Heterogeneity of release probability, facilitation, and depletion at central synapses
Open accessAbstract
Previous studies of short-term plasticity in central nervous systems synapses have largely focused on average synaptic properties. In this study, we use recordings from putative single synaptic release sites in hippocampal slices to show that significant heterogeneity exists in facilitation and depletion among synapses. In particular, the amount of paired-pulse facilitation is inversely related to the initial release probability of the synapse. We also examined depletion at individual synapses using high frequency stimulation, and estimated the size of the readily releasable vesicle pool, which averaged 5.0 +/- 3.0 quanta (n = 13 synapses). In addition, these experiments demonstrate that the release probability at a synapse is directly correlated with the size of its readily releasable vesicle pool.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The number of vesicles adjacent to the presynaptic cleft is proportional to those primed for synaptic transmitter release.
“The area of the postsynaptic density is proportional to the number of postsynaptic receptors (Nusser et al., 1998), while the number of vesicles adjacent to the presynaptic cleft is proportional to those primed for synaptic transmitter release (Dobrunz and Stevens, 1997).”
From The influence of phospho-tau on dendritic spines of cortical pyramidal neurons in patients with Alzheimer’s disease (2013) · cites this paper as Dobrunz and Stevens, 1997
The passage on the physical interpretation of the readily releasable pool (indexed as Abstract; no page given) says that this pool may correspond roughly to morphologically docked vesicles. It explicitly says that identifying the two pools is “far from established” and calls for a demonstration that their sizes vary correspondingly. Thus, it supports a possible relationship, not the claimed proportionality as a settled fact. (LLM, conf=0.88)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Synaptic plasticity in the hippocampus: LTP and LTD
Malenka, R. C. (1994) · Cell · doi:10.1016/0092-8674(94)90517-7 · Cited by 655 · see citing works
Timing of neurotransmission at fast synapses in the mammalian brain
Sabatini, B. L., & Regehr, W. G. (1996) · Nature · doi:10.1038/384170a0 · Cited by 442 · see citing works
Presynaptic Calcium Current Modulation by a Metabotropic Glutamate Receptor
Takahashi, T., Forsythe, I. D., Tsujimoto, T., Barnes-Davies, M., & Onodera, K. (1996) · Science · doi:10.1126/science.274.5287.594 · Cited by 392 · see citing works
Flagged first, then by citations
Research works printed but not linked: 25
- [1]1. Abbott, L.F. ∙ Varela, J.A. ∙ Sen, K. ... Synaptic depression and cortical gain control Science. 1997; 275:220-224 Crossref Scopus (1261) PubMed Google Scholar
- [2]2. Allen, C. ∙ Stevens, C.F. An evaluation of causes for unreliability of synaptic transmission Proc. Natl. Acad. Sci. USA. 1994; 91:10380-10383 Crossref Scopus (324) PubMed Google Scholar
- [3]3. Almers, W. ∙ Tse, F.W. Transmitter release from synapsesdoes a preassembled fusion pore initiate exocytosis? Neuron. 1990; 4:813-818 Full Text (PDF) Scopus (142) PubMed Google Scholar
- [4]4. Barrett, E.F. ∙ Stevens, C.F. The kinetics of transmitter release at the frog neuromuscular junction J. Physiol. 1972; 227:691-708 PubMed Google Scholar
- [5]5. Baskys, A. ∙ Malenka, R.C. Trans-ACPD depresses synaptic transmission in the hippocampus Eur. J. Pharmacol. 1991; 193:131-132 Crossref Scopus (75) PubMed Google Scholar
- [6]6. Bennett, M. ∙ Model, P. ∙ Highstein, S. Stimulation-induced depletion of vesicles, fatigue of transmission and recovery processes at a vertebrate central synapse Cold Spring Harb. Symp. Quant. Biol. 1976; 40:25-35 Crossref Scopus (22) PubMed Google Scholar
- [7]7. Bertolino, M. ∙ Baraldi, M. ∙ Parenti, C. ... Modulation of AMPA/kainate receptors by analogues of diazoxide and cyclothiazide in thin slices of rat hippocampus Recept. Channels. 1993; 1:267-278 PubMed Google Scholar
- [8]8. Borges, S. ∙ Gleason, E. ∙ Turelli, M. ... The kinetics of quantal transmitter release from retinal amacrine cells Proc. Natl. Acad. Sci. USA. 1995; 92:6896-6900 Crossref Scopus (59) PubMed Google Scholar
- [9]9. Borst, J.G.G. ∙ Sakmann, B. Calcium influx and transmitter release in a fast CNS synapse Nature. 1996; 383:431-434 Crossref Scopus (512) PubMed Google Scholar
- [10]10. Choi, S. ∙ Lovinger, D.M. Metabotropic glutamate receptor modulation of voltage-gated Ca2+ channels involves multiple receptor subtypes in cortical neurons J. Neurosci. 1996; 16:36-45 Crossref PubMed Google Scholar
- [11]11. Creager, R. ∙ Dunwiddie, T.V. ∙ Lynch, G. Paired-pulse and frequency facilitation in the CA1 region of the in vitro rat hippocampus J. Physiol. 1980; 299:409-424 PubMed Google Scholar
- [13]13. del Castillo, J. ∙ Katz, B. Quantal components of the end-plate potential J. Physiol. 1954; 124:560-573 PubMed Google Scholar
- [14]14. Eaton, S. ∙ Jane, D. ∙ Jones, P. ... Competitive antagonism at metabotropic glutamate receptors by (S)-4-carboxyphenylglycine and (RS)-alpha-methyl-4-carboxyphenylglycine Eur. J. Pharmacol. 1993; 244:195-197 Crossref Scopus (229) PubMed Google Scholar
- [15]15. Goda, Y. ∙ Stevens, C.F. Two components of transmitter release at a central synapse Proc. Natl. Acad. Sci. USA. 1994; 91:12942-12946 Crossref Scopus (443) PubMed Google Scholar
- [16]16. Hess, G. ∙ Kuhnt, U. ∙ Voronin, L. Quantal analysis of paired-pulse facilitation in guinea pig hippocampal slices Neurosci. Lett. 1987; 77:187-192 Crossref Scopus (121) PubMed Google Scholar
- [17]17. Hessler, N.A. ∙ Shirke, A.M. ∙ Malinow, R. The probability of transmitter release at a mammalian central synapse Nature. 1993; 366:569-572 Crossref Scopus (483) PubMed Google Scholar
- [18]18. Huang, Y.-Y. ∙ Nguyen, P.V. ∙ Abel, T. ... Long-lasting forms of synaptic potentiation in the hippocampus Learning Mem. 1996; 3:74-85 Crossref Scopus (198) PubMed Google Scholar
- [19]19. Larkman, A. ∙ Stratford, K. ∙ Jack, J. Quantal analysis of excitatory synaptic action and depression in hippocampal slices [see comments] Nature. 1991; 350:344-347 Crossref Scopus (135) PubMed Google Scholar
- [20]20. Magleby, K.L. (1987). Short-term changes in synaptic efficacy. In Synaptic Function, G.M. Edelman, V.E. Gall, and K.M. Cowan, eds. (New York: John Wiley and Sons), pp. 21–56. Google Scholar
- [21]21. Malenka, R.C. Synaptic plasticity in the hippocampusLTP and LTD Cell. 1994; 78:535-538 Full Text (PDF) Scopus (563) PubMed Google Scholar
- [22]22. Malinow, R. ∙ Otmakhov, N. ∙ Blum, K.I. ... Visualizing hippocampal synaptic function by optical detection of Ca2+ entry through the N-methyl-D-aspartate channel Proc. Natl. Acad. Sci. USA. 1994; 91:8170-8174 Crossref Scopus (80) PubMed Google Scholar
- [23]23. Mallart, A. ∙ Martin, A.R. The relation between quantal content and facilitation at the neuromuscular junction of frog J. Physiol. 1968; 196:593-604 PubMed Google Scholar
- [24]24. Manabe, T. ∙ Wyllie, D.J. ∙ Perkel, D.J. ... Modulation of synaptic transmission and long-term potentiationeffects on paired pulse facilitation and EPSC variance in the CA1 region of the hippocampus J. Neurophysiol. 1993; 70:1451-1459 PubMed Google Scholar
- [25]25. Markram, H. ∙ Tsodyks, M. Redistribution of synaptic efficacy between neocortical pyramidal neurons Nature. 1996; 382:807-810 Crossref Scopus (644) PubMed Google Scholar
- [26]26. Murphy, T. ∙ Baraban, J. ∙ Wier, W. Mapping miniature synaptic currents to single synapses using calcium imaging reveals heterogeneity in postsynaptic output Neuron. 1995; 15:159-168
Cited by
Sorted by citations
Short-Term Synaptic Plasticity
Zucker, R. S., & Regehr, W. G. (2002) · Annual Review of Physiology · doi:10.1146/annurev.physiol.64.092501.114547 · Cited by 5,068 · see citing works
Plaque-independent disruption of neural circuits in Alzheimer’s disease mouse models
Hsia, A. Y., Masliah, E., McConlogue, L., Yu, G.-Q., Tatsuno, G., Hu, K., Kholodenko, D., Malenka, R. C., Nicoll, R. A., & Mucke, L. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.6.3228 · Cited by 1,123 · see citing works
Single cocaine exposure in vivo induces long-term potentiation in dopamine neurons
Ungless, M. A., Whistler, J. L., Malenka, R. C., & Bonci, A. (2001) · Nature · doi:10.1038/35079077 · Cited by 1,106 · see citing works
Communication in neuronal networks
Laughlin, S. B., & Sejnowski, T. J. (2003) · Science · doi:10.1126/science.1089662 · Cited by 950 · see citing works
Cabin, D. E., Shimazu, K., Murphy, D., Cole, N. B., Gottschalk, W., McIlwain, K. L., Orrison, B., Chen, A., Ellis, C. E., Paylor, R., et al. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-20-08797.2002 · Cited by 865 · see citing works
Predictions not commands: Active inference in the motor system
Adams, R. A., Shipp, S., & Friston, K. J. (2013) · Brain Structure and Function · doi:10.1007/s00429-012-0475-5 · Cited by 765 · see citing works
Cell Type and Pathway Dependence of Synaptic AMPA Receptor Number and Variability in the Hippocampus
Nusser, Z., Lujan, R., Laube, G., Roberts, J. D. B., Molnar, E., & Somogyi, P. (1998) · Neuron · doi:10.1016/s0896-6273(00)80565-6 · Cited by 804 · see citing works
Inactivity produces increases in neurotransmitter release and synapse size
Murthy, V. N., Schikorski, T., Stevens, C. F., & Zhu, Y. (2001) · Neuron · doi:10.1016/s0896-6273(01)00500-1 · Cited by 612 · see citing works
Self-citationReliability and State Dependence of Pyramidal Cell–Interneuron Synapses in the Hippocampus
Csicsvari, J., Hirase, H., Czurko, A., & Buzsáki, G. (1998) · Neuron · doi:10.1016/s0896-6273(00)80525-5 · Cited by 606 · see citing works
Ultrastructure of dendritic spines: correlation between synaptic and spine morphologies
Arellano, J. I. (2007) · Frontiers in Neuroscience · doi:10.3389/neuro.01.1.1.010.2007 · Cited by 529 · see citing works
Amyloid-β as a positive endogenous regulator of release probability at hippocampal synapses
Abramov, E., Dolev, I., Fogel, H., Ciccotosto, G. D., Ruff, E., & Slutsky, I. (2009) · Nature Neuroscience · doi:10.1038/nn.2433 · Cited by 499 · see citing works
Astrocytes Mediate In Vivo Cholinergic-Induced Synaptic Plasticity
Navarrete, M., Perea, G., de Sevilla, D. F., Gómez-Gonzalo, M., Núñez, A., Martín, E. D., & Araque, A. (2012) · PLoS Biology · doi:10.1371/journal.pbio.1001259 · Cited by 387 · see citing works
Distinct functions for direct and transthalamic corticocortical connections
Sherman, S. M., & Guillery, R. W. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00429.2011 · Cited by 336 · see citing works
Structural and synaptic plasticity in stress-related disorders
Christoffel, D. J., Golden, S. A., & Russo, S. J. (2011) · Reviews in the Neurosciences · doi:10.1515/rns.2011.044 · Cited by 334 · see citing works
Efficacy and Stability of Quantal GABA Release at a Hippocampal Interneuron–Principal Neuron Synapse
Kraushaar, U., & Jonas, P. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-15-05594.2000 · Cited by 281 · see citing works
Synaptic Vesicle Pools and Dynamics
Alabi, A. A., & Tsien, R. W. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a013680 · Cited by 284 · see citing works
Hayashi, M. L., Choi, S.-Y., Rao, B. S. S., Jung, H.-Y., Lee, H.-K., Zhang, D., Chattarji, S., Kirkwood, A., & Tonegawa, S. (2004) · Neuron · doi:10.1016/j.neuron.2004.05.003 · Cited by 280 · see citing works
Development of Excitatory Circuitry in the Hippocampus
Hsia, A. Y., Malenka, R. C., & Nicoll, R. A. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.4.2013 · Cited by 279 · see citing works
Synaptic weight set by Munc13-1 supramolecular assemblies
Sakamoto, H., Ariyoshi, T., Kimpara, N., Sugao, K., Taiko, I., Takikawa, K., Asanuma, D., Namiki, S., & Hirose, K. (2018) · Nature Neuroscience · doi:10.1038/s41593-017-0041-9 · Cited by 235 · see citing works
Independent Sources of Quantal Variability at Single Glutamatergic Synapses
Franks, K. M., Stevens, C. F., & Sejnowski, T. J. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-08-03186.2003 · Cited by 224 · see citing works
Self-citationSV2 modulates the size of the readily releasable pool of secretory vesicles
Xu, T., & Bajjalieh, S. M. (2001) · Nature Cell Biology · doi:10.1038/35087000 · Cited by 212 · see citing works
Synaptic vesicle protein 2 enhances release probability at quiescent synapses
Custer, K. L., Austin, N. S., Sullivan, J. M., & Bajjalieh, S. M. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.2699-05.2006 · Cited by 211 · see citing works
Tao, C.-L., Liu, Y.-T., Sun, R., Zhang, B., Qi, L., Shivakoti, S., Tian, C.-L., Zhang, P., Lau, P.-M., Zhou, Z. H., et al. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.1548-17.2017 · Cited by 207 · see citing works
Perea, G., Gómez, R., Mederos, S., Covelo, A., Ballesteros, J. J., Schlosser, L., Hernández-Vivanco, A., Martín-Fernández, M., Quintana, R., Rayan, A., et al. (2016) · eLife · doi:10.7554/elife.20362 · Cited by 194 · see citing works
Properties of Quantal Transmission at CA1 Synapses
Raghavachari, S., & Lisman, J. E. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00258.2004 · Cited by 197 · see citing works
Neurotransmitters and peptides: Whispered secrets and public announcements
Leng, G., & Ludwig, M. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.159103 · Cited by 168 · see citing works
Otsu, Y., Shahrezaei, V., Li, B., Raymond, L. A., Delaney, K. R., & Murphy, T. H. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.4452-03.2004 · Cited by 169 · see citing works
Koponen, E., Võikar, V., Riekki, R., Saarelainen, T., Rauramaa, T., Rauvala, H., Taira, T., & Castrén, E. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.01.006 · Cited by 170 · see citing works
Cotrafficking of SV2 and synaptotagmin at the synapse
Yao, J., Nowack, A., Kensel-Hammes, P., Gardner, R. G., & Bajjalieh, S. M. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4781-09.2010 · Cited by 164 · see citing works
Nicotinic control of axon excitability regulates thalamocortical transmission
Kawai, H., Lazar, R., & Metherate, R. (2007) · Nature Neuroscience · doi:10.1038/nn1956 · Cited by 171 · see citing works
Target cell-specific modulation of transmitter release at terminals from a single axon
Scanziani, M., Gähwiler, B. H., & Charpak, S. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.20.12004 · Cited by 167 · see citing works
Jorgenson, L. A., Sun, M., O'Connor, M., & Georgieff, M. K. (2005) · Hippocampus · doi:10.1002/hipo.20128 · Cited by 162 · see citing works
Merino-Serrais, P., Benavides-Piccione, R., Blazquez-Llorca, L., Kastanauskaite, A., Rábano, A., Avila, J., & DeFelipe, J. (2013) · Brain · doi:10.1093/brain/awt088 · Cited by 134 · see citing works
Synaptic basis for whisker deprivation-induced synaptic depression in rat somatosensory cortex
Bender, K. J., Allen, C. B., Bender, V. A., & Feldman, D. E. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.0175-06.2006 · Cited by 126 · see citing works
Basu, J., Srinivas, K. V., Cheung, S. K., Taniguchi, H., Huang, Z. J., & Siegelbaum, S. A. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.001 · Cited by 122 · see citing works
Taschenberger, H., Woehler, A., & Neher, E. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1606383113 · Cited by 128 · see citing works
Synaptic properties of connections between the primary and secondary auditory cortices in mice
Covic, E. N., & Sherman, S. M. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr029 · Cited by 116 · see citing works
Astroglial networks promote neuronal coordination
Chever, O., Dossi, E., Pannasch, U., Derangeon, M., & Rouach, N. (2016) · Science Signaling · doi:10.1126/scisignal.aad3066 · Cited by 107 · see citing works
Counting the number of releasable synaptic vesicles in a presynaptic terminal
Ikeda, K., & Bekkers, J. M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811017106 · Cited by 99 · see citing works
Bark, C., Bellinger, F. P., Kaushal, A., Mathews, J. R., Partridge, L. D., & Wilson, M. C. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1940-04.2004 · Cited by 101 · see citing works
Gulisano, W., Melone, M., Ripoli, C., Tropea, M. R., Li Puma, D. D., Giunta, S., Cocco, S., Marcotulli, D., Origlia, N., Palmeri, A., et al. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.0163-19.2019 · Cited by 100 · see citing works
Hefft, S., Kraushaar, U., R. P. Geiger, J., & Jonas, P. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2001.013455 · Cited by 79 · see citing works
Galanin receptor-mediated inhibition of glutamate release in the arcuate nucleus of the hypothalamus
Kinney, G. A., Emmerson, P. J., & Miller, R. J. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-10-03489.1998 · Cited by 81 · see citing works
Levetiracetam Reverses Synaptic Deficits Produced by Overexpression of SV2A
Nowack, A., Malarkey, E. B., Yao, J., Bleckert, A., Hill, J., & Bajjalieh, S. M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0029560 · Cited by 81 · see citing works
Masneuf, S., Lowery-Gionta, E., Colacicco, G., Pleil, K. E., Li, C., Crowley, N., Flynn, S., Holmes, A., & Kash, T. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.04.015 · Cited by 69 · see citing works
Haj-Dahmane, S., & Shen, R.-Y. (2009) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.109.153858 · Cited by 69 · see citing works
Electrophysiological identification of medial and lateral perforant path inputs to the dentate gyrus
Petersen, R. P., Moradpour, F., Eadie, B. D., Shin, J. D., Kannangara, T. S., Delaney, K. R., & Christie, B. R. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.07.063 · Cited by 65 · see citing works
Kaempf, N., Kochlamazashvili, G., Puchkov, D., Maritzen, T., Bajjalieh, S. M., Kononenko, N. L., & Haucke, V. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1501627112 · Cited by 63 · see citing works
Imig, C., López-Murcia, F. J., Maus, L., García-Plaza, I. H., Mortensen, L. S., Schwark, M., Schwarze, V., Angibaud, J., Nägerl, U. V., Taschenberger, H., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.09.004 · Cited by 66 · see citing works
Nelson, P. A., Sage, J. R., Wood, S. C., Davenport, C. M., Anagnostaras, S. G., & Boulanger, L. M. (2013) · Learning & Memory · doi:10.1101/lm.031351.113 · Cited by 49 · see citing works
Postnatal maturation of spinal dynorphin circuits and their role in somatosensation
Brewer, C. L., Styczynski, L. M., Serafin, E. K., & Baccei, M. L. (2020) · Pain · doi:10.1097/j.pain.0000000000001884 · Cited by 38 · see citing works
Social experience alters oxytocinergic modulation in the nucleus accumbens of female prairie voles
Borie, A. M., Agezo, S., Lunsford, P., Boender, A. J., Guo, J.-D., Zhu, H., Berman, G. J., Young, L. J., & Liu, R. C. (2022) · Current Biology · doi:10.1016/j.cub.2022.01.014 · Cited by 39 · see citing works
A delayed response enhancement during hippocampal presynaptic plasticity in mice
Jensen, V., Walaas, S. I., Hilfiker, S., Ruiz, A., & Hvalby, Ø. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.131300 · Cited by 33 · see citing works
McCoy, P., Norton, T. T., & McMahon, L. L. (2008) · Journal of Neurophysiology · doi:10.1152/jn.01134.2007 · Cited by 30 · see citing works
- Authors
- Dobrunz, L. E., & Stevens, C. F.
- Affiliations
- Salk Institute for Biological Studies (US)
- Corresponding author
- Stevens, Charles F.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 1997-06
- Volume
- 18
- Issue
- 6
- Pages
- 995-1008
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2019016101
- Cited by
- 1,183
- References
- 3
- Citations by year
- 2026: 21 · 2025: 21 · 2024: 37 · 2023: 27 · 2022: 23 · 2021: 57 · 2020: 32 · 2019: 54 · 2018: 39 · 2017: 38 · 2016: 33 · 2015: 45 · 2014: 46 · 2013: 42 · 2012: 57
- FWCI
- 16.10
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- paired-pulse facilitation, short-term plasticity, hippocampus, central synapses, synaptic heterogeneity
- MeSH terms
- Animals, Brain Stem, Electric Stimulation, Evoked Potentials, Hippocampus, Neural Inhibition, Neuronal Plasticity, Synapses, Synaptic Vesicles, Time Factors, Receptors, Metabotropic Glutamate, Patch-Clamp Techniques, Rats, In Vitro Techniques
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 ›
Are you an author, or do you see a problem with this page? Request a review