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

Kappa opioids inhibit induction of long-term potentiation in the dentate gyrus of the guinea pig hippocampus

Terman, G. W., Wagner, J. J., & Chavkin, C. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-08-04740.1994 · Cited by 82

Functional division of hippocampal area CA1 via modulatory gating of entorhinal cortical inputs

Ito, H., & Schuman, E. M. (2011) · Hippocampus · doi:10.1002/hipo.20909 · Cited by 81

Positive and negative modulation of word learning by reward anticipation

Callan, D. E., & Schweighofer, N. (2008) · Human Brain Mapping · doi:10.1002/hbm.20383 · Cited by 79

Synapse-specific stabilization of plasticity processes: The synaptic tagging and capture hypothesis revisited 10 years later

Barco, Á., de Armentia, M. L., & Alarcón, J. M. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.01.002 · Cited by 81

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

Wolf, M. E. (2010) · Neurotoxicity Research · doi:10.1007/s12640-010-9176-0 · Cited by 80

Depotentiation in the Dentate Gyrus of Freely Moving Rats is Modulated by D1/D5 Dopamine Receptors

Kulla, A. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.6.614 · Cited by 76

Neural systems analysis of decision making during goal-directed navigation

Penner, M. R., & Mizumori, S. J. Y. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.08.010 · Cited by 80

The ascending neuromodulatory systems in learning by reinforcement: comparing computational conjectures with experimental findings

Pennartz, C. M. A. (1995) · Brain Research Reviews · doi:10.1016/0165-0173(95)00014-3 · Cited by 73

Intrinsically regulated learning is modulated by synaptic dopamine signaling

Ripollés, P., Ferreri, L., Herrero, E. M., Alicart, H., Gómez-Andrés, A., Marco‐Pallarés, J., Antonijoan, R. M., Noesselt, T., Valle, M., Riba, J., et al. (2018) · eLife · doi:10.7554/elife.38113 · Cited by 77

Initial memory consolidation and the synaptic tagging and capture hypothesis

Okuda, K., Højgaard, K., Privitera, L., Bayraktar, G., & Takeuchi, T. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14902 · Cited by 74

Trial Outcome and Associative Learning Signals in the Monkey Hippocampus

Wirth, S., Avşar, E., Chiu, C. C., Sharma, V., Smith, A. C., Brown, E. N., & SUZUKI, W. A. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.012 · Cited by 75

Temporal Sensitivity of Protein Kinase A Activation in Late-Phase Long Term Potentiation

Kim, M., Huang, T., Abel, T., & Blackwell, K. T. (2010) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000691 · Cited by 72

drd2‐cre:ribotag mouse line unravels the possible diversity of dopamine d2 receptor‐expressing cells of the dorsal mouse hippocampus

Puighermanal, E., Biever, A., Espallergues, J., Gangarossa, G., Bundel, D. D., & Valjent, E. (2014) · Hippocampus · doi:10.1002/hipo.22408 · Cited by 68

D1/5 receptor-mediated enhancement of LTP requires PKA, Src family kinases, and NR2B-containing NMDARs

Stramiello, M., & Wagner, J. J. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.06.053 · Cited by 71

Computational models of reinforcement learning: the role of dopamine as a reward signal

Samson, R. D., Frank, M. J., & Fellous, J. (2010) · Cognitive Neurodynamics · doi:10.1007/s11571-010-9109-x · Cited by 75

Novelty exposure overcomes foot shock-induced spatial-memory impairment by processes of synaptic-tagging in rats

Almaguer‐Melian, W., Bergado, J. A., Fuentes, N. P., Alberti‐Amador, E., Mercerón‐Martínez, D., & Frey, J. U. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1114198109 · Cited by 71

Imaging-Based Neurochemistry in Schizophrenia: A Systematic Review and Implications for Dysfunctional Long-Term Potentiation

Salavati, B., Rajji, T. K., Price, R., Sun, Y., Graff‐Guerrero, A., & Daskalakis, Z. J. (2014) · Schizophrenia Bulletin · doi:10.1093/schbul/sbu132 · Cited by 71

Ventral Tegmental Area Inactivation Suppresses the Expression of CA1 Long Term Potentiation in Anesthetized Rat

Ghanbarian, E., & Motamedi, F. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058844 · Cited by 71

Mitogen-Activated Protein Kinase-Mediated Reinforcement of Hippocampal Early Long-Term Depression by the Type IV-Specific Phosphodiesterase Inhibitor Rolipram and Its Effect on Synaptic Tagging

Navakkode, S., Sajikumar, S., & Frey, J. U. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2443-05.2005 · Cited by 68

Synaptic consolidation: an approach to long-term learning

Clopath, C. (2011) · Cognitive Neurodynamics · doi:10.1007/s11571-011-9177-6 · Cited by 77

Cocaine-induced modulation of long-term potentiation in the CA1 region of rat hippocampus

THOMPSON, A., Swant, J., & Wagner, J. J. (2005) · Neuropharmacology · doi:10.1016/j.neuropharm.2005.03.005 · Cited by 66

Dopamine transporter blockade increases LTP in the CA1 region of the rat hippocampus via activation of the D3 dopamine receptorPreprint

Swant, J., & Wagner, J. J. (2006) · Learning & Memory · doi:10.1101/lm.63806 · Cited by 64

Modulation of hippocampal plasticity in learning and memory

Fuchsberger, T., & Paulsen, O. (2022) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2022.102558 · Cited by 70

Involvement of β-adrenergic receptors in protein synthesis-dependent late long-term potentiation (LTP) in the dentate gyrus of freely moving rats: the critical role of the LTP induction strength

Straube, T., & Frey, J. U. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00151-9 · Cited by 72

Changes in dopamine D2-receptor binding are associated to symptom reduction after psychotherapy in social anxiety disorder

Červenka, S., Hedman‐Lagerlöf, E., Ikoma, Y., Djurfeldt, D. R., Rück, C., Halldin, C., & Lindefors, N. (2012) · Translational Psychiatry · doi:10.1038/tp.2012.40 · Cited by 67

Obesity and episodic memory function

Loprinzi, P. D., & Frith, E. (2018) · The Journal of Physiological Sciences · doi:10.1007/s12576-018-0612-x · Cited by 63

Behavioral specifications of reward-associated long-term memory enhancement in humans

Wittmann, B. C., Dolan, R. J., & Düzel, E. (2011) · Learning & Memory · doi:10.1101/lm.1996811 · Cited by 62

D1 and D5 dopamine receptors participate on the consolidation of two different memories

Furini, C. R. G., Myskiw, J. C., Schmidt, B. E., Marcondes, L. A., & Izquierdo, I. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.06.027 · Cited by 60

Involvement of the Ventral Tegmental Area in a Rodent Model of Post-Traumatic Stress Disorder

Corral-Frías, N. S., Lahood, R. P., Edelman-Vogelsang, K. E., French, E. D., & Fellous, J. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2012.189 · Cited by 58

Bidirectional Modulation of Hippocampal Long-Term Potentiation under Stress and No-Stress Conditions in Basolateral Amygdala-Lesioned and Intact Rats

Korz, V., & Frey, J. U. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.0910-05.2005 · Cited by 58

The Hippocampal-VTA Loop: The Role of Novelty and Motivation in Controlling the Entry of Information into Long-Term Memory

Otmakhova, N. A., Düzel, E., Deutch, A. Y., & Lisman, J. E. (2012) · Springer eBooks · doi:10.1007/978-3-642-32375-1_10 · Cited by 59

Synaptic Consolidation: From Synapses to Behavioral Modeling

Ziegler, L., Zenke, F., Kastner, D. B., & Wulfram Gerstner, B. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3989-14.2015 · Cited by 55

Change in bi‐directional plasticity at CA1 synapses in hippocampal slices taken from 6‐hydroxydopamine‐treated rats: the role of endogenous norepinephrine

Yang, H., Lin, Y., Yen, C., & Min, M. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02165.x · Cited by 56

Chronic administration of (+)-amphetamine alters the reactivity of midbrain dopaminergic neurons to prefrontal cortex stimulation in the rat

Tong, Z.-Y., Overton, P. G., & Clark, D. T. (1995) · Brain Research · doi:10.1016/0006-8993(94)01439-o · Cited by 56

Synergistic interactions of dopamine D1 and glutamate NMDA receptors in rat hippocampus and prefrontal cortex: Involvement of ERK1/2 signaling

Sarantis, K., Matsokis, N. A., & Angelatou, F. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.07.056 · Cited by 58

Generalizing memories over time: Sleep and reinforcement facilitate transitive inference

Werchan, D. M., & Gómez, R. L. (2012) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2012.12.006 · Cited by 57

Association between striatal and extrastriatal dopamine D2-receptor binding and social desirability

Červenka, S., Gustavsson, P. J., Halldin, C., & Farde, L. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.12.006 · Cited by 54

Dopamine D2 receptors in the hippocampus and amygdala in Alzheimer's disease

Joyce, J. N., Kaeger, C., Ryoo, H., & Goldsmith, S. K. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90199-u · Cited by 53

Group I Metabotropic Glutamate Receptor Signaling via Gαq/Gα11 Secures the Induction of Long-Term Potentiation in the Hippocampal Area CA1

Miura, M., Watanabe, M., Offermanns, S., Simon, M. I., & Kano, M. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-19-08379.2002 · Cited by 53

COMT Val108/158 Met Genotype Affects Neural but not Cognitive Processing in Healthy Individuals

Dennis, N. A., Need, A. C., LaBar, K. S., Waters, S., Cirulli, E. T., Kragel, J. E., Goldstein, D. B., & Cabeza, R. E. L. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp132 · Cited by 53

The Hippocampus Codes the Uncertainty of Cue–Outcome Associations: An Intracranial Electrophysiological Study in Humans

Vanni-Mercier, G., Mauguı̀ere, F., Isnard, J., & Dreher, J. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5298-08.2009 · Cited by 50

Postsynaptic dopamine D3 receptor modulation of evoked IPSCs via GABAA receptor endocytosis in rat hippocampus

Swant, J., Stramiello, M., & Wagner, J. J. (2008) · Hippocampus · doi:10.1002/hipo.20408 · Cited by 51

LTP in cultured hippocampal–entorhinal cortex slices from young adult (P25-30) rats

Leutgeb, J. K., Frey, J. U., & Behnisch, T. (2003) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(03)00228-0 · Cited by 52

Forgetting in Reinforcement Learning Links Sustained Dopamine Signals to Motivation

Kato, A., & Morita, K. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005145 · Cited by 59

Substance P and neurotensin in the limbic system: Their roles in reinforcement and memory consolidation

Lénárd, L., László, K., Kertes, E., Ollmann, T., Péczely, L., Kovács, A., Kállai, V., Zagorácz, O., Gálosi, R., & Karádi, Z. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.09.003 · Cited by 49

Dopamine D2R is Required for Hippocampal-dependent Memory and Plasticity at the CA3-CA1 Synapse

Espadas, I., Ortiz, Ó., García‐Sanz, P., Sanz‐Magro, A., Alberquilla, S., Solís, Ó., Delgado-Garcia, J. M., Gruart, A., & Moratalla, R. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa354 · Cited by 51

Aging impairs amygdala-hippocampus interactions involved in hippocampal LTP

Almaguer, W., Estupiñán, B., Frey, J. U., & Bergado, J. A. (2002) · Neurobiology of Aging · doi:10.1016/s0197-4580(01)00278-0 · Cited by 50

Neurophysiological analysis of long-term potentiation in mammalian brain

Voronin, L. L., Byzov, A. L., Kleschevnikov, A. M., Kozhemyakin, M. B., Kuhnt, U., & Volgushev, M. (1995) · Behavioural Brain Research · doi:10.1016/0166-4328(94)00123-w · Cited by 49

Frequency dependency of NMDA receptor‐dependent synaptic plasticity in the hippocampal CA1 region of freely behaving mice

Buschler, A., Goh, J. J., & Manahan‐Vaughan, D. (2012) · Hippocampus · doi:10.1002/hipo.22041 · Cited by 49

Genetic labeling reveals temporal and spatial expression pattern of D2 dopamine receptor in rat forebrain

Yu, Q., Liu, Y., Zhu, Y., Wang, Y.-Y., Li, Q., & Yin, D. (2019) · Brain Structure and Function · doi:10.1007/s00429-018-01824-2 · Cited by 51

Pathogenesis of Schizophrenic Delusions and Hallucinations: A Neural Model

Ruppin, E., Reggia, J. A., & Horn, D. (1996) · Schizophrenia Bulletin · doi:10.1093/schbul/22.1.105 · Cited by 48

Glutamate receptors and metaplasticity in addiction

Chiamulera, C., Piva, A., & Abraham, W. C. (2020) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2020.09.005 · Cited by 47

Dopamine D2 receptor plays a role in memory function: implications of dopamine–acetylcholine interaction in the ventral hippocampus

Fujishiro, H., Umegaki, H., Suzuki, Y., Kurotani, S., Yamaguchi, Y., & Iguchi, A. (2005) · Psychopharmacology · doi:10.1007/s00213-005-0072-x · Cited by 47

Gradient of Expression of Dopamine D2 Receptors Along the Dorso-Ventral Axis of the Hippocampus

Dubovyk, V., & Manahan‐Vaughan, D. (2019) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2019.00028 · Cited by 49

Protein kinase Mζ is essential for the induction and maintenance of dopamine-induced long-term potentiation in apical CA1 dendritesPreprint

Navakkode, S., Sajikumar, S., Sacktor, T. C., & Frey, J. U. (2010) · Learning & Memory · doi:10.1101/lm.1991910 · Cited by 46

Reduced Threshold for Induction of LTP by Activation of Dopamine D1/D5 Receptors at Hippocampal CA1–Subiculum Synapses

Roggenhofer, E., Fidzinski, P., Shor, O., & Behr, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062520 · Cited by 46

The D1 dopamine receptor agonist SKF-38393 stimulates the release of glutamate in the hippocampus

Bouron, A., & REUTER, H. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00352-8 · Cited by 44

Dopamine D1/D5 receptor activation fails to initiate an activity-independent late-phase LTP in rat hippocampus

Mockett, B. G., Brooks, W. M., Tate, W. P., & Abraham, W. C. (2004) · Brain Research · doi:10.1016/j.brainres.2004.06.039 · Cited by 43

Self-rated intensity of habitual physical activities is positively associated with dopamine D2/3 receptor availability and cognition

Köhncke, Y., Papenberg, G., Jonasson, L. S., Karalija, N., Wåhlin, A., Salami, A., Andersson, M., Axelsson, J., Nyberg, L. H., Riklund, K., et al. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.07.036 · Cited by 48

Activation of Dopaminergic D2/D3 Receptors Modulates Dorsoventral Connectivity in the Hippocampus and Reverses the Impairment of Working Memory after Nerve Injury

Cardoso-Cruz, H., Dourado, M., Monteiro, C., Matos, M. R., & Galhardo, V. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0021-14.2014 · Cited by 39

Modulation of late phases of long-term potentiation in rat dentate gyrus by stimulation of the medial septum

Frey, S., Bergado, J. A., & Frey, J. U. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00029-0 · Cited by 41

Specific Hippocampal Interneurons Shape Consolidation of Recognition Memory

da Cruz, J. F. O., Busquets-García, A., Zhao, Z., Varilh, M., Lavanco, G., Bellocchio, L., Robin, L. M., Cannich, A., Julio‐Kalajzić, F., Lesté-Lasserre, T., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2020.108046 · Cited by 42

Loss of dopamine D2 receptors varies along the rostrocaudal axis of the hippocampal complex in alzheimer's disease

Ryoo, H., & Joyce, J. N. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903480105 · Cited by 40

Hippocampal neural activity reflects the economy of choices during goal‐directed navigation

Tryon, V. L., Penner, M. R., Heide, S. W., King, H. O., Larkin, J. D., & Mizumori, S. J. Y. (2017) · Hippocampus · doi:10.1002/hipo.22720 · Cited by 39

MPTP-meditated hippocampal dopamine deprivation modulates synaptic transmission and activity-dependent synaptic plasticity

Zhu, G., Chen, Y., Huang, Y., Li, Q., & Behnisch, T. (2011) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2011.05.007 · Cited by 39

Modulation of long-term synaptic plasticity at excitatory striatal synapses

Villar, F. D. S., & Walsh, J. P. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00504-1 · Cited by 40

Biochemical Correlates of Long-Term Potentiation in Hippocampal Synapses

Otani, S., & Ben‐Ari, Y. (1993) · International review of neurobiology · doi:10.1016/s0074-7742(08)60567-x · Cited by 40

Synaptic tagging, evaluation of memories, and the distal reward problemPreprint

Päpper, M., Kempter, R., & Leibold, C. (2010) · Learning & Memory · doi:10.1101/lm.2024811 · Cited by 39

Learning and Generalization in Schizophrenia: Effects of Disease and Antipsychotic Drug Treatment

Shohamy, D., Mihalakos, P., Chin, R., Thomas, B. P., Wagner, A. D., & Tamminga, C. A. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.10.025 · Cited by 38

Dopaminergic modulation of hippocampus-dependent learning: Blockade of hippocampal D1-class receptors during learning impairs 1-trial place memory at a 30-min retention delay

Pezze, M. A., & Bast, T. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.05.036 · Cited by 43

Dopamine Rebound-Excitation Theory: Putting Brakes on PTSD

Lee, J. C., Wang, L. P., & Tsien, J. Z. (2016) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2016.00163 · Cited by 42

Role of the hippocampal CA1 region in incremental value learning

Jeong, Y., Huh, N., Lee, J., Yun, I., Lee, J. W., Lee, I., & Jung, M. W. (2018) · Scientific Reports · doi:10.1038/s41598-018-28176-5 · Cited by 40

Alterations in excitatory amino acid‐mediated regulation of midbrain dopaminergic neurones induced by chronic psychostimulant administration and stress: relevance to behavioural sensitization and drug addiction

Clark, D. T., & Overton, P. G. (1998) · Addiction Biology · doi:10.1080/13556219872191 · Cited by 38

Functional correlation between GABAergic and dopaminergic systems of dorsal hippocampus and ventral tegmental area in passive avoidance learning in rats

Nazari-Serenjeh, F., Rezayof, A., & Zarrindast, M. R. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.08.073 · Cited by 38

Effects of endogenous and exogenous D1/D5 dopamine receptor activation on LTP in ventral and dorsal CA1 hippocampal synapses

Papaleonidopoulos, V., Kouvaros, S., & Papatheodoropoulos, C. (2018) · Synapse · doi:10.1002/syn.22033 · Cited by 35

The neuroscience of positive memory deficits in depression

Dillon, D. G. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01295 · Cited by 40

Synaptic Potentiation at Basal and Apical Dendrites of Hippocampal Pyramidal Neurons Involves Activation of a Distinct Set of Extracellular and Intracellular Molecular Cues

Brzdąk, P., Wójcicka, O., Zaręba-Kozioł, M., Minge, D., Henneberger, C., Włodarczyk, J., Mozrzymas, J. W., & Wójtowicz, T. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx324 · Cited by 34

Dopamine D1/D5, But not D2/D3, Receptor Dependency of Synaptic Plasticity at Hippocampal Mossy Fiber Synapses that Is Enabled by Patterned Afferent Stimulation, or Spatial Learning

Hagena, H., & Manahan‐Vaughan, D. (2016) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2016.00031 · Cited by 34

Long-Lasting Hippocampal Plasticity: Cellular Model for Memory Consolidation?

Frey, J. U. (2001) · Results and problems in cell differentiation · doi:10.1007/978-3-540-40025-7_2 · Cited by 35

Specific [3H]l-glutamate binding and [3H]d-aspartate release in the hippocampus of rat after pentylenetetrazol kindling and long-term potentiation

Schröder, H., Schlichthaar, R., & Krug, M. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90247-x · Cited by 35

The 5‐hydroxytryptamine4receptor enables differentiation of informational content and encoding in the hippocampus

Twarkowski, H., Hagena, H., & Manahan‐Vaughan, D. (2016) · Hippocampus · doi:10.1002/hipo.22569 · Cited by 33

Cellular Mechanisms Of Long-Term Potentiation: Late Maintenance

Frey, U. (1997) · Advances in psychology · doi:10.1016/s0166-4115(97)80092-1 · Cited by 33

Dopamine and glutamate receptor genes interactively influence episodic memory in old age

Papenberg, G., Li, S., Nagel, I. E., Nietfeld, W., Schjeide, B. M., Schröder, J., Bertram, L., Heekeren, H. R., Lindenberger, U., & Bäckman, L. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.11.014 · Cited by 32

Cocaine enhancement of long‐term potentiation in the CA1 region of rat hippocampus: Lamina‐specific mechanisms of action

Stramiello, M., & Wagner, J. J. (2010) · Synapse · doi:10.1002/syn.20764 · Cited by 32

Hippocampal synaptic failure is an early event in experimental parkinsonism with subtle cognitive deficit

Belloso-Iguerategui, A., Zamarbide, M., Merino-Galán, L., Rodríguez-Chinchilla, T., Gago, B., Santamaría, E., Fernández‐Irigoyen, J., Cotman, C. W., Prieto, G. A., Quiroga‐Varela, A., et al. (2023) · Brain · doi:10.1093/brain/awad227 · Cited by 33

Temporal phases of long-term potentiation (LTP): myth or fact?

Abbas, A.-K., Villers, A., & Ris, L. (2015) · Reviews in the Neurosciences · doi:10.1515/revneuro-2014-0072 · Cited by 31

Neuropsychopharmacology and Neurogenetic Aspects of Executive Functioning: Should Reward Gene Polymorphisms Constitute a Diagnostic Tool to Identify Individuals at Risk for Impaired Judgment?

Bowirrat, A., Chen, T. J. H., Oscar‐Berman, M., Madigan, M. A., Chen, A. L., Bailey, J. A., Braverman, E. R., Kerner, M., Giordano, J., Morse, S. A., et al. (2012) · Molecular Neurobiology · doi:10.1007/s12035-012-8247-z · Cited by 32

Memory Synapses Are Defined by Distinct Molecular Complexes: A Proposal

Sossin, W. S. (2018) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2018.00005 · Cited by 31

Dopamine D1/D5 receptor signaling regulates synaptic cooperation and competition in hippocampal CA 1 pyramidal neurons via sustained ERK 1/2 activation

Shetty, M. S., Gopinadhan, S., & Sajikumar, S. (2015) · Hippocampus · doi:10.1002/hipo.22497 · Cited by 31

Functional Differences between and across Different Regions of the Apical Branch of Hippocampal CA1 Dendrites with Respect to Long-Term Depression Induction and Synaptic Cross-Tagging

Parvez, S., Ramachandran, B., & Frey, J. U. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5808-09.2010 · Cited by 30

Impairment of Catecholamine Systems during Induction of Long-Term Potentiation at Hippocampal CA1 Synapses in HPC-1/Syntaxin 1A Knock-out Mice

Mishima, T., Fujiwara, T., Kofuji, T., & Akagawa, K. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2911-11.2012 · Cited by 29

Neural Signals Related to Outcome Evaluation Are Stronger in CA1 than CA3

Lee, S.-H., Huh, N., Lee, J. W., Ghim, J.-W., Lee, I., & Jung, M. W. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00040 · Cited by 30

Ventromedial Prefrontal Cortex Activation Is Associated with Memory Formation for Predictable Rewards

Bialleck, K. A., Schaal, H.-P., Kranz, T. A., Fell, J., Elger, C. E., & Axmacher, N. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016695 · Cited by 29

Early-Life Adversity Induces Epigenetically Regulated Changes in Hippocampal Dopaminergic Molecular Pathways

Köhler, J. C., Gröger, N., Lesse, A., Guara Ciurana, S., Rether, K., Fegert, J., Bock, J., & Braun, K. (2019) · Molecular Neurobiology · doi:10.1007/s12035-018-1199-1 · Cited by 28

NMDA and Dopamine Converge on the NMDA-Receptor to Induce ERK Activation and Synaptic Depression in Mature Hippocampus

Kaphzan, H., O’Riordan, K. J., Mangan, K. P., Levenson, J. M., & Rosenblum, K. (2006) · PLoS ONE · doi:10.1371/journal.pone.0000138 · Cited by 28

The maintenance of hippocampal long-term potentiation is paralleled by a dopamine-dependent increase in glycoprotein fucosylation

Angenstein, F., Matthies, H. K., Staeck, S., Reymann, K. G., & Staak, S. (1992) · Neurochemistry International · doi:10.1016/0197-0186(92)90191-s · Cited by 28

Developmental exposure to chlorpyrifos and diazinon differentially affect passive avoidance performance and nitric oxide synthase-containing neurons in the basolateral complex of the amygdala

Vatanparast, J., Naseh, M., Baniasadi, M., & Haghdoost-Yazdi, H. (2012) · Brain Research · doi:10.1016/j.brainres.2012.11.049 · Cited by 27

The psychostimulant modafinil facilitates water maze performance and augments synaptic potentiation in dentate gyrus

Tsanov, M., Lyons, D. G., Barlow, S. H., Reyes, R. E. G., & O’Mara, S. M. (2010) · Neuropharmacology · doi:10.1016/j.neuropharm.2010.03.010 · Cited by 27

Use of Brain Slices to Study Long-Term Potentiation and Depression as Examples of Synaptic Plasticity

Teyler, T. J. (1999) · Methods · doi:10.1006/meth.1999.0764 · Cited by 27

Studies on long-term potentiation of the population spike component of hippocampal field potential by the tetanic stimulation of the perforant path in rats: effects of a dopamine agonist, SKF-38393

Yanagihashi, R., & Ishikawa, T. (1992) · Brain Research · doi:10.1016/0006-8993(92)90744-t · Cited by 26

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