Brain insulin resistance impairs hippocampal synaptic plasticity and memory by increasing GluA1 palmitoylation through FoxO3a.

Salvatore Fusco, Marco Rinaudo, Domenica Donatella Li Puma, Cristian Ripoli, Marcello D'Ascenzo, Claudio Grassi, Matteo Spinelli, Francesca Natale, Andrea Mattera, Rosita Lapenta, Alfonso Grassi

Risultato della ricerca: Contributo in rivistaArticolo in rivistapeer review

71 Citazioni (Scopus)

Abstract

High-fat diet (HFD) and metabolic diseases cause detrimental effects on hippocampal synaptic plasticity, learning, and memory through molecular mechanisms still poorly understood. Here, we demonstrate that HFD increases palmitic acid deposition in the hippocampus and induces hippocampal insulin resistance leading to FoxO3a-mediated overexpression of the palmitoyltransferase zDHHC3. The excess of palmitic acid along with higher zDHHC3 levels causes hyper-palmitoylation of AMPA glutamate receptor subunit GluA1, hindering its activity-dependent trafficking to the plasma membrane. Accordingly, AMPAR current amplitudes and, more importantly, their potentiation underlying synaptic plasticity were inhibited, as well as hippocampal-dependent memory. Hippocampus-specific silencing of Zdhhc3 and, interestingly enough, intranasal injection of the palmitoyltransferase inhibitor, 2-bromopalmitate, counteract GluA1 hyper-palmitoylation and restore synaptic plasticity and memory in HFD mice. Our data reveal a key role of FoxO3a/Zdhhc3/GluA1 axis in the HFD-dependent impairment of cognitive function and identify a novel mechanism underlying the cross talk between metabolic and cognitive disorders.
Lingua originaleEnglish
pagine (da-a)N/A-N/A
Numero di pagine14
RivistaNature Communications
Volume8
DOI
Stato di pubblicazionePubblicato - 2017

Keywords

  • Metabolism
  • Molecular neuroscience
  • Synaptic plasticity

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