Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13442
Title: Cratoxylum formosum Extract Protects against Amyloid-Beta Toxicity in a Caenorhabditis elegans Model of Alzheimer's Disease
Authors: Keowkase R.
Weerapreeyakul N.
Keywords: amyloid beta protein
ascorbic acid
caffeic acid
chlorogenic acid
Cratoxylum formosum extract
gallic acid
Ginkgo biloba extract
heat shock transcription factor 1
hydrogen peroxide
juglone
neuroprotective agent
plant extract
transcription factor FOXO
transcription factor Nrf2
unclassified drug
amyloid beta protein
antioxidant
Caenorhabditis elegans protein
daf-16 protein, C elegans
DNA binding protein
forkhead transcription factor
heat shock factor-1, C elegans
naphthoquinone
plant extract
protective agent
skn-1 protein, C elegans
transcription factor
Alzheimer disease
animal experiment
animal model
animal tissue
antioxidant activity
Article
Caenorhabditis elegans
cell stress
controlled study
Cratoxylum formosum
high performance liquid chromatography
neuroprotection
neurotoxicity
nonhuman
oxidative stress
paralysis
plant stem
plant twig
protein expression
quantitative analysis
survival
temperature stress
transgenic animal
Alzheimer disease
animal
Caenorhabditis elegans
chemistry
Clusiaceae
disease model
drug effects
genetics
metabolism
paralysis
Alzheimer Disease
Amyloid beta-Peptides
Animals
Animals, Genetically Modified
Antioxidants
Caenorhabditis elegans
Caenorhabditis elegans Proteins
Clusiaceae
Disease Models, Animal
DNA-Binding Proteins
Forkhead Transcription Factors
Naphthoquinones
Oxidative Stress
Paralysis
Plant Extracts
Protective Agents
Transcription Factors
Issue Date: 2016
Abstract: Amyloid-β, one of the hallmarks of Alzheimer's disease, is toxic to neurons and causes cell death in the brain. Oxidative stress is known to play an important role in Alzheimer's disease, and there is strong evidence linking oxidative stress to amyloid-β. The herbal plant Tiew kon (Cratoxylum formosum ssp. pruniflorum) is an indigenous vegetable that is grown in Southeast Asia. Many reports suggested that the twig extract from C. formosum possesses an antioxidant property. The purpose of this study was to investigate the protective effect of the twig extract from C. formosum against amyloid-β toxicity using the transgenic Caenorhabditis elegans model. This study demonstrated that the extract significantly delayed amyloid-β-induced paralysis in the C. elegans model of Alzheimer's disease. Using a genetic approach, we found that DAF-16/FOXO transcription factor, heat shock factor 1, and SKN-1 (Nrf2 in mammals) were required for the extract-mediated delayed paralysis. The extract ameliorated oxidative stress by reducing the level of H2O2, which appeared to account for the protective action of the extract. The extract possesses antioxidant activity against juglone-induced oxidative stress as it was shown to increase survival of the stressed worms. In addition, C. formosum decreased the expression of the heat shock protein-16.2 gene which was induced by thermal stress, indicating its ability to reduce cellular stress. The results from this study support the C. elegans model in the search for disease-modifying agents to treat Alzheimer's disease and indicate the potential of the extract from C. formosum ssp. pruniflorum as a source for the development of anti-Alzheimer's drugs. © Georg Thieme Verlag KG Stuttgart · New York.
URI: https://ir.swu.ac.th/jspui/handle/123456789/13442
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957705999&doi=10.1055%2fs-0041-111621&partnerID=40&md5=f95aef1b53bfd998cad65a62d7349375
ISSN: 320943
Appears in Collections:Scopus 1983-2021

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