| Literature DB >> 35657456 |
Yasuyo Miyagi1, Kyoko Fujiwara1, Keigo Hikishima2, Daisuke Utsumi3, Chiaki Katagiri1, Masahiko Nishimura1, Hiroshi Takagi1, Shogo Ishiuchi4.
Abstract
Evidence has accumulated that higher consumption of high-fat diets (HFDs) during the juvenile/adolescent period induces altered hippocampal function and morphology; however, the mechanism behind this phenomenon remains elusive. Using high-resolution structural imaging combined with molecular and functional interrogation, a murine model of obesity treated with HFDs for 12 weeks after weaning mice was shown to change in the glutamate-mediated intracellular calcium signaling and activity, including further selective reduction of gray matter volume in the hippocampus associated with memory recall disturbance. Dysregulation of intracellular calcium concentrations was restored by a non-competitive α-3-hydroxy-5-methyl-4-isoxazole propionic acid receptor (AMPAR) antagonist, followed by normalization of hippocampal volume and memory recall ability, indicating that AMPARs may serve as an attractive therapeutic target for obesity-associated cognitive decline.Entities:
Keywords: CP-AMPAR; Cognitive function; NMDAR; Obesity
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Year: 2022 PMID: 35657456 DOI: 10.1007/s12035-022-02834-2
Source DB: PubMed Journal: Mol Neurobiol ISSN: 0893-7648 Impact factor: 5.682