Cited by 113Neuroscience and Neuropharmacology ResearchMemory and Neural MechanismsGenetics and Neurodevelopmental Disorders

Long‐term potentiation in the rat dentate gyrus is associated with enhanced Arc/Arg3.1 protein expression in spines, dendrites and glia

Rodríguez, J. J., Davies, H. A., Silva, A. T., De Souza, I. E. J., Peddie, C. J., Colyer, F. M., Lancashire, C. L., Fine, A. +3 more·2005·European Journal of Neuroscience

Abstract

Electron microscopic immunocytochemical methods were used to determine the localization, subcellular distribution and expression of activity-regulated cytoskeletal protein (Arc/Arg3.1) in dentate gyrus after unilateral induction of long-term potentiation (LTP) in the perforant pathway of anaesthetized rats. At 2 h post-induction, immunoreaction product was visible in the dentate gyrus in both the granule cell and molecular layers. Arc expression was higher in the potentiated than the unstimulated contralateral hemisphere. Single-section electron microscopy analysis in unstimulated tissue and in tissue prepared 2 and 4 h after LTP induction showed Arc immunoreactivity (Arc-IR) in dendrites, dendritic spines and glia. Arc-IR was associated with synaptic and non-synaptic plasma membrane apposed to axon terminals and with cytoplasmic organelles, including the cytoskeleton. Arc-IR was also present in neuronal perikarya and there was occasional labelling of nuclei and axons. At 2 h post-LTP induction, there were significant increases in Arc-IR within the granule cell and molecular layers of the dentate gyrus and particularly within the middle molecular layer relative to the inner and outer molecular layers. This increase in Arc expression 2 h after LTP induction was blocked by the N-methyl-D-aspartate receptor antagonist (RS)-3-2-carboxypiperazin-4-yl-propyl-1-phosphonic acid. In animals killed 4 h after LTP induction, Arc expression had declined and differences between the potenti…

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Crossref · 10.1111/j.1460-9568.2005.04068.x

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Authors
Rodríguez, J. J., Davies, H. A., Silva, A. T., De Souza, I. E. J., Peddie, C. J., Colyer, F. M., Lancashire, C. L., Fine, A., Errington, M. L., Bliss, T. V. P., & Stewart, M. G.
Affiliations
  • The Open University (GB)
  • National Institute for Medical Research (GB)
Corresponding author
Rodríguez, J. J.
Venue
European Journal of Neuroscience
Publisher
Wiley
Published
2005-05
Volume
21
Issue
9
Pages
2384-2396
ISSN
  • 0953-816X (ISSN-L)
  • 1460-9568
OpenAlex
W2099829314
Cited by
113
References
0
Citations by year
2025: 1 · 2024: 5 · 2023: 8 · 2022: 4 · 2021: 5 · 2020: 3 · 2019: 1 · 2018: 4 · 2017: 6 · 2016: 2 · 2015: 5 · 2014: 8 · 2013: 9 · 2012: 5
FWCI
3.01
Type
journal article
Language
en
Open access
closed
Locations
  • European Journal of Neuroscience (publishedVersion)
  • PubMed (publishedVersion)
  • Research Explorer (The University of Manchester) (submittedVersion)
Funders
Biotechnology and Biological Sciences Research Council
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
Keywords
long-term potentiation, Arc/Arg3.1, dentate gyrus, perforant path, dendritic spines, dendrites, glia, subcellular localization, NMDA receptor, synaptic plasticity, ultrastructure, granule cells, molecular layer
MeSH terms
Animals, Axons, Cytoskeletal Proteins, Dendrites, Male, Microscopy, Electron, Nerve Tissue Proteins, Neuroglia, Neuronal Plasticity, Piperazines, Rats, Sprague-Dawley, Long-Term Potentiation, Immediate-Early Proteins, Excitatory Amino Acid Antagonists, Dentate Gyrus, Dendritic Spines, Rats

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