Key Laboratory of Human Diseases Comparative Medicine, Ministry of Health, Institute of Medical Laboratory Animal Science, Chinese Academy of Medical Sciences (CAMS), Beijing, China.
Key Laboratory of Human Diseases Animal Models, State Administration of Traditional Chinese Medicine, Peking Union Medicine College (PUMC), Beijing, China.
J Alzheimers Dis. 2017;60(4):1241-1257. doi: 10.3233/JAD-170020.
The topic of gut microbiota is currently attracting considerable interest as a potential factor in Alzheimer's disease (AD). However, the extent and time course of alterations in the gut microbiota, and their effects on AD pathology remain uncertain. Herein, we compared the fecal microbiomes and fecal short chain fatty acid composition (SCFAs) between wild-type and AD model mice at different ages under strictly controlled specific pathogen free conditions, and also conducted microscopic investigations of intestinal structures. Our results showed that the microbiota composition and diversity were perturbed and the level of SCFAs was reduced in AD mice, predicting alterations in more than 30 metabolic pathways, which may be associated with amyloid deposition and ultrastructural abnormalities in AD mouse intestine. These findings indicate that AD pathology might not only affect brain function directly, but also exacerbate cognitive deficits through reducing the level of SCFAs via alterations of gut microbiota induced by intestinal amyloid deposition. Our data may support a role of gut microbiota, and suggest a novel route for therapeutic intervention in AD.
肠道微生物组作为阿尔茨海默病(AD)的潜在因素,目前正引起相当大的关注。然而,肠道微生物组的改变程度和时间进程及其对 AD 病理的影响仍不确定。在此,我们在严格控制特定病原体的条件下,比较了不同年龄的野生型和 AD 模型小鼠的粪便微生物组和粪便短链脂肪酸组成(SCFAs),并对肠道结构进行了微观研究。结果表明,AD 小鼠的微生物组成和多样性受到干扰,SCFAs 水平降低,预测超过 30 种代谢途径发生改变,这可能与 AD 小鼠肠道中的淀粉样蛋白沉积和超微结构异常有关。这些发现表明,AD 病理不仅可能直接影响大脑功能,还可能通过肠道淀粉样蛋白沉积引起的肠道微生物组改变,降低 SCFAs 水平,从而加重认知障碍。我们的数据可能支持肠道微生物组的作用,并为 AD 的治疗干预提供新途径。