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Bidirectional Control of Quantal Size by Synaptic Activity in the Hippocampus
Abstract
Analysis of strontium-induced asynchronous release of quanta from stimulated synapses revealed that long-term potentiation and long-term depression in the CA1 region of the mammalian hippocampus are associated with an increase and a decrease, respectively, in quantal size. At a single set of synapses, the increase in quantal size seen with long-term potentiation was completely reversed by depotentiating stimuli. Long-term potentiation and depression are also associated with an increase and decrease, respectively, in the frequency of quantal events, consistent with an all-or-none regulation (up or down) of clusters of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors, a change in the release of transmitter, or both.
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“For instance, the size of “quantal” miniature EPSCs increases after LTP (364, 365).”
From Synaptic memory and CaMKII (2023) · cites this paper as [364]
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Cites
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Self-citationRegulation of Quantal Size by Presynaptic Mechanisms
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“For recording of miniature IPSCs (mIPSCs) in Figure 10, K-gluconate (0 mM) and KCl (150 mM) were used in internal solution, and tetrodotoxin (TTX) was added in the ACSF to block action potentials.”
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“The most widespread use of strontium in the study of synaptic transmission is to desynchronize release to allow examination of the amplitude of evoked quantal events (Abdul-Ghani et al., 1996; Oliet et al., 1996; Choi and Lovinger, 1997; Morishita and Alger, 1997; Otis et al., 1997; Behrends and ten Bruggencate, 1998;…”
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“NMDAR-dependent LTD is expressed via a reduction in synaptic AMPARs and is accompanied by reductions in spine size (Oliet et al., 1996; Carroll et al., 1999; Bredt and Nicoll, 2003; Zhou et al., 2004).”
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“In strontium, evoked EPSCs consist of discrete, temporally dispersed mEPSC-like events (termed SrEPSCs) that represent responses to single, asynchronously released vesicles from stimulated afferents (Miledi and Slater, 1966; Dodge et al., 1969; Goda and Stevens, 1994; Oliet et al., 1996).”
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“For instance, the size of “ quantal ” miniature EPSCs increases after LTP (364, 365).”
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“Synchronous and asynchronous events are thought to originate from the same set of active synapses (Dodge et al. 1969; Goda & Stevens, 1994; Oliet et al. 1996; Otis et al. 1996), the asynchronous events representing unitary quantal currents (Bekkers & Clements, 1999).”
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“Previous work has shown that these locally evoked events, which are due to an evoked asynchronous release of presynaptic glutamate vesicles, can be used to assess the postsynaptic strength of synapses on which the electrically stimulated axons terminate (Bain and Quastel 1992; Goda and Stevens 1998; Miledi 1966; Oliet…”
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“A form of LTD that depends on NMDA receptor activation for its initiation can be induced at these same hippocampal synapses and appears to have a postsynaptic locus of expression (Stevens and Wang, 1994; Selig et al., 1995; Oliet et al., 1996, 1997).”
BackgroundResultBekkers, J. M., & Clements, J. D. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.227aa.x · Cited by 118
“Previous applications of Sr¥ to central synapses have reported that aEPSC and mEPSC amplitude distributions are identical, both for Schaffer collateral—CA1 pyramidal cell inputs (Oliet et al. 1996) and cortical inputs to the striatum (Choi & Lovinger, 1997).”
BackgroundMethodInfluentialChakroborty, S., Kim, J., Schneider, C., Jacobson, C., Molgo, J., & Stutzmann, G. E. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0936-12.2012 · Cited by 118
“mGluR–LTD involves mGluR1/5 activation, which generates IP3 and subsequent ER calcium release (Oliet et al., 1996).”
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Self-citationReyes-Harde, M., Potter, B. V. L., Galione, A., & Stanton, P. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.3.1569 · Cited by 114
“Previous work by our laboratory suggests that a presynaptic ryanodine-sensitive Ca21 store is necessary for the induction of LTD by full LFS (Reyes and Stanton 1996).”
BackgroundResultInfluentialBellingham, M., Lim, R., & Walmsley, B. (1998) · Journal of Physiology · doi:10.1111/j.1469-7793.1998.861bg.x · Cited by 112
“…calyceal synapses show decay time constants which are consistently amongst the fastest recorded in central neurones (Forsythe & Barnes-Davies, 1993; Raman et al. 1994; Isaacson & Walmsley, 1996), our finding of a small absolute decrease in AMPA spontaneous EPSC ôdecay suggests that AMPA receptor…”
BackgroundPresynaptic strontium dynamics and synaptic transmission.
Xu-Friedman, M. A., & Regehr, W. (1999) · Biophysical Journal · doi:10.1016/s0006-3495(99)77360-1 · Cited by 108
“Strontium is often used to isolate individual quantal currents underlying evoked release (Oliet et al., 1996; Choi and Lovinger, 1997; Morishita and Alger, 1997; Otis et al., 1997; Behrends and ten Bruggencate, 1998; Lévénès et al., 1998).”
BackgroundFocal photolysis of caged glutamate produces long-term depression of hippocampal glutamate receptors
Kandler, K., Katz, L. C., & Kauer, J. A. (1998) · Nature Neuroscience · doi:10.1038/368 · Cited by 111
Spontaneous Neurotransmission: An Independent Pathway for Neuronal Signaling?
Kavalali, E. T., Chung, C., Khvotchev, M., Leitz, J., Nosyreva, E., Raingo, J., & Ramirez, D. M. O. (2011) · Physiology · doi:10.1152/physiol.00040.2010 · Cited by 104
“How can a postsynaptic response element distinguish an incoming unitary release event and trigger a distinct signaling pathway if the two forms of release originate from the same location in a terminal and activate the same population of target receptors? Under physiological conditions, unitary synaptic transmission e…”
BackgroundDistinct forms of short-term plasticity at excitatory synapses of hippocampus and neocortex.
Castro-Alamancos, M., & Connors, B. W. (1997) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.94.8.4161 · Cited by 104
Chen, T., Kula, B., Nagy, B., Barzan, R., Gall, A., Ehrlich, I., & Kukley, M. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.09.066 · Cited by 109
“Delayed EPSCs are considered as quantal events in neuronal synapses because those delayed EPSCs have amplitude and kinetics similar to miniature EPSCs [113, 114].”
BackgroundNeocortical synaptic engrams for remote contextual memories
Lee, J., Kim, W. B., Park, E. H., & Cho, J.-H. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01223-1 · Cited by 116
Eye Opening Rapidly Induces Synaptic Potentiation and Refinement
Lü, W., & Constantine‐Paton, M. (2004) · Neuron · doi:10.1016/j.neuron.2004.06.031 · Cited by 101
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
“This approach has been used to determine whether synaptic plasticity involves an increase in the number (frequency) and/or size (amplitude) of the quantal events 34,35 .”
The role of mammalian ionotropic receptors in synaptic plasticity: LTP, LTD and epilepsy
Kullmann, D. M., Asztély, F., & Walker, M. C. (2000) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000640 · Cited by 90
Caillard, O., Ben‐Ari, Y., & Gaïarsa, J. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-17-07568.1999 · Cited by 85
“Because asynchronous release can occur at the subset of synapses that are stimulated, this allows a detailed analysis of quantal events originating from these synapses (Oliet et al., 1996, 1997; Morishita and Alger, 1997; Rumpel and Behrends, 1999).”
BackgroundVikman, K. S., Rycroft, B., & Christie, M. (2008) · Journal of Physiology · doi:10.1113/jphysiol.2007.145581 · Cited by 88
“Desynchronizing individual synaptic quantal events with Sr2+ (Goda & Stevens, 1994) allowed us to measure quantal amplitude and kinetic data in order to evaluate postsynaptic strength pertaining to the particular synapses under investigation (Oliet et al. 1996).”
BackgroundModulation of spontaneous quantal release of neurotransmitters in the hippocampus
Bouron, A. (2001) · Progress in Neurobiology · doi:10.1016/s0301-0082(00)00053-8 · Cited by 74
Spatiotemporal asymmetry of associative synaptic plasticity in fear conditioning pathways.
Shin, R.-M., Tsvetkov, E., & Bolshakov, V. (2006) · Neuron · doi:10.1016/j.neuron.2006.10.010 · Cited by 82
“Second, we obtained quantal size estimates in both cortical and thalamic inputs by measuring the amplitude of asynchronously released single quanta of glutamate when strontium (Sr) was substituted for extracellular Ca (Oliet et al., 1996).”
InfluentialKombian, S. B., Hirasawa, M., Mouginot, D., Chen, X., & Pittman, Q. J. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.5.2542 · Cited by 71
Zones of Enhanced Glutamate Release from Climbing Fibers in the Mammalian Cerebellum
Paukert, M., Huang, Y. H., Tanaka, K., Rothstein, J., & Bergles, D. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5118-09.2010 · Cited by 81
“To test the former possibility, we examined the amplitude and time course of mEPSCs, which were evoked from CFs after replacing extracellular Ca 2 with Sr 2 (Miledi, 1966; Oliet et al., 1996; Xu-Friedman and Regehr, 2000).”
MethodSynaptic mechanism underlying serotonin modulation of transition to cocaine addiction
Li, Y., Simmler, L. D., van Zessen, R., Flakowski, J., Wan, J., Deng, F., Li, Y., Nautiyal, K. M., Pascoli, V., & Lüscher, C. (2021) · Science · doi:10.1126/science.abi9086 · Cited by 97
Cheng, S., Chen, C., Yang, H.-W., Chang, Y.-T., Bai, S.-W., Chen, C., Yen, C., & Min, M. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5564-10.2011 · Cited by 79
“…in which extracellular Ca2 was replaced with 4 mM Sr2 to cause asynchronous release of glutamate from axonal terminals, thereby resulting in aEPSCs, the unitary events comprising synchronous EPSCs evoked at a normal calcium concentration (Oliet et al., 1996; Xu-Friedman and Regehr, 2000).”
BackgroundMethodSynaptic Consolidation Normalizes AMPAR Quantal Size following MAGUK Loss
Levy, J. M., Chen, X., Reese, T. S., & Nicoll, R. A. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.015 · Cited by 83
“When Ca is replaced with Sr, synchronous transmitter release is replaced by asynchronous release, which lasts for a few hundredmilliseconds after the stimulus (Miledi, 1966;Oliet et al., 1996;Xu-Friedmanand Regehr, 2000).”
Self-citationConti, R., & Lisman, J. (2003) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.0630290100 · Cited by 77
Functional Maturation of the First Synapse in Olfaction: Development and Adult Neurogenesis
Grubb, M. S., Nissant, A., Murray, K., & Lledo, P. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5550-07.2008 · Cited by 72
“We therefore replaced all calcium (2 mM) in the extracellular medium with strontium (2 mM), a change that alters evoked synaptic release from smoothly synchronous to largely asynchronous, with quantal stimulated strontium EPSCs (SrEPSCs) strung out individually over a window of a few hundred milliseconds after stimula…”
Neural plasticity and emotional memory
Post, R., Weiss, S. R., Li, H., Smith, M. A., Zhang, L.-X., Xing, G., Osuch, E., & Mccann, U. (1998) · Development and Psychopathology · doi:10.1017/s0954579498001898 · Cited by 75
Nicoll, R. A., Oliet, S. H. R., & Malenka, R. C. (1998) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1998.3838 · Cited by 71
Self-citationGlasgow, S. D., Labrecque, S., Beamish, I. V., Aufmkolk, S., Gibon, J., Han, D., Harris, S. N., Dufresne, P., Wiseman, P., McKinney, R., et al. (2018) · bioRxiv · doi:10.1101/330688 · Cited by 73
Divergent pallidal pathways underlying distinct Parkinsonian behavioral deficits
Lilascharoen, V., Wang, E. H.-J., Do, N., Pate, S. C., Tran, A. N., Yoon, C. D., Choi, J.-H., Wang, X.-Y., Pribiag, H., Park, Y.-G., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00810-y · Cited by 88
Enhanced Visual Activity In Vivo Forms Nascent Synapses in the Developing Retinotectal Projection
Aizenman, C. D., & Cline, H. T. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00452.2006 · Cited by 63
Deng, P.-Y., Xiao, Z.-Y., Jha, A., Ramonet, D., Matsui, T., Leitges, M., Shin, H.-S., Porter, J., Geiger, J., & Lei, S. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5711-09.2010 · Cited by 68
“We next measured the effects of CCK on the quantal properties of glutamate release at the PP-GC synapses using the method of replacing extracellular Ca 2 with strontium (Sr 2 ) to induce asynchronous transmitter release (Goda and Stevens, 1994; Oliet et al., 1996).”
MethodLi, Y., Li, C., Wang, X., Jin, S., Wu, Z.-H., Jiang, P., Dong, P., He, X., Xu, F., Duan, S., et al. (2019) · Neuron · doi:10.1016/j.neuron.2018.12.012 · Cited by 74
Maturation of Excitatory Synaptic Transmission of the Rat Nucleus Accumbens From Juvenile to Adult
Kasanetz, F., & Manzoni, O. J. (2009) · Journal of Neurophysiology · doi:10.1152/jn.91039.2008 · Cited by 70
A Modular Organization of LRR Protein-Mediated Synaptic Adhesion Defines Synapse Identity.
Schroeder, A., Vanderlinden, J., Vints, K., Ribeiro, L. F., Vennekens, K. M., Gounko, N. V., Wierda, K. D., & de Wit, J. (2018) · Neuron · doi:10.1016/j.neuron.2018.06.026 · Cited by 60
“We replaced Ca in the extracellular solution with Sr, which enters the presynaptic terminal through calcium channels and triggers neurotransmitter release, albeit with lower efficiency (Bekkers and Clements, 1999; Oliet et al., 1996).”
Learning and reconsolidation implicate different synaptic mechanisms
Li, Y., Meloni, E. G., Carlezon, W. A., Milad, M. R., Pitman, R. K., Nader, K., & Bolshakov, V. Y. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1217878110 · Cited by 61
“Asynchronous EPSCs may be observed for hundreds of milliseconds following the presynaptic stimulation pulse, thus permitting analysis of quantal responses in specific projections to the target area (36).”
BackgroundVlachos, A., Becker, D., Jedlička, P., Winkels, R., Roeper, J., & Deller, T. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032883 · Cited by 61
“In contrast to conventional mEPSC recordings, which are based on a stochastic release of presynaptic vesicles, asynchronous EPSCs (aEPSCs) are induced by local electrical stimulation and can thus be attributed to the stimulated afferents [37,38].”
BackgroundMethodInfluentialYamaguchi, K., Tanaka, M., Mizoguchi, A., Hirata, Y., Ishizaki, H., Kaneko, K., Miyoshi, J., & Takai, Y. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.212511399 · Cited by 58
Tominaga-Yoshino, K., Urakubo, T., Okada, M., Matsuda, H., & Ogura, A. (2008) · Hippocampus · doi:10.1002/hipo.20391 · Cited by 55
“contrarily to the event observed in LTP (Manabe et al., 1992; Oliet et al., 1996).”
ResultGlutamate Receptor Trafficking in Synaptic Plasticity
Contractor, A., & Heinemann, S. F. (2002) · Science Signaling · doi:10.1126/stke.2002.156.re14 · Cited by 50
“The AMPA-mediated component of the excitatory postsynaptic current (EPSC) is selectively increased after induction of LTP (20) and dramatically decreased after induction of LTD (21).”
BackgroundNorris, C., & Foster, T. (1999) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1998.3864 · Cited by 55
“The importance of this finding may be considerable, since theoretical reports and empirical data indicate that synaptic function is regulated by the interaction of LTP and LTD mechanisms (Hrabetva & Saktor, 1996; Mayford, Wang, Kandel, & O’Dell, 1995; Oliet, Malenka, & Nicoll, 1996; Oliet, Malenka, & Nicoll, 1997).”
BackgroundHendricson, A. W., Sibbald, J., & Morrisett, R. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00997.2003 · Cited by 53
“Ethanol Alters the Frequency, Amplitude, and Decay Kinetics of Sr2 - Supported, Asynchronous NMDAR mEPSCs in Rat Hippocampal Slices”
BackgroundMethodWildburger, N. C., & Laezza, F. (2012) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2012.00080 · Cited by 52
“, 2010), for example, might contribute to the mechanisms underling LTD expression (Oliet et al., 1996; Beattie et al., 2000).”
BackgroundZhang, J., Yang, Y., Li, H., Cao, J., & Xu, L. (2005) · Brain Research · doi:10.1016/j.brainres.2005.05.032 · Cited by 49
Metadata
- Authors
- Oliet, S. H. R., Malenka, R. C., & Nicoll, R. A.
- Affiliations
- University of California, San Francisco (US)
- Venue
- Science
- Published
- 1996-03
- Volume
- 271
- Issue
- 5253
- Pages
- 1294-1297
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2057637786
- Cited by
- 209
- References
- 0
- Citations by year
- 2025: 7 · 2024: 3 · 2023: 3 · 2022: 2 · 2021: 5 · 2020: 3 · 2019: 8 · 2018: 6 · 2017: 7 · 2016: 3 · 2015: 6 · 2014: 3 · 2013: 6 · 2012: 6
- FWCI
- 7.29
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- quantal size, synaptic transmission, long-term potentiation, long-term depression, hippocampal CA1, depotentiation, synaptic plasticity
- MeSH terms
- Animals, Calcium, Electric Stimulation, Evoked Potentials, Guinea Pigs, Hippocampus, Synaptic Transmission, Neuronal Plasticity, Neurons, Strontium, Synapses, Rats, Sprague-Dawley, Long-Term Potentiation, Receptors, AMPA, Patch-Clamp Techniques, Rats, In Vitro Techniques
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