Hippocampus-specific knockdown of Shati/Nat8l impairs cognitive function and electrophysiological response in mice

Naotaka Izuo, Daiki Ikejima, Kyosuke Uno, Takashi Asano, Shin Ichi Muramatsu, Atsumi Nitta*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Shati/Nat8l was identified as an upregulated molecule in the nucleus accumbens (NAc) of mice following repeated methamphetamine administration. Region-specific roles of this molecule are associated with psychiatric disorders. In the present study, we examined the importance of Shati/Nat8l in the hippocampus because of its high expression in this region. Mice with a hippocampus-specific knockdown of Shati/Nat8l (hippocampal Shati-cKD) were prepared by the microinjection of adeno-associated virus (AAV) vectors carrying Cre into the hippocampus of Shati/Nat8lflox/flox mice, and their phenotypes were investigated. Drastic reduction in the expression and function of Shati/Nat8l in the hippocampus was observed in Shati-cKD mice. These mice exhibited cognitive dysfunction in behavioral experiments and impaired the electrophysiological response to the stimuli, which elicits long-term potentiation. Shati/Nat8l in the hippocampus is suggested to possibly play an important role in synaptic plasticity to maintain cognitive function. This molecule could be a therapeutic target for hippocampus-related disorders such as dementia.

Original languageEnglish
Article number150435
JournalBiochemical and Biophysical Research Communications
Volume736
DOIs
StatePublished - 2024/12/03

Keywords

  • Cognitive function
  • Hippocampus
  • N-acetylaspartate
  • Shati/Nat8l
  • Synaptic plasticity

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

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