Cited by 43Neuroscience and Neuropharmacology ResearchMemory and Neural MechanismsNeural dynamics and brain function

The supramammillary nucleus contributes to associative EPSP‐spike potentiation in the rat dentate gyrus in vivo

Nakanishi, Kosuke, Saito, Hiroshi, Abe, Kazuho·2001·European Journal of Neuroscience

Abstract

The supramammillary nucleus (SUM) of the hypothalamus sends neural projections to the hippocampus and is supposed to be involved in learning and memory. To test the possibility that SUM afferents modulate hippocampal functions, we investigated the effect of electrical stimulation of the SUM on the induction of long-term potentiation (LTP) at medial perforant path (PP)--granule cell synapses in the dentate gyrus (DG) of anaesthetized rats. High-frequency stimulation of the SUM (100 pulses at 100 Hz) alone did not change PP--DG field potentials. However, when the SUM stimulation was applied simultaneously with weak tetanic stimulation of the PP (20 pulses at 20 Hz) which alone did not induce any potentiation, it produced a long-lasting potentiation of the population spike, without an accompanying increase in the population excitatory postsynaptic potential (EPSP). The EPSP-spike (E-S) potentiation induced by pairing SUM and PP stimulation was abolished by lesions of the fimbria--fornix, a major pathway of SUM afferents. SUM stimulation applied 1 s before or after PP stimulation failed to produce E-S potentiation, and SUM stimulation augmented PP--DG field potentials during tetanic stimulation. Furthermore, the E-S potentiation was abolished by blocking GABAergic neurotransmission with picrotoxin. These results suggest that coactivation of SUM and PP inputs produces a long-lasting increase of granule cell excitability by modulating GABAergic inhibition. SUM afferents may contribute to associative memory processing by modulating hippocampal excitability.

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Crossref · 10.1046/j.1460-9568.2001.01446.x

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  • Input from the hypothalamus and the locus coeruleus, via activation of β-adrenergic receptors, as well as dopaminergic innervation of the hippocampus from the VTA and local release of CRH, all appear to contribute to the rapid stress-induced enhancement of hippocampal LTP.

    “In addition, input from the hypothalamus (Nakanishi et al. [216]) and the locus coeruleus (Harley and Sara [217]; Sara et al. [218]; Kitchigina et al. [219]; Bouret and Sara [220]), via activation of β-adrenergic receptors (Ikegaya et al. [221]; Vermetten and Bremner [8]; Strange and Dolan [222]; Nathan et al. [189]; Hurlemann et al. [223]), as well as the dopaminergic innervation of the”

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Authors
Nakanishi, K., Saito, H., & Abe, K.
Affiliations
  • The University of Tokyo (JP)
  • Hoshi University (JP)
Corresponding author
Abe, Kazuho
Venue
European Journal of Neuroscience
Publisher
Wiley
Published
2001-02
Volume
13
Issue
4
Pages
793-800
ISSN
  • 0953-816X (ISSN-L)
  • 1460-9568
OpenAlex
W2016072986
Cited by
43
References
1
Citations by year
2026: 2 · 2024: 2 · 2023: 2 · 2022: 3 · 2021: 3 · 2020: 2 · 2019: 2 · 2018: 2 · 2016: 1 · 2015: 2 · 2014: 1
FWCI
1.11
Type
journal article
Language
en
Open access
closed
Locations
  • European Journal of 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
supramammillary nucleus, dentate gyrus, perforant path, long-term potentiation, associative memory, GABAergic inhibition, fimbria-fornix, hippocampal excitability, population spike, picrotoxin
MeSH terms
Animals, Electric Stimulation, gamma-Aminobutyric Acid, Hypothalamus, Posterior, Male, Picrotoxin, Receptors, GABA-A, Rats, Wistar, Long-Term Potentiation, GABA Antagonists, Dentate Gyrus, Perforant Pathway, Excitatory Postsynaptic Potentials, Rats

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