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[Dysfunction of Na+/Ca2+ exchangers is associated with cognitive decline in Alzheimer's disease].

Abstract
Na+/Ca2+ exchanger (NCX) is mainly expressed in the plasma membrane and mediates electrogenical exchange of one Ca2+ for three Na+, depending on the electrochemical gradients across the plasma membrane. NCX has three different isoforms (NCX1, NCX2, NCX3) encoded by distinct genes in mammals. Here, we report that NCX2 and NCX3 protein levels are relatively reduced in hippocampal CA1 of Alzheimer's disease model mice. Likewise, NCX2+/- or NCX3+/- mice exhibited impaired hippocampal LTP and memory-related behaviors. In immunoblot analyses, calcium/calmodulin-dependent protein kinase II (CaMKII) autophosphorylation significantly decreased in hippocampal CA1 of NCX2+/- mice compared to wild-type mice. By contrast, NCX2+/- mice was correlated with elevated calcineurin (CaN) activity and rescued by treatment with the calcineurin inhibitor FK506. Taken together, the imbalance of CaMKII and CaN activities with concomitant LTP impairment likely accounts for the learning disability observed in NCX2+/- mice.
AuthorsShigeki Moriguchi, Satomi Kita, Takahiro Iwamoto, Kohji Fukunaga
JournalNihon yakurigaku zasshi. Folia pharmacologica Japonica (Nihon Yakurigaku Zasshi) 2018 Vol. 152 Issue 6 Pg. 299-305 ISSN: 0015-5691 [Print] Japan
PMID30531101 (Publication Type: Journal Article)
Chemical References
  • NCX1 protein, mouse
  • Sodium-Calcium Exchanger
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Calcium
Topics
  • Alzheimer Disease
  • Animals
  • Calcium
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Cognitive Dysfunction
  • Memory
  • Mice
  • Sodium-Calcium Exchanger

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