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1000 Titel
  • d-Cycloserine enhances the bidirectional range of NMDAR-dependent hippocampal synaptic plasticity
1000 Autor/in
  1. Vestring, Stefan |
  2. Dorner, Alexandra |
  3. Scholliers, Jonas |
  4. Ehrenberger, Konstantin |
  5. Kiss, Andrea |
  6. Arenz, Luis |
  7. Theiss, Alice |
  8. Rossner, Paul |
  9. Frase, Sibylle |
  10. Du Vinage, Catherine |
  11. Wendler, Elisabeth |
  12. Serchov, Tsvetan |
  13. Domschke, Katharina |
  14. Bischofberger, Josef |
  15. Normann, Claus |
1000 Verlag Nature Publishing Group UK
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-01-09
1000 Erschienen in
1000 Quellenangabe
  • 14(1):18
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1038/s41398-023-02725-7 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10776623/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:p>The partial N-methyl-D-aspartate receptor (NMDAR) agonist <jats:sc>d</jats:sc>-Cycloserine (DCS) has been evaluated for the treatment of a wide variety of psychiatric disorders, including dementia, schizophrenia, depression and for the augmentation of exposure-based psychotherapy. Most if not all of the potential psychiatric applications of DCS target an enhancement or restitution of cognitive functions, learning and memory. Their molecular correlate is long-term synaptic plasticity; and many forms of synaptic plasticity depend on the activation of NMDA receptors. Here, we comprehensively examined the modulation of different forms of synaptic plasticity in the hippocampus by DCS and its mechanism. We found that DCS positively modulates NMDAR-dependent forms of long-term synaptic plasticity (long-term synaptic potentiation, LTP, and long-term synaptic depression, LTD) in hippocampal brain slices of juvenile rats without affecting basal synaptic transmission. DCS binds to the <jats:sc>d</jats:sc>-serine/glycine binding site of the NMDAR. Pharmacological inhibition of this site prevented the induction of LTP, whereas agonism at the <jats:sc>d</jats:sc>-serine/glycine binding site augmented LTP and could functionally substitute for weak LTP induction paradigms. The most probable origin of endogenous <jats:sc>d</jats:sc>-serine are astrocytes, and its exocytosis is regulated by astrocytic metabotropic glutamate receptors (mGluR1). Functional eradication of astrocytes, inhibition of mGluR1 receptors and G-protein signaling in astrocytes adjacent to postsynaptic neurons prevented the induction of NMDAR-dependent forms of LTP and LTD. Our results support the enhancement of a bidirectional range of NMDAR-dependent hippocampal synaptic plasticity by DCS and <jats:sc>d</jats:sc>-serine-mediated gliotransmission. Therefore, the <jats:sc>d</jats:sc>-serine/glycine-binding site in NMDAR is a major target for psychopharmacological interventions targeting plasticity-related disorders.</jats:p>
1000 Sacherschließung
lokal Cycloserine/pharmacology [MeSH]
lokal Receptors, N-Methyl-D-Aspartate [MeSH]
lokal Humans [MeSH]
lokal /9/74
lokal Rats [MeSH]
lokal Serine [MeSH]
lokal /631/378/1595/1554
lokal Animals [MeSH]
lokal /64/60
lokal Hippocampus [MeSH]
lokal /692/699/476/1414
lokal Article
lokal Glycine [MeSH]
lokal Neuronal Plasticity [MeSH]
lokal article
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0001-9150-8712|https://frl.publisso.de/adhoc/uri/RG9ybmVyLCBBbGV4YW5kcmE=|https://frl.publisso.de/adhoc/uri/U2Nob2xsaWVycywgSm9uYXM=|https://frl.publisso.de/adhoc/uri/RWhyZW5iZXJnZXIsIEtvbnN0YW50aW4=|https://frl.publisso.de/adhoc/uri/S2lzcywgQW5kcmVh|https://frl.publisso.de/adhoc/uri/QXJlbnosIEx1aXM=|https://frl.publisso.de/adhoc/uri/VGhlaXNzLCBBbGljZQ==|https://frl.publisso.de/adhoc/uri/Um9zc25lciwgUGF1bA==|https://frl.publisso.de/adhoc/uri/RnJhc2UsIFNpYnlsbGU=|https://frl.publisso.de/adhoc/uri/RHUgVmluYWdlLCBDYXRoZXJpbmU=|https://frl.publisso.de/adhoc/uri/V2VuZGxlciwgRWxpc2FiZXRo|https://orcid.org/0000-0002-2234-2875|https://orcid.org/0000-0002-2550-9132|https://frl.publisso.de/adhoc/uri/QmlzY2hvZmJlcmdlciwgSm9zZWY=|https://orcid.org/0000-0001-5693-8936
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1000 Erstellt am 2025-02-03T23:09:00.005+0100
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