Reference - Detail
| RRC ID | 87292 |
|---|---|
| Author | Findley CA, McFadden SA, Hill T, Peck MR, Quinn K, Hascup KN, Hascup ER. |
| Title | Sexual dimorphism, altered hippocampal glutamatergic neurotransmission, and cognitive impairment in APP knock-in mice. |
| Journal | J Alzheimers Dis |
| Abstract |
BACKGROUND:It is well established that glutamatergic neurotransmission plays an essential role in learning and memory. Previous studies indicate that glutamate dynamics shift with Alzheimer's disease (AD) progression, contributing to negative cognitive outcomes. OBJECTIVE:In this study, we characterized hippocampal glutamatergic signaling with age and disease progression in a knock-in mouse model of AD (APPNL-F/NL--F). METHODS:At 2-4 and 18+ months old, male and female APPNL/NL, APPNL-F/NL-F, and C57BL/6 mice underwent cognitive assessment using Morris water maze (MWM) and Novel Object Recognition (NOR). Then, basal and 70 mM KCl stimulus-evoked glutamate release was measured in the dentate gyrus (DG), CA3, and CA1 regions of the hippocampus using a glutamate-selective microelectrode in anesthetized mice. RESULTS:Glutamate recordings support elevated stimulus-evoked glutamate release in the DG and CA3 of young APPNL-F/NL-F male mice that declined with age compared to age-matched control mice. Young female APPNL-F/NL-F mice exhibited increased glutamate clearance in the CA1 that slowed with age compared to age-matched control mice. Male and female APPNL-F/NL-F mice exhibited decreased CA1 basal glutamate levels, while males also showed depletion in the CA3. Cognitive assessment demonstrated impaired spatial cognition in aged male and female APPNL-F/NL-F mice, but only aged females displayed recognition memory deficits compared to age-matched control mice. CONCLUSIONS:These findings confirm a sex-dependent hyper-to-hypoactivation glutamatergic paradigm in APPNL-F/NL-F mice. Further, data illustrate a sexually dimorphic biological aging process resulting in a more severe cognitive phenotype for female APPNL-F/NL-F mice than their male counterparts. Research outcomes mirror that of human AD pathology and provide further evidence of divergent AD pathogenesis between sexes. |
| Volume | 102(2) |
| Pages | 491-505 |
| Published | 2024-11-1 |
| DOI | 10.3233/JAD-240795 |
| PMID | 39543985 |
| PMC | PMC11639043 |
| MeSH | Alzheimer Disease / genetics Alzheimer Disease / metabolism Amyloid beta-Protein Precursor* / genetics Amyloid beta-Protein Precursor* / metabolism Animals Cognitive Dysfunction* / genetics Cognitive Dysfunction* / metabolism Disease Models, Animal Female Gene Knock-In Techniques* Glutamic Acid* / metabolism Hippocampus* / metabolism Male Maze Learning / physiology Mice Mice, Inbred C57BL* Mice, Transgenic* Sex Characteristics* Synaptic Transmission* / physiology |
| IF | 3.909 |
| Resource | |
| Mice | RBRC06342 RBRC06343 |