Freire-Regatillo Alejandra, Diaz-Pacheco Sonia, Frago Laura M, Arévalo María-Ángeles, Argente Jesús, Garcia-Segura Luis M, de Ceballos María L, Chowen Julie A
Department of Endocrinology, Instituto de Investigación la Princesa, Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
Department of Pediatrics, Universidad Aútonoma de Madrid, Madrid, Spain.
Front Neuroanat. 2022 Jul 26;16:910477. doi: 10.3389/fnana.2022.910477. eCollection 2022.
The propensity to develop neurodegenerative diseases is influenced by diverse factors including genetic background, sex, lifestyle, including dietary habits and being overweight, and age. Indeed, with aging, there is an increased incidence of obesity and neurodegenerative processes, both of which are associated with inflammatory responses, in a sex-specific manner. High fat diet (HFD) commonly leads to obesity and markedly affects metabolism, both peripherally and centrally. Here we analyzed the metabolic and inflammatory responses of middle-aged (11-12 months old) transgenic amyloid precursor protein (TgAPP) mice of both sexes to HFD for 18 weeks (starting at 7-8 months of age). We found clear sex differences with females gaining significantly more weight and fat mass than males, with a larger increase in circulating leptin levels and expression of inflammatory markers in visceral adipose tissue. Glycemia and insulin levels increased in HFD fed mice of both sexes, with TgAPP mice being more affected than wild type (WT) mice. In the hypothalamus, murine amyloid β (Aβ) levels were increased by HFD intake exclusively in males, reaching statistical significance in TgAPP males. On a low fat diet (LFD), TgAPP males had significantly lower mRNA levels of the anorexigenic neuropeptide proopiomelanocortin (POMC) than WT males, with HFD intake decreasing the expression of the orexigenic neuropeptides Agouti-related peptide (AgRP) and neuropeptide Y (NPY), especially in TgAPP mice. In females, HFD increased POMC mRNA levels but had no effect on AgRP or NPY mRNA levels, and with no effect on genotype. There was no effect of diet or genotype on the hypothalamic inflammatory markers analyzed or the astrogliosis marker glial acidic protein (GFAP); however, levels of the microglial marker Iba-1 increased selectively in male TgAPP mice. In summary, the response to HFD intake was significantly affected by sex, with fewer effects due to genotype. Hypothalamic inflammatory cytokine expression and astrogliosis were little affected by HFD in middle-aged mice, although in TgAPP males, which showed increased Aβ, there was microglial activation. Thus, excess intake of diets high in fat should be avoided because of its possible detrimental consequences.
神经退行性疾病的发病倾向受多种因素影响,包括遗传背景、性别、生活方式(包括饮食习惯和超重情况)以及年龄。事实上,随着年龄增长,肥胖和神经退行性病变的发病率都会上升,且二者均与炎症反应相关,且存在性别特异性。高脂饮食(HFD)通常会导致肥胖,并显著影响外周和中枢的代谢。在此,我们分析了中年(11 - 12个月大)的转基因淀粉样前体蛋白(TgAPP)雌雄小鼠在18周(从7 - 8个月大开始)高脂饮食后的代谢和炎症反应。我们发现了明显的性别差异,雌性小鼠比雄性小鼠体重和脂肪量增加得更多,循环瘦素水平升高,内脏脂肪组织中炎症标志物的表达增加。高脂饮食喂养的雌雄小鼠血糖和胰岛素水平均升高,TgAPP小鼠比野生型(WT)小鼠受影响更大。在雄性小鼠中,仅高脂饮食摄入会使下丘脑小鼠淀粉样β(Aβ)水平升高,在TgAPP雄性小鼠中达到统计学显著水平。在低脂饮食(LFD)条件下,TgAPP雄性小鼠厌食神经肽阿黑皮素原(POMC)的mRNA水平显著低于WT雄性小鼠,高脂饮食摄入会降低促食欲神经肽刺鼠相关肽(AgRP)和神经肽Y(NPY)的表达,尤其是在TgAPP小鼠中。在雌性小鼠中,高脂饮食会增加POMC mRNA水平,但对AgRP或NPY mRNA水平没有影响,且对基因型也没有影响。饮食或基因型对所分析的下丘脑炎症标志物或星形胶质细胞增生标志物胶质纤维酸性蛋白(GFAP)没有影响;然而,小胶质细胞标志物离子钙结合衔接分子1(Iba - 1)的水平仅在雄性TgAPP小鼠中选择性升高。总之,高脂饮食摄入的反应受性别显著影响,受基因型影响较小。中年小鼠下丘脑炎症细胞因子表达和星形胶质细胞增生受高脂饮食影响较小,尽管在显示Aβ增加的TgAPP雄性小鼠中存在小胶质细胞激活。因此,应避免过量摄入高脂肪饮食,因为其可能产生有害后果。