Department of Neuroscience & Experimental Therapeutics, Albany Medical College, 47 New Scotland Avenue; MC-136, Albany, NY, 12208, USA.
Department of Psychology & Neuroscience, Nova Southeastern University, 3301 College Avenue, Fort Lauderdale, FL, 33314, USA.
J Neuroinflammation. 2022 May 14;19(1):110. doi: 10.1186/s12974-022-02466-2.
Approximately 70% of Alzheimer's disease (AD) patients have co-morbid vascular contributions to cognitive impairment and dementia (VCID); this highly prevalent overlap of dementia subtypes is known as mixed dementia (MxD). AD is more prevalent in women, while VCID is slightly more prevalent in men. Sex differences in risk factors may contribute to sex differences in dementia subtypes. Unlike metabolically healthy women, diabetic women are more likely to develop VCID than diabetic men. Prediabetes is 3× more prevalent than diabetes and is linked to earlier onset of dementia in women, but not men. How prediabetes influences underlying pathology and cognitive outcomes across different dementia subtypes is unknown. To fill this gap in knowledge, we investigated the impact of diet-induced prediabetes and biological sex on cognitive function and neuropathology in mouse models of AD and MxD.
Male and female 3xTg-AD mice received a sham (AD model) or unilateral common carotid artery occlusion surgery to induce chronic cerebral hypoperfusion (MxD model). Mice were fed a control or high fat (HF; 60% fat) diet from 3 to 7 months of age. In both sexes, HF diet elicited a prediabetic phenotype (impaired glucose tolerance) and weight gain.
In females, but not males, metabolic consequences of a HF diet were more severe in AD or MxD mice compared to WT. In both sexes, HF-fed AD or MxD mice displayed deficits in spatial memory in the Morris water maze (MWM). In females, but not males, HF-fed AD and MxD mice also displayed impaired spatial learning in the MWM. In females, but not males, AD or MxD caused deficits in activities of daily living, regardless of diet. Astrogliosis was more severe in AD and MxD females compared to males. Further, AD/MxD females had more amyloid beta plaques and hippocampal levels of insoluble amyloid beta 40 and 42 than AD/MxD males. In females, but not males, more severe glucose intolerance (prediabetes) was correlated with increased hippocampal microgliosis.
High-fat diet had a wider array of metabolic, cognitive, and neuropathological consequences in AD and MxD females compared to males. These findings shed light on potential underlying mechanisms by which prediabetes may lead to earlier dementia onset in women.
约 70%的阿尔茨海默病(AD)患者存在认知障碍和痴呆症的血管性共病(VCID);这种常见的痴呆亚型重叠被称为混合性痴呆(MxD)。AD 在女性中更为常见,而 VCID 在男性中略为常见。危险因素的性别差异可能导致痴呆亚型的性别差异。与代谢健康的女性不同,患有糖尿病的女性比男性更容易发生 VCID。前驱糖尿病的患病率是糖尿病的 3 倍,并且与女性痴呆症的发病年龄更早有关,但与男性无关。前驱糖尿病如何影响不同痴呆亚型的潜在病理和认知结果尚不清楚。为了填补这一知识空白,我们研究了饮食诱导的前驱糖尿病和生物性别对 AD 和 MxD 小鼠模型认知功能和神经病理学的影响。
雄性和雌性 3xTg-AD 小鼠接受假手术(AD 模型)或单侧颈总动脉闭塞手术以诱导慢性脑灌注不足(MxD 模型)。从 3 到 7 个月大时,小鼠分别喂食对照或高脂肪(HF;60%脂肪)饮食。在两性中,HF 饮食都会引起前驱糖尿病表型(葡萄糖耐量受损)和体重增加。
在女性中,但不在男性中,HF 饮食对 AD 或 MxD 小鼠的代谢后果比 WT 更严重。在两性中,HF 喂养的 AD 或 MxD 小鼠在 Morris 水迷宫(MWM)中显示出空间记忆缺陷。在女性中,但不在男性中,HF 喂养的 AD 和 MxD 小鼠在 MWM 中也显示出空间学习障碍。在女性中,但不在男性中,AD 或 MxD 引起的日常生活活动缺陷与饮食无关。与男性相比,AD 和 MxD 女性的星形胶质细胞增生更为严重。此外,AD/MxD 女性的海马淀粉样β斑块和不溶性淀粉样β 40 和 42 水平高于 AD/MxD 男性。在女性中,但不在男性中,更严重的葡萄糖耐量受损(前驱糖尿病)与海马小胶质细胞增生增加相关。
与男性相比,HF 饮食对 AD 和 MxD 女性具有更广泛的代谢、认知和神经病理学后果。这些发现揭示了前驱糖尿病可能导致女性痴呆症更早发病的潜在机制。