Synaptic plasticity in the hippocampus: LTP and LTD

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

The Medial Temporal Lobe Memory System

Squire, L. R., & Zola-Morgan, S. (1991) · Science · doi:10.1126/science.1896849 · Cited by 3,282

Dynamics of the Hippocampal Ensemble Code for Space

Wilson, M. A., & McNaughton, B. L. (1993) · Science · doi:10.1126/science.8351520 · Cited by 2,350

Mechanisms underlying induction of homosynaptic long-term depression in area CA1 of the hippocampus

Mulkey, R. M., & Malenka, R. C. (1992) · Neuron · doi:10.1016/0896-6273(92)90248-c · Cited by 1,113

Involvement of a calcineurin/ inhibitor-1 phosphatase cascade in hippocampal long-term depression

Mulkey, R. M., Endo, S., Shenolikar, S., & Malenka, R. C. (1994) · Nature · doi:10.1038/369486a0 · Cited by 1,083

NMDA-receptor-dependent synaptic plasticity: multiple forms and mechanisms

Malenka, R. C., & Nicoll, R. A. (1993) · Trends in Neurosciences · doi:10.1016/0166-2236(93)90197-t · Cited by 904

Nitric Oxide and Synaptic Function

Schuman, E. M., & Madison, D. V. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.001101 · Cited by 774

Induction of LTP in the hippocampus needs synaptic activation of glutamate metabotropic receptors

Bashir, Z. I., Bortolotto, Z. A., Davies, C. H., Berretta, N., Irving, A. J., Seal, A., Henley, J. M., Jane, D. E., Watkins, J. C., & Collingridge, G. L. (1993) · Nature · doi:10.1038/363347a0 · Cited by 733

An Essential Role for Protein Phosphatases in Hippocampal Long-Term Depression

Mulkey, R. M., Herron, C. E., & Malenka, R. C. (1993) · Science · doi:10.1126/science.8394601 · Cited by 699

Arachidonic acid induces a long-term activity-dependent enhancement of synaptic transmission in the hippocampus

Williams, J. H., Errington, M., Lynch, M., & Bliss, T. (1989) · Nature · doi:10.1038/341739a0 · Cited by 630

Gedächtnisdefizite nach Läsionen des medialen Temporallappens

Finke, C. (2013) · Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver · doi:10.17169/refubium-8387

ENVOLVIMENTO DA GUANILATO CICLASE SOLÚVEL E DE CANAIS DE POTÁSSIO SENSÍVEIS AO CÁLCIO NA HIPORRESPONSIVIDADE DE LONGA DURAÇÃO À FENILEFRINA INDUZIDA PELO ÓXIDO NÍTRICO NA MUSCULATURA LISA VASCULAR

Terluk, M. R. (2000) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Functional Regulation of Glutamate Receptor GluR1: Long Term Potentiation and Depression of GluR1 by Post Translational Modification

Elahi, S., Kaleem, A., Ahmad, I., & Shakoori, A. R. (2009) · Pakistan Journal of Zoology

Synaptic plasticity in mice (Mus musculus L., 1758) deficient in cell adhesion or extracellular matrix molecules: in vivo and in vitro electrophysiological analysis

der Fakultät, B. (2008)

SHORT COMMUNICATION Induction of long-term potentiation at spinal synapses by noxious stimulation or nerve injury

Liu, X. (1998)

UNIVERSIDADE FEDERAL DO RIO GRANDE DO SUL INSTITUTO DE CIÊNCIAS BÁSICAS DA SAÚDE CURSO DE PÓS-GRADUAÇÃO EM NEUROCIÊNCIAS EPILEPSIA EXPERIMENTAL E FÁRMACOS ANTIEPILÉPTICOS: EFEITO NA MEMÓRIA ESPACIAL E NA POTENCIAÇÃO DE LONGA DURAÇÃO INDUZIDA IN VITRO

Pedroso, M. F. (2005)

The role of L-type voltage-gated calcium channels in hippocampal CA1 neuron glutamate and GABA-A receptor-mediated synaptic plasticity following chronic benzodiazepine administration

Xiang, K. (2007) · OhioLink ETD Center (Ohio Library and Information Network)

Neural Plasticity in the Ventral Tegmental Area and Alcohol Addiction*Portions of this chapter were prepared by U.S. government employee in connection with their official duties, and therefore copyright protection is not available in the United States for such portions of the chapter pursuant to 17 U.S.C. Section 105.*

Whitaker, L. R., Hendrickson, L. M., & Morikawa, H. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405941-2.00012-2

Physiological properties of cerebellar circuits in a mouse model for Angelman Syndrome and modulation of inhibitory transmission by NMDA receptor activation in the mouse hippocampus

Xue, J. G. (2011) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/51022

The Regulatory Properties of α5 Subunit-Containing γ-Aminobutyric Acid Subtype A Receptors in Learning and Synaptic Plasticity

Martin, L. J. (2010) · TSpace (University of Toronto)

Intracellular Message Chains

Coward, L. A. (2013) · Springer eBooks · doi:10.1007/978-94-007-7107-9_5

Cellular Mechanisms of Memory: Complex Circuits

Eichenbaum, H. (2002) · doi:10.1093/acprof:oso/9780195141740.003.0003

Long‐Term Potentiation

Eichenbaum, H. (2010) · The Corsini Encyclopedia of Psychology · doi:10.1002/9780470479216.corpsy0514

Facilitation of Declarative Memory and Congruent Brain States by Applications of Weak, Patterned Magnetic Fields: The Future of Memory Access?

Corradini, P. L., Collins, M., & Persinger, M. A. (2014)

Basic Research Low-Level Baroreceptor Stimulation Suppresses Atrial Fibrillation by Inhibiting Ganglionated Plexus Activity

Liao, K., Yu, L., Zhou, X., Saren, G., Wang, S., Wang, Z., Huang, B. S., Yang, K., & Jiang, H. (2015)

The Roles of Neurotrophins in Novel Object Recognition

Kelly, Á. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812012-5.00030-6

Computational Examination of Synaptic Plasticity and Metaplasticity in Hippocampal Dentate Granule Neurons

Shirrafiardekani, A., Frauendiener, J., Moustafa, A. A., & Beňušková, Ľ. (2018) · Springer series in computational neuroscience · doi:10.1007/978-3-319-99103-0_20

Mechanisms Underlying Maintenance of Adult Visual Receptive Fields

Mudd, D. B. (2022) · Digital Archive @ GSU · doi:10.57709/14967304

Effect of an Ethanol Extract of Cassia obtusifolia Seeds on Alcohol-induced Memory Impairment

Kwon, H., Cho, E., Jeon, J., Lee, Y. C., & Kim, D. H. (2019) · JoLS Journal of Life Sciences · doi:10.5352/jls.2019.29.5.564

Not all is lost; prenatal ethanol exposure impairs bidirectional synaptic plasticity in the juvenile dentate gyrus

Fontaine, C. J. (2018) · UVic’s Research and Learning Repository (University of Victoria)

Approaches for unveiling the kinetic mechanisms of voltage gated ion channels in neurons

Navarro, M. A. (2019) · doi:10.32469/10355/75029

Disinhibitory and neuromodulatory regulation of hippocampal synaptic plasticityPreprint

Guerreiro, I. C., Gu, Z., Yakel, J. L., & Gutkin, B. S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.13.337188

Presynaptic LTP in Blockade of NMDA2B Receptors

Kudryashova, I. V. (2020) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-020-00999-8

Structural Development of Hippocampal CA3 Pyramidal Neurons and Relation to the Development of Spatial Learning and Memory in Rats

Mahdi, M. (2015) · doi:10.22215/etd/2015-11122

NMDAR-PSD95-nNOS Axis-Mediated Molecular Mechanisms in the Basolateral Amygdala Underlying Fear Consolidation

Patel, J. (2021) · IUScholarWorks (Indiana University) · doi:10.7912/c2/2085

Development of Spatial Function in Rats and Associated C-Fos Patterns in the Hippocampal CA1 and CA3 Regions

Comba, R. (2013) · doi:10.22215/etd/2013-09893

Relationship between monocular form deprivation amblyopia and activity-regulated cytoskeleton-associated in visual cortex of kittensPreprint

Fan, H., Wang, Y., Zou, Y., Song, W., Chen, S., Tang, X., & Xie, J. (2022) · Research Square · doi:10.21203/rs.3.rs-2301462/v1

Double-Forming Mechanism of TaOx-Based Resistive Memory Device and Its Synaptic Applications

Ju, D., Kim, S., Lee, S., & Kim, S. (2023) · Materials · doi:10.3390/ma16186184

The functional role of VEGF secretion during neuronal development

Nicholson, L. (2023) · Publication Server of Goethe University Frankfurt am Main (Goethe University Frankfurt) · doi:10.21248/gups.79200

Impairment of LTP, LTD and Metaplasticity During the Early Stages of Alzheimer'S Disease: a Computational Study

Shirrafiardekani, A., Mirjalili, A., Alashwal, H., & Moustafa, A. A. (2023) · International Conference on Machine Learning and Cybernetics · doi:10.1109/icmlc58545.2023.10327966

Live FRET-FLIM Imaging to Study Metabotropic Signaling via the NMDA Receptor

Manikkoth, M., & Doré, K. (2024) · Neuromethods · doi:10.1007/978-1-0716-3742-5_4

Adaptive synaptic mechanisms: The role of metaplasticity in synaptic tagging and capture

Jayapragas, S., Yin, L. S., & Sajikumar, S. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00065-1

Neuromodulation Through Axonal Stimulations in Brain

Feng, Z. (2025) · Springer eBooks · doi:10.1007/978-981-95-4145-4_9

Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts

Martins, M. (2013) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

Actin at the Synapse: Contribution to Pre- and Postsynaptic Functions

Liao, D. (2010) · Advances in neurobiology · doi:10.1007/978-1-4419-7368-9_10

FOOD INTAKE TAEES FACILIATES BRAIN PLASTICITY

Oomura, Y. (2015) · Medical academic journal · doi:10.17816/maj15154-62

Activation of oligodendrocyte precursor cells triggers cognitive dysfunction and synaptic defects in SAE

Wu, Y., Yang, Z., Liu, H., Li, J., Liu, R., Li, Y., Yu, C., & Su, B. (2026) · Experimental Neurology · doi:10.1016/j.expneurol.2026.115670 · Cited by 1

Dynamique des interactions entre excitation et inhibition périsomatique dans le circuit hippocampique normal et épileptique in vivo

Dubanet, O. (2019) · theses.fr (ABES) · doi:10.70675/0359faf0z0c04z4868z91c1z3346cb326678

Altérations des synapses et des corps cellulaires neuronaux chez les souris APPxPS1-KI et dans la Maladie d'Alzheimer

Androuin, A. (2018) · theses.fr (ABES) · doi:10.70675/a4392b1fz1293z4debzbe98ze28194a21801

Roles of astroglial cannabinoid type 1 receptors (CB1) in memory and synaptic plasticity

Robin, L. M. (2018) · theses.fr (ABES) · doi:10.70675/1fd1dda8z3f4bz404azbdf6z5b648e4c4053

Noyaux réuniens et rhomboïde du thalamus et persistance d'un souvenir chez le rat

Quet, É. (2019) · theses.fr (ABES) · doi:10.70675/4038aabbzab3ez41dbz98c0za1e03d07a65b

Pathophysiological consequences of a Fragile X missense mutation

Garcia, M. P. (2020) · theses.fr (ABES) · doi:10.70675/b8e86263z5926z4a83zbaf6z0f61bf2d15f9

Effets des ions bromures dans les modèles murins d'autisme et sur la signalisation des récepteurs couplés aux protéines G

Derieux, C. (2021) · theses.fr (ABES) · doi:10.70675/e9ba9584z22eez4cbbzb118za3ef2dae7731

Evaluation dynamique et fonctionnelle de l'inhibition périsomatique dans le circuit hippocampique au cours du développement normal et pathologique chez la souris in vivo

Silva, A. F. G. D. (2022) · theses.fr (ABES) · doi:10.70675/2aded2d4z39f7z4f70zbfa6z87186f05a59c

From Erythropoiesis to Circuit Rewiring: Erythropoietin as a Precision Tool for Neurorestoration

Almaguer‐Melian, W., Mercerón‐Martínez, D., Acosta, B. B., & Bergado, J. A. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27104329

Tracking long-term natural changes in hippocampal excitatory to inhibitory synapses from spikesPreprint

Ren, N., Mankili, A., & Stevenson, I. H. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.27.728158

Synaptic neurotransmitter concentration modulation during learning in bio-inspired spiking neural network

Yadav, S., Gehlot, N., Chaudhary, S., Kumar, R., & Nkomozepi, P. (2026) · Cognitive Neurodynamics · doi:10.1007/s11571-026-10489-1

Entorhinal Cortex Hyperexcitability Drives Selective Hippocampal Injury and Cognitive Impairment After Global Cerebral Ischemia

Chen, Y., Yan, Z., Wei, Z., Xu, J., Li, A., & Zhu, Q. (2026) · Journal of the American Heart Association · doi:10.1161/jaha.125.045208

Fascin in dendritic protrusions is required for synaptic plasticity

Zheng, J. Q., Joubert, S., Gonzalez-Islas, C. E., Ogawa, Y., Poddar, A., Penas, A. B., Liu, E., Wenner, P., & Myers, K. R. (2026) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2026.113465

The study of adolescent to adult neural development (SAND): Examining the neurobehavioral impacts of poverty-related adversity in the future of families and child wellbeing cohort

Hyde, L. W., Mitchell, C., McLoyd, V. C., Meier, H. C. S., Neblett, E. W., & Monk, C. S. (2026) · Brain and Environment · doi:10.1016/j.braen.2026.100036

Episodic memory, semantic memory, and amnesia

Squire, L. R., & Zola, S. M. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1998)8:3

Untitled work

(2000) · doi:10.1002/1098-1063(2000)10:6

Hippocampal Synaptic Enhancement as a Basis for Learning and Memory:A Selected Review of Current Evidence from Behaving Animals

Barnes, C. A., Erickson, C. A., Davis, S., & McNaughton, B. L. (1995) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195082944.003.0016 · Cited by 11

Long-term potentiation: What's learning got to do with it?

Shors, T. J., & Matzel, L. D. (1997) · Behavioral and Brain Sciences · doi:10.1017/s0140525x97001593 · Cited by 320

Pretraining and the Function of Hippocampal Long-Term Potentiation

Moser, M., & Moser, E. I. (2000) · Neuron · doi:10.1016/s0896-6273(00)81192-7 · Cited by 17

Physiological significance of long-term potentiation.

Esposito, E., & Pulvirenti, L. (1992) · PubMed · Cited by 4

Hippocampal synaptic enhancement and information storage within a distributed memory system

McNaughton, B. L., & Morris, R. G. M. (1987) · Trends in Neurosciences · doi:10.1016/0166-2236(87)90011-7 · Cited by 1,304