Dopaminergic antagonists prevent long-term maintenance of posttetanic LTP in the CA1 region of rat hippocampal slices

Long‐lasting potentiation of synaptic transmission in the dentate area of the unanaesthetized rabbit following stimulation of the perforant path

Bliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,424

NMDA receptors - their role in long-term potentiation

Collingridge, G. L., & Bliss, T. (1987) · Trends in Neurosciences · doi:10.1016/0166-2236(87)90175-5 · Cited by 1,178

The role of dopamine in locomotor activity and learning

Beninger, R. J. (1983) · Brain Research Reviews · doi:10.1016/0165-0173(83)90038-3 · Cited by 848

Anisomycin, an inhibitor of protein synthesis, blocks late phases of LTP phenomena in the hippocampal CA1 region in vitro

Frey, U., Krug, M., Reymann, K. G., & Matthies, H. (1988) · Brain Research · doi:10.1016/0006-8993(88)90008-x · Cited by 806

The current excitement in long term potentiation

Nicoll, R. A., Kauer, J. A., & Malenka, R. C. (1988) · Neuron · doi:10.1016/0896-6273(88)90193-6 · Cited by 535

Anisomycin blocks the late phase of long-term potentiation in the dentate gyrus of freely moving rats

Krug, M., Lössner, B., & Ott, T. (1984) · Brain Research Bulletin · doi:10.1016/0361-9230(84)90005-4 · Cited by 509

Temporally distinct pre- and post-synaptic mechanisms maintain long-term potentiation

Davies, S. N., Lester, R. A. J., Reymann, K. G., & Collingridge, G. L. (1989) · Nature · doi:10.1038/338500a0 · Cited by 478

NMDA application potentiates synaptic transmission in the hippocampus

Kauer, J. A., Malenka, R. C., & Nicoll, R. A. (1988) · Nature · doi:10.1038/334250a0 · Cited by 423

Long-term potentiation as a candidate mnemonic device

Teyler, T. J., & DiScenna, P. G. (1984) · Brain Research Reviews · doi:10.1016/0165-0173(84)90027-4 · Cited by 371

Reduction of long‐term potentiation in the dentate gyrus of the rat following selective depletion of monoamines.

Bliss, T. V. P., Goddard, G. V., & Riives, M. L. (1983) · The Journal of Physiology · doi:10.1113/jphysiol.1983.sp014507 · Cited by 294

A Novel and Selective Dopamine Transporter Inhibitor, (S)-MK-26, Promotes Hippocampal Synaptic Plasticity and Restores Effort-Related Motivational Dysfunctions

Kouhnavardi, S., Ecevitoglu, A., Dragačević, V., Sanna, F., Arias‐Sandoval, E., Kalaba, P., Kirchhofer, M., Lubec, J., Niello, M., Holy, M., et al. (2022) · Biomolecules · doi:10.3390/biom12070881 · Cited by 24

MPTP modulates hippocampal synaptic transmission and activity‐dependent synaptic plasticity via dopamine receptors

Zhu, G., Huang, Y., Chen, Y., Zhuang, Y., & Behnisch, T. (2012) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2012.07815.x · Cited by 24

Low dopamine D5 receptor density in hippocampus in an animal model of attention-deficit/hyperactivity disorder (ADHD)

Medin, T., Rinholm, J. E., Owe, S. G., Sagvolden, T., GJEDDE, A. H., Storm‐Mathisen, J., & Bergersen, L. H. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.03.036 · Cited by 27

Neuregulin links dopaminergic and glutamatergic neurotransmission to control hippocampal synaptic plasticity

Neddens, J., Vullhorst, D., & Buonanno, A. (2009) · Communicative & Integrative Biology · doi:10.4161/cib.2.3.7825 · Cited by 25

Effect of prenatal malnutrition on release of monoamines from hippocampal slices

Chen, J., Turiák, G., Galler, J. R., & Volicer, L. (1995) · Life Sciences · doi:10.1016/0024-3205(95)02119-4 · Cited by 24

Hippocampal synaptic plasticity as a biological substrate underlying episodic psychosis

Port, R. L., & Seybold, K. S. (1995) · Biological Psychiatry · doi:10.1016/0006-3223(94)00128-p · Cited by 24

Increased Resting-State Perfusion after Repeated Encoding Is Related to Later Retrieval of Declarative Associative Memories

Grön, G., Sokolov, A. N., Jonas, C., Roebling, R., & Spitzer, M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019985 · Cited by 25

Principles of Intelligence: On Evolutionary Logic of the Brain

Tsien, J. Z. (2016) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00186 · Cited by 24

Blockade of dopamine D2 receptors disrupts intrahippocampal connectivity and enhances pain‐related working memory deficits in neuropathic pain rats

Cardoso-Cruz, H., Dourado, M., Monteiro, C., & Galhardo, V. (2018) · European Journal of Pain · doi:10.1002/ejp.1186 · Cited by 23

Molecular and cell biology of addiction.

Hyman, S. E. (1993) · PubMed · Cited by 23

Hippocampal convergence during anticipatory midbrain activation promotes subsequent memory formation

Poh, J.-H., Vu, M.-A. T., Stanek, J. K., Hsiung, A., Egner, T., & Adcock, R. A. (2022) · Nature Communications · doi:10.1038/s41467-022-34459-3 · Cited by 24

Phasic locus coeruleus activity enhances trace fear conditioning by increasing dopamine release in the hippocampus

Wilmot, J. H., Diniz, C. R. A. F., Crestani, A. P., Puhger, K. R., Roshgadol, J., Tian, L., & Wiltgen, B. J. (2023) · eLife · doi:10.7554/elife.91465 · Cited by 38

Effects of antipsychotic D2 antagonists on long-term potentiation in animals and implications for human studies

Price, R., Salavati, B., Graff‐Guerrero, A., Blumberger, D. M., Mulsant, B. H., Daskalakis, Z. J., & Rajji, T. K. (2014) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2014.05.001 · Cited by 26

Ibogaine Signals Addiction Genes and Methamphetamine Alteration of Long‐Term Potentiation

Onaivi, E. S., Ali, S. F., Chirwa, S., Zwiller, J., Thiriet, N., Akinshola, B. E., & Ishiguro, H. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb04149.x · Cited by 22

Amphetamine Effects on Striatal Neurons: Implications for Models of Dopamine Function

Haracz, J. L. (1998) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(97)00057-2 · Cited by 22

Exploring the Neurophysiological Effects of Self-Controlled Practice in Motor Skill Learning

Leiker, A. M., Pathania, A., Miller, M. W., & Lohse, K. R. (2018) · Journal of Motor Learning and Development · doi:10.1123/jmld.2017-0051 · Cited by 22

Neuromodulator-dependent synaptic tagging and capture retroactively controls neural coding in spiking neural networks

Lehr, A. B., Luboeinski, J., & Tetzlaff, C. (2022) · Scientific Reports · doi:10.1038/s41598-022-22430-7 · Cited by 20

Dopamine-induced tyrosine phosphorylation of NR2B (Tyr1472) is essential for ERK1/2 activation and processing of novel taste information

David, O., Barrera, I., Adaikkan, C., Kaphzan, H., Nakazawa, T., Yamamoto, T. S., & Rosenblum, K. (2014) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2014.00066 · Cited by 22

How do stupendous cannabinoids modulate memory processing via affecting neurotransmitter systems?

Vaseghi, S., Nasehi, M., & Zarrindast, M. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.10.018 · Cited by 21

Cognitive and emotional information processing: protein synthesis and gene expression

Sajikumar, S., Navakkode, S., Korz, V., & Frey, J. U. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.140087 · Cited by 21

Postsynaptic burst reactivation of hippocampal neurons enables associative plasticity of temporally discontiguous inputs

Fuchsberger, T., Clopath, C., Jarzębowski, P., Brzosko, Z., Wang, H., & Paulsen, O. (2022) · eLife · doi:10.7554/elife.81071 · Cited by 19

Loss of Catecholaminergic Neuromodulation of Persistent Forms of Hippocampal Synaptic Plasticity with Increasing Age

Twarkowski, H., & Manahan‐Vaughan, D. (2016) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2016.00030 · Cited by 20

NMDA receptors in the midbrain play a critical role in dopamine‐mediated hippocampal synaptic potentiation caused by morphine

Hu, L., Jing, X., Cui, C., Xing, G., & Zhu, B. (2012) · Addiction Biology · doi:10.1111/adb.12010 · Cited by 19

Effects of zinc on spatial reference memory and brain dopamine (D1) receptor binding kinetics in rats

Turner, T. Y., & Soliman, M. R. I. (2000) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(00)00128-7 · Cited by 19

Modulation of extracellular monoamine transmitter concentrations in the hippocampus after weak and strong tetanization of the perforant path in freely moving rats

Neugebauer, F., Korz, V., & Frey, J. U. (2009) · Brain Research · doi:10.1016/j.brainres.2009.03.055 · Cited by 18

Haloperidol-induced blockade of induction of long-term potentiation in perforant path-dentate gyrus pathway in chronically prepared rabbits

Jibiki, I., 脇田, 茂., Kubota, T., Kurokawa, K., Fukushima, T., & Yamaguchi, N. (1993) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(93)90211-b · Cited by 18

Phasic locus coeruleus activity enhances trace fear conditioning by increasing dopamine release in the hippocampus

Wilmot, J. H., Diniz, C. R. A. F., Crestani, A. P., Puhger, K. R., Roshgadol, J., Tian, L., & Wiltgen, B. J. (2024) · eLife · doi:10.7554/elife.91465.3 · Cited by 17

Involvement of the dopaminergic system in the consolidation of fear conditioning in hippocampal CA3 subregion

Wen, J.-L., Li, X., Wang, R., Chen, Z.-X., Shi, Y., & Zhao, H. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.10.049 · Cited by 17

Modulating the map

Werlen, E., & Jones, M. W. (2015) · Progress in brain research · doi:10.1016/bs.pbr.2015.03.002 · Cited by 16

Reduced expression of dopamine D2 receptors on astrocytes in R6/1 HD mice and HD post-mortem tissue

Harris, K. L., Mason, S., Vallin, B., & Barker, R. A. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.136289 · Cited by 16

The effects of neurosteroid allopregnanolone on synaptic dysfunction in the hippocampus in experimental parkinsonism rats: An electrophysiological and molecular study

Sheibani, V., Rajizadeh, M. A., Bejeshk, M. A., Haghparast, E., Nozari, M., Esmaeili‐Mahani, S., & Nezhadi, A. (2022) · Neuropeptides · doi:10.1016/j.npep.2022.102229 · Cited by 17

Dopamine receptor pharmacology

Mailman, R. B., & Huang, X. (2007) · Handbook of clinical neurology · doi:10.1016/s0072-9752(07)83004-1 · Cited by 17

Remembering rewarding futures: A simulation‐selection model of the hippocampus

Jung, M. W., Lee, H., Jeong, Y., Lee, J. W., & Lee, I. (2018) · Hippocampus · doi:10.1002/hipo.23023 · Cited by 16

Carbamazepine-induced blockade of induction of long-term potentiation in the perforant path-dentate gyrus pathway in chronically prepared rabbits

Kubota, T., Jibiki, I., Fukushima, T., Kurokawa, K., & Yamaguchi, N. (1994) · Neuroscience Letters · doi:10.1016/0304-3940(94)90266-6 · Cited by 16

Haloperidol and loxapine but not clozapine increase synaptic responses in the hippocampus

Baskys, A., Wang, S. Z., Remington, G. J., & Wojtowicz, J. M. (1993) · European Journal of Pharmacology · doi:10.1016/0014-2999(93)90151-7 · Cited by 16

Dopaminergic D1 receptor agonist SKF 38393 induces GAP-43 expression and long-term potentiation in hippocampus in vivo

Williams, S. C., Mmbaga, N., & Chirwa, S. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2006.03.075 · Cited by 16

The striatum and beyond: contributions of the hippocampus to decision making

Wimmer, G. E., & Shohamy, D. (2011) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780199600434.003.0013 · Cited by 14

Hippocampal place cell responses to distal and proximal cue manipulations in dopamine D2 receptor-knockout mice

Nguyen, C. L., Tran, A. H., Matsumoto, J., Hori, E., Uwano, T., Ono, T., & Nishijo, H. (2014) · Brain Research · doi:10.1016/j.brainres.2014.04.023 · Cited by 14

Dexpramipexole enhances hippocampal synaptic plasticity and memory in the rat

Coppi, E., Lana, D., Cherchi, F., Fusco, I., Buonvicino, D., Urru, M., Ranieri, G., Muzzi, M., Iovino, L., Giovannini, M. G., et al. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.10.003 · Cited by 14

Cocaine facilitates protein synthesis-dependent LTP: The role of metabotropic glutamate receptors

Fole, A., Miguéns, M., Higuera‐Matas, A., Alguacil, L. F., Ambrosio, E., & Olmo, N. D. (2013) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2013.10.013 · Cited by 13

Hippocampal receptor complexes paralleling LTP reinforcement in the spatial memory holeboard test in the rat

Subramaniyan, S., Hajali, V., Scherf, T., Sase, S., Sialana, F. J., Gröger, M., Bennett, K. L., Pollak, A. J., Li, L., Korz, V., et al. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.01.036 · Cited by 13

Bidirectional Regulation of Hippocampal Synaptic Plasticity and Modulation of Cumulative Spatial Memory by Dopamine D2-Like Receptors

Caragea, V.-M., & Manahan‐Vaughan, D. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.803574 · Cited by 14

Activation of D1/D5 receptors ameliorates decreased intrinsic excitability of hippocampal neurons induced by neonatal blockade of N‐methyl‐ d ‐aspartate receptors

Griego, E., Hernández‐Frausto, M., Márquez, L. A., Lara-Valderrábano, L., López‐Rubalcava, C., & Galván, E. J. (2021) · British Journal of Pharmacology · doi:10.1111/bph.15735 · Cited by 13

Modulation of fear memory by retrieval and extinction: a clue for memory deconsolidation

Hong, I., Kim, J., Song, B., Park, S., Lee, J., Kim, J., An, B., Lee, S., & Choi, S. (2011) · Reviews in the Neurosciences · doi:10.1515/rns.2011.023 · Cited by 13

Dopamine increases protein synthesis in hippocampal neurons enabling dopamine-dependent LTPPreprint

Fuchsberger, T., Stockwell, I., Woods, M., Brzosko, Z., Greger, I. H., & Paulsen, O. (2024) · eLife · doi:10.7554/elife.100822 · Cited by 13

Dopamine D5 receptors are localized at asymmetric synapses in the rat hippocampus

Medin, T., Owe, S. G., Rinholm, J. E., Larsson, M., Sagvolden, T., Storm‐Mathisen, J., & Bergersen, L. H. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.06.056 · Cited by 12

The modulatory role of accumbens and hippocampus D2 receptors in anxiety and memory

Ebrahimi-Ghiri, M., Nasehi, M., & Zarrindast, M. (2018) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-018-1534-0 · Cited by 12

In utero cocaine exposure decreases dopamine D1 receptor modulation of hippocampal long-term potentiation in the rabbit

Little, J. Z., & Teyler, T. J. (1996) · Neuroscience Letters · doi:10.1016/0304-3940(96)12960-8 · Cited by 12

The effects of ladasten on dopaminergic neurotransmission and hippocampal synaptic plasticity in rats

Mikhaylova, M., Vakhitova, J. V., Yamidanov, R. S., Салимгареева, М. Х., Середенин, С. Б., & Behnisch, T. (2007) · Neuropharmacology · doi:10.1016/j.neuropharm.2007.07.001 · Cited by 12

Alterations in the hippocampal and striatal catecholaminergic fiber densities of heterozygous reeler mice

Nullmeier, S., Panther, P., Frotscher, M., Zhao, S., & Schwegler, H. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.06.027 · Cited by 10

The Role of the Locus Coeruleus in Cellular and Systems Memory Consolidation

Eschenko, O. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812028-6.00018-5 · Cited by 10

Associative memory in three aplysiids: correlation with heterosynaptic modulation.

Hoover, B. A., Nguyen, H., Thompson, L., & Wright, W. G. (2006) · Learning & Memory · doi:10.1101/lm.284006 · Cited by 9

Case-Based Decision Neuroscience

Bhui, R. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812098-9.00004-8 · Cited by 10

Visuospatial functioning is associated with sleep disturbance and hallucinations in nondemented patients with Parkinson’s disease

Specketer, K., Zabetian, C. P., Edwards, K. L., Tian, L., Quinn, J. F., Peterson‐Hiller, A. L., Chung, K. A., Hu, S., Montine, T. J., & Cholerton, B. (2019) · Journal of Clinical and Experimental Neuropsychology · doi:10.1080/13803395.2019.1623180 · Cited by 9

A Multicomponent Learning Model of Drug Abuse: Drug Taking and Craving May Involve Separate Brain Circuits Underlying Instrumental and Classical Conditioning, Respectively

Haracz, J. L., Mash, D. C., & Sircar, R. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09329.x · Cited by 7

Comparison of the Role of D1- and D2-Like Receptors in the CA1 Region of the Hippocampus in the Reinstatement Induced by a Subthreshold Dose of Morphine and Forced Swim Stress in Extinguished Morphine-CPP in Rats

Nazari-Serenjeh, F., Rezaee, L., Zarrabian, S., & Haghparast, A. (2018) · Neurochemical Research · doi:10.1007/s11064-018-2631-7 · Cited by 9

NMDA receptor delayed maturation and schizophrenia

Ruppin, E. (2000) · Medical Hypotheses · doi:10.1054/mehy.1999.0928 · Cited by 9

GABAa receptor-mediated field potentials are enhanced in area CA1 following prenatal cocaine exposure

Little, J. Z., & Teyler, T. J. (1998) · Developmental Brain Research · doi:10.1016/s0165-3806(98)00100-x · Cited by 9

Long-lasting memory of sounds combined with reward in rats

Watanabe, S., Kudoh, M., Ohnishi, K., & Shibuki, K. (2001) · Neuroscience Letters · doi:10.1016/s0304-3940(01)02121-8 · Cited by 8

The hippocampus contributes to retroactive stimulus associations during trace fear conditioning

Puhger, K. R., Crestani, A. P., Diniz, C. R. A. F., & Wiltgen, B. J. (2024) · iScience · doi:10.1016/j.isci.2024.109035 · Cited by 10

Cannabinoids and monoaminergic system: implications for learning and memory

Zhao, S., Gu, Z.-L., Yue, Y.-N., Zhang, X., & Dong, Y. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1425532 · Cited by 7

Strain-dependent regulation of hippocampal long-term potentiation by dopamine D1/D5 receptors in mice

Hagena, H., Stacho, M., Laja, A., & Manahan‐Vaughan, D. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.1023361 · Cited by 7

Methylphenidate induces state-dependency of social recognition learning: Central components

Zinn, C. G., Bühler, L., Cavalcante, L. E. S., Schmidt, S. D., Ferreira, F. F., Zanini, M. L., Furini, C. R. G., Myskiw, J. D. C., & Izquierdo, I. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.02.002 · Cited by 7

The Influence of Hippocampal Dopamine D2 Receptors on Episodic Memory Is Modulated byBDNFandKIBRAPolymorphisms

Papenberg, G., Karalija, N., Salami, A., Andersson, M., Axelsson, J., Riklund, K., Lindenberger, U., Nyberg, L. H., & Bäckman, L. (2019) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01429 · Cited by 7

Phasic locus coeruleus activity enhances trace fear conditioning by increasing dopamine release in the hippocampusPreprint

Wilmot, J. H., Diniz, C. R. A. F., Crestani, A. P., Puhger, K. R., Roshgadol, J., Tian, L., & Wiltgen, B. J. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.17.512590 · Cited by 6

Stimulation of the nucleus raphe medialis modifies basal synaptic transmission at the dentate gyrus, but not long-term potentiation or its reinforcement by stimulation of the basolateral amygdala

Bergado, J. A., Scherf, T., Almaguer‐Melian, W., Frey, S., Lopez‐Rojas, J., & Frey, J. U. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.08.034 · Cited by 5

Effect of hippocampal 6-OHDA lesions on the contextual modulation of taste recognition memory

Grau-Perales, A. B., Gámiz, F., & Gallo, M. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113320 · Cited by 5

Regulation of AMPA Receptor Trafficking in the Nucleus Accumbens by Dopamine and Cocaine

Wolf, M. E. (2010) · Springer eBooks · doi:10.1007/978-1-4614-0785-0_21 · Cited by 5

Associative Reactivation of Place–Reward Information in the Hippocampal–Ventral Striatal Circuitry

Lansink, C. S., & Pennartz, C. M. A. (2014) · Springer series in computational neuroscience · doi:10.1007/978-1-4939-1969-7_4 · Cited by 4

Integrating information at single synaptic connections.

Montague, P. R. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.7.2424 · Cited by 5

Synaptic Plasticity in the Hippocampus

Bliss, T., Collingridge, G. L., Cooke, S. F., Georgiou, J., & Morris, R. (2025) · Oxford University Press eBooks · doi:10.1093/med/9780190065324.003.0010 · Cited by 4

Modeling Emergent Dynamics Arising from Synaptic Tagging and Capture at the Network Level

Luboeinski, J., & Tetzlaff, C. (2024) · Springer eBooks · doi:10.1007/978-3-031-54864-2_23 · Cited by 4

Subcortical nuclei of the human ascending arousal system encode anticipated reward but do not predict subsequent memory

Lloyd, B., Miletić, S., Bazin, P., Isherwood, S. J., Tse, D. H. Y., Haberg, A. K., Forstmann, B. U., & Nieuwenhuis, S. (2025) · Cerebral Cortex · doi:10.1093/cercor/bhaf101 · Cited by 3

Dopamine and Memory

LaLumiere, R. T. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-408139-0.00005-5 · Cited by 4

Amphetamine Self-Administration and Its Extinction Alter the 5-HT1B Receptor Protein Levels in Designated Structures of the Rat Brain

Miszkiel, J., Jastrzębska, J., Filip, M., & Przegaliński, E. (2018) · Neurotoxicity Research · doi:10.1007/s12640-018-9950-y · Cited by 5

Dopaminergic Neuromodulation in Synaptic Tagging and Capture

Navakkode, S. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1761-7_8 · Cited by 4

Dexpramipexole Enhances K+ Currents and Inhibits Cell Excitability in the Rat Hippocampus In Vitro

Coppi, E., Buonvicino, D., Ranieri, G., Cherchi, F., Venturini, M., Pugliese, A. M., & Chiarugi, A. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02300-5 · Cited by 4

Haloperidol reduces K+-evoked Ca2+-dependentd-[3H]aspartate release from rat hippocampal slices

Tzavara, E. T., Svarna, R., & Palaiologos, G. (1995) · Neurochemical Research · doi:10.1007/bf00995147 · Cited by 4

The Role of Synaptic Tagging and Capture for Memory Dynamics in Spiking Neural Networks

Luboeinski, J. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-463 · Cited by 4

Hippocampal long-term potentiation is modulated by exercise-induced alterations in dopaminergic synaptic transmission in mice selectively bred for high voluntary wheel running

Phan, J. M.-P., Yi, J., Foote, J. H. A., Ayabe, A. R. K., Guan, K., Garland, T., & Parfitt, K. D. (2024) · Restorative Neurology and Neuroscience · doi:10.1177/09226028241290400 · Cited by 3

Neural Network Simulations of a Possible Role of the Hippocampus in Pavlovian Conditioning

Burgos, J. E., & Galeazzi, J. M. (2021) · Springer eBooks · doi:10.1007/978-3-030-61721-9_23 · Cited by 3

Changing Reward Expectation Transforms Spatial Encoding and Retrieval in the HippocampusPreprint

Krishnan, S., Cherian, C., & Sheffield, M. E. J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.13.295469 · Cited by 3

Dopamine increases protein synthesis in hippocampal neurons enabling dopamine-dependent LTP

Fuchsberger, T., Stockwell, I., Woods, M., Brzosko, Z., Greger, I. H., & Paulsen, O. (2024) · eLife · doi:10.7554/elife.100822.3 · Cited by 20

Long-term potentiation in the brain: a synaptic memory mechanism

Moreno, A. R., & Paulsen, O. (2026) · Physiological Reviews · doi:10.1152/physrev.00028.2025 · Cited by 2

The effect of external rewards on declarative memory

Wang, S., Cheng, S., JIANG, T., Liu, X., & ZHANG, M. (2022) · Advances in Psychological Science · doi:10.3724/sp.j.1042.2023.00078 · Cited by 2

Effects of zotepine on excitatory synaptic responses in the perforant path–dentate gyrus pathway in chronically prepared rabbits

Kubota, T., Jibiki, I., & Kurokawa, S. (2002) · European Journal of Pharmacology · doi:10.1016/s0014-2999(02)02447-0 · Cited by 2

Effects of L-Dopa and Dopamine D2 Agonists on Recollection and Familiarity in Idiopathic Nondementing Parkinson’s Disease

Edelstyn, N. M. J., Shepherd, T. A., Mayes, A. R., Sherman, S. M., & Ellis, S. J. (2011) · Neuroscience & Medicine · doi:10.4236/nm.2011.24042 · Cited by 2

Learning and Representation of Declarative Memories by Single Neurons in the Human Brain

Rutishauser, U. (2008) · CaltechTHESIS (California Institute of Technology) · doi:10.7907/gx3n-qd05 · Cited by 2

Phorbol ester-induced changes in rat hippocampal glycoprotein fucosylation

Angenstein, F., Staak, S., & Jork, R. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90453-e · Cited by 2

Investigating the Contributions of Hippocampal Memory and Reward Valuation Systems to Cost-Benefit Decision Making

Tryon, V. L. (2017) · ResearchWorks at the University of Washington (University of Washington) · Cited by 2

Short-Term Exercise Ameliorates Cognitive Deficits and Upregulates the Hippocampal BDNF Pathway in Rats with Chronic Sleep Deprivation

Wen, Y., Wei, W., Huang, H., He, X., Chen, Q., Zhong, Q., & Zhao, M. (2026) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2026.101237 · Cited by 1

Reward Processing in Motivational and Affective Disorders

Skandali, N. (2016) · Frontiers research topics · doi:10.3389/978-2-88919-986-0 · Cited by 1

Langzeitpotenzierung im Hippokampus: Entdeckung, Mechanismen und Funktion

Bliss, T., Collingridge, G. L., Morris, R., & Reymann, K. G. (2018) · e-Neuroforum · doi:10.1515/nf-2017-0059 · Cited by 1

Dopamine and Synaptic Tagging and Capture: A Neuromodulatory Interplay That Shapes Associative Plasticity

Navakkode, S. (2024) · Springer eBooks · doi:10.1007/978-3-031-54864-2_15 · Cited by 1

Interactions between memory and reward systems

Poh, J.-H., & Adcock, R. A. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00049-3 · Cited by 1

D1/D5Dopamine Agonists as Pharmacotherapy for Schizophrenia

Boyd, K. N., & Mailman, R. B. (2012) · Wiley eBooks · doi:10.1002/9781118309421.ch3 · Cited by 1

Chapter 3.8 The multiple roles of dopaminergic neurotransmission in episodic memory

Schott, B. H., & Düzel, E. (2008) · Handbook of behavioral neuroscience · doi:10.1016/s1569-7339(08)00221-x · Cited by 1

Aging and functional reorganization of striatum- and Medial-Temporal Lobe-dependent memory systems

Schuck, N. W. (2013) · doi:10.18452/16773 · Cited by 1

Mechanisms underlying memory enhancement in humans

Granados, M. D. M. Y. (2017) · UPM Digital Archive (Technical University of Madrid) · doi:10.20868/upm.thesis.47030 · Cited by 1

The contribution of the hippocampus to language processing

Alamri, S. (2017) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · Cited by 1

The effect of dopaminergic D1 receptor blockade during tetanization on the expression of long-term potentiation in the rat CA1 region in vitro

Frey, U., Matthies, H., Reymann, K. G., & Matthies, H. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90732-9 · Cited by 314

Dopamine D1-deficient mutant mice do not express the late phase of hippocampal long-term potentiation

Matthies, H., Becker, A., Schröeder, H., Kraus, J., Höllt, V., & Krug, M. (1997) · Neuroreport · doi:10.1097/00001756-199711100-00023 · Cited by 106

Domperidone, an inhibitor of the D2-receptor, blocks a late phase of an electrically induced long-term potentiation in the CA1-region in rats.

Frey, U., Hartmann, S., & Matthies, H. K. (1989) · PubMed · Cited by 51

Long-term potentiation in rat prefrontal slices facilitated by phased application of dopamine

Blond, O., Crépel, F., & Otani, S. (2002) · European Journal of Pharmacology · doi:10.1016/s0014-2999(02)01291-8 · Cited by 52

Dopaminergic modulation of LTP induction in the dentate gyrus of intact brain

Kusuki, T., Imahori, Y., Ueda, S., & Inokuchi, K. (1997) · Neuroreport · doi:10.1097/00001756-199705260-00046 · Cited by 66