학술논문

Fasting-mimicking diet cycles reduce neuroinflammation to attenuate cognitive decline in Alzheimer’s models
Document Type
article
Source
Cell Reports. 40(13)
Subject
Biochemistry and Cell Biology
Biological Sciences
Neurosciences
Brain Disorders
Alzheimer's Disease
Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD)
Nutrition
Acquired Cognitive Impairment
Neurodegenerative
Aging
Stem Cell Research
Dementia
Stem Cell Research - Nonembryonic - Non-Human
Neurological
Alzheimer Disease
Amyloid beta-Peptides
Animals
Cognitive Dysfunction
Disease Models
Animal
Fasting
Mice
Mice
Transgenic
NADPH Oxidases
Neuroinflammatory Diseases
Superoxides
tau Proteins
Alzheimer’s disease
CP: Metabolism
CP: Neuroscience
NADPH oxidase
amyloid beta
fasting
fasting-mimicking diet
hyperphosphorylated tau
microglia
neuroinflammation
protein restriction
superoxide
Medical Physiology
Biological sciences
Language
Abstract
The effects of fasting-mimicking diet (FMD) cycles in reducing many aging and disease risk factors indicate it could affect Alzheimer's disease (AD). Here, we show that FMD cycles reduce cognitive decline and AD pathology in E4FAD and 3xTg AD mouse models, with effects superior to those caused by protein restriction cycles. In 3xTg mice, long-term FMD cycles reduce hippocampal Aβ load and hyperphosphorylated tau, enhance genesis of neural stem cells, decrease microglia number, and reduce expression of neuroinflammatory genes, including superoxide-generating NADPH oxidase (Nox2). 3xTg mice lacking Nox2 or mice treated with the NADPH oxidase inhibitor apocynin also display improved cognition and reduced microglia activation compared with controls. Clinical data indicate that FMD cycles are feasible and generally safe in a small group of AD patients. These results indicate that FMD cycles delay cognitive decline in AD models in part by reducing neuroinflammation and/or superoxide production in the brain.