Visualization of changes in presynaptic function during long-term synaptic plasticity
Abstract
Controversy exists regarding the site of modification of synaptic transmission during long-term plasticity in the mammalian hippocampus. Here we used a fluorescent marker of presynaptic activity, FM 1-43, to directly image changes in presynaptic function during both short-term and long-term forms of plasticity at presynaptic boutons of CA3-CA1 excitatory synapses in acute hippocampal slices. We demonstrated enhanced presynaptic function during long-term potentiation (LTP) induced either chemically (with tetraethylammonium), or by high-frequency (200-Hz) electrical stimulation. Both of these forms of LTP required activation of L-type voltage-gated calcium channels and NMDA receptors in the postsynaptic CA1 neuron. These results thus implied that a long-lasting increase in the efficacy of synaptic transmission is likely to depend, at least in part, on enhanced transmitter release from the presynaptic neuron.
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Destaining curves of FM1-43 were superimposable before and after tetanic induction of NMDAR-dependent LTP in CA1 neurons at 50-100 Hz.
“Just as with MK-801, the destaining curves were superimposable before and after tetanic induction of NMDAR-dependent LTP in CA1 neurons at 50 -100 Hz (Zakharenko et al. 2001).”
From NMDA receptor-dependent long-term potentiation and long-term depression (LTP/LTD). (2012) · cites this paper as Zakharenko et al. 2001
At CA1 excitatory synapses, both NMDAR-dependent and NMDAR-independent forms of LTP can coexist under certain conditions.
“There is even evidence that at CA1 excitatory synapses both NMDAR-dependent and NMDAR-independent forms of LTP can coexist under certain conditions (49–51).”
From Synaptic memory and CaMKII (2023) · cites this paper as [50]
With intense induction protocols for LTP, a component of LTP requires the activation of VDCCs.
“with intense induction protocols for LTP a component of LTP requires the activation of VDCCs (49–51, 193, 196).”
From Synaptic memory and CaMKII (2023) · cites this paper as [50]
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- Authors
- Zakharenko, S. S., Zablow, L., & Siegelbaum, S. A.
- Affiliations
- Howard Hughes Medical Institute (US)
- Corresponding author
- Siegelbaum, Steven A.
- Venue
- Nature Neuroscience
- Published
- 2001-07
- Volume
- 4
- Issue
- 7
- Pages
- 711-717
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- OpenAlex
- W1488440012
- Cited by
- 305
- References
- 49
- Citations by year
- 2026: 2 · 2025: 1 · 2024: 6 · 2023: 6 · 2022: 5 · 2021: 6 · 2020: 10 · 2019: 5 · 2018: 2 · 2017: 20 · 2016: 10 · 2015: 10 · 2014: 13 · 2013: 15 · 2012: 14
- FWCI
- 7.00
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- 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
- long-term potentiation, presynaptic function, synaptic plasticity, hippocampus, CA3-CA1 synapses, FM1-43, presynaptic terminals, neurotransmitter release, L-type calcium channels, NMDA receptor, tetraethylammonium, high-frequency stimulation, short-term plasticity
- MeSH terms
- Quaternary Ammonium Compounds, Animals, Electric Stimulation, Fluorescent Dyes, Hippocampus, Microscopy, Fluorescence, Neuronal Plasticity, Pyridinium Compounds, Presynaptic Terminals, Long-Term Potentiation, Microscopy, Confocal, Excitatory Postsynaptic Potentials, Mice, In Vitro Techniques
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