Cocaine Exposure Modulates Perineuronal Nets and Synaptic Excitability of Fast-Spiking Interneurons in the Medial Prefrontal Cortex
Open accessAbstract
Abstract We previously reported that perineuronal nets (PNNs) are required for cocaine-associated memories. Perineuronal nets are extracellular matrix that primarily surrounds parvalbumin (PV)-containing, GABAergic fast-spiking interneurons (FSIs) in the medial prefrontal cortex (mPFC). Here we measured the impact of acute (1 d) or repeated (5 d) cocaine exposure on PNNs and PV cells within the prelimbic and infralimbic regions of the mPFC. Adult rats were exposed to 1 or 5 d of cocaine and stained for PNNs (using Wisteria floribunda agglutinin) and PV intensity 2 or 24 h later. In the prelimbic and infralimbic PFC, PNN staining intensity decreased 2 h after 1 d of cocaine exposure but increased after 5 d of cocaine exposure. Cocaine also produced changes in PV intensity, which generally lagged behind that of PNNs. In the prelimbic PFC, both 1 and 5 d of cocaine exposure increased GAD65/67 puncta near PNN-surrounded PV cells, with an increase in the GAD65/67-to-VGluT1 puncta ratio after 5 d of cocaine exposure. In the prelimbic PFC, slice electrophysiology studies in FSIs surrounded by PNNs revealed that both 1 and 5 d of cocaine exposure reduced the number of action potentials 2 h later. Synaptic changes demonstrated that 5 d of cocaine exposure increased the inhibition of FSIs, potentially reducing the inhibition of pyramidal neurons and contributing to their hyperexcitability during relapse behavior. These early and rapid responses to cocaine may alter the network stability of PV FSIs that partially mediate the persistent and chronic nature of drug addiction.
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
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?
Ethanol, nicotine, cocaine, and heroin alter the intensity or number of PNNs in various brain regions.
“Several classes of drugs, including ethanol, nicotine, cocaine, and heroin, alter the intensity or number of PNNs in various brain regions, including the mPFC [154, 155], anterior cingulate cortex [131], orbitofrontal cortex [156], barrel cortex [157], insula [158], hypothalamus [159, 160], ventral tegmental area [156], and cerebellum [161–164].”
From The extracellular matrix and perineuronal nets in memory (2022) · cites this paper as [154]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
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
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 · see citing works
Parvalbumin neurons and gamma rhythms enhance cortical circuit performance
Sohal, V. S., Zhang, F., Yizhar, O., & Deisseroth, K. (2009) · Nature · doi:10.1038/nature07991 · Cited by 2,606 · see citing works
Self-citationReactivation 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
Modulation of Neuronal Interactions Through Neuronal Synchronization
Womelsdorf, T., Schoffelen, J.-M., Oostenveld, R., Singer, W., Desimone, R., Engel, A. K., & Fries, P. (2007) · Science · doi:10.1126/science.1139597 · Cited by 1,367 · 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
Parvalbumin-expressing basket-cell network plasticity induced by experience regulates adult learning
Donato, F., Rompani, S. B., & Caroni, P. (2013) · Nature · doi:10.1038/nature12866 · Cited by 703 · see citing works
Kawaguchi, Y., & Kubota, Y. (1993) · Journal of Neurophysiology · doi:10.1152/jn.1993.70.1.387 · Cited by 558 · 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
Limbic and Motor Circuitry Underlying Footshock-Induced Reinstatement of Cocaine-Seeking Behavior
McFarland, K., Davidge, S. B., Lapish, C. C., & Kalivas, P. W. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4177-03.2004 · Cited by 524 · see citing works
Perineuronal nets protect fast-spiking interneurons against oxidative stress
Cabungcal, J.-H., Steullet, P., Morishita, H., Kraftsik, R., Cuenod, M., Hensch, T. K., & Do, K. Q. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1300454110 · Cited by 512 · 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
Role of the calcium-binding protein parvalbumin in short-term synaptic plasticity
Caillard, O., Moreno, H., Schwaller, B., Llano, I., Celio, M. R., & Marty, A. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.230362997 · Cited by 406 · 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
Extracellular matrix and perineuronal nets in CNS repair
Kwok, J. C. F., Dick, G., Wang, D., & Fawcett, J. W. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20974 · Cited by 395 · see citing works
McLaughlin, J., & See, R. E. (2002) · Psychopharmacology · doi:10.1007/s00213-002-1196-x · Cited by 392 · see citing works
The perineuronal net and the control of CNS plasticity
Wang, D., & Fawcett, J. (2012) · Cell and Tissue Research · doi:10.1007/s00441-012-1375-y · Cited by 373 · 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
Ma, Y.-Y., Lee, B. R., Wang, X., Guo, C., Liu, L., Cui, R., Lan, Y., Balcita-Pedicino, J. J., Wolf, M. E., Sesack, S. R., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.023 · Cited by 344 · 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
Perineuronal nets potentially protect against oxidative stress
Morawski, M., Brückner, M. K., Riederer, P., Brückner, G., & Arendt, T. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.04.017 · Cited by 246 · see citing works
Cabungcal, J.-H., Steullet, P., Kraftsik, R., Cuenod, M., & Do, K. Q. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.09.020 · Cited by 232 · 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
Cocaine and Cognition: A Systematic Quantitative Review
Potvin, S., Stavro, K., Rizkallah, É., & Pelletier, J. (2014) · Journal of Addiction Medicine · doi:10.1097/adm.0000000000000066 · Cited by 220 · see citing works
Perineuronal Nets Enhance the Excitability of Fast-Spiking Neurons
Balmer, T. S. (2016) · eneuro · doi:10.1523/eneuro.0112-16.2016 · Cited by 220 · 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
Self-citationPyramidal Neurons in Prefrontal Cortex Receive Subtype-Specific Forms of Excitation and Inhibition
Lee, A. T., Gee, S. M., Vogt, D., Patel, T., Rubenstein, J. L., & Sohal, V. S. (2014) · Neuron · doi:10.1016/j.neuron.2013.10.031 · Cited by 201 · see citing works
Modulation of Perineuronal Nets and Parvalbumin with Developmental Song Learning
Balmer, T. S., Carels, V. M., Frisch, J. L., & Nick, T. A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2974-09.2009 · Cited by 181 · 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
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
Dietrich, J.-B., Mangeol, A., Revel, M.-O., Burgun, C., Aunis, D., & Zwiller, J. (2005) · Neuropharmacology · doi:10.1016/j.neuropharm.2005.01.018 · Cited by 168 · cited 1× · see citing works
“A key mechanism that may link cocaine exposure to changes in PNN and/or PV intensity is cocaine-induced oxidative stress (Dietrich et al., 2005; Jang et al., 2015).”
BackgroundSuttkus, A., Rohn, S., Weigel, S., Glöckner, P., Arendt, T., & Morawski, M. (2014) · Cell Death & Disease · doi:10.1038/cddis.2014.25 · Cited by 168 · see citing works
Prefrontal cortex plasticity mechanisms in drug seeking and relapse
van den Oever, M. C., Spijker, S., Smit, A. B., & Vries, T. J. D. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.11.016 · Cited by 163 · see citing works
The neural rejuvenation hypothesis of cocaine addiction
Dong, Y., & Nestler, E. J. (2014) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2014.05.005 · Cited by 163 · 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
The ability of the mesocortical dopamine system to operate in distinct temporal modes
Lapish, C. C., Kroener, S., Durstewitz, D., Lavı́n, A., & Seamans, J. K. (2006) · Psychopharmacology · doi:10.1007/s00213-006-0527-8 · Cited by 153 · see citing works
Brain ageing changes proteoglycan sulfation, rendering perineuronal nets more inhibitory
Foscarin, S., Raha-Chowdhury, R., Fawcett, J. W., & Kwok, J. C. F. (2017) · Aging · doi:10.18632/aging.101256 · Cited by 139 · see citing works
Vo, T., Carulli, D., Ehlert, E., Kwok, J. C. F., Dick, G., Mecollari, V., Moloney, E. B., Neufeld, G., de Winter, F., Fawcett, J. W., et al. (2013) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2013.04.009 · 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
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
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
Moine, C. L., & Gaspar, P. (1998) · Molecular Brain Research · doi:10.1016/s0169-328x(98)00118-1 · Cited by 117 · see citing works
Repeated 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
Molecular control of brain plasticity and repair
Fawcett, J. (2009) · Progress in Brain Research · doi:10.1016/s0079-6123(09)17534-9 · Cited by 105 · 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
Yamada, J., Ohgomori, T., & Jinno, S. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12792 · Cited by 99 · 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
Self-citationHuang, C., Lin, H., & Hsu, K. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhl096 · Cited by 84 · 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
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
Involvement of reactive oxygen species in cocaine‐taking behaviors in rats
Jang, E. Y., Ryu, Y., Lee, B. H., Chang, S., Yeo, M. J., Kim, S. H., Folsom, R. J., Schilaty, N. D., Kim, K. J., Yang, C. H., et al. (2015) · Addiction Biology · doi:10.1111/adb.12159 · Cited by 70 · 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
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
Hegarty, D. M., Tonsfeldt, K. J., Hermes, S. M., Helfand, H., & Aicher, S. A. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22414 · Cited by 47 · see citing works
Self-citationCerebellar 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
Altered Dopamine Modulation of Inhibition in the Prefrontal Cortex of Cocaine-Sensitized Rats
Kroener, S., & Lavı́n, A. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.107 · Cited by 41 · 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
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
Time of day alters long-term sensitization to cocaine in rats
Sleipness, E. P., Sorg, B. A., & Jansen, H. T. (2005) · Brain Research · doi:10.1016/j.brainres.2005.10.017 · Cited by 36 · see citing works
Self-citationHegarty, D. M., Hermes, S. M., Largent‐Milnes, T. M., & Aicher, S. A. (2014) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2014.06.006 · Cited by 25 · see citing works
Self-citationCampanac, E., & Hoffman, D. A. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00596.2012 · Cited by 20 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- Yamada J, Ohgomori T, Jinno S (2015) Perineuronal nets affect parvalbumin expression in GABAergic neurons of the mouse hippocampus. Eur J Neurosci 41: 368– 378. 25411016
Cited by
Sorted by citations
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-citationAn Extracellular Perspective on CNS Maturation: Perineuronal Nets and the Control of Plasticity
Carulli, D., & Verhaagen, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052434 · Cited by 123 · see citing works
Cerebellar plasticity and associative memories are controlled by perineuronal nets
Carulli, D., Broersen, R., de Winter, F., Muir, E. M., Mešković, M., de Waal, M., de Vries, S., Boele, H.-J., Canto, C. B., De Zeeuw, C. I., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1916163117 · Cited by 110 · 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
Drzewiecki, C. M., & Juraska, J. M. (2020) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2020.173044 · Cited by 67 · see citing works
Tanti, A., Belliveau, C., Nagy, C., Maitra, M., Denux, F., Perlman, K., Chen, F. Y., Mpai, R., Canonne, C., Théberge, S., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01372-y · Cited by 65 · 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-citationMolecular profiling of the hippocampus of children with autism spectrum disorder
Rexrode, L., Hartley, J., Showmaker, K. C., Challagundla, L., Vandewege, M. W., Martin, B. E., Blair, E., Bollavarapu, R., Antonyraj, R. B., Hilton, K., et al. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02441-8 · Cited by 70 · see citing works
Incubation of food craving in rats: A review
Grimm, J. W. (2019) · Journal of the Experimental Analysis of Behavior · doi:10.1002/jeab.561 · Cited by 31 · see citing works
Learning-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
Kupferschmidt, D. A., Cummings, K. A., Joffe, M. E., MacAskill, A. F., Malik, R., Sánchez-Bellot, C., Tejeda, H. A., & Yarur, H. E. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1136-22.2022 · Cited by 29 · see citing works
Shi, P., Nie, J., Liu, H., Li, Y., Lu, X., Shen, X., Ge, F., Yuan, T., & Guan, X. (2019) · The FASEB Journal · doi:10.1096/fj.201802192rr · Cited by 28 · see citing works
Altered Relationship Between Parvalbumin and Perineuronal Nets in an Autism Model
Xia, D., Li, L., Yang, B., & Zhou, Q. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.597812 · Cited by 27 · 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
Quantitative changes in perineuronal nets in development and posttraumatic condition
Lipachev, N., Arnst, N., Melnikova, A. A., Jäälinoja, H. T., Kochneva, A., Zhigalov, A., Kulesskaya, N., Aganov, A. V., Олегович, М. М., Rauvala, H., et al. (2019) · Journal of Molecular Histology · doi:10.1007/s10735-019-09818-y · Cited by 26 · 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-citationLeyrer‐Jackson, J. M., Hood, L. E., & Olive, M. F. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.703655 · 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
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-citationJorgensen, 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-citationExtracellular 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
Yaw, A. M., Prosser, R. A., Jones, P. C., Garcia, B. J., Jacobson, D., & Glass, J. D. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.02.043 · Cited by 19 · see citing works
Hazlett, M. F., Hall, V. L., Patel, E. M., Halvorsen, A. T., Calakos, N., & West, A. E. (2024) · Biological Psychiatry · doi:10.1016/j.biopsych.2024.02.003 · Cited by 18 · 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
Zhang, X., Hashimoto, J. G., Han, X., Zhang, F., Linhardt, R. J., & Guizzetti, M. (2021) · Neurochemical Research · doi:10.1007/s11064-020-03195-9 · Cited by 17 · see citing works
Self-citationExtrasynaptic therapeutic targets in substance use and stress disorders
Hodebourg, R., Kalivas, P. W., & Kruyer, A. (2021) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2021.10.006 · 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
Trnski, S., Nikolić, B., Ilić, K., Drlje, M., Bobić‐Rasonja, M., Darmopil, S., Petanjek, Z., Hranilović, D., & Milošević, N. J. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.810980 · Cited by 15 · see citing works
Wingert, J. C., Ramos, J. D., Reynolds, S., Gonzalez, A. E., Rose, R. M., Hegarty, D. M., Aicher, S. A., Bailey, L. G., Brown, T. E., Abbas, A. I., et al. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.0468-24.2024 · Cited by 15 · see citing works
Self-citationBarrett, M. S., Hegarty, D. M., Habecker, B. A., & Aicher, S. A. (2022) · Physiological Reports · doi:10.14814/phy2.15334 · Cited by 14 · see citing works
Self-citationDynamic regulation of the extracellular matrix in reward memory processes: a question of time
Valeri, J., Gisabella, B., & Pantazopoulos, H. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1208974 · Cited by 13 · see citing works
Gonzalez, A. E., Jorgensen, E. T., Ramos, J. D., Harkness, J. H., Aadland, J. A., Brown, T. E., & Sorg, B. A. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.932391 · Cited by 13 · see citing works
Self-citationHuang, D., & Ma, Y. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.06.002 · Cited by 13 · 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
Cross-species conservation in the regulation of parvalbumin by perineuronal nets
Wang, A. S., Wan, X., Storch, D.-S., Li, V. Y., Cornez, G., Balthazart, J., Cisneros-Franco, J. M., de Villers‐Sidani, E., & Sakata, J. T. (2023) · Frontiers in Neural Circuits · doi:10.3389/fncir.2023.1297643 · Cited by 12 · see citing works
Gandhi, T., Liu, C., Adeyelu, T. T., Canepa, C. R., & Lee, C. C. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2023.1114789 · Cited by 12 · see citing works
Moschak, T. M., & Carelli, R. M. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01024-3 · Cited by 11 · see citing works
Wingert, J. C., Anguiano, J. N., Ramos, J. D., Blacktop, J. M., Gonzalez, A. E., Churchill, L., & Sorg, B. A. (2023) · Addiction Biology · doi:10.1111/adb.13334 · Cited by 9 · see citing works
Self-citationLançon, K., Tian, J., Bach, H., Drapeau, P., Poulin, J.-F., & Séguéla, P. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2502558122 · Cited by 8 · see citing works
Cocaine and habit training cause dendritic spine rearrangement in the prelimbic cortex
Sequeira, M. K., Swanson, A. M., Kietzman, H. W., & Gourley, S. L. (2023) · iScience · doi:10.1016/j.isci.2023.106240 · Cited by 8 · see citing works
O'Dell, D. E., Schreurs, B. G., Smith-Bell, C., & Wang, D. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107358 · Cited by 8 · 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
Rose, T. R., de Velasco, E. M. F., Vo, B. N., Tipps, M. E., & Wickman, K. D. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2606-20.2020 · Cited by 7 · see citing works
Perineuronal Net Microscopy: From Brain Pathology to Artificial Intelligence
Николаевич, П. М., Egorchev, A. A., Musin, F., Lipachev, N., Melnikova, A. A., Gimadutdinov, R. M., Kashipov, A., Molotkov, D. A., Chickrin, D. E., & Aganov, A. V. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25084227 · Cited by 7 · see citing works
Brinks, A. S., Carrica, L. K., Tagler, D. J., Gulley, J. M., & Juraska, J. M. (2024) · Developmental Neuroscience · doi:10.1159/000538608 · Cited by 6 · 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
Shi, S., Chen, T., Su, H., & Zhao, M. (2025) · The Neuroscientist · doi:10.1177/10738584241310156 · 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
Young, L., Webber-Waugh, A., & Thaxter, K. (2021) · Journal of Behavioral and Brain Science · doi:10.4236/jbbs.2021.117011 · Cited by 3 · see citing works
Liu, Y., Zhao, T., Yao, J., Zhang, Q., Cui, Y., Li, F., Yong, Y., & Li, C.-Q. (2026) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2026.178737 · Cited by 1 · see citing works
Four hypothalamic peptides and their impact on drug-seeking behaviour: A prefrontal cortex view
Perry, C. J., & Cornish, J. L. (2022) · Addiction Neuroscience · doi:10.1016/j.addicn.2022.100018 · Cited by 1 · see citing works
The Medial Prefrontal Cortex (mPFC) and Addictions
Pérez-Rando, M., & Guirado, R. (2022) · Springer eBooks · doi:10.1007/978-3-030-67928-6_25-1 · Cited by 1 · see citing works
Quantitative Anatomical Approaches to Examining Plasticity in Neural Circuits
Hegarty, D. M., Gonzalez, A. E., Harkness, J. H., Sorg, B. A., & Aicher, S. A. (2019) · Microscopy and Microanalysis · doi:10.1017/s1431927619006354
Self-citationRose, T. R., de Velasco, E. M. F., Vo, B. N., Tipps, M. E., & Wickman, K. D. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.04.134486
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
The Medial Prefrontal Cortex (mPFC) and Addictions
Pérez-Rando, M., & Guirado, R. (2022) · Springer eBooks · doi:10.1007/978-3-030-92392-1_25
Lüttig, A., Perl, S., Franz, D., Kotyra, M., Morawski, M., Köhling, R., & Richter, A. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111486
Ventral pallidal perineuronal nets regulate opioid relapsePreprint
Nogueira, M., Giannotti, G., Miller, C. N., Guaderrama, S. D., Kregar, N. P., Wiedmeyer, B., Fayette, N., & Heinsbroek, J. A. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.21.700926
Disruption of psychostimulant-associated memories by single, low dose ketamine in rats
Gonzalez, A. E., Ramos, J. D., Anderson, Z., Sewell, C. M., Modaberi, S., Hentges, S. T., Brown, T. E., & Sorg, B. A. (2026) · Neuropharmacology · doi:10.1016/j.neuropharm.2026.110912
Self-citationECM remodeling in the mPFC exacerbates cocaine-induced hyperactivity and impairs threat vigilance
Lin, X., Huo, Y., Wang, X., Yu, J., Liu, Z., Fan, X., Guo, S., Ye, X., Zhang, X., Li, Y., et al. (2026) · Translational Psychiatry · doi:10.1038/s41398-026-04014-5
Houff, J., Williams, A., Allen, O., Gisabella, B., Pantazopoulos, H., & Arco, A. D. (2026) · European Journal of Neuroscience · doi:10.1111/ejn.70574
Dejeux, M. I. H., Jewanee, S., Moutos, S., Trehan, A., Golbarani, M., Kwak, J., Farach, E., Cheng, N., Kasaram, S. V., Ogden, A., et al. (2026) · Frontiers in Neuroscience · doi:10.3389/fnins.2026.1821692
Nashawi, H., Foltz, C. T., Oh, N., Santiago, E. A., Selm, D. R., Herman, J. P., & Ulrich‐Lai, Y. M. (2026) · Brain Structure and Function · doi:10.1007/s00429-026-03141-5
Jenike, A. E., Brown, T. E., Impey, S., Sorg, B. A., & Aicher, S. A. (2026) · Brain Research · doi:10.1016/j.brainres.2026.150507
Self-citation
- Authors
- 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.
- Affiliations
- Washington State University Vancouver (US)
- University of Wyoming (US)
- Oregon Health & Science University (US)
- Rensselaer Polytechnic Institute (US)
- Corresponding author
- Sorg, Barbara A.
- ORCID
- Venue
- eneuro
- Publisher
- Society for Neuroscience
- Published
- 2018-09
- Volume
- 5
- Issue
- 5
- Pages
- ENEURO.0221-18.2018
- ISSN
- 2373-2822 (ISSN-L)
- PMC
- PMC6171740
- OpenAlex
- W2892965632
- Cited by
- 64
- References
- 65
- Citations by year
- 2026: 8 · 2025: 3 · 2024: 7 · 2023: 7 · 2022: 10 · 2021: 14 · 2020: 9 · 2019: 6
- FWCI
- 3.30
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- eNeuro (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute on Drug Abuse (R01DA040965, R01DA033404)
- National Institute of General Medical Sciences (P30GM103398)
- National Institute of Neurological Disorders and Stroke (P30NS061800)
- 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 › Neural dynamics and brain function
- Keywords
- cocaine exposure, perineuronal nets, fast-spiking interneurons, parvalbumin, medial prefrontal cortex, prelimbic cortex, infralimbic cortex, synaptic inhibition, GAD65/67, VGLUT1, extracellular matrix, drug addiction, relapse, synaptic plasticity
- MeSH terms
- Animals, Cocaine, Extracellular Matrix, Interneurons, Male, Nerve Net, Neurons, Parvalbumins, Synapses, Rats, Sprague-Dawley, Prefrontal Cortex
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