.20651 · Cited by 46 · see citing works
Bernard Katz, quantal transmitter release and the foundations of presynaptic physiology
Augustine, G. J., & Kasai, H. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.123224 · Cited by 33 · see citing works
Robinson, M. J., Armson, M. J., & Franklin, K. B. J. (2011) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2011.00042 · Cited by 28 · see citing works
Chefer, V. I., Wang, R., & Shippenberg, T. S. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.89 · Cited by 25 · see citing works
Optogenetically evoked gamma oscillations are disturbed by cocaine administration
Dilgen, J. E., Tompa, T., Saggu, S., Naselaris, T., & Lavı́n, A. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00213 · Cited by 22 · see citing works
Campanac, E., & Hoffman, D. A. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00596.2012 · Cited by 20 · see citing works
Itzhak, Y., & Anderson, K. L. (2011) · Addiction Biology · doi:10.1111/j.1369-1600.2011.00334.x · Cited by 19 · see citing works
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Tran, A. P., Warren, P. M., & Silver, J. (2018) · Physiological Reviews · doi:10.1152/physrev.00017.2017 · Cited by 883 · see citing works
The roles of perineuronal nets and the perinodal extracellular matrix in neuronal function
Fawcett, J. W., Oohashi, T., & Pizzorusso, T. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0196-3 · Cited by 589 · see citing works
Casting a Wide Net: Role of Perineuronal Nets in Neural Plasticity
Sorg, B. A., Berretta, S., Blacktop, J. M., Fawcett, J. W., Kitagawa, H., Kwok, J. C. F., & Miquel, M. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.2351-16.2016 · Cited by 454 · see citing works
Self-citationPerineuronal Nets: Plasticity, Protection, and Therapeutic Potential
Reichelt, A. C., Hare, D. J., Bussey, T. J., & Saksida, L. M. (2019) · Trends in Neurosciences · doi:10.1016/j.tins.2019.04.003 · Cited by 219 · see citing works
The extracellular matrix and perineuronal nets in memory
Fawcett, J. W., Fyhn, M., Jendelova, P., Kwok, J. C. F., Ruzicka, J., & Sorg, B. A. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01634-3 · Cited by 169 · see citing works
Self-citationPerineuronal Nets in the Adult Sensory Cortex Are Necessary for Fear Learning
Banerjee, S. B., Gutzeit, V. A., Baman, J., Aoued, H. S., Doshi, N. K., Liu, R. C., & Ressler, K. J. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.007 · Cited by 163 · see citing works
Miyata, S., & Kitagawa, H. (2017) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2017.06.010 · Cited by 171 · see citing works
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Mayne, P., & Burne, T. H. J. (2019) · Trends in Neurosciences · doi:10.1016/j.tins.2019.01.003 · Cited by 162 · see citing works
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Testa, D., Prochiantz, A., & Nardo, A. A. D. (2018) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2018.09.011 · Cited by 141 · see citing works
Lensjø, K. K., Christensen, A. C., Tennøe, S., Fyhn, M., & Hafting, T. (2017) · eneuro · doi:10.1523/eneuro.0379-16.2017 · Cited by 133 · see citing works
Wingert, J. C., & Sorg, B. A. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.673210 · Cited by 129 · see citing works
Self-citationShifting Developmental Trajectories During Critical Periods of Brain Formation
Dehorter, N., & del Pino, I. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00283 · Cited by 134 · see citing works
Oohashi, T., Edamatsu, M., Bekku, Y., & Carulli, D. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.09.010 · Cited by 131 · see citing works
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Carulli, D., & Verhaagen, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052434 · Cited by 123 · see citing works
Shi, W., Wei, X., Wang, X., Du, S., Liu, W., Song, J., & Wang, Y. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1902680116 · Cited by 122 · see citing works
Wiera, G., & Mozrzymas, J. W. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00427 · Cited by 117 · see citing works
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Bernard, C., & Prochiantz, A. (2016) · Neural Plasticity · doi:10.1155/2016/7931693 · Cited by 102 · see citing works
Haubrich, J., & Nader, K. (2016) · Current topics in behavioral neurosciences · doi:10.1007/7854_2016_463 · Cited by 100 · see citing works
Baker, K., Gray, A. R., & Richardson, R. (2017) · Behavioral Neuroscience · doi:10.1037/bne0000203 · Cited by 89 · see citing works
Bozzelli, P. L., Alaiyed, S., Kim, E., Villapol, S., & Conant, K. E. (2018) · Neural Plasticity · doi:10.1155/2018/5735789 · Cited by 90 · see citing works
Caccavano, A., Bozzelli, P. L., Forcelli, P. A., Pak, D. T. S., Wu, J., Conant, K. E., & Vicini, S. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0425-20.2020 · Cited by 85 · see citing works
Santiago, A. N., Lim, K. Y., Opendak, M., Sullivan, R. M., & Aoki, C. (2018) · Journal of Comparative Neurology · doi:10.1002/cne.24522 · Cited by 87 · see citing works
Slaker, M. L., Harkness, J. H., & Sorg, B. A. (2016) · IBRO Reports · doi:10.1016/j.ibror.2016.10.001 · Cited by 86 · see citing works
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Chen, H., & Lasek, A. W. (2020) · Addiction Biology · doi:10.1111/adb.12821 · Cited by 73 · see citing works
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Lasek, A. W., Chen, H., & Chen, W.-Y. (2018) · Trends in Genetics · doi:10.1016/j.tig.2017.12.004 · Cited by 71 · see citing works
Chondroitin 6-sulphate is required for neuroplasticity and memory in ageing
Yang, S., Gigout, S., Molinaro, A., Naito-Matsui, Y., Hilton, S., Foscarin, S., Nieuwenhuis, B., Tan, C. L., Verhaagen, J., Pizzorusso, T., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01208-9 · Cited by 70 · see citing works
Signals from the Fourth Dimension Regulate Drug Relapse
Mulholland, P. J., Chandler, L. J., & Kalivas, P. W. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.04.007 · Cited by 67 · see citing works
Drzewiecki, C. M., Willing, J., & Juraska, J. M. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02137-z · Cited by 67 · see citing works
Reichelt, A. C., Gibson, G. D., Abbott, K. N., & Hare, D. J. (2019) · Food & Function · doi:10.1039/c8fo02118j · Cited by 65 · see citing works
Slaker, M. L., Jorgensen, E. T., Hegarty, D. M., Liu, X., Kong, Y., Zhang, F., Linhardt, R. J., Brown, T. E., Aicher, S. A., & Sorg, B. A. (2018) · eneuro · doi:10.1523/eneuro.0221-18.2018 · Cited by 64 · see citing works
Self-citationBlocking human fear memory with the matrix metalloproteinase inhibitor doxycycline
Bach, D. R., Tzovara, A., & Vunder, J. (2018) · Molecular Psychiatry · doi:10.1038/mp.2017.65 · Cited by 64 · see citing works
Drzewiecki, C. M., & Juraska, J. M. (2020) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2020.173044 · Cited by 67 · see citing works
Koskinen, M.-K., van Mourik, Y., Smit, A. B., Riga, D., & Spijker, S. (2020) · Scientific Reports · doi:10.1038/s41598-020-73173-2 · Cited by 61 · see citing works
Effects of Ethanol on Brain Extracellular Matrix: Implications for Alcohol Use Disorder
Lasek, A. W. (2016) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.13200 · Cited by 57 · see citing works
Slaker, M. L., Barnes, J., Sorg, B. A., & Grimm, J. W. (2016) · PLoS ONE · doi:10.1371/journal.pone.0168256 · Cited by 57 · see citing works
Self-citationIncubation of depression: ECM assembly and parvalbumin interneurons after stress
Spijker, S., Koskinen, M.-K., & Riga, D. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.07.015 · Cited by 55 · see citing works
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Sun, Z. Y., Bozzelli, P. L., Caccavano, A., Allen, M., Balmuth, J., Vicini, S., Wu, J., & Conant, K. E. (2017) · Hippocampus · doi:10.1002/hipo.22804 · Cited by 55 · see citing works
Diurnal changes in perineuronal nets and parvalbumin neurons in the rat medial prefrontal cortex
Harkness, J. H., Gonzalez, A. E., Bushana, P. N., Jorgensen, E. T., Hegarty, D. M., Nardo, A. A. D., Prochiantz, A., Wisor, J. P., Aicher, S. A., Brown, T. E., et al. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02229-4 · Cited by 51 · see citing works
Self-citationHärtig, W., Mages, B., Aleithe, S., Nitzsche, B., Altmann, S., Barthel, H., Krueger, M., & Michalski, D. (2017) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2017.00015 · Cited by 53 · see citing works
Caught in the Net: Perineuronal Nets and Addiction
Slaker, M. L., Blacktop, J. M., & Sorg, B. A. (2016) · Neural Plasticity · doi:10.1155/2016/7538208 · Cited by 50 · see citing works
Self-citationAllen, M., Ghosh, S., Ahern, G. P., Villapol, S., Maguire‐Zeiss, K. A., & Conant, K. E. (2016) · Scientific Reports · doi:10.1038/srep35497 · Cited by 49 · see citing works
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Manto, M. U., Adamaszek, M., Apps, R., Carlson, E. S., Guarque‐Chabrera, J., Heleven, E., Kakei, S., Khodakhah, K., Kuo, S., Lin, C.-Y. R., et al. (2024) · The Cerebellum · doi:10.1007/s12311-024-01702-0 · Cited by 50 · see citing works
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Laham, B. J., & Gould, E. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.814287 · Cited by 47 · see citing works
A potential role for glia‐derived extracellular matrix remodeling in postinjury epilepsy
Kim, S. Y., Porter, B. E., Friedman, A., & Kaufer, D. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23758 · Cited by 47 · see citing works
The Physiology of Homeoprotein Transduction
Nardo, A. A. D., Fuchs, J., Joshi, R. L., Moya, K. L., & Prochiantz, A. (2018) · Physiological Reviews · doi:10.1152/physrev.00018.2017 · Cited by 41 · see citing works
Haubrich, J., Bernabo, M., Baker, A. G., & Nader, K. (2020) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-091319-024636 · Cited by 44 · see citing works
Prefrontal cortex development and its implications in mental illness
Goodpaster, C. M., Christensen, C. R., Alturki, M.-B., & DeNardo, L. A. (2025) · Neuropsychopharmacology · doi:10.1038/s41386-025-02154-8 · Cited by 53 · see citing works
Reconsolidation blockade for the treatment of addiction: challenges, new targets, and opportunitiesPreprint
Exton-McGuinness, M. T. J., & Milton, A. L. (2018) · Learning & Memory · doi:10.1101/lm.046771.117 · Cited by 43 · see citing works
Cerebellar perineuronal nets in cocaine-induced pavlovian memory: Site matters
Carbo‐Gas, M., Moreno, J. M. M., Guarque‐Chabrera, J., Vazquez-Sanroman, D. B., Gil‐Miravet, I., Carulli, D., Hoebeek, F. E., Zeeuw, C. I. D., Sanchis‐Segura, C., & Miquel, M. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.07.009 · Cited by 44 · see citing works
Blacktop, J. M., Todd, R. P., & Sorg, B. A. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.03.018 · Cited by 43 · see citing works
Self-citationVazquez‐Sanroman, D. B., Monje, R. D., & Bardo, M. T. (2017) · Addiction Biology · doi:10.1111/adb.12437 · Cited by 40 · see citing works
Blacktop, J. M., & Sorg, B. A. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-018-0212-8 · Cited by 40 · see citing works
Self-citationMolecular and circuit mechanisms regulating cocaine memory
Bender, B. N., & Torregrossa, M. M. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03498-8 · Cited by 39 · see citing works
García-Pardo, M. P., Roger-Sánchez, C., Rodríguez‐Arias, M., Miñarro, J., & Aguilar, M. A. (2016) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2016.03.065 · Cited by 39 · see citing works
Dingess, P. M., Darling, R. A., Derman, R. C., Wulff, S. S., Hunter, M. L., Ferrario, C. R., & Brown, T. E. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.57 · Cited by 38 · see citing works
Self-citationSleep disruption elevates oxidative stress in parvalbumin-positive cells of the rat cerebral cortex
Harkness, J. H., Bushana, P. N., Todd, R. P., Clegern, W. C., Sorg, B. A., & Wisor, J. P. (2018) · SLEEP · doi:10.1093/sleep/zsy201 · Cited by 39 · see citing works
Self-citationZhang, T., Yanagida, J., Kamii, H., Wada, S., Domoto, M., Sasase, H., Deyama, S., Takarada, T., Hinoi, E., Sakimura, K., et al. (2019) · Addiction Biology · doi:10.1111/adb.12723 · Cited by 39 · see citing works
Perineuronal nets gain prominence for their role in learning, memory, and plasticity
Shen, H. H. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1815273115 · Cited by 38 · see citing works
Bitanihirwe, B. K. Y., Mauney, S. A., & Woo, T.-U. W. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.03.1047 · Cited by 37 · see citing works
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Dingess, P. M., Harkness, J. H., Slaker, M. L., Zhang, Z., Wulff, S. S., Sorg, B. A., & Brown, T. E. (2018) · Neural Plasticity · doi:10.1155/2018/2108373 · Cited by 37 · see citing works
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Paylor, J. W., Wendlandt, E., Freeman, T. S., Greba, Q., Marks, W. N., Howland, J. G., & Winship, I. R. (2018) · eNeuro · doi:10.1523/eneuro.0253-18.2018 · Cited by 37 · see citing works
Zhang, L., Gao, Y.-Z., Zhao, C., Xia, J., Yang, J., & Ji, M. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109382 · Cited by 37 · see citing works
Cocaine-induced plasticity in the cerebellum of sensitised mice
Vazquez-Sanroman, D. B., Carbo‐Gas, M., Leto, K., Cerezo, M., Gil‐Miravet, I., Sanchis‐Segura, C., Carulli, D., Rossi, F., & Miquel, M. (2015) · Psychopharmacology · doi:10.1007/s00213-015-4072-1 · Cited by 37 · see citing works
From molecules to behavior: Implications for perineuronal net remodeling in learning and memory
Sanchez, B., Kraszewski, P., Lee, S., & Cope, E. C. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.16036 · Cited by 37 · see citing works
Cornez, G., Madison, F. N., der Linden, A. V., Cornil, C. A., Yoder, K. M., Ball, G. F., & Balthazart, J. (2017) · Developmental Neurobiology · doi:10.1002/dneu.22485 · Cited by 36 · see citing works
Blanco, I., & Conant, K. E. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14910 · Cited by 37 · see citing works
Modelos animales de adicción a las drogas
García-Pardo, M. P., Sánchez, C. R., Ortí, J. E. D. L. R., & Calpe, M. A. A. (2017) · Adicciones · doi:10.20882/adicciones.862 · Cited by 35 · see citing works
Li, Y., Ge, S., Li, N., Chen, L., Zhang, S., Wang, J., Wu, H., Wang, X., & Wang, X. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.11.063 · Cited by 33 · see citing works
Lubbers, B. R., Matos, M. R., Horn, A., Visser, E., Van der Loo, R. C., Gouwenberg, Y., Meerhoff, G. F., Frischknecht, R., Seidenbecher, C. I., Smit, A. B., et al. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2015.361 · Cited by 34 · see citing works
Reinhard, S. M., Rais, M., Afroz, S., Hanania, Y., Pendi, K., Espinoza, K., Rosenthal, R., Binder, D. K., Ethell, I. M., & Razak, K. A. (2019) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2019.107042 · Cited by 33 · see citing works
Alonso‐Caraballo, Y., Fetterly, T. L., Jorgensen, E. T., Nieto, A. M., Brown, T. E., & Ferrario, C. R. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-0781-1 · Cited by 33 · see citing works
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Eill, G. J., Sinha, A., Morawski, M., Viapiano, M. S., & Matthews, R. T. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.010830 · Cited by 32 · see citing works
Mascio, G., Notartomaso, S., Martinello, K., Liberatore, F., Bucci, D., Imbriglio, T., Cannella, M., Antenucci, N., Scarselli, P., Lattanzi, R., et al. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1714-21.2022 · Cited by 32 · see citing works
The protein tyrosine phosphatase RPTPζ/phosphacan is critical for perineuronal net structure
Eill, G. J., Sinha, A., Morawski, M., Viapiano, M. S., & Matthews, R. T. (2020) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)49907-8 · Cited by 32 · see citing works
Distinct roles for hyaluronan in neural stem cell niches and perineuronal nets
Su, W., Matsumoto, S. G., Sorg, B. A., & Sherman, L. S. (2018) · Matrix Biology · doi:10.1016/j.matbio.2018.01.022 · Cited by 32 · see citing works
Self-citationLearning-induced intrinsic and synaptic plasticity in the rodent medial prefrontal cortex
Porter, J. T., & Sepulveda-Orengo, M. T. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2019.107117 · Cited by 30 · see citing works
Muñiz, J. A., Prieto, J. P., González, B., Sosa, M. H., Cadet, J. L., Scorza, C., Urbano, F. J., & Bisagno, V. (2017) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2017.00200 · Cited by 30 · see citing works
Miquel, M., Gil‐Miravet, I., & Guarque‐Chabrera, J. (2020) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2020.586574 · Cited by 30 · see citing works
Sexually dimorphic perineuronal nets in the rodent and primate reproductive circuit
Ciccarelli, A., Weijers, D., Kwan, W. C., Warner, C. E., Bourne, J. A., & Gross, C. T. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25167 · Cited by 28 · see citing works
Addiction and the cerebellum with a focus on actions of opioid receptors
Ranjbar, H., Soti, M., Banazadeh, M., Saleki, K., Kohlmeier, K. A., & Shabani, M. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.09.021 · Cited by 28 · see citing works
Perineuronal nets affect memory and learning after synapse withdrawal
Růžička, J., Dalecká, M., Safrankova, K., Peretti, D., Mallucci, G. R., Jendelová, P., Kwok, J. C. F., & Fawcett, J. W. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-02226-z · Cited by 27 · see citing works
Cornez, G., Jonckers, E., ter Haar, S. M., der Linden, A. V., Cornil, C. A., & Balthazart, J. (2018) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2018.0849 · Cited by 27 · see citing works
NPY-Y1 receptor signaling controls spatial learning and perineuronal net expression
Bertocchi, I., Mele, P., Ferrero, G., Oberto, A., Carulli, D., & Eva, C. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.108425 · Cited by 26 · see citing works
A Role for Matrix Metalloproteases in Antidepressant Efficacy
Alaiyed, S., & Conant, K. E. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00117 · Cited by 25 · see citing works
Liu, L., Zhang, Y., Men, S., Li, X., Hou, S., & Ju, J. (2023) · Hippocampus · doi:10.1002/hipo.23503 · Cited by 26 · see citing works
Li, X., Wu, X., Lu, T., Kuang, C., Si, Y., Zheng, W., Li, Z., & Xue, Y.-X. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25063412 · Cited by 25 · see citing works
Net gain and loss: influence of natural rewards and drugs of abuse on perineuronal nets
Brown, T. E., & Sorg, B. A. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01337-x · Cited by 25 · see citing works
Self-citationThe Mechanisms and Boundary Conditions of Drug Memory Reconsolidation
Chen, L., He, Y., Wang, Y., He, Z., Leng, Q., Huang, S., Wu, F., Feng, X., & Yan, J. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.717956 · Cited by 23 · see citing works
Roura-Martínez, D., Díaz-Bejarano, P., Ucha, M., Paiva, R. R., Ambrosio, E., & Higuera-Matas, A. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.108290 · Cited by 23 · see citing works
Sultana, R., Brooks, C. B., Shrestha, A., Ogundele, O. M., & Lee, C. C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222011140 · Cited by 21 · see citing works
Gil‐Miravet, I., Eixea, I. M., Arias‐Sandoval, E., Vásquez-Celaya, L., Guarque‐Chabrera, J., Olucha-Bordonau, F. E., & Miquel, M. (2019) · Addiction Biology · doi:10.1111/adb.12834 · Cited by 21 · see citing works
Sex and region-specific effects of high fat diet on PNNs in obesity susceptible rats
Dingess, P. M., Zhang, Z., Sorg, B. A., Ferrario, C. R., & Brown, T. E. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.112963 · Cited by 21 · see citing works
Self-citationPerineuronal Net Receptor PTPσ Regulates Retention of Memories
Lesnikova, A., Casarotto, P., Moliner, R., Fred, S. M., Biojone, C., & Castrén, E. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.672475 · Cited by 21 · see citing works
Jorgensen, E. T., Gonzalez, A. E., Harkness, J. H., Hegarty, D. M., Thakar, A., Burchi, D. J., Aadland, J. A., Aicher, S. A., Sorg, B. A., & Brown, T. E. (2020) · Addiction Biology · doi:10.1111/adb.12947 · Cited by 20 · see citing works
Self-citation
- Authors
- Slaker, M., Churchill, L., Todd, R. P., Blacktop, J. M., Zuloaga, D. G., Raber, J., Darling, R. A., Brown, T. E., & Sorg, B. A.
- Affiliations
- Washington State University Vancouver (US)
- Washington State University (US)
- Oregon Health & Science University (US)
- Oregon National Primate Research Center (US)
- University of Wyoming (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2015-03-11
- Volume
- 35
- Issue
- 10
- Pages
- 4190-4202
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC4355195
- OpenAlex
- W2059869176
- Cited by
- 208
- References
- 64
- Citations by year
- 2026: 12 · 2025: 15 · 2024: 21 · 2023: 13 · 2022: 18 · 2021: 20 · 2020: 32 · 2019: 19 · 2018: 19 · 2017: 18 · 2016: 15 · 2015: 6
- FWCI
- 8.98
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Aeronautics and Space Administration (#NNJ12ZSA001N)
- Washington State University
- National Institute on Drug Abuse (DA030647, R21DA030647, DA033404, T32DA007262, R01DA033404)
- National Institute of General Medical Sciences (P30 GM103398-32128, P30GM103398)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- perineuronal nets, medial prefrontal cortex, prelimbic cortex, cocaine, conditioned place preference, memory reconsolidation, memory acquisition, parvalbumin interneurons, fast-spiking interneurons, pyramidal neurons, c-fos, extracellular matrix, cocaine-seeking behavior, addiction treatment targets
- MeSH terms
- Animals, Association Learning, Brain Injuries, Cocaine, Conditioning, Operant, Extinction, Psychological, Male, Memory Disorders, Nerve Net, Nerve Tissue Proteins, Neuronal Plasticity, Time Factors, Proto-Oncogene Proteins c-fos, Rats, Sprague-Dawley, Prefrontal Cortex, Microscopy, Confocal, Dopamine Uptake Inhibitors, Chondroitin ABC Lyase, Receptors, N-Acetylglucosamine, Plant Lectins, Rats
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