Cited by 246Neuroscience and Neuropharmacology ResearchNerve injury and regenerationMemory and Neural Mechanisms

Induction of long-term potentiation and depression is reflected by corresponding changes in secretion of endogenous brain-derived neurotrophic factor

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Aicardi, Giorgio, Argilli, Emanuela, Cappello, Silvia, Santi, Spartaco, Riccio, Massimo, Thoenen, Hans, Canossa, Marco·2004·Proceedings of the National Academy of Sciences

Abstract

Neurotrophins play an important role in modulating activity-dependent neuronal plasticity. In particular, threshold levels of brain-derived neurotrophic factor (BDNF) are required to induce long-term potentiation (LTP) in acute hippocampal slices. Conversely, the administration of exogenous BDNF prevents the induction of long-term depression (LTD) in the visual cortex. A long-standing missing link in the analysis of this modulatory role of BDNF was the determination of the time-course of endogenous BDNF secretion in the same organotypic preparation in which LTP and LTD are elicited. Here, we fulfilled this requirement in slices of perirhinal cortex. Classical theta-burst stimulation patterns evoking LTP lasting >180 min elicited a large increase in BDNF secretion that persisted 5-12 min beyond the stimulation period. Weaker theta-burst stimulation patterns leading only to the initial phase of LTP (≈35 min) were accompanied by a smaller increase in BDNF secretion lasting <1 min. Sequestration of BDNF by TrkB-IgG receptor bodies prevented LTP. Low-frequency stimulations leading to LTD were accompanied by reductions in BDNF secretion that never lasted beyond the duration of the stimulation.

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Crossref · 10.1073/pnas.0406960101

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  • The secretion of BDNF is responsive to the synchrony of synaptic input and postsynaptic spikes.

    “Because BDNF secretion is not induced by a 1-Hz spike train alone (22, 23), our data suggest that the secretion of this neurotrophin is responsive to the synchrony of synaptic input and postsynaptic spikes.”

    From Protein synthesis and neurotrophin-dependent structural plasticity of single dendritic spines (2008) · cites this paper as [23]

    The cited paper’s Results (‘Decrease of Endogenous BDNF Secretion During LTD’) report that 1-Hz stimulation reduced BDNF secretion rather than increasing it. That supports the cited premise that 1-Hz stimulation does not induce secretion, but the paper stimulated afferent fibers; it did not test a postsynaptic spike train alone or whether synchrony with synaptic input governs secretion. The synchrony statement is presented as the citing authors’ inference, not as a finding directly attributed to this source. (LLM, conf=0.84)

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  • BDNF secretion is not induced by a 1-Hz spike train alone.

    “Because BDNF secretion is not induced by a 1-Hz spike train alone (22, 23), our data suggest that the secretion of this neurotrophin is responsive to the synchrony of synaptic input and postsynaptic spikes.”

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Cites

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Research works printed but not linked: 7

  1. Korte, M., Carroll, P., Wolf, E., Brem, G., Thoenen, H. & Bonhoeffer, T. (1995) Proc. Natl. Acad. Sci. USA 92, 8856-8860.
  2. Korte, M., Griesbeck O., Gravel, C., Carroll, P., Staiger, V., Thoenen, H. & Bonhoeffer, T. (1996) Proc. Natl. Acad. Sci. USA 29, 12547-12552.
  3. Zafra, F., Castren, E., Thoenen, H. & Lindholm, D. (1991) Proc. Natl. Acad. Sci. USA 88, 10037-10041.
  4. Canossa, M., Griesbeck, O., Berninger, B., Campana, G., Kolbeck, R. & Thoenen, H. (1997) Proc. Natl. Acad. Sci. USA 94, 13279-13286.
  5. Gartner, A. & Staiger, V. (2002) Proc. Natl. Acad. Sci. USA 99, 6386-6391.
  6. Canossa, M., Giordano, E., Cappello, S., Guarnirei, C. & Ferri, S. (2002) Proc. Natl. Acad. Sci. USA 99, 3282-3287.
  7. Kruttgen, A., Moller, J. C., Heymach, J.V. & Shooter, E. M. (1998) Proc. Natl. Acad. Sci. USA 95, 9614-9619.

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Authors
Aicardi, G., Argilli, E., Cappello, S., Santi, S., Riccio, M., Thoenen, H., & Canossa, M.
Affiliations
Istituto Ortopedico Rizzoli (IT)
Corresponding author
  • Aicardi, Giorgio
  • Argilli, Emanuela
  • Cappello, Silvia
  • Canossa, Marco
Venue
Proceedings of the National Academy of Sciences
Published
2004-10-25
Volume
101
Issue
44
Pages
15788-15792
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2016843660
Cited by
246
References
4
Citations by year
2026: 3 · 2025: 4 · 2024: 2 · 2023: 8 · 2022: 10 · 2021: 6 · 2020: 7 · 2019: 14 · 2018: 9 · 2017: 12 · 2016: 15 · 2015: 15 · 2014: 13 · 2013: 23 · 2012: 5
FWCI
5.05
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • IRIS UNIMORE (University of Modena and Reggio Emilia) (submittedVersion, cc-by)
  • Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) (submittedVersion)
Funders
  • Regeneron Pharmaceuticals
  • Ministero dell’Istruzione, dell’Università e della Ricerca
  • Max-Planck-Gesellschaft
  • Università di Bologna
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Keywords
brain-derived neurotrophic factor, long-term potentiation, long-term depression, BDNF secretion, theta burst stimulation, perirhinal cortex, TrkB receptor, neurotrophins, activity-dependent plasticity, low-frequency stimulation, hippocampus
MeSH terms
Animals, Brain, Electrophysiology, Hippocampus, Male, Rats, Sprague-Dawley, Long-Term Potentiation, Entorhinal Cortex, Brain-Derived Neurotrophic Factor, Long-Term Synaptic Depression, Rats, In Vitro Techniques

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