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Correlation between the Pharmacology of Long-Term Potentiation and the Pharmacology of Memory
Abstract
The pharmacology of memory has been recently studied by the infusion of drugs into the hippocampus (HIP), amygdala (AMY), medial septum (MS), and entorhinal cortex (EC) at various times after training or at the time of retention testing. It was found to be remarkably similar to that of long-term potentiation (LTP). Memory and LTP are blocked early on by antagonists of glutamate N-methyl-D-aspartate (NMDA) or metabotropic receptors (mGLUs), by the antagonist of the presynaptic membrane receptor to PAF, BN 52021, by the inhibitor of heme oxygenase, ZnPP, by the inhibitor of NO synthase, N-nitro-arginine, by GABA type A receptor agonists, or by muscarinic blockers. Both memory and LTP are enhanced, at this early stage, by glutamate, mGLU agonists, GABA-A antagonists, muscarinic agonists, and norepinephrine. In the next 1-3 h, memory and LTP are accompanied by enhanced activity of protein kinases and are blocked by specific inhibitors of calcium/calmodulin dependent protein kinase II and protein kinase C. At the time of expression, memory and LTP are blocked by antagonists of glutamate AMPA receptors and are accompanied by an enhanced sensitivity of these receptors. Memories that depend on HIP are affected by drugs given into the HIP but not the MS or AMY, memories that depend on the AMY are affected by drugs given into the AMY, and memories that depend on the HIP, AMY, and MS are affected by drugs given into the three structures.(ABSTRACT TRUNCATED AT 250 WORDS)
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“For example, the release of PFC-mediated inhibition over locus coeruleus cell activity will increase norepinephrine release throughout the forebrain, which would be manifested behaviorally as an enhancement of attention, and physiologically as enhanced memory-related neuroplasticity in the amygdala and hippocampus (Izquierdo and Medina [435]; Roozendaal [436]; McGaugh [437]; Strange and Dolan [222”
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 Izquierdo and Medina [435]
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Li, Z., & Richter‐Levin, G. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00021 · Cited by 35
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Scaini, G., Teodorak, B. P., Jeremias, I. C., Morais, M. O. D. S., Mina, F., Dominguini, D., Pescador, B., Comim, C. M., Schuck, P. F., Ferreira, G. C., et al. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.03.004 · Cited by 31
Valvassori, S. S., Dal-Pont, G. C., Varela, R. B., Resende, W. R., Gava, F. F., Mina, F., Budni, J., & Quevedo, J. (2020) · Journal of Affective Disorders · doi:10.1016/j.jad.2020.12.190 · Cited by 31
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Zanatta, M. S., Quillfeldt, J. A., Schaeffer, E. L., Schmitz, P. K., Quevedo, J., Medina, J. H., & Izquierdo, I. (1997) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x1997000200012 · Cited by 32
Self-citationLand, C. L., & Riccio, D. C. (1997) · Psychobiology · doi:10.3758/bf03331929 · Cited by 29
Hughes, R. N. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.10.028 · Cited by 29
Billard, J. (2018) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2018.00106 · Cited by 28
Sharp, B. M., Yatsula, M. S., & Fu, Y. (2004) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.103.063586 · Cited by 28
Moshfegh, A., Babaei, P., Oryan, S., Tehrani, B. S., & Zarrindast, M. (2010) · Neuroscience Letters · doi:10.1016/j.neulet.2010.07.079 · Cited by 27
Rubin, M. A., Jurach, A., Zanolla, G. R., Boemo, R. L., Souza, D. O., & Mello, C. F. (1997) · Neuroreport · doi:10.1097/00001756-199712010-00011 · Cited by 27
Soto‐Moyano, R., Burgos, H., Flores, F. J., Valladares, L., Sierralta, W. D., FERNANDEZ, V., Pérez, H., HERNANDEZ, P., & Hernández, A. (2006) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2006.09.009 · Cited by 26
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Sun, C., Yin, Z., Chen, J., Wang, W., Zheng, G., Li, J., Chen, L., & Zhang, Q. (2021) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202101002 · Cited by 25
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Bianchin, M. M., Spanis, C. W., Roesler, R., McGaugh, J. L., & Izquierdo, I. (2000) · Brain Research · doi:10.1016/s0006-8993(99)02220-9 · Cited by 24
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Sadowski, R. N., Canal, C. E., & Gold, P. E. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.03.007 · Cited by 23
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Korol, D. L., & Gold, P. E. (2007) · Hippocampus · doi:10.1002/hipo.20372 · Cited by 23
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Zarrindast, M., Khodjastehfar, E., Oryan, S., & Torkaman‐Boutorabi, A. (2001) · European Journal of Pharmacology · doi:10.1016/s0014-2999(00)00906-7 · Cited by 23
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Liang, K. (2001) · American Psychological Association eBooks · doi:10.1037/10413-009 · Cited by 23
Ézrokhi, V. L., Zosimovskiĭ, V. A., Korshunov, V. A., & Markevich, V. A. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00232-2 · Cited by 23
Venero, C., & Sandi, C. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb00759.x · Cited by 23
Benes, F. M., Burke, R. E., Walsh, J., Berretta, S., Matzilevich, D., Minns, M., & Konradi, C. L. (2004) · Molecular Psychiatry · doi:10.1038/sj.mp.4001524 · Cited by 23
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Immunohistochemical localization of the neural cannabinoid receptor in rat brain
Pettit, D. A. D., Harrison, M. P., Olson, J. M., Spencer, R. F., & Cabral, G. A. (1998) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19980201)51:3 · Cited by 228
Gaskin, S., & White, N. M. (2007) · Hippocampus · doi:10.1002/hipo.20295 · Cited by 22
Lin, S.-Y., Chen, G., Liao, J.-M., Pan, S.-F., Chen, M.-J., Chen, J. C., Peng, H., Ho, Y., Ho, Y., Huang, P.-C., et al. (2006) · Endocrinology · doi:10.1210/en.2005-1378 · Cited by 22
Alvarez, E. O., & Banzán, A. M. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.12.015 · Cited by 21
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Men, D., McCarty, R. C., & Gold, P. E. (1999) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1998.3880 · Cited by 21
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Babu, C. S., Kesavanarayanan, K. S., Kalaivani, P., Ranju, V., & Ramanathan, M. (2011) · Chromatography Research International · doi:10.4061/2011/732409 · Cited by 20
Tuon, L., Comim, C. M., Petronilho, F. C., Barichello, T., Izquierdo, I., Quevedo, J., & Dal‐Pizzol, F. (2008) · Critical Care · doi:10.1186/cc7103 · Cited by 20
Self-citationBevilaqua, L., Ardenghi, P., Schröder, N., Bromberg, E., Quevedo, J., Schmitz, P., Bianchin, M., Walz, R., Schaeffer, E., Medina, J., et al. (1997) · Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas · doi:10.1590/s0100-879x1997000800009 · Cited by 22
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Kaitsuka, T., Fukunaga, K., Soeda, F., Shirasaki, T., Miyamoto, E., & Takahama, K. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.10.051 · Cited by 19
Han, C. J., Pierre-Louis, J., Scheff, A., & Robinson, J. K. (2000) · European Journal of Pharmacology · doi:10.1016/s0014-2999(00)00480-5 · Cited by 19
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Liao, J.-M., Huang, P.-C., Pan, S.-F., Chen, M.-J., Tung, K., Peng, H., Shyu, J., Liou, Y., Chen, G., & Lin, T.-B. (2007) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00443.2006 · Cited by 19
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Neugebauer, F., Korz, V., & Frey, J. U. (2009) · Brain Research · doi:10.1016/j.brainres.2009.03.055 · Cited by 18
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Gomes, K. M., Comim, C., Valvassori, S., Réus, G. Z., Inácio, C. G., Martins, M. R., Souza, R. P., & Quevedo, J. (2010) · Journal of neural transmission · doi:10.1007/s00702-010-0385-8 · Cited by 19
Zvara, P., Braas, K. M., May, V., & Vizzard, M. A. (2006) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1317.092 · Cited by 17
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Billard, J., & Fréret, T. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14586 · Cited by 14
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Krug, M., Brödemann, R., Matthies, R., Rüthrich, H., & Wagner, M. (2001) · Hippocampus · doi:10.1002/hipo.1033 · Cited by 10
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Schröder, N., de Mattos-Dutra, Â., de Freitas, M. S., Lisboa, C. S. F., Zilles, A. C., Pessoa‐Pureur, R., & Izquierdo, I. (1997) · Brain Research · doi:10.1016/s0006-8993(96)01250-4 · Cited by 8
Self-citationGilbert, M. E. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06874.x · Cited by 8
Kaikai, N.-E., Ba-M’hamed, S., Bennis, M., & Ghanima, A. (2019) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2019.103309 · Cited by 7
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İ. Okulicz-Kozaryn, Mikołajczak, P. Ł., Szczawinska, K., Kamińska, E., & Kus, K. (2001) · Journal of Basic and Clinical Physiology and Pharmacology · doi:10.1515/jbcpp.2001.12.3.197 · Cited by 6
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Park, J. Y., Park, J., Baek, J., Chang, J. W., Kim, Y. G., & Chang, W. S. (2023) · Scientific Reports · doi:10.1038/s41598-023-45600-7 · Cited by 5
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Hughes, R. N. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.07.026 · Cited by 4
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Cid, F. M. (2016) · Dialnet (Universidad de la Rioja) · Cited by 2
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DeGracia, D. J. (1999) · Cited by 2
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McLean, T. A. B., Jin, Z., Hategan, L. A., Creighton, S. D., Luo, J., Pirri, F., Dahi, T. A., Neira-Diaz, L., Winston, S. M., Brimble, M. A., et al. (2026) · Neuropsychopharmacology · doi:10.1038/s41386-026-02479-y · Cited by 1
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Bonini, J. S. (2006) · Americanae (AECID Library) · Cited by 1
Kerimoglu, C. (2012) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3197 · Cited by 1
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Farooqui, A. A. (2008) · Springer eBooks · doi:10.1007/978-0-387-09693-3_3 · Cited by 1
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Rabinak, C. A. (2009) · Deep Blue (University of Michigan)
Cassini, L. F. (2013) · Americanae (AECID Library) · doi:10.13140/rg.2.2.13877.01766
Metadata
- Authors
- Izquierdo, I., & Medina, J. H.
- Affiliations
- Universidade Federal do Rio Grande do Sul (BR)
- Venue
- Neurobiology of Learning and Memory
- Publisher
- Elsevier BV
- Published
- 1995-01
- Volume
- 63
- Issue
- 1
- Pages
- 19-32
- ISSN
- 1074-7427 (ISSN-L)
- OpenAlex
- W2046474139
- Cited by
- 230
- References
- 0
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 2 · 2023: 2 · 2022: 4 · 2021: 2 · 2020: 2 · 2019: 3 · 2018: 4 · 2017: 2 · 2016: 2 · 2015: 5 · 2014: 5 · 2013: 6 · 2012: 7
- FWCI
- 7.86
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neurobiology of Learning and Memory (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 › Memory Processes and Influences
- Keywords
- long-term potentiation, hippocampus, amygdala, medial septum, entorhinal cortex, NMDA receptor antagonists, metabotropic glutamate receptors, PAF receptor antagonists, heme oxygenase inhibition, nitric oxide synthase inhibition, GABAA receptor, muscarinic receptors, norepinephrine, protein kinases, calcium/calmodulin-dependent protein kinase II, protein kinase C, AMPA receptors, memory expression, memory consolidation
- MeSH terms
- Amygdala, Animals, Brain, Brain Mapping, Hippocampus, Memory, Septum Pellucidum, Neurotransmitter Uptake Inhibitors, Long-Term Potentiation, Receptors, Neurotransmitter, Neurotransmitter Agents, Entorhinal Cortex
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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