Bistable parvalbumin circuits pivotal for brain plasticity

Cortical interneurons that specialize in disinhibitory control

Pi, H.-J., Hangya, B., Kvitsiani, D., Sanders, J. I., Huang, Z. J., & Kepecs, A. (2013) · Nature · doi:10.1038/nature12676 · Cited by 1,136 · see citing works

A disinhibitory microcircuit for associative fear learning in the auditory cortex

Letzkus, J. J., Wolff, S. B. E., Meyer, E. M. M., Tovote, P., Courtin, J., Herry, C., & Lüthi, A. (2011) · Nature · doi:10.1038/nature10674 · Cited by 840 · 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

Balancing Plasticity/Stability Across Brain Development

Takesian, A. E., & Hensch, T. K. (2013) · Progress in Brain Research · doi:10.1016/b978-0-444-63327-9.00001-1 · Cited by 667 · see citing works

Common circuit defect of excitatory-inhibitory balance in mouse models of autism

Gogolla, N., LeBlanc, J. J., Quast, K. B., Südhof, T. C., Fagiolini, M., & Hensch, T. K. (2009) · Journal of Neurodevelopmental Disorders · doi:10.1007/s11689-009-9023-x · Cited by 610 · see citing works

Learning-related feedforward inhibitory connectivity growth required for memory precision

Ruediger, S., Vittori, C. G., Bednarek, E., Genoud, C., Strata, P., Sacchetti, B., & Caroni, P. (2011) · Nature · doi:10.1038/nature09946 · Cited by 282 · see citing works

Choroid-Plexus-Derived Otx2 Homeoprotein Constrains Adult Cortical Plasticity

Spatazza, J., Lee, H. H. C., Di Nardo, A. A., Tibaldi, L., Joliot, A., Hensch, T. K., & Prochiantz, A. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.05.014 · Cited by 176 · see citing works

Obligatory Role for the Immediate Early Gene NARP in Critical Period Plasticity

Gu, Y., Huang, S., Chang, M., Worley, P. F., Kirkwood, A., & Quinlan, E. M. (2013) · Neuron · doi:10.1016/j.neuron.2013.05.016 · Cited by 117 · see citing works

Processing of Neuregulin-1 by Neuropsin Regulates GABAergic Neuron to Control Neural Plasticity of the Mouse Hippocampus

Tamura, H., Kawata, M., Hamaguchi, S., Ishikawa, Y., & Shiosaka, S. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2542-12.2012 · Cited by 68 · see citing works

Regionalized Loss of Parvalbumin Interneurons in the Cerebral Cortex of Mice with Deficits in GFRα1 Signaling

Canty, A. J., Dietze, J., Harvey, M., Enomoto, H., Milbrandt, J., & Ibáñez, C. F. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2658-09.2009 · Cited by 65 · see citing works

Bidirectional perisomatic inhibitory plasticity of a Fos neuronal network

Yap, E.-L., Pettit, N. L., Davis, C. P., Nagy, M. A., Harmin, D. A., Golden, E., Dağliyan, O., Lin, C., Rudolph, S., Sharma, N., et al. (2020) · Nature · doi:10.1038/s41586-020-3031-0 · Cited by 149 · see citing works

Mechanisms of Action and Persistent Neuroplasticity by Drugs of Abuse

Korpi, E. R., den Hollander, B., Farooq, U., Vashchinkina, E., Rajkumar, R., Nutt, D. J., Hyytiä, P., & Dawe, G. S. (2015) · Pharmacological Reviews · doi:10.1124/pr.115.010967 · Cited by 148 · see citing works

MECP2 regulates cortical plasticity underlying a learned behaviour in adult female mice

Krishnan, K., Lau, B. Y. B., Ewall, G., Huang, Z. J., & Shea, S. D. (2017) · Nature Communications · doi:10.1038/ncomms14077 · Cited by 94 · see citing works

Leveraging Neuroscience to Inform Adolescent Health: The Need for an Innovative Transdisciplinary Developmental Science of Adolescence

Suleiman, A. B., & Dahl, R. E. (2017) · Journal of Adolescent Health · doi:10.1016/j.jadohealth.2016.12.010 · Cited by 95 · see citing works

Becoming a sexual being: The “elephant in the room” of adolescent brain development

Suleiman, A. B., Galván, A., Harden, K. P., & Dahl, R. E. (2017) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2016.09.004 · Cited by 89 · see citing works

iPlasticity: Induced juvenile‐like plasticity in the adult brain as a mechanism of antidepressants

Umemori, J., Winkel, F., Didio, G., Llach Pou, M., & Castrén, E. (2018) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.12683 · Cited by 80 · see citing works

Chondroitin Sulfate Is Required for Onset and Offset of Critical Period Plasticity in Visual Cortex

Hou, X., Yoshioka, N., Tsukano, H., Sakai, A., Miyata, S., Watanabe, Y., Yanagawa, Y., Sakimura, K., Takeuchi, K., Kitagawa, H., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-04007-x · Cited by 75 · see citing works

Epigenetic basis of sensitization to stress, affective episodes, and stimulants: implications for illness progression and prevention

Post, R. M. (2016) · Bipolar Disorders · doi:10.1111/bdi.12401 · Cited by 73 · see citing works

Incubation 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

Damaged Neocortical Perineuronal Nets Due to Experimental Focal Cerebral Ischemia in Mice, Rats and Sheep

Härtig, 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

Synapse-Selective Control of Cortical Maturation and Plasticity by Parvalbumin-Autonomous Action of SynCAM 1

Ribic, A., Crair, M. C., & Biederer, T. (2019) · Cell Reports · doi:10.1016/j.celrep.2018.12.069 · Cited by 47 · see citing works

Overinhibition mediated by parvalbumin interneurons might contribute to depression-like behavior and working memory impairment induced by lipopolysaccharide challenge

Ji, M., Zhang, L., Mao, M., Zhang, H., Yang, J., & Qiu, L.-L. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.112509 · Cited by 47 · see citing works

Γ-Aminobutyric acid in adult brain: an update

Siucińska, E. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112224 · Cited by 41 · see citing works

Parvalbumin - Positive Neurons in the Neocortex: A Review

Druga, R., Salaj, M., & Al‐Redouan, A. (2023) · Physiological Research · doi:10.33549/physiolres.935005 · Cited by 42 · see citing works

Firing dynamics in hybrid coupled populations of bistable neurons

Uzuntarla, M. (2019) · Neurocomputing · doi:10.1016/j.neucom.2019.07.099 · Cited by 30 · see citing works

A Late Critical Period for Frequency Modulated Sweeps in the Mouse Auditory System

Bhumika, S., Nakamura, M., Valerio, P., Sołyga, M., Lindén, H., & Barkat, T. R. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz262 · Cited by 30 · see citing works

Alternative splicing of neurexins 1–3 is modulated by neuroinflammation in the prefrontal cortex of a murine model of multiple sclerosis

Marchese, E., Valentini, M., Sante, G. D., Cesari, E., Adinolfi, A., Corvino, V., Ria, F., Sette, C., & Geloso, M. C. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113497 · Cited by 29 · see citing works

Ketamine and its metabolite 2 R ,6 R ‐hydroxynorketamine promote ocular dominance plasticity and release tropomyosin‐related kinase B from inhibitory control without reducing perineuronal nets enwrapping parvalbumin interneurons

Cannarozzo, C., Rubiolo, A., Casarotto, P. C., & Ċastrén, E. (2023) · European Journal of Neuroscience · doi:10.1111/ejn.15929 · Cited by 24 · see citing works

The role of parvalbumin interneuron dysfunction across neurodegenerative dementias

Smeralda, C. L., Pandit, S., Turrini, S., Reilly, J., Palmisano, A., Sprugnoli, G., Hampel, H. J., Benussi, A., Borroni, B., Press, D. Z., et al. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102509 · Cited by 24 · see citing works

Experience-dependent central vision deficits: Neurobiology and visual acuity

Williams, K., Balsor, J. L., Beshara, S. P., Beston, B. R., Jones, D. G., & Murphy, K. M. (2015) · Vision Research · doi:10.1016/j.visres.2015.01.021 · Cited by 16 · see citing works

Molecular, Pathophysiological, and Clinical Aspects of Corticosteroid-Induced Neuropsychiatric Effects: From Bench to Bedside

Avendaño-Lopez, S. S., Rodríguez-Marín, A. J., Lara-Castillo, M., Agresott-Carrillo, J., Lara-Cortés, L. E., Sánchez-Almanzar, J. F., Villamil-Cruz, S., Rojas-Rodríguez, L. C., Ariza-Salamanca, D. F., Gaviria-Carrillo, M., et al. (2024) · Biomedicines · doi:10.3390/biomedicines12092131 · Cited by 13 · see citing works

Type 2 diabetes alters hippocampal gamma oscillations: A potential mechanism behind impaired cognition

Lietzau, G., Darsalia, V., Pintana, H., Östenson, C., Nyström, T., Fisahn, A., & Patrone, C. (2017) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2017.04.012 · Cited by 13 · see citing works

Developmental stage‐dependent impact of midazolam on calbindin, calretinin and parvalbumin expression in the immature rat medial prefrontal cortex during the brain growth spurt

Osterop, S. F., Virtanen, M. A., Loepke, J. R., Joseph, B., Loepke, A. W., & Vutskits, L. (2015) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2015.04.002 · Cited by 13 · see citing works

Transcriptional Response and Morphological Features of the Neurovascular Unit and Associated Extracellular Matrix After Experimental Stroke in Mice

Aleithe, S., Blietz, A., Mages, B., Hobusch, C., Härtig, W., & Michalski, D. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-1604-4 · Cited by 11 · see citing works

Developmental Age Differentially Mediates the Calcium-Binding Protein Parvalbumin in the Rat: Evidence for a Selective Decrease in Hippocampal Parvalbumin Cell Counts

Honeycutt, J. A., Keary, K. M., Kania, V. M., & Chrobak, J. J. (2016) · Developmental Neuroscience · doi:10.1159/000444447 · Cited by 11 · see citing works

Enriched environmental exposure reduces the onset of action of the serotonin norepinephrin reuptake inhibitor venlafaxine through its effect on parvalbumin interneurons plasticity in mice

Coutens, B., Lejards, C., Bouisset, G., Verret, L., Rampon, C., & Guiard, B. P. (2023) · Translational Psychiatry · doi:10.1038/s41398-023-02519-x · Cited by 10 · see citing works

Role of neuropsin in parvalbumin immunoreactivity changes in hippocampal basket terminals of mice reared in various environments

Suzuki, H., Kanagawa, D., Nakazawa, H., Tawara-Hirata, Y., Kogure, Y., Shimizu‐Okabe, C., Takayama, C., Ishikawa, Y., & Shiosaka, S. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00420 · Cited by 10 · see citing works

Overexpression of the schizophrenia risk gene C4 in PV cells drives sex-dependent behavioral deficits and circuit dysfunction

Fournier, L. A., Phadke, R. A., Salgado, M., Brack, A., Nocon, J. C., Bolshakova, S., Grant, J. R., Padró-Luna, N. M., Sen, K., & Cruz‐Martín, A. (2024) · iScience · doi:10.1016/j.isci.2024.110800 · Cited by 9 · see citing works

FriendlyClearMap: an optimized toolkit for mouse brain mapping and analysis

Negwer, M., Bosch, B., Bormann, M., Hesen, R., Lütje, L., Aarts, L., Rossing, C., Kasri, N. N., & Schubert, D. (2022) · GigaScience · doi:10.1093/gigascience/giad035 · Cited by 5 · see citing works

Cofilin1 Controls Transcolumnar Plasticity in Dendritic Spines in Adult Barrel Cortex

Tsubota, T., Okubo-Suzuki, R., Ohashi, Y., Tamura, K., Ogata, K., Yaguchi, M., Matsuyama, M., Inokuchi, K., & Miyashita, Y. (2015) · PLoS Biology · doi:10.1371/journal.pbio.1002070 · Cited by 5 · see citing works

Exploring Cortical Interneurons in Substance Use Disorder: From Mechanisms to Therapeutic Perspectives

Shi, S., Chen, T., Su, H., & Zhao, M. (2025) · The Neuroscientist · doi:10.1177/10738584241310156 · Cited by 4 · see citing works

Parvalbumin-Immunoreactive Cells in the Superior Colliculus in Dog: Distribution, Colocalization with GABA, and Effect of Monocular Enucleation

Lee, J.-Y., Jeong, S.-J., & Jeon, C. (2014) · ZOOLOGICAL SCIENCE · doi:10.2108/zs140073 · Cited by 2 · see citing works

Ketamine and its metabolite 2R,6R-hydroxynorketamine promote ocular dominance plasticity and release TRKB from inhibitory control without changing perineuronal nets enwrapping parvalbumin interneurons

Cannarozzo, C., Rubiolo, A., Casarotto, P., & Castrén, E. (2022) · doi:10.1101/2022.04.06.487292 · Cited by 2 · see citing works

Inflammation and the Newborn Brain

Gressèns, P. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-10513-5.00017-6 · Cited by 1 · see citing works

Non-cell autonomous OTX2 in the piriform cortex regulates parvalbumin cell maturation states and olfactory-driven behaviorPreprint

Gibel-Russo, R., & Nardo, A. A. D. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.04.578782 · Cited by 1 · see citing works

Development of the Nervous System During Adolescence

Aigbogho, U. G. (2026) · Advances in experimental medicine and biology · doi:10.1007/978-981-95-7000-3_5

Altérations anatomo-fonctionnelles des interneurones à parvalbumine dans un modèle murin de la maladie d'Alzheimer

Cattaud, V. (2018) · theses.fr (ABES) · doi:10.70675/ab9d6bfaz7490z4ae6zb7f3z525493f6bba4

Implication du tPA cérébral dans la régulation des comportements et le remodelage des perineuronal nets

Douceau, S. (2020) · theses.fr (ABES) · doi:10.70675/6f1007f2z8468z4365zb07dz7d863bf32cd5

Stratégies non pharmacologiques et réponse aux antidépresseurs dans un modèle murin de dépression : effets comportementaux et mécanismes neurobiologiques

Coutens, B. (2022) · theses.fr (ABES) · doi:10.70675/7ffbfd7ezefb5z4e4ez82f4z42a6ac0ff754

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

The highs and lows of memory

Allen, K. L., & Monyer, H. (2013) · Nature · doi:10.1038/504228a · Cited by 4 · see citing works

[Nerve cell plasticity during learning].

Гусельников, В. И., & Pivovarov, A. S. (1980) · PubMed

Early- and Late-Born Parvalbumin Basket Cell Subpopulations Exhibiting Distinct Regulation and Roles in Learning

Donato, F., Chowdhury, A., Lahr, M., & Caroni, P. (2015) · Neuron · doi:10.1016/j.neuron.2015.01.011 · Cited by 159 · see citing works

A cellular mechanism makes switches in brain states compatible with synaptic plasticity

Jacquerie, K., & Drion, G. (2019)