Effects of Menopause and High Fat Diet on Metabolic Outcomes in a Mouse Model of Alzheimer's Disease.

更年期和高脂饮食对阿尔茨海默病小鼠模型代谢结果的影响

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作者:Abi-Ghanem Charly, Salinero Abigail E, Smith Rachel M, Kelly Richard D, Belanger Kasey M, Richard Riane N, Paul Aaron S, Herzog Ava A, Thrasher Christina A, Rybka Krystyna A, Riccio David, Gannon Olivia J, Kordit David, Kyaw Nyi-Rein, Mansour Febronia M, Groom Emily, Brooks Heddwen L, Robison Lisa S, Pumiglia Kevin, Zuloaga Damian G, Zuloaga Kristen L
BACKGROUND: About two-thirds of those with Alzheimer's disease (AD) are women, most of whom are post-menopausal. Menopause accelerates dementia risk by increasing the risk for metabolic, cardiovascular, and cerebrovascular diseases. Mid-life metabolic disease (obesity, diabetes/prediabetes) is a well-known risk factor for dementia. A high fat diet can lead to poor metabolic health in both humans and rodents. OBJECTIVE: Our goal was to determine the effects of a high fat diet on metabolic outcomes in the AppNL-F knock-in mouse model of AD and assess the effects of menopause. METHODS: First, 3-month-old AppNL-F and WT female mice were placed on either a control or a high fat diet until 10 months of age then assessed for metabolic outcomes. Next, we did a more extensive assessment in AppNL-F mice that were administered VCD (4-vinylcyclohexene diepoxide) or vehicle (oil) and placed on a control or high fat diet for 7 months. VCD was used to model menopause by causing accelerated ovarian failure. RESULTS: Compared to WT controls, AD female mice had worse glucose intolerance. Menopause led to metabolic impairment (weight gain and glucose intolerance) and further exacerbated obesity in response to a high fat diet. There were interactions between diet and menopause on some metabolic health serum biomarkers and the expression of hypothalamic markers related to energy balance. CONCLUSIONS: This work highlights the need to model endocrine aging in animal models of dementia and will contribute to further understanding the interaction between menopause and metabolic health in the context of AD.

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