Releasing Addiction Memories Trapped in Perineuronal Nets
Open accessAbstract
Drug addiction can be conceptualized at a basic level as maladaptive learning and memory. Addictive substances elicit changes in brain circuitry involved in reward, cognition, and emotional state, leading to the formation and persistence of strong drug-associated memories that lead to craving and relapse. Recently, perineuronal nets (PNNs), extracellular matrix (ECM) structures surrounding neurons, have emerged as regulators of learning, memory, and addiction behaviors. PNNs do not merely provide structural support to neurons but are dynamically remodeled in an experience-dependent manner by metalloproteinases. They function in various brain regions through constituent proteins such as brevican that are implicated in neural plasticity. Understanding the function of PNN components in memory processes may lead to new therapeutic approaches to treating addiction.
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Drugs of abuse can either decrease or increase PNNs.
“Several studies have shown that drugs of abuse can either decrease or increase PNNs (see [153] for review).”
From The extracellular matrix and perineuronal nets in memory (2022) · cites this paper as [153]
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1 retracted
Matrix Metalloproteinase (MMP) 9 Transcription in Mouse Brain Induced by Fear Learning
Ganguly, K., Rejmak, E., Mikosz, M., Nikolaev, E., Knapska, E., & Kaczmarek, L. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.457903 · Cited by 100 · see citing works
RetractedRemodelling the extracellular matrix in development and disease
Bonnans, C., Chou, J., & Werb, Z. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3904 · Cited by 4,367 · 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
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
Contextual and temporal modulation of extinction: behavioral and biological mechanisms
Bouton, M. E., Westbrook, R. F., Corcoran, K. A., & Maren, S. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.12.015 · Cited by 671 · see citing works
The ADAMTS (A Disintegrin and Metalloproteinase with Thrombospondin motifs) family
Kelwick, R. J. R., Desanlis, I., Wheeler, G. N., & Edwards, D. R. (2015) · Genome biology · doi:10.1186/s13059-015-0676-3 · Cited by 654 · see citing works
Matrix metalloproteinase-9 is required for hippocampal late-phase long-term potentiation and memory
Nagy, V., Bozdagi, O., Matynia, A., Balcerzyk, M., Okulski, P., Dzwonek, J., Costa, R. M., Silva, A. J., Kaczmarek, L., & Huntley, G. W. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4359-05.2006 · Cited by 499 · see citing works
Animals lacking link protein have attenuated perineuronal nets and persistent plasticity
Carulli, D., Pizzorusso, T., Kwok, J. C. F., Putignano, E., Poli, A., Forostyak, S., Andrews, M. R., Deepa, S. S., Glant, T. T., & Fawcett, J. W. (2010) · Brain · doi:10.1093/brain/awq145 · Cited by 495 · 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
Favuzzi, E., Marques-Smith, A., Deogracias, R., Winterflood, C. M., Sánchez-Aguilera, A., Mantoan, L., Maeso, P., Fernandes, C., Ewers, H., & Rico, B. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.028 · Cited by 397 · 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
Carulli, D., Rhodes, K. E., Brown, D. J., Bonnert, T. P., Pollack, S. J., Oliver, K., Strata, P., & Fawcett, J. W. (2006) · Journal of Comparative Neurology · doi:10.1002/cne.20822 · Cited by 341 · see citing works
Seif, T., Chang, S., Simms, J. A., Gibb, S. L., Dadgar, J., Chen, B. T., Harvey, B. K., Dorit Ron, A., Messing, R. O., Bonci, A., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3445 · Cited by 310 · see citing works
Synaptic circuit remodelling by matrix metalloproteinases in health and disease
Huntley, G. W. (2012) · Nature reviews. Neuroscience · doi:10.1038/nrn3320 · Cited by 282 · see citing works
Meighan, S. E., Meighan, P. C., Choudhury, P., Davis, C. J., Olson, M. L., Zornes, P. A., Wright, J. W., & Harding, J. W. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03565.x · Cited by 281 · see citing works
Sensory Deprivation Alters Aggrecan and Perineuronal Net Expression in the Mouse Barrel Cortex
McRae, P. A., Rocco, M. M., Kelly, G., Brumberg, J. C., & Matthews, R. T. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5425-06.2007 · Cited by 272 · see citing works
Tenascins and the Importance of Adhesion ModulationPreprint
Chiquet‐Ehrismann, R., & Tucker, R. P. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a004960 · Cited by 272 · see citing works
Perineuronal Nets Suppress Plasticity of Excitatory Synapses on CA2 Pyramidal Neurons
Carstens, K. E., Phillips, M. L., Pozzo-Miller, L., Weinberg, R. J., & Dudek, S. M. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.0245-16.2016 · Cited by 271 · see citing works
Weber, P., Bartsch, U., Rasband, M. N., Czaniera, R., Lang, Y., Bluethmann, H., Margolis, R. U., Levinson, S. R., Shrager, P., Montag, D., et al. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-11-04245.1999 · Cited by 247 · see citing works
Romberg, C., Yang, S., Melani, R., Andrews, M. R., Horner, A. E., Spillantini, M. G., Bussey, T. J., Fawcett, J. W., Pizzorusso, T., & Saksida, L. M. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.6267-11.2013 · Cited by 231 · see citing works
Kochlamazashvili, G., Henneberger, C., Bukalo, O., Dvoretskova, E., Senkov, O., Lievens, P. M.-J., Westenbroek, R., Engel, A. K., Catterall, W. A., Rusakov, D. A., et al. (2010) · Neuron · doi:10.1016/j.neuron.2010.05.030 · Cited by 215 · see citing works
Slaker, M., Churchill, L., Todd, R. P., Blacktop, J. M., Zuloaga, D. G., Raber, J., Darling, R. A., Brown, T. E., & Sorg, B. A. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.3592-14.2015 · Cited by 208 · see citing works
Perineuronal net formation and structure in aggrecan knockout mice
Giamanco, K. A., Morawski, M., & Matthews, R. T. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.08.032 · Cited by 207 · 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
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
Coleman, L. G., Liu, W., Oguz, I., Styner, M., & Crews, F. T. (2014) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.11.021 · Cited by 170 · see citing works
Perineuronal 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
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
Giamanco, K. A., & Matthews, R. T. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.05.055 · Cited by 138 · see citing works
Structural and Functional Aberrations in the Cerebral Cortex of Tenascin-C Deficient Mice
Irintchev, A., Rollenhagen, A., Troncoso, E., Kiss, J. Z., & Schachner, M. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhh195 · Cited by 137 · see citing works
Extracellular matrix protein expression is brain region dependent
Dauth, S., Grevesse, T., Pantazopoulos, H., Campbell, P. H., Maoz, B. M., Berretta, S., & Parker, K. K. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.23965 · Cited by 134 · see citing works
Synaptic plasticity mediating cocaine relapse requires matrix metalloproteinases
Smith, A. C. W., Kupchik, Y. M., Scofield, M. D., Gipson, C. D., Wiggins, A., Thomas, C. A., & Kalivas, P. W. (2014) · Nature Neuroscience · doi:10.1038/nn.3846 · Cited by 133 · 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
Pyka, M., Wetzel, C., Aguado, A., Geissler, M., Hatt, H., & Faissner, A. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07690.x · Cited by 131 · 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
Experience-dependent plasticity and modulation of growth regulatory molecules at central synapses
Foscarin, S., Ponchione, D., Pajaj, E., Leto, K., Gawlak, M., Wilczynski, G. M., Rossi, F., & Carulli, D. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016666 · Cited by 128 · 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
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
Mash, D. C., ffrench‐Mullen, J. M. H., Adi, N., Qin, Y., Buck, A., & Pablo, J. P. (2007) · PLoS ONE · doi:10.1371/journal.pone.0001187 · Cited by 119 · see citing works
Genome-Wide Association Study of Alcohol Dependence Implicates KIAA0040 on Chromosome 1q
Zuo, L., Gelernter, J. E., Zhang, H., Zhao, H., Lu, L., Kranzler, H. R., Malison, R. T., Li, C.-S. R., Wang, F., Zhang, X., et al. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.229 · Cited by 115 · see citing works
Nowicka, D., Soulsby, S., Skangiel‐Kramska, J., & Glazewski, S. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06996.x · Cited by 110 · see citing works
Nagy, V., Bozdagi, O., & Huntley, G. W. (2007) · Learning & Memory · doi:10.1101/lm.678307 · Cited by 107 · see citing works
Wegner, F., Härtig, W., Bringmann, A., Grosche, J., Wohlfarth, K., Zuschratter, W., & Brückner, G. (2003) · Experimental Neurology · doi:10.1016/s0014-4886(03)00313-3 · Cited by 107 · see citing works
Morellini, F., Sivukhina, E., Stoenica, L., Oulianova, E., Bukalo, O., Jakovcevski, I., Dityatev, A., Irintchev, A., & Schachner, M. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq017 · Cited by 104 · see citing works
Rossier, J., Bernard, A., Cabungcal, J.-H., Perrenoud, Q., Savoye, A., Gallopin, T., Hawrylycz, M., Cuénod, M., Do, K., Urban, A., et al. (2015) · Molecular Psychiatry · doi:10.1038/mp.2014.162 · Cited by 101 · see citing works
Distribution of pyramidal cells associated with perineuronal nets in the neocortex of rat
Alpár, A., Gärtner, U., Härtig, W., & Brückner, G. (2006) · Brain Research · doi:10.1016/j.brainres.2006.08.069 · Cited by 93 · see citing works
Baker, K., Gray, A. R., & Richardson, R. (2017) · Behavioral Neuroscience · doi:10.1037/bne0000203 · Cited by 89 · see citing works
Reward Learning Requires Activity of Matrix Metalloproteinase-9 in the Central Amygdala
Knapska, E., Lioudyno, V. I., Kiryk, A., Mikosz, M., Górkiewicz, T., Michaluk, P., Gawlak, M., Chaturvedi, M., Mochol, G., Balcerzyk, M., et al. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5239-12.2013 · Cited by 87 · see citing works
Ethanol-induced impairment of spatial memory and brain matrix metalloproteinases
Wright, J. W., Masino, A. J., Reichert, J. R., Turner, G. D., Meighan, S. E., Meighan, P. C., & Harding, J. W. (2003) · Brain Research · doi:10.1016/s0006-8993(02)04036-2 · Cited by 85 · see citing works
Madinier, A., Quattromani, M. J., Sjölund, C., Ruscher, K., & Wieloch, T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0093121 · Cited by 82 · see citing works
Severe cognitive and motor coordination deficits in Tenascin‐R‐deficient mice
Sallaz, M., & Montag, D. (2003) · Genes Brain & Behavior · doi:10.1034/j.1601-183x.2003.00003.x · Cited by 80 · see citing works
Repeated Binge Drinking Increases Perineuronal Nets in the Insular Cortex
Chen, H., He, D., & Lasek, A. W. (2015) · Alcoholism: Clinical and Experimental Research · doi:10.1111/acer.12847 · Cited by 77 · see citing works
Self-citationParvalbumin neurons and perineuronal nets in the mouse prefrontal cortex
Ueno, H., Suemitsu, S., Okamoto, M., Matsumoto, Y., & Ishihara, T. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.11.035 · Cited by 76 · see citing works
Metalloproteinase inhibition prevents inhibitory synapse reorganization and seizure genesis
Pollock, E., Everest, M., Brown, A., & Poulter, M. O. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.06.003 · Cited by 75 · see citing works
Mizoguchi, H., Yamada, K., Niwa, M., Mouri, A., Mizuno, T., Noda, Y., Nitta, A., Itohara, S., Banno, Y., & Nabeshima, T. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04288.x · Cited by 75 · see citing works
Morikawa, S., Ikegaya, Y., Narita, M., & Tamura, H. (2017) · Scientific Reports · doi:10.1038/srep46024 · Cited by 74 · see citing works
Mizoguchi, H., Yamada, K., Mouri, A., Niwa, M., Mizuno, T., Noda, Y., Nitta, A., Itohara, S., Banno, Y., & Nabeshima, T. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04623.x · Cited by 71 · see citing works
Inhibition of hippocampal matrix metalloproteinase-3 and -9 disrupts spatial memory
Wright, J. W., Brown, T. E., & Harding, J. W. (2007) · Neural Plasticity · doi:10.1155/2007/73813 · Cited by 71 · see citing works
Stefaniuk, M., Beroun, A., Lebitko, T., Markina, O. A., Łęski, S., Meyza, K. Z., Grzywacz, A., Samochowiec, J., Samochowiec, A., Radwańska, K., et al. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.12.026 · Cited by 70 · see citing works
Horii‐Hayashi, N., Sasagawa, T., Matsunaga, W., & Nishi, M. (2015) · Neural Plasticity · doi:10.1155/2015/256389 · Cited by 66 · see citing works
Increased metalloproteinase activity in the hippocampus following status epilepticus
Dubey, D., McRae, P. A., Rankin-Gee, E. K., Baranov, E., Wandrey, L., Rogers, S., & Porter, B. E. (2017) · Epilepsy Research · doi:10.1016/j.eplepsyres.2017.02.021 · Cited by 65 · see citing works
Zhang, X., Bhattacharyya, S., Kusumo, H., Goodlett, C. R., Tobacman, J. K., & Guizzetti, M. (2013) · Glia · doi:10.1002/glia.22604 · Cited by 65 · see citing works
Bekku, Y., Saito, M., Moser, M., Fuchigami, M., Maehara, A., Nakayama, M., Kusachi, S., Ninomiya, Y., & Oohashi, T. (2012) · Journal of Comparative Neurology · doi:10.1002/cne.23009 · Cited by 65 · see citing works
Brown, T. E., Forquer, M. R., Harding, J. W., Wright, J. W., & Sorg, B. A. (2008) · Synapse · doi:10.1002/syn.20562 · Cited by 61 · see citing works
Stamenković, V., Stamenković, S., Jaworski, T., Gawlak, M., Jovanović, M., Jakovčevski, I., Wilczynski, G. M., Kaczmarek, L., Schachner, M., Radenović, L., et al. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1224-y · Cited by 60 · see citing works
Yamada, J., & Jinno, S. (2017) · Journal of Comparative Neurology · doi:10.1002/cne.24132 · Cited by 59 · 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
The cerebellum on cocaine: plasticity and metaplasticity
Vazquez-Sanroman, D. B., Leto, K., Cerezo, M., Carbo‐Gas, M., Sanchis‐Segura, C., Carulli, D., Rossi, F., & Miquel, M. (2015) · Addiction Biology · doi:10.1111/adb.12223 · Cited by 57 · see citing works
Region-specific impairments in parvalbumin interneurons in social isolation-reared mice
Ueno, H., Suemitsu, S., Murakami, S., Kitamura, N., Wani, K., Okamoto, M., Matsumoto, Y., & Ishihara, T. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.07.016 · Cited by 56 · see citing works
Samochowiec, A., Grzywacz, A., Kaczmarek, L., Bieńkowski, P., Samochowiec, J., Mierzejewski, P., Preuss, U. W., Grochans, E., & Ciechanowicz, A. (2010) · Brain Research · doi:10.1016/j.brainres.2010.02.072 · Cited by 54 · see citing works
Hyaluronan-based extracellular matrix under conditions of homeostatic plasticity
Valenzuela, J. C., Heise, C., Franken, G., Singh, J. B., Schweitzer, B., Seidenbecher, C. I., & Frischknecht, R. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0606 · Cited by 46 · see citing works
Smith, A. C. W., Nealey, K. A., Wright, J. W., & Walker, B. M. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.04.011 · Cited by 45 · see citing works
Ueno, H., Suemitsu, S., Okamoto, M., Matsumoto, Y., & Ishihara, T. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.04.041 · Cited by 45 · 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
Vazquez‐Sanroman, D. B., Monje, R. D., & Bardo, M. T. (2017) · Addiction Biology · doi:10.1111/adb.12437 · Cited by 40 · see citing works
Levy, C., Brooks, J. M., Chen, J., Su, J., & Fox, M. A. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23701 · Cited by 38 · 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
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
Natarajan, R., Harding, J. W., & Wright, J. W. (2013) · Journal of Experimental Neuroscience · doi:10.4137/jen.s11381 · Cited by 31 · see citing works
Alterations in serum MMP and TIMP concentrations following chronic heroin abuse
Kovatsi, L., Batzios, S., Nikolaou, K., Fragou, D., Njau, S., Tsatsakis, A., Karakiulakis, G., & Papakonstantinou, E. (2013) · Toxicology Mechanisms and Methods · doi:10.3109/15376516.2012.758681 · Cited by 21 · see citing works
Morellini, F., Malyshev, A. Y., Volgushev, M., Chistiakova, M., Papashvili, G., Fellini, L., KLEENE, R. B., Schachner, M., & Dityatev, A. E. (2017) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2017.00016 · Cited by 16 · see citing works
Enriched environment alters the behavioral profile of tenascin-C deficient mice
Stamenković, V., Milenkovic, I., Galjak, N., Todorović, V., & Anđjus, P. R. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.05.047 · Cited by 13 · see citing works
Postnatal development of perineuronal nets in wild-type mice and in a mutant deficient in tenascin-R
Br�ckner, G., Grosche, J., Schmidt, S., H�rtig, W., Margolis, R. U., Delpech, B., Seidenbecher, C. I., Czaniera, R., & Schachner, M. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20001225)428:4
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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
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Carulli, D., & Verhaagen, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052434 · Cited by 123 · see citing works
Tewari, B. P., Chaunsali, L., Prim, C. E., & Sontheimer, H. W. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.1022754 · Cited by 107 · see citing works
Krishnaswamy, V. R., Benbenishty, A., Blinder, P., & Sagi, I. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03182-6 · Cited by 92 · see citing works
Harris, S. E., Cox, S. R., Bell, S., Marioni, R. E., Prins, B. P., Pattie, A., Corley, J., Maniega, S. M., Hernández, M. D. C. V., Morris, Z., et al. (2020) · Nature Communications · doi:10.1038/s41467-019-14161-7 · Cited by 78 · see citing works
Extracellular Matrix in Neural Plasticity and Regeneration
Chelyshev, Y. A., Kabdesh, I. M., & Mukhamedshina, Y. O. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00986-0 · Cited by 76 · see citing works
Circadian Rhythms of Perineuronal Net Composition
Pantazopoulos, H., Gisabella, B., Rexrode, L., Benefield, D., Yıldız, E., Seltzer, P., Valeri, J., Chelini, G., Reich, A., Ardelt, M., et al. (2020) · eNeuro · doi:10.1523/eneuro.0034-19.2020 · Cited by 73 · see citing works
Perineuronal Nets: Subtle Structures with Large Implications
Carceller, H., Gramuntell, Y., Klimczak, P., & Nácher, J. (2022) · The Neuroscientist · doi:10.1177/10738584221106346 · Cited by 48 · 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
Extracellular Metalloproteinases in the Plasticity of Excitatory and Inhibitory Synapses
Wiera, G., & Mozrzymas, J. W. (2021) · Cells · doi:10.3390/cells10082055 · Cited by 36 · 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
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
Orsini, C. A., Brown, T. E., Hodges, T. E., Alonso‐Caraballo, Y., Winstanley, C. A., & Becker, J. B. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1378-22.2022 · 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
Cell-type specific transcriptional adaptations of nucleus accumbens interneurons to amphetamine
Gallegos, D. A., Minto, M. S., Liu, F., Hazlett, M. F., Yousefzadeh, S. A., Bartelt, L. C., & West, A. E. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01466-1 · Cited by 24 · 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
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
Matrix metalloproteinase‐9: A magic drug target in neuropsychiatry?
Kaczmarek, K., Protokowicz, K., & Kaczmarek, L. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15976 · Cited by 23 · see citing works
Sullivan, E. V., Zhao, Q., Pohl, K. M., Zahr, N. M., & Pfefferbaum, A. (2021) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2021.01.053 · Cited by 23 · 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
Extracellular matrix abnormalities in the hippocampus of subjects with substance use disorder
Valeri, J., Stiplosek, C., O'Donovan, S. M., Sinclair, D., Grant, K. A., Bollavarapu, R., Platt, D. M., Stockmeier, C. A., Gisabella, B., & Pantazopoulos, H. (2024) · Translational Psychiatry · doi:10.1038/s41398-024-02833-y · Cited by 19 · see citing works
HITZEMANN, R. J., Phillips, T. J., Lockwood, D. R., Darakjian, P., & Searles, R. P. (2020) · Genomics · doi:10.1016/j.ygeno.2020.08.004 · Cited by 19 · see citing works
Differential regulation of alcohol consumption and reward by the transcriptional cofactor LMO4
Maiya, R., Pomrenze, M. B., Tran, T. N. A., Tiwari, G. R., Beckham, A., Paul, M. T., Mayfield, R. D., & Messing, R. O. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0706-8 · Cited by 17 · see citing works
Sanchez-Hernandez, A., Nicolas, C., Gil‐Miravet, I., Guarque‐Chabrera, J., Solinas, M., & Miquel, M. (2021) · Psychopharmacology · doi:10.1007/s00213-020-05752-0 · Cited by 17 · see citing works
Anderson, M. D., Paylor, J. W., Scott, G. A., Greba, Q., Winship, I. R., & Howland, J. G. (2020) · Learning & Memory · doi:10.1101/lm.050245.119 · Cited by 16 · see citing works
Pasqualitto, F., Panin, F., Maidhof, C., Thompson, N., & Fachner, J. C. (2023) · Brain Sciences · doi:10.3390/brainsci13020259 · Cited by 16 · see citing works
Catale, C., Martini, A., Piscitelli, R. M., Senzasono, B., Iacono, L. L., Mercuri, N. B., Guatteo, E., & Carola, V. (2022) · European Journal of Neuroscience · doi:10.1111/ejn.15825 · Cited by 17 · see citing works
The Role of the Cerebellum in Drug Reward: A Review
Wang, Y., & Yan, L. (2023) · Journal of Integrative Neuroscience · doi:10.31083/j.jin2206147 · Cited by 15 · see citing works
Huang, S., Liu, X., Li, Z., Si, Y., Yang, L., Deng, J., Luo, Y., Xue, Y.-X., & Lü, L. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01294-z · Cited by 14 · see citing works
Guarque‐Chabrera, J., Sanchez-Hernandez, A., Ibáñez-Marín, P., Eixea, I. M., & Miquel, M. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109210 · Cited by 14 · see citing works
Gisabella, B., Babu, J., Valeri, J., Rexrode, L., & Pantazopoulos, H. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.646678 · Cited by 13 · see citing works
Storage and erasure of behavioural experiences at the single neuron level
Dyakonova, T. L., Sultanakhmetov, G. S., Mezheritskiy, M., Sakharov, D. A., & Dyakonova, V. E. (2019) · Scientific Reports · doi:10.1038/s41598-019-51331-5 · Cited by 12 · see citing works
Galán‐Llario, M., Gramage, E., García‐Guerra, A., Torregrosa, A. B., Gasparyan, A., Navarro, D., Navarrete, F., García‐Gutiérrez, M. S., Manzanares, J., & Herradón, G. (2024) · Neuropharmacology · doi:10.1016/j.neuropharm.2024.109850 · Cited by 12 · see citing works
Modulation of stress-, pain-, and alcohol-related behaviors by perineuronal nets
Aguilar, J. S., & Lasek, A. W. (2024) · Neurobiology of Stress · doi:10.1016/j.ynstr.2024.100692 · Cited by 10 · see citing works
Self-citationMueller-Buehl, C., Pakusch, J., Bader, V., Winklhofer, K. F., Mark, M. D., & Faissner, A. (2025) · Scientific Reports · doi:10.1038/s41598-025-89580-2 · Cited by 9 · see citing works
Circadian Rhythms of Perineuronal Net CompositionPreprint
Pantazopoulos, H., Gisabella, B., Rexrode, L., Benefield, D., Yildiz, E., Seltzer, P., Valeri, J., Chelini, G., Reich, A., Ardelt, M., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.21.053751 · Cited by 9 · see citing works
Chen, Z., Tang, S., Xiao, X., Hong, Y., Fu, B., Li, X., Shao, Y.-W., Chen, L., Yuan, D., Long, Y., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.115074 · Cited by 8 · see citing works
Zhu, Z., Wang, H., Jiang, Y., Hua, T., & Zhang, C. (2020) · Neuroscience Letters · doi:10.1016/j.neulet.2020.134819 · Cited by 7 · see citing works
A Pathway-Based Genomic Approach to Identify Medications: Application to Alcohol Use Disorder
Ferguson, L. B., Patil, S., Moskowitz, B. A., Ponomarev, I., Harris, R. A., Mayfield, R. D., & Messing, R. O. (2019) · Brain Sciences · doi:10.3390/brainsci9120381 · Cited by 7 · see citing works
Sakata, J. T., Alonge, K. M., Diethorn, E. J., Krishnan, K., Milman, N., Ramsaran, A. I., Wan, X., & Sorg, B. A. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1367-25.2025 · Cited by 6 · see citing works
Tau Protein Modulates Perineuronal Extracellular Matrix Expression in the TauP301L-acan Mouse Model
Schmidt, S., Holzer, M., Arendt, T., Sonntag, M., & Morawski, M. (2022) · Biomolecules · doi:10.3390/biom12040505 · Cited by 7 · see citing works
Perineuronal nets: Cruise from a honeycomb to the safety nets
John, U., Patro, N., & Patro, I. K. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2022.10.004 · Cited by 6 · see citing works
Towner, T. T., Coleman, H. J., Goyden, M. A., Vore, A. S., Papastrat, K. M., Varlinskaya, E. I., & Werner, D. F. (2024) · Neuropharmacology · doi:10.1016/j.neuropharm.2024.110195 · Cited by 6 · see citing works
Galán‐Llario, M., Rodríguez‐Zapata, M., Fontán‐Baselga, T., Cañeque‐Rufo, H., García‐Guerra, A., Fernández, B., Gramage, E., & Herradón, G. (2024) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.70159 · Cited by 5 · see citing works
Roflumilast treatment during forced abstinence reduces relapse to methamphetamine seeking and taking
Baek, J. J., Kline, H. L., Deveau, C., & Yamamoto, B. K. (2021) · Addiction Biology · doi:10.1111/adb.13082 · Cited by 5 · see citing works
Patton, M. S., Sheats, S. H., Wulff, A. B., McKeon, P. N., VanRyzin, J. W., Patton, M. H., Heckman, M. M., Siclair, A. N., Iffland, P. H., & Mathur, B. N. (2026) · Biological Psychiatry · doi:10.1016/j.biopsych.2026.02.006 · Cited by 4 · see citing works
Yao, J., Zhao, T.-S., Guo, Z., Lu, X.-Y., Lu, X.-Y., Zou, G.-J., Zhaorong, C., Liu, Y., Cui, Y.-H., Li, F., et al. (2024) · Behavioural Brain Research · doi:10.1016/j.bbr.2024.115152 · Cited by 4 · see citing works
Qi, Y., Fan, S., Sun, Y. H., Shi, H., Li, H., Xiao, G., & Shen, Q. (2025) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.70588 · Cited by 4 · see citing works
Schreurs, B. G., O’Dell, D. E., & Wang, D. (2024) · Biology · doi:10.3390/biology13030200 · Cited by 4 · see citing works
Shi, S., Chen, T., Su, H., & Zhao, M. (2025) · The Neuroscientist · doi:10.1177/10738584241310156 · Cited by 4 · see citing works
WFA-labeled perineuronal nets in the macaque claustrum
Pletikos, M., & Rockland, K. S. (2018) · Claustrum · doi:10.1080/20023294.2018.1536104 · Cited by 4 · see citing works
Schob, S., Puchta, J., Winter, K., Michalski, D., Mages, B., Martens, H., Emmer, A., Hoffmann, K., Gaunitz, F., Meinicke, A., et al. (2021) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2021.102036 · Cited by 4 · see citing works
Eisele, B. S., Wu, A. J., Luka, Z., Hale, A. T., & York, J. D. (2021) · Advances in Biological Regulation · doi:10.1016/j.jbior.2021.100858 · Cited by 3 · see citing works
Huang, Y.-F., Liu, C., Liu, Z., Zhuang, X., Chen, J.-H., Zhang, Z.-N., Shen, C., & Hu, Y. (2026) · Brain · doi:10.1093/brain/awag058 · Cited by 2 · see citing works
Amphetamine produces sex- and subregion-selective neuroplasticity in the amygdala of Wistar rats
Cadeddu, D., Lucente, E., Ericson, M., & Adermark, L. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.178302 · Cited by 1 · see citing works
Lucente, E., Domi, A., Ericson, M., & Adermark, L. (2026) · Neuropharmacology · doi:10.1016/j.neuropharm.2026.110879 · Cited by 1 · see citing works
Sun, F., Tian, X., Li, Z., Yu, N., Cai, H., Fu, Z., Peng, L., Zhao, J., Ma, C., Wang, T., et al. (2026) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2026.106567 · Cited by 1 · see citing works
Adult vitamin D deficiency and adverse brain outcomes
Mayne, P., Bradford, D., Groves, N. J., McGrath, J. J., & Burne, T. H. J. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-91386-7.00035-0 · Cited by 1 · see citing works
Modeling Brain Gene Expression in Alcohol Use Disorder with Genetic Animal Models
HITZEMANN, R. J., Ozburn, A. R., Lockwood, D. R., & Phillips, T. J. (2023) · Current topics in behavioral neurosciences · doi:10.1007/7854_2023_455 · Cited by 1 · see citing works
Gai, C., Guo, Z., Guo, K., Yang, S., Zhang, Y., Zhu, H., Kan, F., Sun, H., & Hu, D. (2024) · Journal of Traditional Chinese Medical Sciences · doi:10.1016/j.jtcms.2024.09.006 · Cited by 1 · see citing works
Harris, S. E., Cox, S. R., Bell, S., Marioni, R. E., Prins, B. P., Pattie, A., Corley, J., Maniega, S. M., Hernández, M. D. C. V., Morris, Z., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/692459
Schob, S., Puchta, J., Winter, K., Michalski, D., Mages, B., Martens, H., Emmer, A., Hoffmann, K., Gaunitz, F., Meinicke, A., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-747032/v1
Addictions and neurodegenerative diseases: Common targets in the search for new therapies
Gil-Gallardo, G. H. (2024) · Anales de la Real Academia Nacional de Farmacia · doi:10.53519/analesranf.2024.90.01.05
Electroacupuncture facilitates remote fear memory erasure via promoting perineuronal net degradation
Teng, S.-W., Guo, W.-B., Song, B.-F., He, Y., Wang, K., Gao, S.-B., Li, W., & Chen, Z.-Y. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03789-3
Etude du rôle du Syndécan à la jonction neuromusculaire de Caenorhabditis elegans
Vachon, C. (2020) · theses.fr (ABES) · doi:10.70675/4f34af1dzeed7z426dzbab2zb1e21a201491
Role of extracellular space in neurodegenerative diseases
Estaún‐Panzano, J. (2024) · doi:10.70675/98d1d96eza025z406ezba93z33e0820c3cf3
Context-dependent effects of microglial MyD88 removal on voluntary ethanol consumption in mice
Dziabis, J. E., Rogers, N., Horvath, B. L., Patton, M. S., Jonathan, I. O., Freeman, E. J., Sun, W., Moulden, J., Zhang, G., & Bilbo, S. D. (2026) · Neuropharmacology · doi:10.1016/j.neuropharm.2026.111076
Yao, J., Wu, X.-Y., Guo, Z.-R., Wang, X., Liu, X.-X., Li, J., Yang, J.-J., Tang, W., Cui, Y., Li, F., et al. (2026) · Neuropharmacology · doi:10.1016/j.neuropharm.2026.111145
- Authors
- Lasek, A. W., Chen, H., & Chen, W.-Y.
- Affiliations
- University of Illinois Chicago (US)
- Corresponding author
- Lasek, Amy W.
- Venue
- Trends in Genetics
- Publisher
- Elsevier BV
- Published
- 2018-03
- Volume
- 34
- Issue
- 3
- Pages
- 197-208
- ISSN
- 0168-9525 (ISSN-L)
- PMC
- PMC5834377
- OpenAlex
- W2777683237
- Cited by
- 71
- References
- 85
- Citations by year
- 2026: 6 · 2025: 6 · 2024: 13 · 2023: 5 · 2022: 13 · 2021: 10 · 2020: 11 · 2019: 5 · 2018: 2
- FWCI
- 0.61
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Trends in Genetics (acceptedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Alcohol Abuse and Alcoholism (U01 020912)
- Center for Alcohol Research in Epigenetics (P50 AA022538)
- National Institute on Drug Abuse (R01 DA033429)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- drug addiction, perineuronal nets, extracellular matrix, drug-associated memory, maladaptive learning, metalloproteinases, brevican, neuroplasticity, relapse, craving, memory consolidation
- MeSH terms
- Animals, Brain, Extracellular Matrix, Humans, Memory, Models, Neurological, Nerve Net, Neuronal Plasticity, Neurons, Substance-Related Disorders
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