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A post-tetanic time window for the reinforcement of long-term potentiation by appetitive and aversive stimuli
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Current theories on the encoding and storage of information in the brain commonly suppose that a short-term memory is converted into a lasting one; thus, it becomes consolidated over time. Within a finite period after training, such a short-term memory can be reinforced by behavioral and humoral stimuli. We have found that, long-term potentiation (LTP), a likely candidate for a memory-encoding mechanism at the cellular level, displays similar features. LTP in the dentate gyrus of freely moving rats was reinforced after its induction by appetitive and aversive stimuli. The efficacy of these stimuli terminates about 1 h after tetanization, which may reflect the time constants of the mechanisms underlying the consolidation that takes place. The reinforcement by appetitive and aversive stimulation was blocked by the β-adrenergic antagonist propranolol, implicating norepinephrine in the underlying cellular processes.
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“Numerous other studies have replicated and extended this finding to show that a variety of arousing experiences, such as water immersion, exposure to novel places and objects, and spatial learning occurring around the time of the delivery of tetanizing stimulation, all increased the duration of LTP in CA1 and DG (e.g., Seidenbecher et al. [202]; Frey [203]; Li et al. [204]; Straube et al. [205];”
From The Temporal Dynamics Model of Emotional Memory Processing: A Synthesis on the Neurobiological Basis of Stress-Induced Amnesia, Flashbulb and Traumatic Memories, and the Yerkes-Dodson Law (2007) · cites this paper as Seidenbecher et al. [202]
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Citations
Cites
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
Bliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,424
Morris, R. G. M., Anderson, E., Lynch, G. S., & Baudry, M. (1986) · Nature · doi:10.1038/319774a0 · Cited by 3,640
McGaugh, J. L. (1966) · Science · doi:10.1126/science.153.3742.1351 · Cited by 1,468
β-Adrenergic activation and memory for emotional events
Cahill, L., Prins, B., Weber, M., & McGaugh, J. L. (1994) · Nature · doi:10.1038/371702a0 · Cited by 1,271
The Structure and Organization of Memory
Squire, L. R., Knowlton, B. J., & Musen, G. (1993) · Annual Review of Psychology · doi:10.1146/annurev.ps.44.020193.002321 · Cited by 1,159
Neurobiology of learning and memory
Delacour, J. (1985) · Neuropsychologia · doi:10.1016/0028-3932(85)90073-9 · Cited by 1,026
A motivational view of learning, performance, and behavior modification.
Bindra, D. (1974) · Psychological Review · doi:10.1037/h0036330 · Cited by 594
Involvement Of Hormonal And Neuromodulatory Systems In The Regulation Of Memory Storage
McGaugh, J. L. (1989) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.12.030189.001351 · Cited by 566
Inescapable versus escapable shock modulates long-term potentiation in the rat hippocampus
Shors, T. J., Seib, T. B., Levine, S., & Thompson, R. F. (1989) · Science · doi:10.1126/science.2704997 · Cited by 458
Research works printed but not linked: 4
- 10.1037/0735-7044.108.6.1053 · DOI
- 10.1113/jphysiol.1973.sp010273 · DOI · Paper page
- 10.1037/0735-7044.108.1.44 · DOI
- R C Malenka, R A Nicoll Semin Neurosci 2, 335–343 (1990).
Cited by
Sorted by citations
Memory - A century of consolidation
McGaugh, J. L. (2000) · Science · doi:10.1126/science.287.5451.248 · Cited by 4,250
The locus coeruleus and noradrenergic modulation of cognition
Sara, S. J. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2573 · Cited by 1,848
Mechanisms of emotional arousal and lasting declarative memory.
Cahill, L., & McGaugh, J. L. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01214-9 · Cited by 1,575
Making memories last: the synaptic tagging and capture hypothesis
Redondo, R. L., & Morris, R. G. M. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn2963 · Cited by 792
Diamond, D. M., Campbell, A. M., Park, C. R., Halonen, J., & Zoladz, P. R. (2007) · Neural Plasticity · doi:10.1155/2007/60803 · Cited by 762
“In brief, rats were handled for three days and then they were given a single session of water maze training to find a hidden platform located in 1 of 6 swim arms.”
MethodSynaptic tagging: implications for late maintenance of hippocampal long-term potentiation
Frey, U., & Morris, R. G. M. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01189-2 · Cited by 615
Dopamine-dependent facilitation of LTP induction in hippocampal CA1 by exposure to spatial novelty
Li, S., Cullen, W. K., Anwyl, R., & Rowan, M. J. (2003) · Nature Neuroscience · doi:10.1038/nn1049 · Cited by 568
Hippocampal-Neocortical Interactions in Memory Formation, Consolidation, and Reconsolidation
Wang, S., & Morris, R. (2009) · Annual Review of Psychology · doi:10.1146/annurev.psych.093008.100523 · Cited by 570
A neuromodulatory role of interleukin-1β in the hippocampus
Schneider, H., Pitossi, F., Balschun, D., Wagner, A., del Rey, A., & Besedovsky, H. O. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.13.7778 · Cited by 498
Self-citationNeuromodulated Spike-Timing-Dependent Plasticity, and Theory of Three-Factor Learning Rules
Frémaux, N., & Wulfram Gerstner, B. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00085 · Cited by 449
O’Donnell, J., Zeppenfeld, D., McConnell, E., Pena, S., & Nedergaard, M. (2012) · Neurochemical Research · doi:10.1007/s11064-012-0818-x · Cited by 399
Late-associativity, synaptic tagging, and the role of dopamine during LTP and LTD
Sajikumar, S. (2004) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.03.003 · Cited by 345
Reymann, K. G., & Frey, J. U. (2007) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.07.026 · Cited by 331
Self-citationInterleukin‐6: a cytokine to forget
Balschun, D., Wetzel, W., del Rey, A., Pitossi, F. J., Schneider, H., Zuschratter, W., & Besedovsky, H. O. (2004) · The FASEB Journal · doi:10.1096/fj.04-1625fje · Cited by 317
Self-citationLong-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
Gourley, S. L., Wu, F. J., Kiraly, D. D., Ploski, J. E., Kedves, A. T., Duman, R. S., & Taylor, J. R. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.07.016 · Cited by 287
Akirav, I., & Maroun, M. (2007) · Neural Plasticity · doi:10.1155/2007/30873 · Cited by 293
Hippocampal theta rhythm: A tag for short‐term memory
Vertes, R. P. (2005) · Hippocampus · doi:10.1002/hipo.20118 · Cited by 319
Frey, S., Bergado, J. A., Seidenbecher, T., Pape, H., & Frey, J. U. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-10-03697.2001 · Cited by 260
Self-citationHow long will long-term potentiation last?
Abraham, W. C. (2003) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2002.1222 · Cited by 271
McIntyre, C. K., Miyashita, T., Setlow, B., Marjon, K. D., Steward, O., Guzowski, J. F., & McGaugh, J. L. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504436102 · Cited by 253
Dopaminergic modulation of the persistence of one-trial hippocampus-dependent memoryPreprint
O’Carroll, C., Martin, S. J., Sandin, J., Frenguelli, B. G., & Morris, R. G. M. (2006) · Learning & Memory · doi:10.1101/lm.321006 · Cited by 243
Xu, L., Hölscher, C., Anwyl, R., & Rowan, M. J. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.6.3204 · Cited by 234
Mechanisms of Amygdala Modulation of Hippocampal Plasticity
Akirav, I., & Richter‐Levin, G. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-22-09912.2002 · Cited by 225
Interacting brain systems modulate memory consolidation
McIntyre, C. K., McGaugh, J. L., & Williams, C. L. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.11.001 · Cited by 243
Gourley, S. L., Kiraly, D. D., Howell, J. L., Olausson, P., & Taylor, J. R. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.06.016 · Cited by 219
Emotional tagging of memory formation—in the search for neural mechanisms
Richter‐Levin, G., & Akirav, I. (2003) · Brain Research Reviews · doi:10.1016/j.brainresrev.2003.08.005 · Cited by 203
Behavioural pharmacology and its contribution to the molecular basis of memory consolidation
Izquierdo, I., & McGaugh, J. L. (2000) · Behavioural Pharmacology · doi:10.1097/00008877-200011000-00001 · Cited by 188
Swanson-Park, J. L., Coussens, C. M., Mason-Parker, S. E., Raymond, C. R., Hargreaves, E. L., Dragunow, M., Cohen, A. S., & Abraham, W. C. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00010-x · Cited by 175
Balschun, D., Wolfer, D. P., Bertocchini, F., Barone, V., Conti, A., Zuschratter, W., Missiaen, L., Lipp, H., Frey, J. U., & Sorrentino, V. (1999) · The EMBO Journal · doi:10.1093/emboj/18.19.5264 · Cited by 175
Self-citationHagena, H., Hansen, N., & Manahan‐Vaughan, D. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv330 · Cited by 174
Korz, V., & Frey, J. U. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-19-07281.2003 · Cited by 155
Straube, T., Korz, V., Balschun, D., & Frey, J. U. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.049452 · Cited by 157
Self-citationRole of the Basolateral Amygdala in Memory Consolidation
McINTYRE, C. K., POWER, A. E., ROOZENDAAL, B., & McGAUGH, J. L. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07088.x · Cited by 147
Frey, S., & Frey, J. U. (2008) · Progress in brain research · doi:10.1016/s0079-6123(07)00007-6 · Cited by 139
Norepinephrine and the dentate gyrus
Harley, C. W. (2007) · Progress in brain research · doi:10.1016/s0079-6123(07)63018-0 · Cited by 149
Vagus nerve stimulation potentiates hippocampal LTP in freely-moving rats
Zuo, Y., Smith, D. C., & Jensen, R. A. (2007) · Physiology & Behavior · doi:10.1016/j.physbeh.2006.11.009 · Cited by 135
Diamond, D. M., Park, C. R., Campbell, A. M., & Woodson, J. C. (2005) · Hippocampus · doi:10.1002/hipo.20107 · Cited by 128
Akbari, E., Naghdi, N., & Motamedi, F. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.05.028 · Cited by 126
Norepinephrine and Dopamine as Learning Signals
Harley, C. W. (2004) · Neural Plasticity · doi:10.1155/np.2004.191 · Cited by 124
Accounting for immediate emotional memory enhancement
Talmi, D., & McGarry, L. M. (2011) · Journal of Memory and Language · doi:10.1016/j.jml.2011.07.009 · Cited by 121
Walling, S. G., & Harley, C. W. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.4426-03.2004 · Cited by 117
Inhibition of mGluR5 blocks hippocampal LTP in vivo and spatial learning in rats
Balschun, D., & Wetzel, W. (2002) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(02)00847-x · Cited by 116
Self-citationSelbach, O., Doreulee, N., Bohla, C., Eriksson, K. S., Sergeeva, O. A., Poelchen, W., Brown, R. E., & Haas, H. L. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.05.012 · Cited by 113
Noradrenergic Action in Prefrontal Cortex in the Late Stage of Memory ConsolidationPreprint
Tronel, S., Feenstra, M. G. P., & Sara, S. J. (2004) · Learning & Memory · doi:10.1101/lm.74504 · Cited by 112
Long-term potentiation in the hippocampus: discovery, mechanisms and function
Bliss, T., Collingridge, G. L., Morris, R., & Reymann, K. G. (2018) · e-Neuroforum · doi:10.1515/nf-2017-a059 · Cited by 122
Self-citationLong-Term Effects of Brief Acute Stress on Cellular Signaling and Hippocampal LTP
Ahmed, T., Frey, J. U., & Korz, V. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4901-05.2006 · Cited by 111
Bidirectional modulation of long-term potentiation by novelty-exploration in rat dentate gyrus
Straube, T., Korz, V., & Frey, J. U. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(03)00349-5 · Cited by 106
Hernández-Rabaza, V., Hontecillas-Prieto, L., Velázquez-Sánchez, C., Ferragud, A., Pérez-Villaba, A., Arcusa, A., Barcia, J. A., Trejo, J. L., & Canales, J. J. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.06.008 · Cited by 114
Akbari, E., Naghdi, N., & Motamedi, F. (2006) · Peptides · doi:10.1016/j.peptides.2006.11.002 · Cited by 100
Noradrenaline is a stress-associated metaplastic signal at GABA synapses
Inoue, W., Baimoukhametova, D. V., Füzesi, T., Cusulin, J. I. W., Koblinger, K., Whelan, P. J., Pittman, Q. J., & Bains, J. S. (2013) · Nature Neuroscience · doi:10.1038/nn.3373 · Cited by 94
Brown, R. A. M., Walling, S. G., Milway, J. S., & Harley, C. W. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4307-04.2005 · Cited by 98
Hansen, N., & Manahan‐Vaughan, D. (2015) · Hippocampus · doi:10.1002/hipo.22436 · Cited by 92
Emotional tagging—A simple hypothesis in a complex reality
Bergado, J. A., Lucas, M., & Richter‐Levin, G. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.03.004 · Cited by 98
Relationship of hippocampal theta and gamma oscillations to potentiation of synaptic transmission
Bikbaev, A. F. (2008) · Frontiers in Neuroscience · doi:10.3389/neuro.01.010.2008 · Cited by 90
A locus coeruleus to dentate gyrus noradrenergic circuit modulates aversive contextual processing
Seo, D.-O., Zhang, E. T., Piantadosi, S. C., Marcus, D. J., Motard, L. E., Kan, B. K., Gomez, A. M., Nguyen, T. K., Li, X., & Bruchas, M. R. (2021) · Neuron · doi:10.1016/j.neuron.2021.05.006 · Cited by 83
Neuroplasticity Regulation by Noradrenaline in Mammalian Brain
Marzo, A., Bai, J., & Otani, S. (2009) · Current Neuropharmacology · doi:10.2174/157015909790031193 · Cited by 89
Reinforcement of rat hippocampal LTP by holeboard trainingPreprint
Uzakov, S., Frey, J. U., & Korz, V. (2005) · Learning & Memory · doi:10.1101/lm.89305 · Cited by 83
Physiological Dissociation in Hippocampal Subregions in Response to Amygdala Stimulation
Vouimba, R., & Richter‐Levin, G. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhi058 · Cited by 80
Barco, Á., de Armentia, M. L., & Alarcón, J. M. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.01.002 · Cited by 81
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
Vouimba, R., Yaniv, D., & Richter‐Levin, G. (2006) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.07.007 · Cited by 71
Taylor, F., & Cahill, L. F. (2002) · Journal of Traumatic Stress · doi:10.1023/a:1020145610914 · Cited by 68
Kukushkin, N. V., & Carew, T. J. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.029 · Cited by 72
Bergado, J. A., Frey, S., Lopez‐Rojas, J., Almaguer‐Melian, W., & Frey, J. U. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.05.003 · Cited by 66
Dahl, M. J., Kulesza, A., Werkle‐Bergner, M., & Mather, M. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105358 · Cited by 67
Stress modulation of hippocampal activity – Spotlight on the dentate gyrus
Fa, M., Li, X., Anunu, R., Kehat, O., Kriebel, M., Volkmer, H., & Richter‐Levin, G. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.04.008 · Cited by 62
Korz, V., & Frey, J. U. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.0910-05.2005 · Cited by 58
The Tagging and Capture Hypothesis from Synapse to Memory
Viola, H., Ballarini, F., Martínez, M. C., & Moncada, D. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-420170-5.00013-1 · Cited by 60
Aging and Synaptic Plasticity: A Review
Bergado, J. A., & Almaguer, W. (2002) · Neural Plasticity · doi:10.1155/np.2002.217 · Cited by 55
Almaguer-Melian, W., Martínez-Martí, L., Frey, J. U., & Bergado, J. A. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00867-9 · Cited by 50
Miyashita, T., & Williams, C. L. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.11.005 · Cited by 49
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
Alzheimer’s Disease, Neural Plasticity, and Functional Recovery
Mercerón‐Martínez, D., Ibaceta-González, C., Salazar, C., Almaguer‐Melian, W., Bergado, J. A., & Palacios, A. G. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-201178 · Cited by 48
Spatial and emotional memory in aged rats: a behavioral-statistical analysis
Bergado, J. A., Almaguer, W., Rojas, Y., Capdevila, V., & Frey, J. U. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.10.064 · Cited by 47
Zhu, L., Sacco, T., Strata, P., & Sacchetti, B. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016673 · Cited by 47
Distinct Roles of Dopamine and Noradrenaline in Incidental Memory
Hauser, T. U., Eldar, E., Purg, N., Moutoussis, M., & Dolan, R. J. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.0401-19.2019 · Cited by 47
Schulz, K., & Korz, V. (2010) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2010.00187 · Cited by 43
Almaguer‐Melian, W., Rojas-Reyes, Y., Alvare, A., Rosillo, J. C., Frey, J. U., & Bergado, J. A. (2004) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.08.002 · Cited by 42
Bass, D. I., Partain, K. N., & Manns, J. R. (2011) · Behavioral Neuroscience · doi:10.1037/a0026462 · Cited by 42
Memory consolidation and improvement by synaptic tagging and capture in recurrent neural networks
Luboeinski, J., & Tetzlaff, C. (2021) · Communications Biology · doi:10.1038/s42003-021-01778-y · Cited by 41
Frey, S., Bergado, J. A., & Frey, J. U. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00029-0 · Cited by 41
Korz, V., & Frey, J. U. (2007) · Learning & Memory · doi:10.1101/lm.459807 · Cited by 37
Li, Z., & Richter‐Levin, G. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00021 · Cited by 35
The perseveration-consolidation hypothesis: Mueller and Pilzecker, 1900
McGaugh, J. L. (1999) · Brain Research Bulletin · doi:10.1016/s0361-9230(99)00126-4 · Cited by 35
Jas, J., Almaguer, W., Frey, J. U., & Bergado, J. A. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02037-0 · 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
Brief novelty exposure facilitates dentate gyrus LTP in aged rats
Sierra‐Mercado, D., Dieguez, D., & Barea-Rodríguez, E. J. (2008) · Hippocampus · doi:10.1002/hipo.20447 · Cited by 33
Effect of emotional context in auditory-cortex processing
Alexandrov, Y. I., Klucharev, V. A., & Sams, M. E. (2007) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2007.05.004 · Cited by 31
Lashgari, R., Khakpour-Taleghani, B., Motamedi, F., & Shahidi, . (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.05.012 · Cited by 27
Bergado, J. A., Almaguer‐Melian, W., Kostenko, S., Frey, S., & Frey, J. U. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(03)00943-1 · Cited by 27
Factors That Determine the Non-Linear Amygdala Influence on Hippocampus-Dependent Memory
Akirav, I., & Richter‐Levin, G. (2006) · Dose-Response · doi:10.2203/dose-response.004.01.003.akirav · Cited by 26
EPO induces changes in synaptic transmission and plasticity in the dentate gyrus of rats
Almaguer‐Melian, W., Mercerón‐Martínez, D., Delgado‐Ocaña, S., Fuentes, N. P., Ledón, N., & Bergado, J. A. (2016) · Synapse · doi:10.1002/syn.21895 · Cited by 23
Epinephrine converts long‐term potentiation from transient to durable form in awake rats
Korol, D. L., & Gold, P. E. (2007) · Hippocampus · doi:10.1002/hipo.20372 · Cited by 23
Almaguer‐Melian, W., Cruz-Aguado, R., de la Riva, C., Kendrick, K. M., Frey, J. U., & Bergado, J. A. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.12.085 · Cited by 23
Emotional modulation of the synapse
McReynolds, J. R., & McIntyre, C. K. (2012) · Reviews in the Neurosciences · doi:10.1515/revneuro-2012-0047 · Cited by 23
Kenney, J. (2013) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2013.00010 · Cited by 22
Learning-Related Hippocampal Long-Term Potentiation and Long-Term Depression
Manahan‐Vaughan, D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21104-8 · Cited by 22
Amer, A., & Martin, J. H. (2022) · Brain stimulation · doi:10.1016/j.brs.2022.07.005 · Cited by 21
Tanaka, T., Kai, N., Kobayashi, K., Takano, Y., & Hironaka, N. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.05.032 · Cited by 20
Metadata
- Authors
- Seidenbecher, T., Reymann, K. G., & Balschun, D.
- Affiliations
- Leibniz Institute for Neurobiology (DE)
- ORCID
- Balschun, Detlef
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1997-02-18
- Volume
- 94
- Issue
- 4
- Pages
- 1494-1499
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC19819
- OpenAlex
- W1974502920
- Cited by
- 154
- References
- 35
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 4 · 2023: 2 · 2022: 4 · 2021: 5 · 2020: 2 · 2019: 4 · 2018: 3 · 2017: 6 · 2016: 4 · 2015: 4 · 2014: 5 · 2013: 6 · 2012: 3
- FWCI
- 2.95
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- long-term potentiation, post-tetanic potentiation, memory consolidation, dentate gyrus, appetitive stimuli, aversive stimuli, norepinephrine, beta-adrenergic blockade, propranolol, short-term memory, synaptic plasticity
- MeSH terms
- Adrenergic beta-Antagonists, Animals, Appetitive Behavior, Male, Memory, Memory, Short-Term, Propranolol, Punishment, Reinforcement, Psychology, Reward, Tetany, Time Factors, Rats, Wistar, Long-Term Potentiation, Dentate Gyrus, Rats
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