Shenzhen Key Laboratory of Drug Addiction, Shenzhen Neher Neural Plasticity Laboratory, the Brain Cognition and Brain Disease Institute (BCBDI), Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences (CAS), Shenzhen-Hong Kong Institute of Brain Science-Shenzhen Fundamental Research Institutions, Shenzhen, China.
University of Chinese Academy of Sciences, Beijing, China.
CNS Neurosci Ther. 2022 Apr;28(4):580-592. doi: 10.1111/cns.13779. Epub 2021 Dec 10.
Alzheimer's disease (AD) is the most common neurodegenerative disorder that causes dementia and affects millions of people worldwide. Although it has devastating outcomes for patients and tremendous economic costs to society, there is currently no effective treatment available.
The high-fat, low-carbohydrate ketogenic diet (KD) is an established treatment for refractory epilepsy with a proven efficacy. Although the considerable interest has emerged in recent years for applying KD in AD patients, only few interventional studies in animals and humans have addressed the effects of KD on cognitive impairments, and the results were inconclusive. The aim of this study was to explore the impact of KD on cognitive functions and AD pathology in 5XFAD mice-a validated animal model of AD.
Four months of a ketogenic diet improved spatial learning, spatial memory and working memory in 5XFAD mice. The improvement in cognitive functions was associated with a restored number of neurons and synapses in both the hippocampus and the cortex. Ketogenic diet treatment also reduced amyloid plaque deposition and microglial activation, resulting in reduced neuroinflammation. The positive effect of ketogenic diet on cognitive functions depended on the starting time and the duration of the diet. A shorter period (2 months) of ketogenic diet treatment had a weaker effect. Ketogenic diet initiated at late stage of AD (9 months of age) displayed no effect on cognitive improvement.
These findings indicate positive effects of ketogenic diet on both cognitive function and histopathology in Alzheimer's disease, which could be due to reduced microglial activation and neuroinflammation. Our findings provide new insights and therapeutic interventions for the treatment of Alzheimer's disease.
阿尔茨海默病(AD)是最常见的神经退行性疾病,可导致痴呆并影响全球数百万人。尽管它给患者带来了毁灭性的后果,给社会带来了巨大的经济成本,但目前尚无有效的治疗方法。
高脂肪、低碳水化合物生酮饮食(KD)是治疗难治性癫痫的既定方法,具有已证实的疗效。尽管近年来人们对将 KD 应用于 AD 患者产生了浓厚的兴趣,但只有少数动物和人类的干预研究探讨了 KD 对认知障碍的影响,结果尚无定论。本研究旨在探索 KD 对 5XFAD 小鼠(AD 的一种验证动物模型)认知功能和 AD 病理的影响。
4 个月的生酮饮食改善了 5XFAD 小鼠的空间学习、空间记忆和工作记忆。认知功能的改善与海马和皮质中神经元和突触数量的恢复有关。生酮饮食治疗还减少了淀粉样斑块沉积和小胶质细胞激活,从而减少了神经炎症。生酮饮食对认知功能的积极影响取决于饮食的开始时间和持续时间。较短的(2 个月)生酮饮食治疗效果较弱。在 AD 晚期(9 个月龄)开始的生酮饮食对认知改善没有影响。
这些发现表明生酮饮食对阿尔茨海默病的认知功能和组织病理学均有积极影响,这可能是由于小胶质细胞激活和神经炎症减少所致。我们的研究结果为阿尔茨海默病的治疗提供了新的见解和治疗干预措施。