Long-term potentiation depends on release of d-serine from astrocytes

A synaptic model of memory: long-term potentiation in the hippocampus

Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566

Astrocytes, from brain glue to communication elements: the revolution continues

Volterra, A., & Meldolesi, J. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1722 · Cited by 1,837

Synaptic scaling mediated by glial TNF-α

Stellwagen, D., & Malenka, R. C. (2006) · Nature · doi:10.1038/nature04671 · Cited by 1,715

Protoplasmic Astrocytes in CA1 Stratum Radiatum Occupy Separate Anatomical Domains

Bushong, E. A., Martone, M. E., Jones, Y. Z., & Ellisman, M. H. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-01-00183.2002 · Cited by 1,578

Astrocytic Purinergic Signaling Coordinates Synaptic Networks

Pascual, O., Casper, K. B., Kubera, C., Zhang, J., Revilla-Sanchez, R., Sul, J.-Y., Takano, H., Moss, S. J., McCarthy, K., & Haydon, P. G. (2005) · Science · doi:10.1126/science.1116916 · Cited by 1,280

D-serine is an endogenous ligand for the glycine site of the N-methyl-D-aspartate receptor.

Mothet, J., Parent, A., Wolosker, H., Brady, R., Linden, D. J., Ferris, C., Rogawski, M., & Snyder, S. (2000) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.97.9.4926 · Cited by 1,164

Prostaglandins stimulate calcium-dependent glutamate release in astrocytes

Bezzi, P., Carmignoto, G., Pasti, L., Vesce, S., Rossi, D., Rizzini, B. L., Pozzan, T., & Volterra, A. (1998) · Nature · doi:10.1038/34651 · Cited by 1,143

CXCR4-activated astrocyte glutamate release via TNFα: amplification by microglia triggers neurotoxicity

Bezzi, P., Domercq, M., Brambilla, L., Galli, R., Schols, D., De Clercq, E., Vescovi, A., Bagetta, G., Kollias, G., Meldolesi, J., et al. (2001) · Nature Neuroscience · doi:10.1038/89490 · Cited by 1,102

Neuronal Synchrony Mediated by Astrocytic Glutamate through Activation of Extrasynaptic NMDA Receptors

Fellin, T., Pascual, O., Gobbo, S., Pozzan, T., Haydon, P. G., & Carmignoto, G. (2004) · Neuron · doi:10.1016/j.neuron.2004.08.011 · Cited by 1,005

Glia-Derived d-Serine Controls NMDA Receptor Activity and Synaptic Memory

Panatier, A., Theodosis, D. T., Mothet, J.-P., Touquet, B., Pollegioni, L., Poulain, D. A., & Oliet, S. H. R. (2006) · Cell · doi:10.1016/j.cell.2006.02.051 · Cited by 934

Astrocytic Actions on Extrasynaptic Neuronal Currents

Pál, B. Z. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00474 · Cited by 29

The Paradox of Astroglial Ca2 + Signals at the Interface of Excitation and Inhibition

Caudal, L. C., Gobbo, D., Scheller, A., & Kirchhoff, F. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.609947 · Cited by 28

Impact of maternal immune activation on dendritic spine development

Pękała, M., Doliwa, M., & Kalita, K. B. (2020) · Developmental Neurobiology · doi:10.1002/dneu.22804 · Cited by 27

Modification of Glial Cell Activation through Dendritic Cell Vaccination: Promises for Treatment of Neurodegenerative Diseases

Sabahi, M., Joshaghanian, A., Dolatshahi, M., Jabbari, P., Rahmani, F., & Rezaei, N. (2021) · Journal of Molecular Neuroscience · doi:10.1007/s12031-021-01818-6 · Cited by 26

Astrocytes as Drivers and Disruptors of Behavior: New Advances in Basic Mechanisms and Therapeutic Targeting

Barnett, D., Bohmbach, K., Grelot, V., Charlet, A., Dallérac, G. M., Ju, Y. H., Nagai, J., & Orr, A. G. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1376-23.2023 · Cited by 27

Neurochemical Analysis of Primary Motor Cortex in Chronic Low Back Pain

Sharma, N. K., Brooks, W. M., Popescu, E. A., Dillen, L. V., George, S. Z., McCarson, K. E., Gajewski, B. J., Gorman, P., & Cirstea, C. M. (2012) · Brain Sciences · doi:10.3390/brainsci2030319 · Cited by 26

Motor and Premotor Cortices in Subcortical Stroke

Craciunas, S. C., Brooks, W. M., Nudo, R. J., Popescu, E. A., Choi, I., Lee, P., Yeh, H., Savage, C. R., & Cirstea, C. M. (2013) · Neurorehabilitation and neural repair · doi:10.1177/1545968312469835 · Cited by 26

Basal Synaptic Transmission: Astrocytes Rule!

Navarrete, M., & Araque, A. (2011) · Cell · doi:10.1016/j.cell.2011.08.006 · Cited by 26

Evidence for a Role of Proline and Hypothalamic Astrocytes in the Regulation of Glucose Metabolism in Rats

Arrieta‐Cruz, I., Su, Y., Knight, C. M., Lam, T. K. T., & Juárez, R. G. (2012) · Diabetes · doi:10.2337/db12-0228 · Cited by 26

Running Opposes the Effects of Social Isolation on Synaptic Plasticity and Transmission in a Rat Model of Depression

Gómez‐Galán, M., Femenía, T., Åberg, E., Graae, L., Eeckhaut, A. V., Smolders, I. J., Brené, S., & Lindskog, M. (2016) · PLoS ONE · doi:10.1371/journal.pone.0165071 · Cited by 26

Astroglial Ca2+ signaling is generated by the coordination of IP3R and store-operated Ca2+ channels.

Sakuragi, S., Niwa, F., Oda, Y., Mikoshiba, K., & Bannai, H. (2017) · Biochemical and Biophysical Research Communications - BBRC · doi:10.1016/j.bbrc.2017.03.096 · Cited by 22

Rearing‐environment‐dependent hippocampal local field potential differences in wild‐type and inositol trisphosphate receptor type 2 knockout mice

Tanaka, M., Wang, X., Mikoshiba, K., Hirase, H., & Shinohara, Y. (2017) · The Journal of Physiology · doi:10.1113/jp274573 · Cited by 26

Spatiotemporal Localization of d -Amino Acid Oxidase and d -Aspartate Oxidases during Development in Caenorhabditis elegans

Saitoh, Y., Katane, M., Kawata, T., Maeda, K., Sekine, M., Furuchi, T., Kobuna, H., Sakamoto, T., Inoue, T., Arai, H., et al. (2012) · Molecular and Cellular Biology · doi:10.1128/mcb.06513-11 · Cited by 26

Transcranial direct current stimulation alters cerebrospinal fluid-interstitial fluid exchange in mouse brain

Wang, Y., & Monai, H. (2024) · Brain stimulation · doi:10.1016/j.brs.2024.04.009 · Cited by 25

Chemotherapy-induced cognitive impairment and glia: A new take on chemobrain?

Barbosa-Azevedo, M., Dias-Carvalho, A., Carvalho, F. D., & Costa, V. M. (2024) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2024.117085 · Cited by 25

The role of astrocytes from synaptic to non-synaptic plasticity

Sanz-Gálvez, R., Falardeau, D., Kolta, A., & Inglebert, Y. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1477985 · Cited by 27

cAMP-Dependent Calcium Oscillations of Astrocytes: An Implication for Pathology

Ujita, S., Sasaki, T., Asada, A., Funayama, K., Gao, M., Mikoshiba, K., Matsuki, N., & Ikegaya, Y. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv310 · Cited by 28

Astrocytic Ca2+ responses in the spinal dorsal horn by noxious stimuli to the skin

Yoshihara, K., Matsuda, T., Kohro, Y., Tozaki‐Saitoh, H., Inoue, K., & Tsuda, M. (2018) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2018.04.007 · Cited by 25

Massive efflux of adenosine triphosphate into the extracellular space immediately after experimental traumatic brain injury

Moro, N., Ghavim, S. S., & Sutton, R. (2021) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2021.10007 · Cited by 25

Npas3 deficiency impairs cortical astrogenesis and induces autistic-like behaviors

Li, Y., Fan, T., Li, X., Liu, L., Mao, F., Li, Y., Miao, Z., Zeng, C., Song, W., Pan, J., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111289 · Cited by 25

EEG biomarkers of activation of the lymphatic drainage system of the brain during sleep and opening of the blood-brain barrier

SEMYACHKINA-GLUSHKOVSKAYA, O. V., Karavaev, A. S., Prokhorov, M. D., Евгеньевна, Р. А., Borovkova, E. I., Yu.M., I., Hramkov, A. N., Kulminskiy, D. D., Игоревна, С. Н., Sergeev, K. S., et al. (2022) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2022.12.019 · Cited by 26

Afferent Input Selects NMDA Receptor Subtype to Determine the Persistency of Hippocampal LTP in Freely Behaving Mice

Ballesteros, J. J., Buschler, A., Köhr, G., & Manahan‐Vaughan, D. (2016) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2016.00033 · Cited by 25

Does rapid and physiological astrocyte–neuron signalling amplify epileptic activity?

Henneberger, C. (2016) · The Journal of Physiology · doi:10.1113/jp271958 · Cited by 25

What Non-neuronal Mechanisms Should Be Studied to Understand Epileptic Seizures?

Janigro, D., & Walker, M. C. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-94-017-8914-1_20 · Cited by 25

Astrocyte Dysfunctions in Obsessive Compulsive Disorder: Rethinking Neurobiology and Therapeutic Targets

Gonzalez, L., & Bezzi, P. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70092 · Cited by 24

Integrated Brain Circuits: Neuron-Astrocyte Interaction in Sleep-Related Rhythmogenesis

Halassa, M. M., Maschio, M. D., Beltramo, R., Haydon, P. G., Benfenati, F., & Fellin, T. (2010) · The Scientific World JOURNAL · doi:10.1100/tsw.2010.130 · Cited by 25

Cryptococcus neoformans–astrocyte interactions: effect on fungal blood brain barrier disruption, brain invasion, and meningitis progression

Woo, Y. H., & Martinez, L. R. (2021) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2020.1869178 · Cited by 24

Astrocytic α4-containing nAChR signaling in the hippocampus governs the formation of temporal association memory

Ma, W., Si, T., Wang, Z., Wen, P., Zhu, Z., Liu, Q., Wang, J., Xu, F., & Li, Q. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112674 · Cited by 24

Astrocyte and Neuronal Plasticity in the Somatosensory System

Sims, R. E., Butcher, J. B., Parri, H. R., & Glazewski, S. (2015) · Neural Plasticity · doi:10.1155/2015/732014 · Cited by 28

New players in the neurovascular unit: Insights from experimental and clinical epilepsy

Bertini, G., Bramanti, P., Constantin, G., Pellitteri, M., Radu, B. M., Radu, M., & Fabene, P. F. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.08.001 · Cited by 25

Regulation of rhythm genesis by volume-limited, astroglia-like signals in neural networks

Savtchenko, L. P., & Rusakov, D. A. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0614 · Cited by 25

Nuclear Compartmentalization of Serine Racemase Regulates d-Serine Production

Kolodney, G., Dumin, E., Safory, H., Rosenberg, D., Mori, H., Radzishevsky, I. S., & Wolosker, H. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.699496 · Cited by 24

Identification of Novel d -Aspartate Oxidase Inhibitors by in Silico Screening and Their Functional and Structural Characterization in Vitro

Katane, M., Yamada, S., Kawaguchi, G., Chinen, M., Matsumura, M., Ando, T., Doi, I., Nakayama, K., Kaneko, Y., Matsuda, S., et al. (2015) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.5b00871 · Cited by 24

Changes in the Striatal Proteome of YAC128Q Mice Exhibit Gene–Environment Interactions between Mutant Huntingtin and Manganese

Węgrzynowicz, M., Holt, H. K., Friedman, D. B., & Bowman, A. B. (2011) · Journal of Proteome Research · doi:10.1021/pr200839d · Cited by 24

The Effects of Alpha Boswellic Acid on Reelin Expression and Tau Phosphorylation in Human Astrocytes

Fathi, E., Katouli, F. H., Riazi, G. H., Shasaltaneh, M. D., Parandavar, E., Bayati, S., Afrasiabi, A., & Nazari, R. (2016) · NeuroMolecular Medicine · doi:10.1007/s12017-016-8437-3 · Cited by 24

Drugs Based on NMDAR Hypofunction Hypothesis in Schizophrenia

Wu, Q., Huang, J., & Wu, R. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.641047 · Cited by 24

The role of D-serine as co-agonist of NMDA receptors in the nucleus accumbens: relevance to cocaine addiction

Dâ€TMAscenzo, M., Podda, M. V., & Grassi, C. (2014) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2014.00016 · Cited by 24

d-Serine: A key to synaptic plasticity?

Henneberger, C., Bard, L., & Rusakov, D. A. (2012) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2012.01.005 · Cited by 24

The tripartite synapse

Halassa, M. M., & Haydon, P. G. (2008) · Springer eBooks · doi:10.1007/978-0-387-79492-1_15 · Cited by 24

Ketamine Metabolites Enantioselectively Decrease Intracellular D-Serine Concentrations in PC-12 Cells

Singh, N. S., Rutkowska, E., Plazinska, A., Khadeer, M., Moaddel, R., Jozwiak, K., Bernier, M., & Wainer, I. W. (2016) · PLOS ONE · doi:10.1371/journal.pone.0149499 · Cited by 23

d-Serine in the nucleus accumbens region modulates behavioral sensitization and extinction of conditioned place preference

Liu, Z.-Q., Gu, X.-H., Yang, Y.-J., Yin, X.-P., Xu, L.-J., & Wang, W. (2016) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2016.02.002 · Cited by 23

Implications of Gliotransmission for the Pharmacotherapy of CNS Disorders

Rossi, D., Martorana, F., & Brambilla, L. (2011) · CNS Drugs · doi:10.2165/11593090-000000000-00000 · Cited by 24

WONOEP appraisal: Optogenetic tools to suppress seizures and explore the mechanisms of epileptogenesis

Ritter, L. M., Golshani, P., Takahashi, K. U., Dufour, S., Valiante, T. A., & Kokaia, M. (2014) · Epilepsia · doi:10.1111/epi.12804 · Cited by 23

Sleep-Awake Profile Related Circadian D-Alanine Rhythm in Human Serum and Urine

MORIKAWA, A., Fukuoka, H., Uezono, K., Mita, M., Koyanagi, S., Ohdo, S., Zaitsu, K., & Hamase, K. (2017) · Chromatography · doi:10.15583/jpchrom.2017.003 · Cited by 23

Multi-Dimensional HPLC Analysis of Metabolic Related Chiral Amino Acids -Method Development and Biological/Clinical Applications-

Koga, R., Yoshida, H., Nohta, H., & Hamase, K. (2019) · Chromatography · doi:10.15583/jpchrom.2019.002 · Cited by 23

Increased excitation-inhibition balance and loss of GABAergic synapses in the serine racemase knockout model of NMDA receptor hypofunction

Jami, S. A., Cameron, S., Wong, J. M., Daly, E. R., McAllister, A. K., & Gray, J. A. (2021) · Journal of Neurophysiology · doi:10.1152/jn.00661.2020 · Cited by 25

ASC Transporters Mediate D-Serine Transport into Astrocytes Adjacent to Synapses in the Mouse Brain

Krishnan, K. S., & Billups, B. (2023) · Biomolecules · doi:10.3390/biom13050819 · Cited by 23

d-Cycloserine enhances the bidirectional range of NMDAR-dependent hippocampal synaptic plasticity

Vestring, S., Dorner, A., Scholliers, J., Ehrenberger, K., Kiss, A., Arenz, L., Theiß, A., Rossner, P., Frase, S., du Vinage, C., et al. (2024) · Translational Psychiatry · doi:10.1038/s41398-023-02725-7 · Cited by 24

Serine racemase deletion abolishes light‐evoked NMDA receptor currents in retinal ganglion cells

Sullivan, S. J., Esguerra, M., Wickham, R. J., Romero, G. E., Coyle, J. T., & Miller, R. F. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.217059 · Cited by 24

Astrocytic Target Mechanisms in Epilepsy

Héja, L. (2014) · Current Medicinal Chemistry · doi:10.2174/0929867320666131119160445 · Cited by 25

Imaging microcircuit function in healthy and diseased brain

Garaschuk, O. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.02.009 · Cited by 24

Astroglial Networks and Implications for Therapeutic Neuromodulation of Epilepsy

Witcher, M. R., & Ellis, T. L. (2012) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2012.00061 · Cited by 23

How do Glial Cells Contribute to Motor Control?

Christensen, R. K., Petersen, A. V., & Perrier, J. (2013) · Current Pharmaceutical Design · doi:10.2174/13816128113199990384 · Cited by 25

Glia: dos velhos conceitos às novas funções de hoje e as que ainda virão

Gomes, F. C. A., Tortelli, V., & Diniz, L. P. (2013) · Estudos Avançados · doi:10.1590/s0103-40142013000100006 · Cited by 29

The nature of early astroglial protection—Fast activation and signaling

Kardos, J., Héja, L., Jemnitz, K., Kovács, R., & Palkovits, M. (2017) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2017.03.005 · Cited by 23

Heterogeneity and function of hippocampal macroglia

Seifert, G., & Steinhäuser, C. (2017) · Cell and Tissue Research · doi:10.1007/s00441-017-2746-1 · Cited by 25

The Role of Astrocytic Calcium Signaling in the Aged Prefrontal Cortex

Guerra‐Gomes, S., Viana, J. F., Nascimento, D. S. M., Correia, J. S., Sardinha, V. M., Caetano, I., Sousa, N., Pinto, L., & Oliveira, J. F. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00379 · Cited by 23

Diacylglycerol lipase alpha in astrocytes is involved in maternal care and affective behaviors

Schüle, L., Glasmacher, S., Gertsch, J., Roggan, M. D., Transfeld, J. L., Bîndilă, L., Lutz, B., Kolbe, C., Bilkei‐Gorzó, A., Zimmer, A., et al. (2020) · Glia · doi:10.1002/glia.23903 · Cited by 25

A Rationally and Computationally Designed Fluorescent Biosensor for d -Serine

Vongsouthi, V., Whitfield, J. H., Unichenko, P., Mitchell, J. A., Breithausen, B., Khersonsky, O., Kremers, L., Janovjak, H., Monai, H., Hirase, H., et al. (2021) · ACS Sensors · doi:10.1021/acssensors.1c01803 · Cited by 23

The Role of Astrocytes in the Molecular Pathophysiology of Schizophrenia: Between Neurodevelopment and Neurodegeneration

Vellucci, L., Mazza, B., Barone, A., Nasti, A., Simone, G. D., Iasevoli, F., & de Bartolomeis, A. (2025) · Biomolecules · doi:10.3390/biom15050615 · Cited by 23

An Active Role for Astrocytes in Synaptic Plasticity?

Wenker, I. C. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00429.2010 · Cited by 22

Computational modeling of opioid-induced synaptic plasticity in hippocampus

Borjkhani, M., Bahrami, F., & Janahmadi, M. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193410 · Cited by 22

Rapid, enantioselective and colorimetric detection of D-arginine

Yu, X., Zhang, B., Fan, C., Yan, Q., Wang, S., Hu, H., Dong, Q., Du, G., Gao, Y., & Zeng, C. (2022) · iScience · doi:10.1016/j.isci.2022.104964 · Cited by 22

Spontaneous and multifaceted ATP release from astrocytes at the scale of hundreds of synapses

Hatashita, Y., Wu, Z., Fujita, H., Kumamoto, T., Livet, J., Li, Y., Tanifuji, M., & Inoue, T. (2023) · Glia · doi:10.1002/glia.24392 · Cited by 23

Glial modulation of the parallel memory formation

Kanaya, T., Ito, R., Morizawa, Y. M., Sasaki, D., Yamao, H., Ishikane, H., Hiraoka, Y., Tanaka, K., & Matsui, K. (2023) · Glia · doi:10.1002/glia.24431 · Cited by 22

Two-dimensional LC-MS/MS and three-dimensional LC analysis of chiral amino acids and related compounds in real-world matrices

Ishii, C., & Hamase, K. (2023) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2023.115627 · Cited by 22

Astrocytic activation and an inhibition of MAP kinases are required for proteinase‐activated receptor‐2‐mediated protection from neurotoxicity

Greenwood, S. M., & Bushell, T. J. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06737.x · Cited by 22

A Theoretical Study on the Role of Astrocytic Activity in Neuronal Hyperexcitability by a Novel Neuron-Glia Mass Model

Garnier, A., Vidal, A. C., & Benali, H. (2016) · The Journal of Mathematical Neuroscience · doi:10.1186/s13408-016-0042-0 · Cited by 22

Determination of Chiral Amino Acids in Various Fermented Products Using a Two-Dimensional HPLC-MS/MS System

Ishii, C., Akita, T., Nagano, M., Mita, M., & Hamase, K. (2019) · Chromatography · doi:10.15583/jpchrom.2019.011 · Cited by 22

Effects of arsenic exposure on d-serine metabolism in the hippocampus of offspring mice at different developmental stages

Wang, Y., Yang, X., Yu, H., Wang, H., Qi, Y., & Geng, M. (2019) · Archives of Toxicology · doi:10.1007/s00204-019-02616-1 · Cited by 22

Tau-Mediated Dysregulation of Neuroplasticity and Glial Plasticity

Koller, E. J., & Chakrabarty, P. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00151 · Cited by 23

Morphine-induced inhibition of Ca2+ -dependent d -serine release from astrocytes suppresses excitability of GABAergic neurons in the nucleus accumbens: d -serine in morphine addiction

Wu, J., Zhao, R., Guo, L., & Zhen, X. (2017) · Addiction Biology · doi:10.1111/adb.12417 · Cited by 21

The Effects of Modified Curcumin Preparations on Glial Morphology in Aging and Neuroinflammation

Ullah, F., Gamage, R. V., Sen, M. K., & Gyengési, E. (2022) · Neurochemical Research · doi:10.1007/s11064-021-03499-4 · Cited by 21

Disrupting cortical astrocyte Ca 2+ signaling in developing brain induces social deficits and depressive‐like behaviors

Luo, R., Zhou, B., Liao, P. S., Zuo, Y., & Jiang, R. (2023) · Glia · doi:10.1002/glia.24358 · Cited by 21

Glial Cell Modulation of Dendritic Spine Structure and Synaptic Function

Rasia‐Filho, A. A., Calcagnotto, M. E., & Halbach, O. V. B. U. (2023) · Advances in neurobiology · doi:10.1007/978-3-031-36159-3_6 · Cited by 21

Genome-wide association study of NMDA receptor coagonists in human cerebrospinal fluid and plasma

Luykx, J. J., Bakker, S. C., Visser, W. F., Verhoeven‐Duif, N. M., Buizer‐Voskamp, J. E., den Heijer, J. M., Boks, M. P., Sul, J. H., Eskin, E., Ori, A. P. S., et al. (2015) · Molecular Psychiatry · doi:10.1038/mp.2014.190 · Cited by 21

Pharmacological Tools to Study the Role of Astrocytes in Neural Network Functions

Peña‐Ortega, F., Rivera‐Angulo, A., & Lorea-Hernández, J. J. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-40764-7_3 · Cited by 23

A Compartmental Model to Investigate Local and Global Ca2+ Dynamics in Astrocytes

Cresswell-Clay, E., Crock, N., Tabak, J., & Erlebacher, G. (2018) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2018.00094 · Cited by 21

Estimating integrated information in bidirectional neuron-astrocyte communication

Abrego, L., Gordleeva, S., Игоревич, К. О., Krivonosov, M., & Zaikin, A. A. (2021) · Physical review. E · doi:10.1103/physreve.103.022410 · Cited by 21

Aging-Associated Cognitive Decline is Reversed by D-Serine Supplementation

Nava-Gomez, L. J., Calero-Vargas, I., Higinio-Rodríguez, F., Vázquez-Prieto, B., Olivares-Moreno, R., Ortíz-Retana, J. J., Aranda, P., Hernández‐Chan, N. G., Rojas‐Piloni, G., Alcauter, S., et al. (2022) · eNeuro · doi:10.1523/eneuro.0176-22.2022 · Cited by 21

Na+–Ca2+ exchanger mediates ChR2-induced [Ca2+]i elevation in astrocytes

Yang, J., Yu, H. Q., Zhou, D., Zhu, K., Lou, H., Duan, S., & Wang, H. (2015) · Cell Calcium · doi:10.1016/j.ceca.2015.06.008 · Cited by 21

D-Serine in Neuropsychiatric Disorders: New Advances

Durrant, A. R., & Heresco‐Levy, U. (2014) · Advances in Psychiatry · doi:10.1155/2014/859735 · Cited by 21

D-Amino Acid Aberrations in Cerebrospinal Fluid and Plasma of Smokers

Luykx, J. J., Bakker, S. C., van Boxmeer, L., Vinkers, C. H., Smeenk, H. E., Visser, W. F., Verhoeven‐Duif, N. M., Strengman, E., Buizer‐Voskamp, J. E., de Groene, L., et al. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.103 · Cited by 20

Rescue of synaptic and cognitive functions in polysialic acid-deficient mice and dementia models by short polysialic acid fragments

Varbanov, H., Jia, S., Kochlamazashvili, G., Bhattacharya, S., Buabeid, M. A., El‐Tabbal, M., Hayani, H., Stoyanov, S., Sun, W., Thiesler, H., et al. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106079 · Cited by 22

Diverse impact of acute and long-term extracellular proteolytic activity on plasticity of neuronal excitability

Wójtowicz, T., Brzdąk, P., & Mozrzymas, J. W. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00313 · Cited by 20

d-Serine rescues the deficits of hippocampal long-term potentiation and learning and memory induced by sodium fluoroacetate

Han, H., Yan, P., & Dong, Z. (2015) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2015.03.017 · Cited by 21

In Vivo Astrocytic Ca 2+ Signaling In Health and Brain Disorders

Ding, S. (2013) · Future Neurology · doi:10.2217/fnl.13.38 · Cited by 21

Hedgehog Signaling Modulates the Release of Gliotransmitters from Cultured Cerebellar Astrocytes

Okuda, H., Tatsumi, K., Takemura, S., Nakahara, K., Nochioka, K., Shinjo, T., Terada, Y., & Wanaka, A. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1791-y · Cited by 20

Activity-dependent changes in transporter and potassium currents in hippocampal astrocytes

Lebedeva, A., Plata, A., Nosova, O., Tyurikova, O., & Semyanov, A. V. (2017) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2017.08.015 · Cited by 20

Presynaptic mGluRs Control the Duration of Endocannabinoid-Mediated DSI

Colmers, P. L. W., & Bains, J. S. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1097-18.2018 · Cited by 20

Persistent activation of histamine H1 receptors in the hippocampal CA1 region enhances NMDA receptor-mediated synaptic excitation and long-term potentiation in astrocyte- and D-serine-dependent manner

Masuoka, T., Ikeda, R., & Konishi, S. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.03.036 · Cited by 20

Chemogenetic manipulation of astrocytic activity: Is it possible to reveal the roles of astrocytes?

Shen, W., Chen, S., Liu, Y., Han, P., Ma, T., & Zeng, L. (2021) · Biochemical Pharmacology · doi:10.1016/j.bcp.2021.114457 · Cited by 21

Expression and cellular function of vSNARE proteins in brain astrocytes

Ropert, N., Jalil, A., & Li, D. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.10.036 · Cited by 21

Astrocytes Shape Axonal Signaling

Debanne, D., & Rama, S. (2011) · Science Signaling · doi:10.1126/scisignal.2001884 · Cited by 20

The Role of Astrocytes in Synaptic Dysfunction and Memory Deficits in Alzheimer’s Disease

de León-López, C. A. M., Navarro‐Lobato, I., & Khan, Z. U. (2025) · Biomolecules · doi:10.3390/biom15070910 · Cited by 19

Excitatory and inhibitory D-serine binding to the NMDA receptor

Yovanno, R. A., Chou, T., Brantley, S. J., Furukawa, H., & Lau, A. Y. (2022) · eLife · doi:10.7554/elife.77645 · Cited by 19

Advances in the Electrophysiological Recordings of Long-Term Potentiation

Jiang, F., Bello, S. T., Gao, Q., Lai, Y., Li, X., & He, L. S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24087134 · Cited by 19

Astrocyte coverage of excitatory synapses correlates to measures of synapse structure and function in ferret primary visual cortex

Thomas, C. I., Ryan, M. A., McNabb, M. C., Kamasawa, N., & Scholl, B. (2024) · Glia · doi:10.1002/glia.24582 · Cited by 19

Calcium‐Dependent Signaling in Astrocytes: Downstream Mechanisms and Implications for Cognition

Veiga, A., Abreu, D. S., Dias, J. D., Azenha, P., Barsanti, S., & Oliveira, J. F. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70019 · Cited by 21

On the Evolution of Memory: A Time for Clocks

Gerstner, J. R. (2012) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2012.00023 · Cited by 20

Contribution of astrocytes to hippocampal long-term potentiation through release of d -serine

Yang, Y., Ge, W., Chen, Y., Zhang, Z., Shen, W., Wu, C., Poo, M., & Duan, S. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2431073100 · Cited by 533

Astrocytes as aide-mémoires

Santello, M., & Volterra, A. (2010) · Nature · doi:10.1038/463169a · Cited by 31

Astrocytes release d-serine by a large vesicle

Kang, N., Peng, H., Yu, Y., Stanton, P. K., Guilarte, T. R., & Kang, J. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.02.029 · Cited by 60

With a little help from glia

Wiedemann, C. G. (2010) · Nature reviews. Neuroscience · doi:10.1038/nrn2818 · Cited by 2

Astrocytes control hippocampal synaptic plasticity through the vesicular-dependent release of D-serine

Abreu, D. S., Gomes, J. I., Ribeiro, F. F., Diógenes, M. J., Sebastião, A. M., & Vaz, S. H. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1282841 · Cited by 32