Kelliny Sally, Lin Liying, Deng Isaac, Xiong Jing, Zhou Fiona, Al-Hawwas Mohammed, Bobrovskaya Larisa, Zhou Xin-Fu
Health and Biomedical Innovation, Clinical and Health Sciences, University of South Australia, Adelaide, SA, 5000, Australia.
Faculty of Pharmacy, Assiut University, Assiut, Egypt.
Mol Neurobiol. 2021 Aug;58(8):3692-3711. doi: 10.1007/s12035-021-02338-5. Epub 2021 Apr 2.
Alzheimer's disease (AD) is the most common cause of dementia among elderly people. Majority of AD cases are sporadic (SAD) with unknown cause. Transgenic animal models closely reflect the familial (genetic) aspect of the disease but not the sporadic type. However, most new drug candidates which are tested positive in transgenic animal models failed in clinical studies so far. Herein, we aim to develop an AD animal model that combines most of the neuropathological features seen in sporadic AD in humans with amyloid plaques observed in transgenic mice. Four-month-old wild-type and APP/PS1 AD mice were given a single intracerebroventricular (ICV) injection of 3 mg/kg streptozotocin (STZ), a diabetogenic agent. Three weeks later, their cognitive behavior was assessed, and their brain tissues were collected for biochemical and histological analysis. STZ produced cognitive deficits in both non-transgenic mice and AD mice. Biochemical analysis showed a severe decline in synaptic proteins, increase in tau phosphorylation, oxidative stress, disturbed brain insulin signaling with extensive neuroinflammation, and cell death. Significant increase was also observed in the level of the soluble beta amyloid precursor protein (APP) fragments and robust accumulation of amyloid plaques in AD mice compared to the control. These results suggest that STZ ICV treatment causes disturbance in multiple metabolic and cell signaling pathways in the brain that facilitated amyloid plaque accumulation and tau phosphorylation. Therefore, this animal model can be used to evaluate new AD therapeutic agents for clinical translation.
阿尔茨海默病(AD)是老年人痴呆最常见的病因。大多数AD病例为散发性(SAD),病因不明。转基因动物模型能密切反映该疾病的家族性(遗传)特征,但不能反映散发性类型。然而,目前大多数在转基因动物模型中测试呈阳性的新药候选物在临床研究中均告失败。在此,我们旨在开发一种AD动物模型,该模型结合了人类散发性AD中所见的大多数神经病理学特征以及转基因小鼠中观察到的淀粉样斑块。对4月龄的野生型和APP/PS1 AD小鼠进行单次脑室内(ICV)注射3 mg/kg链脲佐菌素(STZ),一种致糖尿病药物。三周后,评估它们的认知行为,并收集脑组织进行生化和组织学分析。STZ在非转基因小鼠和AD小鼠中均产生了认知缺陷。生化分析显示突触蛋白严重下降、tau蛋白磷酸化增加、氧化应激、脑胰岛素信号传导紊乱并伴有广泛的神经炎症以及细胞死亡。与对照组相比,AD小鼠中可溶性β淀粉样前体蛋白(APP)片段水平也显著增加,且淀粉样斑块大量积聚。这些结果表明,STZ脑室内注射治疗会导致大脑中多种代谢和细胞信号通路紊乱,从而促进淀粉样斑块积聚和tau蛋白磷酸化。因此,该动物模型可用于评估用于临床转化的新型AD治疗药物。