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Cratoxylum formosum Extract Protects against Amyloid-Beta Toxicity in a Caenorhabditis elegans Model of Alzheimer's Disease

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dc.contributor.author Keowkase R.
dc.contributor.author Weerapreeyakul N.
dc.date.accessioned 2021-04-05T03:23:58Z
dc.date.available 2021-04-05T03:23:58Z
dc.date.issued 2016
dc.identifier.issn 320943
dc.identifier.other 2-s2.0-84957705999
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/13442
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957705999&doi=10.1055%2fs-0041-111621&partnerID=40&md5=f95aef1b53bfd998cad65a62d7349375
dc.description.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.
dc.subject amyloid beta protein
dc.subject ascorbic acid
dc.subject caffeic acid
dc.subject chlorogenic acid
dc.subject Cratoxylum formosum extract
dc.subject gallic acid
dc.subject Ginkgo biloba extract
dc.subject heat shock transcription factor 1
dc.subject hydrogen peroxide
dc.subject juglone
dc.subject neuroprotective agent
dc.subject plant extract
dc.subject transcription factor FOXO
dc.subject transcription factor Nrf2
dc.subject unclassified drug
dc.subject amyloid beta protein
dc.subject antioxidant
dc.subject Caenorhabditis elegans protein
dc.subject daf-16 protein, C elegans
dc.subject DNA binding protein
dc.subject forkhead transcription factor
dc.subject heat shock factor-1, C elegans
dc.subject naphthoquinone
dc.subject plant extract
dc.subject protective agent
dc.subject skn-1 protein, C elegans
dc.subject transcription factor
dc.subject Alzheimer disease
dc.subject animal experiment
dc.subject animal model
dc.subject animal tissue
dc.subject antioxidant activity
dc.subject Article
dc.subject Caenorhabditis elegans
dc.subject cell stress
dc.subject controlled study
dc.subject Cratoxylum formosum
dc.subject high performance liquid chromatography
dc.subject neuroprotection
dc.subject neurotoxicity
dc.subject nonhuman
dc.subject oxidative stress
dc.subject paralysis
dc.subject plant stem
dc.subject plant twig
dc.subject protein expression
dc.subject quantitative analysis
dc.subject survival
dc.subject temperature stress
dc.subject transgenic animal
dc.subject Alzheimer disease
dc.subject animal
dc.subject Caenorhabditis elegans
dc.subject chemistry
dc.subject Clusiaceae
dc.subject disease model
dc.subject drug effects
dc.subject genetics
dc.subject metabolism
dc.subject paralysis
dc.subject Alzheimer Disease
dc.subject Amyloid beta-Peptides
dc.subject Animals
dc.subject Animals, Genetically Modified
dc.subject Antioxidants
dc.subject Caenorhabditis elegans
dc.subject Caenorhabditis elegans Proteins
dc.subject Clusiaceae
dc.subject Disease Models, Animal
dc.subject DNA-Binding Proteins
dc.subject Forkhead Transcription Factors
dc.subject Naphthoquinones
dc.subject Oxidative Stress
dc.subject Paralysis
dc.subject Plant Extracts
dc.subject Protective Agents
dc.subject Transcription Factors
dc.title Cratoxylum formosum Extract Protects against Amyloid-Beta Toxicity in a Caenorhabditis elegans Model of Alzheimer's Disease
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Planta Medica. Vol 82, No.6 (2016), p.516-523
dc.identifier.doi 10.1055/s-0041-111621


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