Ketogenic diet ameliorates cognitive impairment and neuroinflammation in a mouse model of Alzheimer’s disease

Introduction 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. Aim...

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Published inCNS neuroscience & therapeutics Vol. 28; no. 4; pp. 580 - 592
Main Authors Xu, Yunlong, Jiang, Chenyu, Wu, Junyan, Liu, Peidong, Deng, Xiaofei, Zhang, Yadong, Peng, Bo, Zhu, Yingjie
Format Journal Article
LanguageEnglish
Published England John Wiley & Sons, Inc 01.04.2022
John Wiley and Sons Inc
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Abstract Introduction 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. Aims 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. Results 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. Conclusions 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. Ketogenic diet improved cognitive functions, decreased amyloid plaque deposition and microglial activation, restored synaptic and neuronal density, and reduced neuroinflammation.
AbstractList IntroductionAlzheimer'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.AimsThe 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.ResultsFour 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.ConclusionsThese 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.
Introduction 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. Aims 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. Results 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. Conclusions 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. Ketogenic diet improved cognitive functions, decreased amyloid plaque deposition and microglial activation, restored synaptic and neuronal density, and reduced neuroinflammation.
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.INTRODUCTIONAlzheimer'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.AIMSThe 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.RESULTSFour 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.CONCLUSIONSThese 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.
Ketogenic diet improved cognitive functions, decreased amyloid plaque deposition and microglial activation, restored synaptic and neuronal density, and reduced neuroinflammation.
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.
Author Xu, Yunlong
Zhang, Yadong
Wu, Junyan
Deng, Xiaofei
Peng, Bo
Liu, Peidong
Jiang, Chenyu
Zhu, Yingjie
AuthorAffiliation 5 State Key Laboratory of Medical Neurobiology MOE Frontiers Center for Brain Science Institute for Translational Brain Research Fudan University Shanghai China
8 CAS Key Laboratory of Brain Connectome and Manipulation The Brain Cognition and Brain Disease Institute (BCBDI) Shenzhen Institute of Advanced Technology (SIAT) Chinese Academy of Sciences (CAS) Shenzhen China
4 Medical College of Acupuncture‐Moxibustion and Rehabilitation Guangzhou University of Chinese Medicine Guangzhou China
3 The First Affiliated Hospital Sun Yat‐sen University Guangzhou China
7 CAS Center for Excellence in Brain Science and Intelligence Technology Chinese Academy of Sciences Shanghai China
6 Faculty of Life and Health Sciences Shenzhen Institute of Advanced Technology Chinese Academy of Sciences Shenzhen China
2 University of Chinese Academy of Sciences Beijing China
1 Shenzhen Key Laboratory of Drug Addiction Shenzhen Neher Neural Plasticity Laboratory the Brain Cognition and Brain Disease Institute (BCBDI) S
AuthorAffiliation_xml – name: 2 University of Chinese Academy of Sciences Beijing China
– name: 1 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
– name: 6 Faculty of Life and Health Sciences Shenzhen Institute of Advanced Technology Chinese Academy of Sciences Shenzhen China
– name: 5 State Key Laboratory of Medical Neurobiology MOE Frontiers Center for Brain Science Institute for Translational Brain Research Fudan University Shanghai China
– name: 8 CAS Key Laboratory of Brain Connectome and Manipulation The Brain Cognition and Brain Disease Institute (BCBDI) Shenzhen Institute of Advanced Technology (SIAT) Chinese Academy of Sciences (CAS) Shenzhen China
– name: 7 CAS Center for Excellence in Brain Science and Intelligence Technology Chinese Academy of Sciences Shanghai China
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  givenname: Yunlong
  surname: Xu
  fullname: Xu, Yunlong
  organization: University of Chinese Academy of Sciences
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  givenname: Chenyu
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  fullname: Jiang, Chenyu
  organization: University of Chinese Academy of Sciences
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  givenname: Junyan
  surname: Wu
  fullname: Wu, Junyan
  organization: Guangzhou University of Chinese Medicine
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  givenname: Yingjie
  orcidid: 0000-0002-0783-0897
  surname: Zhu
  fullname: Zhu, Yingjie
  email: yj.zhu1@siat.ac.cn
  organization: Chinese Academy of Sciences (CAS)
BackLink https://www.ncbi.nlm.nih.gov/pubmed/34889516$$D View this record in MEDLINE/PubMed
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Issue 4
Keywords cognitive impairment
ketogenic diet
neuroinflammation
Alzheimer's disease
microglial activation
Language English
License Attribution
2021 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd.
This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
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Notes Yunlong Xu and Chenyu Jiang Contributed equally to this work.
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Snippet Introduction Alzheimer's disease (AD) is the most common neurodegenerative disorder that causes dementia and affects millions of people worldwide. Although it...
Alzheimer's disease (AD) is the most common neurodegenerative disorder that causes dementia and affects millions of people worldwide. Although it has...
IntroductionAlzheimer's disease (AD) is the most common neurodegenerative disorder that causes dementia and affects millions of people worldwide. Although it...
Ketogenic diet improved cognitive functions, decreased amyloid plaque deposition and microglial activation, restored synaptic and neuronal density, and reduced...
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StartPage 580
SubjectTerms Alzheimer Disease - pathology
Alzheimer's disease
Amyloid
Animal cognition
Animal models
Animals
Brain
Carbohydrates
Cognitive ability
Cognitive Dysfunction - etiology
cognitive impairment
Dementia
Dementia disorders
Diet
Diet, Ketogenic
Disease Models, Animal
Epilepsy
Ethanol
High carbohydrate diet
High fat diet
Humans
Inflammation
Ketogenesis
ketogenic diet
Laboratories
Low carbohydrate diet
Low fat diet
Memory
Mice
Mice, Transgenic
microglial activation
Neurodegenerative diseases
neuroinflammation
Neuroinflammatory Diseases
Nutrient deficiency
Original
Patients
Plaque, Amyloid
Proteins
Short term memory
Spatial discrimination learning
Spatial memory
Synapses
Therapeutic applications
Transgenic animals
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Title Ketogenic diet ameliorates cognitive impairment and neuroinflammation in a mouse model of Alzheimer’s disease
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fcns.13779
https://www.ncbi.nlm.nih.gov/pubmed/34889516
https://www.proquest.com/docview/2640028166
https://www.proquest.com/docview/2608539691
https://pubmed.ncbi.nlm.nih.gov/PMC8928920
Volume 28
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