Capsaicin consumption reduces brain amyloid-beta generation and attenuates Alzheimer's disease-type pathology and cognitive deficits in APP/PS1 mice

Alzheimer's disease (AD) is the most common cause of age-related dementia and is currently incurable. The failures of current clinical trials and the establishment of modifiable risk factors have shifted the AD intervention from treatment to prevention in the at-risk population. Previous studie...

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Published inTranslational psychiatry Vol. 10; no. 1; p. 230
Main Authors Wang, Jun, Sun, Bin-Lu, Xiang, Yang, Tian, Ding-Yuan, Zhu, Chi, Li, Wei-Wei, Liu, Yu-Hui, Bu, Xian-Le, Shen, Lin-Lin, Jin, Wang-Sheng, Wang, Zhen, Zeng, Gui-Hua, Xu, Wei, Chen, Li-Yong, Chen, Xiao-Wei, Hu, Zhian, Zhu, Zhi-Ming, Song, Weihong, Zhou, Hua-Dong, Yu, Jin-Tai, Wang, Yan-Jiang
Format Journal Article
LanguageEnglish
Published United States Nature Publishing Group 13.07.2020
Nature Publishing Group UK
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Abstract Alzheimer's disease (AD) is the most common cause of age-related dementia and is currently incurable. The failures of current clinical trials and the establishment of modifiable risk factors have shifted the AD intervention from treatment to prevention in the at-risk population. Previous studies suggest that there is a geographic overlap between AD incidence and spicy food consumption. We previously reported that capsaicin-rich diet consumption was associated with better cognition and lower serum Amyloid-beta (Aβ) levels in people aged 40 years and over. In the present study, we found that intake of capsaicin, the pungent ingredient in chili peppers, reduced brain Aβ burden and rescued cognitive decline in APP/PS1 mice. Our in vivo and in vitro studies revealed that capsaicin shifted Amyloid precursor protein (APP) processing towards α-cleavage and precluded Aβ generation by promoting the maturation of a disintegrin and metalloproteinase 10 (ADAM10). We also found that capsaicin alleviated other AD-type pathologies, such as tau hyperphosphorylation, neuroinflammation and neurodegeneration. The present study suggests that capsaicin is a potential therapeutic candidate for AD and warrants clinical trials on chili peppers or capsaicin as dietary supplementation for the prevention and treatment of AD.
AbstractList Alzheimer’s disease (AD) is the most common cause of age-related dementia and is currently incurable. The failures of current clinical trials and the establishment of modifiable risk factors have shifted the AD intervention from treatment to prevention in the at-risk population. Previous studies suggest that there is a geographic overlap between AD incidence and spicy food consumption. We previously reported that capsaicin-rich diet consumption was associated with better cognition and lower serum Amyloid-beta (Aβ) levels in people aged 40 years and over. In the present study, we found that intake of capsaicin, the pungent ingredient in chili peppers, reduced brain Aβ burden and rescued cognitive decline in APP/PS1 mice. Our in vivo and in vitro studies revealed that capsaicin shifted Amyloid precursor protein (APP) processing towards α-cleavage and precluded Aβ generation by promoting the maturation of a disintegrin and metalloproteinase 10 (ADAM10). We also found that capsaicin alleviated other AD-type pathologies, such as tau hyperphosphorylation, neuroinflammation and neurodegeneration. The present study suggests that capsaicin is a potential therapeutic candidate for AD and warrants clinical trials on chili peppers or capsaicin as dietary supplementation for the prevention and treatment of AD.
Abstract Alzheimer’s disease (AD) is the most common cause of age-related dementia and is currently incurable. The failures of current clinical trials and the establishment of modifiable risk factors have shifted the AD intervention from treatment to prevention in the at-risk population. Previous studies suggest that there is a geographic overlap between AD incidence and spicy food consumption. We previously reported that capsaicin-rich diet consumption was associated with better cognition and lower serum Amyloid-beta (Aβ) levels in people aged 40 years and over. In the present study, we found that intake of capsaicin, the pungent ingredient in chili peppers, reduced brain Aβ burden and rescued cognitive decline in APP/PS1 mice. Our in vivo and in vitro studies revealed that capsaicin shifted Amyloid precursor protein (APP) processing towards α-cleavage and precluded Aβ generation by promoting the maturation of a disintegrin and metalloproteinase 10 (ADAM10). We also found that capsaicin alleviated other AD-type pathologies, such as tau hyperphosphorylation, neuroinflammation and neurodegeneration. The present study suggests that capsaicin is a potential therapeutic candidate for AD and warrants clinical trials on chili peppers or capsaicin as dietary supplementation for the prevention and treatment of AD.
ArticleNumber 230
Author Shen, Lin-Lin
Jin, Wang-Sheng
Wang, Zhen
Wang, Yan-Jiang
Tian, Ding-Yuan
Zhu, Zhi-Ming
Bu, Xian-Le
Wang, Jun
Xu, Wei
Xiang, Yang
Chen, Li-Yong
Chen, Xiao-Wei
Zeng, Gui-Hua
Yu, Jin-Tai
Li, Wei-Wei
Sun, Bin-Lu
Liu, Yu-Hui
Hu, Zhian
Zhu, Chi
Song, Weihong
Zhou, Hua-Dong
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  organization: Department of Neurology and Center for Clinical Neuroscience, Daping Hospital, Third Military Medical University, 400042, Chongqing, China. qywangjun@163.com
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  organization: Department of Neurology and Center for Clinical Neuroscience, Daping Hospital, Third Military Medical University, 400042, Chongqing, China
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  organization: Department of Neurology, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, 610072, Chengdu, China
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  organization: Department of Neurology and Center for Clinical Neuroscience, Daping Hospital, Third Military Medical University, 400042, Chongqing, China
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  givenname: Yu-Hui
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  orcidid: 0000-0002-2331-3339
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  organization: Department of anaesthesiology, Daping Hospital, Third Military Medical University, 400042, Chongqing, China
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  fullname: Zeng, Gui-Hua
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  surname: Xu
  fullname: Xu, Wei
  organization: Department of Neurology, Qingdao Municipal Hospital, Qingdao University, 266071, Qingdao, China
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  organization: Department of Physiology and Institute of Brain and Intelligence, Third Military Medical University, 400038, Chongqing, China
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  givenname: Zhi-Ming
  surname: Zhu
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  organization: Center for Hypertension and Metabolic Diseases, Department of Hypertension and Endocrinology, Daping Hospital, Third Military Medical University, 400042, Chongqing, China
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  organization: Townsend Family Laboratories, Department of Psychiatry, Brain Research Center, The University of British Columbia, Vancouver, BC, V6T 1Z3, Canada
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  givenname: Yan-Jiang
  orcidid: 0000-0002-6227-6112
  surname: Wang
  fullname: Wang, Yan-Jiang
  email: yanjiang_wang@tmmu.edu.cn, yanjiang_wang@tmmu.edu.cn, yanjiang_wang@tmmu.edu.cn
  organization: Center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, 200031, Shanghai, China. yanjiang_wang@tmmu.edu.cn
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Snippet Alzheimer's disease (AD) is the most common cause of age-related dementia and is currently incurable. The failures of current clinical trials and the...
Abstract Alzheimer’s disease (AD) is the most common cause of age-related dementia and is currently incurable. The failures of current clinical trials and the...
Alzheimer’s disease (AD) is the most common cause of age-related dementia and is currently incurable. The failures of current clinical trials and the...
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crossref
pubmed
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Aggregation Database
Index Database
StartPage 230
SubjectTerms Alzheimer Disease - drug therapy
Alzheimer Disease - prevention & control
Alzheimer's disease
Amyloid beta-Peptides - metabolism
Amyloid beta-Protein Precursor - metabolism
Animals
Brain - metabolism
Capsaicin - pharmacology
Clinical trials
Cognition
Cognitive Dysfunction - drug therapy
Cognitive Dysfunction - prevention & control
Disease Models, Animal
Mice
Mice, Transgenic
Presenilin-1 - metabolism
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Title Capsaicin consumption reduces brain amyloid-beta generation and attenuates Alzheimer's disease-type pathology and cognitive deficits in APP/PS1 mice
URI https://www.ncbi.nlm.nih.gov/pubmed/32661266
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Volume 10
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