Department of Neuroscience, Osaka City University Graduate School of Medicine, 1-4-3 Asahimachi, Abeno-ku, Osaka 545-8585, Japan.
Life Sci. 2012 Dec 10;91(23-24):1169-76. doi: 10.1016/j.lfs.2011.12.022. Epub 2012 Jan 17.
Hypercholesterolemia is known to be a risk factor for Alzheimer's disease (AD), and diet-induced hypercholesterolemia has been shown to accelerate amyloid pathology in animals. While growing evidence has shown that synaptic and cognitive dysfunction in AD is associated with intraneuronal accumulation of Aβ, the relationships between hypercholesterolemia, memory impairment, and intraneuronal Aβ remains unclear. The present study aims to clarify this association.
Transgenic mice expressing amyloid precursor protein (APP) harboring the Osaka (E693∆) mutation (APP(OSK)-Tg mice) were used. These mice exhibit intraneuronal Aβ oligomers and memory impairment from 8months of age. Five-month-old male APP(OSK)-Tg mice and non-Tg littermates were fed a high-cholesterol diet for 1 month to induce hypercholesterolemia. At 6 months of age, their cognitive function was evaluated by the Morris water maze. Intraneuronal Aβ, synaptic density, and tau phosphorylation were examined by immunohistochemistry.
Serum and brain cholesterol levels were significantly higher in APP(OSK)-Tg mice and non-Tg littermates that were fed a high-cholesterol diet than in control mice that were fed normal chow, indicating that hypercholesterolemia was successfully induced. Hypercholesterolemic APP(OSK)-Tg mice, but not control APP(OSK)-Tg mice or hypercholesterolemic non-Tg littermates, exhibited impaired spatial reference memory, which was accompanied with intraneuronal accumulation of Aβ oligomers, reduced synaptophysin immunoreactivity, and abnormal tau phosphorylation in the hippocampus. Hypercholesterolemia-accelerated accumulation of intraneuronal Aβ oligomers was also observed in another model mouse, Tg2576.
Our findings suggest that hypercholesterolemia accelerates intraneuronal accumulation of Aβ oligomers and subsequent synapse loss, resulting in memory impairment.
高胆固醇血症是阿尔茨海默病(AD)的一个已知风险因素,饮食诱导的高胆固醇血症已被证明可加速动物的淀粉样蛋白病理学。虽然越来越多的证据表明 AD 中的突触和认知功能障碍与 Aβ 在内神经元中的积累有关,但高胆固醇血症、记忆障碍和 Aβ 在内神经元中的关系仍不清楚。本研究旨在阐明这种关联。
使用表达淀粉样前体蛋白(APP)的转基因小鼠,该 APP 携带大阪(E693∆)突变(APP(OSK)-Tg 小鼠)。这些小鼠从 8 月龄开始表现出 Aβ 寡聚物在内神经元中的积累和记忆障碍。将 5 月龄的雄性 APP(OSK)-Tg 小鼠和非-Tg 同窝仔鼠喂食高胆固醇饮食 1 个月以诱导高胆固醇血症。在 6 月龄时,通过 Morris 水迷宫评估它们的认知功能。通过免疫组织化学检查 Aβ 在内神经元中的含量、突触密度和 tau 磷酸化。
与喂食正常饲料的对照组相比,喂食高胆固醇饮食的 APP(OSK)-Tg 小鼠和非-Tg 同窝仔鼠的血清和脑胆固醇水平显著升高,表明成功诱导了高胆固醇血症。高胆固醇血症的 APP(OSK)-Tg 小鼠,而不是对照组 APP(OSK)-Tg 小鼠或高胆固醇血症的非-Tg 同窝仔鼠,表现出空间参考记忆受损,这伴随着 Aβ 寡聚物在内神经元中的积累、突触小体素免疫反应性降低和海马 tau 磷酸化异常。在另一种模型小鼠 Tg2576 中也观察到高胆固醇血症加速的 Aβ 寡聚物在内神经元中的积累。
我们的研究结果表明,高胆固醇血症加速 Aβ 寡聚物在内神经元中的积累,随后导致突触丢失,从而导致记忆障碍。