Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Key Laboratory of Basic Pharmacology of Ministry of Education and Joint International Research Lab of Ethnomedicine of Ministry of Education, Zunyi Medical University, Zunyi, China.
J Alzheimers Dis. 2020;75(2):385-395. doi: 10.3233/JAD-200063.
Alzheimer's disease (AD) is a highly age-related cognitive decline frequently attacking the elderly. Senescence-accelerated mouse-prone 8 (SAMP8) is an ideal model to study AD, displaying age-related learning and memory disorders. SAMP8 mice exhibit most features of pathogenesis of AD, including an abnormal expression of anti-aging factors, oxidative stress, inflammation, amyloid-β (Aβ) deposits, tau hyperphosphorylation, endoplasmic reticulum stress, abnormal autophagy activity, and disruption of intestinal flora. SAMP8 mice, therefore, have visualized the understanding of AD, and also provided effective ways to find new therapeutic targets. This review focused on the age-related pathogenesis in SAMP8 mice, to advance the understanding of age-related learning and memory decline and clarify the mechanisms. Furthermore, this review will provide extensive foundations for SAMP8 mice used in therapeutics for AD.
阿尔茨海默病(AD)是一种与年龄高度相关的认知能力下降,常发生于老年人。快速老化小鼠品系 8(SAMP8)是研究 AD 的理想模型,表现出与年龄相关的学习和记忆障碍。SAMP8 小鼠表现出 AD 发病机制的大多数特征,包括抗衰老因子的异常表达、氧化应激、炎症、β淀粉样蛋白(Aβ)沉积、tau 过度磷酸化、内质网应激、异常自噬活性以及肠道菌群失调。因此,SAMP8 小鼠为 AD 的发病机制提供了可视化的理解,并为寻找新的治疗靶点提供了有效的途径。本综述重点介绍了 SAMP8 小鼠与年龄相关的发病机制,以加深对与年龄相关的学习和记忆减退的理解,并阐明其机制。此外,本综述将为 SAMP8 小鼠在 AD 治疗中的应用提供广泛的基础。